J. Cowell

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WAVE3 promotes cell motility and invasion through the regulation of MMP-1, MMP-3, and MMP-9 expression.

Andrei V Bakin, K. Sossey-Alaoui, T. Ranalli, 2005, Experimental cell research.

Identification of YAC clones for human chromosome 1p32 and physical mapping of the infantile neuronal ceroid lipofuscinosis (INCL) locus.

L. Peltonen, A. Palotie, S. Mead, 1995, Genomics.

Identification of genes involved in squamous cell carcinoma of the lung using synchronized data from DNA copy number and transcript expression profiling analysis.

L. Hawthorn, J. Cowell, K. Lo, 2008, Lung cancer.

Application of spectral karyotyping to the analysis of the human chromosome complement of interspecies somatic cell hybrids.

Michael R Rossi, S. Matsui, J. Cowell, 2003, Cancer genetics and cytogenetics.

Molecular characterization of the t(3;9) associated with immortalization in the MCF10A cell line.

N. Nowak, S. Matsui, J. Cowell, 2005, Cancer genetics and cytogenetics.

Predisposition to retinoblastoma due to a translocation within the 4.7R locus.

J. Cowell, C. Mitchell, 1989, Oncogene.

Isolation of chromosome-specific DNA sequences from an Alu polymerase chain reaction library to define the breakpoint in a patient with a constitutional translocation t(1;13) (q22;q12) and ganglioneuroblastoma.

J. Cowell, F. Cotter, A. Michalski, 1992, Oncogene.

Integration of the physical and genetic linkage map for human chromosome 13.

L. Hawthorn, J. Cowell, 1995, Genomics.

Characterisation of a human chromosome 1 somatic cell hybrid mapping panel and regional assignment of 6 novel STS

T. Roberts, R. S. Mead, J. Cowell, 1996, Annals of human genetics.

Regional assignment of EST sequences on human chromosome 13.

L. Hawthorn, J. Cowell, 1996, Cytogenetics and cell genetics.

Molecular characterization of the t(8;13)(p11;q12) translocation associated with an atypical myeloproliferative disorder: evidence for three discrete loci involved in myeloid leukemias on 8p11.

R. Stone, J. Cowell, D. Hurd, 1997, Blood.

Molecular characterization of the 1p22 breakpoint region spanning the constitutional translocation breakpoint in a neuroblastoma patient with a t(1;10)(p22;q21).

T. Roberts, J. Cowell, O. Chernova, 1998, Cancer genetics and cytogenetics.

Isolation and regional localisation of DNA sequences from a human chromosome 11-specific cosmid library

P. Little, J. Cowell, R. Wadey, 1990, Human Genetics.

Essential roles of leucine-rich glioma inactivated 1 in the development of embryonic and postnatal cerebellum

N. Zhang, Lin Zhou, J. Cowell, 2015, Scientific Reports.

Ploidy status and copy number aberrations in primary glioblastomas defined by integrated analysis of allelic ratios, signal ratios and loss of heterozygosity using 500K SNP Mapping Arrays

Y. Turpaz, P. Gardina, J. Cowell, 2008, BMC Genomics.

Promotion of invasion by mutant RAS is dependent on activation of the WASF3 metastasis promoter gene

J. Cowell, Yong Teng, L. Ngoka, 2017, Genes, chromosomes & cancer.

Targeting the WASF3-CYFIP1 Complex Using Stapled Peptides Suppresses Cancer Cell Invasion.

Laura E. Hanold, E. Kennedy, Da-yong Dong, 2015, Cancer research.

WASF3 provides the conduit to facilitate invasion and metastasis in breast cancer cells through HER2/HER3 signaling

Y. Wang, J. Cowell, Yong Teng, 2015, Oncogene.

Homozygous Deletion of the LGI1 Gene in Mice Leads to Developmental Abnormalities Resulting in Cortical Dysplasia

J. Cowell, Suash J Sharma, Jeane Silva, 2015, Brain pathology.

Cloning and characterization of the TATA-less promoter from the human GFI1 proto-oncogene.

J. Cowell, S. Liu, 2000, Annals of human genetics.

Acute Progression of BCR-FGFR1 Induced Murine B-Lympho/Myeloproliferative Disorder Suggests Involvement of Lineages at the Pro-B Cell Stage

J. Cowell, Suash J Sharma, M. Ren, 2012, PloS one.

WAVE3-mediated Cell Migration and Lamellipodia Formation Are Regulated Downstream of Phosphatidylinositol 3-Kinase*

K. Sossey-Alaoui, T. Ranalli, Xiurong Li, 2005, Journal of Biological Chemistry.

Identification of the promoter, genomic structure, and mouse ortholog of LGI1

Y. Shoshan, J. Cowell, Siqing Liu, 2000, Mammalian Genome.

Partial inactivation of the RB product in a family with incomplete penetrance of familial retinoblastoma and benign retinal tumors.

F. Kaye, R. Kratzke, G. Otterson, 1994, Oncogene.

Ponatinib suppresses the development of myeloid and lymphoid malignancies associated with FGFR1 abnormalities

J. Cowell, H. Qin, M. Ren, 2012, Leukemia.

Molecular analysis of chromosome region 11p13 in patients with Drash syndrome

T. Barratt, J. Cowell, C. Mitchell, 1991, Human Genetics.

ZNF198, a zinc finger protein rearranged in myeloproliferative disease, localizes to the PML nuclear bodies and interacts with SUMO-1 and PML.

S. Chin, C. Caldas, J. Cowell, 2006, Experimental cell research.

Arsenic Trioxide Affects Signal Transducer and Activator of Transcription Proteins through Alteration of Protein Tyrosine Kinase Phosphorylation

P. Wallace, J. Cowell, H. Baumann, 2006, Clinical Cancer Research.

Antisense oligonucleotides suppress B-cell lymphoma growth in a SCID-hu mouse model.

P. Johnson, J. Cowell, F. Cotter, 1994, Oncogene.

Antisense telomerase treatment: induction of two distinct pathways, apoptosis and differentiation

G. Barnett, Y. Kondo, S. Kondo, 1998, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Telomerase activity in pancreatic endocrine tumors

Shou-Jiang Tang, M. Goormastic, J. Cowell, 2002, American Journal of Gastroenterology.

Telomerase activity in pancreatic endocrine tumors.

Shou-Jiang Tang, M. Goormastic, J. Cowell, 2002 .

HIF1A induces expression of the WASF3 metastasis‐associated gene under hypoxic conditions

J. Cowell, Pushpankur Ghoshal, Y. Teng, 2012, International journal of cancer.

LGI1: from zebrafish to human epilepsy.

J. Cowell, 2014, Progress in brain research.

Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11.

J. Cowell, R. Wadey, J. Pritchard, 1990, Oncogene.

aCGHViewer: A Generic Visualization Tool For aCGH data

N. Nowak, J. Conroy, J. Cowell, 2006, Cancer informatics.

Overlay analysis of the oligonucleotide array gene expression profiles and copy number abnormalities as determined by array comparative genomic hybridization in medulloblastomas

S. Pomeroy, J. Cowell, M. Rossi, 2007, Genes, chromosomes & cancer.

LGI1, a Putative Tumor Metastasis Suppressor Gene, Controls in Vitro Invasiveness and Expression of Matrix Metalloproteinases in Glioma Cells through the ERK1/2 Pathway*

L. Hawthorn, J. Cowell, P. Kunapuli, 2004, Journal of Biological Chemistry.

Genome Wide Copy Number Abnormalities in Pediatric Medulloblastomas as Assessed by Array Comparative Genome Hybridization

C. Eberhart, J. Cowell, M. Rossi, 2007, Brain pathology.

HSPA1A is an important regulator of the stability and function of ZNF198 and its oncogenic derivative, ZNF198–FGFR1

J. Cowell, P. Kunapuli, C. Kasyapa, 2007, Journal of cellular biochemistry.

Isolation and characterisation of a panel of cosmids which allows unequivocal identification of chromosome deletions involving the RB1 gene using fluorescence in situ hybridisation.

J. Cowell, H. Kempski, R. Jaju, 1994, Journal of medical genetics.

Structural rearrangements of the WT1 gene in Wilms' tumour cells.

D. Housman, D. Haber, K. Call, 1991, Oncogene.

Insulin-like growth factor-II gene expression in Wilms' tumour and embryonic tissues

J. Scott, G. Bell, J. Cowell, 1985, Nature.

Dysregulated signaling pathways in the development of CNTRL-FGFR1-induced myeloid and lymphoid malignancies associated with FGFR1 in human and mouse models.

E. Kitamura, J. Cowell, H. Qin, 2013, Blood.

Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome.

J. Cowell, P. Baird, L. Jadresić, 1992, Human molecular genetics.

Analysis of the RB1 gene in children with retinoblastoma having residential connections to West Cumbria, England

J. Cowell, E. Tawn, J. Morris, 2005, Journal of radiological protection : official journal of the Society for Radiological Protection.

Phosphorylation of the SSBP2 and ABL proteins by the ZNF198‐FGFR1 fusion kinase seen in atypical myeloproliferative disorders as revealed by phosphopeptide‐specific MS

T. Gu, J. Cowell, R. Polakiewicz, 2009, Proteomics.

Investigation of LGI1 as the antigen in limbic encephalitis previously attributed to potassium channels: a case series

R. Balice-Gordon, J. Dalmau, J. Cowell, 2010, The Lancet Neurology.

Epilepsy research gets new guidance

J. Cowell, 2002, Nature Medicine.

Homozygous inactivation of the LGI1 gene results in hypomyelination in the peripheral and central nervous systems

J. Cowell, Y. E. Yu, Suash J Sharma, 2010, Journal of neuroscience research.

Lgi1 null mutant mice exhibit myoclonic seizures and CA1 neuronal hyperexcitability.

L. Mei, A. Pao, K. Sossey-Alaoui, 2010, Human molecular genetics.

Mass Spectrometry Identifies LGI1-Interacting Proteins that Are Involved in Synaptic Vesicle Function in the Human Brain

J. Cowell, L. Kazim, G. Jang, 2009, Journal of Molecular Neuroscience.

Effect of the esterase-D phenotype on its in vitro enzyme activity

M. Jay, J. Cowell, J. Hungerford, 1986, Human Genetics.

An assessment of the usefulness of electrophoretic variants of esterase-D in the antenatal diagnosis of retinoblastoma in the United Kingdom.

M. Jay, J. Cowell, J. Hungerford, 1987, British Journal of Cancer.

Anassessment oftheusefulness ofelectrophoretic variants ofesterase-D intheantenatal diagnosis ofretinoblastoma intheUnited Kingdom

M. Jay, J. Cowell, P. Rutland, 1987 .

Characterization of the breakpoints in a t(8;13)(p11;q12) translocation from a patient with myeloproliferative disease using fluorescence in situ hybridization

J. Cowell, M. Kalaycio, O. Chernova, 1998, Genes, chromosomes & cancer.

A truncated derivative of FGFR1 kinase cooperates with FLT3 and KIT to transform hematopoietic stem cells in syndromic and de novo AML

J. Cowell, Yun Liu, Xuexiu Fang, 2022, Molecular cancer.

Molecular evidence that the esterase-D gene lies proximal to the retinoblastoma susceptibility locus in chromosome region 13q14

J. Cowell, C. Mitchell, 1988, Human Genetics.

Genomic organization and expression profile of the human and mouse WAVE gene family

N. Nowak, K. Sossey-Alaoui, J. Cowell, 2003, Mammalian Genome.

Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumour

P. Scambler, J. Cowell, R. Grundy, 1998, Oncogene.

Molecular analysis of two putative tumour suppressor genes, PTEN and DMBT, which have been implicated in glioblastoma multiforme disease progression

Y. Shoshan, G. Barnett, C. Eng, 1998, Oncogene.

Loss of Zebrafish lgi1b Leads to Hydrocephalus and Sensitization to Pentylenetetrazol Induced Seizure-Like Behavior

Xiayang Xie, J. Cowell, J. Mumm, 2011, PloS one.

Detection of heterozygous mutations in the RB1 gene in retinoblastoma patients using single-strand conformation polymorphism analysis and polymerase chain reaction sequencing.

A. Hogg, J. Cowell, Z. Onadim, 1992, Oncogene.

Identification and molecular characterization of de novo translocation t(8;14)(q22.3;q13) associated with a vascular and tissue overgrowth syndrome

P. Szafranski, A. Baldini, D. Driscoll, 2001, Cytogenetic and Genome Research.

Aberrant expression of the tumour suppressor gene p53 is very frequent in Wilms' tumours

N. Lemoine, J. Cowell, C. Hughes, 1992, The Journal of pathology.

Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype.

A. Hogg, J. Cowell, Z. Onadim, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Characterization of FAM10A4, a member of the ST13 tumor suppressor gene family that maps to the 13q14.3 region associated with B-Cell leukemia, multiple myeloma, and prostate cancer.

E. Kitamura, K. Sossey-Alaoui, J. Cowell, 2002, Genomics.

Inhibition of telomerase increases the susceptibility of human malignant glioblastoma cells to cisplatin-induced apoptosis

Yoshikazu Tanaka, Y. Kondo, S. Kondo, 1998, Oncogene.

RHOA-regulated IGFBP2 promotes invasion and drives progression of BCR-ABL1 chronic myeloid leukemia

E. Kitamura, J. Cowell, Yun Liu, 2022, Haematologica.

Distinct signaling programs associated with progression of FGFR1 driven leukemia in a mouse model of stem cell leukemia lymphoma syndrome.

L. Hawthorn, E. Kitamura, J. Cowell, 2019, Genomics.

Transformation of human CD34+ hematopoietic progenitor cells with DEK-NUP214 induces AML in an immunocompromized mouse model

S. Malek, J. Cowell, H. Qin, 2016, Oncogene.

Radiation‐Induced Meningioma: A Distinct Molecular Genetic Pattern?

Y. Shoshan, G. Barnett, J. Cowell, 2000, Journal of neuropathology and experimental neurology.

Transgelin increases metastatic potential of colorectal cancer cells in vivo and alters expression of genes involved in cell motility

J. Lee, J. Cowell, Yuan-yuan Fang, 2016, BMC Cancer.

Occurrence and evolution of homogeneously staining regions may be due to breakage-fusion-bridge cycles following telomere loss

J. Cowell, O. Miller, O. J. Miller, 2004, Chromosoma.

Inactivation of LGI1 expression accompanies early stage hyperplasia of prostate epithelium in the TRAMP murine model of prostate cancer.

E. Karasik, B. Foster, J. Cowell, 2010, Experimental and molecular pathology.

Isolation and regional localization of 25 anonymous DNA probes on a chromosome 13 hybrid panel.

C. James, W. Cavenee, J. Buchanan, 1991, Cytogenetics and cell genetics.

A somatic cell hybrid mapping panel for regional assignment of human chromosome 13 DNA sequences.

J. Cowell, C. Mitchell, 1989, Cytogenetics and cell genetics.

Rapid detection of allelic losses in brain tumours using microsatellite repeat markers and high-performance liquid chromatography

G. Barnett, J. Cowell, O. Chernova, 2003, British Journal of Cancer.

Molecular mechanisms of oncogenic mutations in tumors from patients with bilateral and unilateral retinoblastoma.

A. Hogg, J. Cowell, Z. Onadim, 1993, Proceedings of the National Academy of Sciences of the United States of America.

THE EXPRESSION PATTERN OF WILMS' TUMOUR GENE (WT1) PRODUCT IN NORMAL TISSUES AND PAEDIATRIC RENAL TUMOURS

P. Ramani, J. Cowell, 1996, The Journal of pathology.

Molecular alterations in the neurofibromatosis type 2 gene and its protein rarely occurring in meningothelial meningiomas.

Y. Shoshan, M. Golubić, J. Cowell, 2001, Journal of neurosurgery.

A rapid method for accurate DNA measurements in single cells in situ using a simple microfluorimeter and Hoechst 33258 as a quantitative fluorochrome.

J. Cowell, L. M. Franks, 1980, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Cloning of the human Gfi-1 gene and its mapping to chromosome region 1p22

T. Roberts, J. Cowell, 1997, Oncogene.

A photographic representation of the variability in the G-banded structure of the chromosomes in the mouse karyotype

J. Cowell, 2004, Chromosoma.

Suppression of the cell proliferation and invasion phenotypes in glioma cells by the LGI1 gene

J. Cowell, K. Chitta, P. Kunapuli, 2003, Oncogene.

The Oncogenic Fusion Protein-tyrosine Kinase ZNF198/Fibroblast Growth Factor Receptor-1 Has Signaling Function Comparable with Interleukin-6 Cytokine Receptors*

J. Cowell, H. Baumann, E. Tracy, 2003, The Journal of Biological Chemistry.

The t(8;13) atypical myeloproliferative disorder: further analysis of the ZNF198 gene and lack of evidence for multiple genes disrupted on chromosome 13.

J. Cowell, I. Still, 1998, Blood.

Cloning and characterization of the TATA‐less promoter from the human GFI1 Proto‐oncogene

J. Cowell, S. Liu, 2000 .

Selective inactivation of LGI1 in neuronal precursor cells leads to cortical dysplasia in mice

J. Cowell, H. Qin, Jeane Silva, 2019, Genesis.

Telomeres and telomerase in ageing and cancer

J. Cowell, 1999, AGE.

Colon carcinoma cells harboring PIK3CA mutations display resistance to growth factor deprivation induced apoptosis

J. Willson, J. Hauser, K. Kuropatwinski, 2007, Molecular Cancer Therapeutics.

Changes in DNA content during in vitro transformation of mouse salivary gland epithelium.

J. Cowell, C. Wigley, 1980, Journal of the National Cancer Institute.

Critical individual roles of the BCR and FGFR1 kinase domains in BCR‐FGFR1‐driven stem cell leukemia/lymphoma syndrome

J. Cowell, H. Qin, Yun Liu, 2020, International journal of cancer.

Genetic counseling in retinoblastoma.

J. Cowell, 1991, The British journal of ophthalmology.

The ability of normal mouse cells to reduce the malignant potential of transformed mouse bladder epithelial cells depends on their somatic origin

J. Cowell, L. M. Franks, 1984, International Journal of Cancer.

lymphoma Development of a murine model for blastoid variant mantle-cell

L. Hawthorn, A. Multani, J. Cowell, 2013 .

Development of a murine model for blastoid variant mantle-cell lymphoma.

L. Hawthorn, A. Multani, J. Cowell, 2007, Blood.

Ubiquitin-conjugating enzyme UBE2C: molecular biology, role in tumorigenesis, and potential as a biomarker

Hui Zhang, John Cowell, J. Cowell, 2012, Tumor Biology.

Mutations in the PAX6 gene in patients with hereditary aniridia.

J. Cowell, A. Davis, Alison F. Davis, 1993, Human molecular genetics.

Correction: The pleiotropic effects of TNFα in breast cancer subtypes is regulated by TNFAIP3/A20

M. Wicha, J. Gestwicki, J. Cowell, 2019, Oncogene.

The pleiotropic effects of TNFα in breast cancer subtypes is regulated by TNFAIP3/A20

M. Wicha, J. Gestwicki, J. Cowell, 2018, Oncogene.

Chromosome changes associated with the progression of cell lines from preneoplastic to tumorigenic phenotype during transformation of mouse salivary gland epithelium in vitro.

J. Cowell, C. Wigley, 1982, Journal of the National Cancer Institute.

Loss of heterozygosity at 11p13 in Wilms' tumours does not necessarily involve mutations in the WT1 gene.

J. Cowell, P. Baird, N. Groves, 1993, British Journal of Cancer.

Targeted therapy of human malignant glioma in a mouse model by 2-5A antisense directed against telomerase RNA

R. Silverman, Y. Kondo, S. Kondo, 1998, Oncogene.

Tumour suppressor genes.

J. Cowell, J K Cowell, 1992, Annals of oncology : official journal of the European Society for Medical Oncology.

Molecular Study of Malignant Gliomas Treated with Epidermal Growth Factor Receptor Inhibitors: Tissue Analysis from North American Brain Tumor Consortium Trials 01-03 and 00-01

Susan M. Chang, R. Wilson, M. Prados, 2005, Clinical Cancer Research.

Molecular Study of Malignant Gliomas Treated with Epidermal Growth Factor Receptor Inhibitors : Tissue Analysis fromNorth

Susan M. Chang, R. Wilson, M. Prados, 2005 .

Distinct molecular signatures in pediatric infratentorial glioblastomas defined by aCGH.

J. Cowell, S. Peiper, Y. Mei, 2010, Experimental and molecular pathology.

Frequent Constitutional C to T Mutations in CGA-Arginine Codons in the RB1 Gene Produce Premature Stop Codons in Patients with Bilateral (Hereditary) Retinoblastoma

J. Cowell, B. Bia, T. Smith, 1994, European journal of human genetics : EJHG.

Downregulation of PUMA underlies resistance to FGFR1 inhibitors in the stem cell leukemia/lymphoma syndrome

J. Cowell, Yun Liu, M. Ren, 2020, Cell Death & Disease.

Constitutive Notch pathway activation in murine ZMYM2-FGFR1-induced T-cell lymphomas associated with atypical myeloproliferative disease.

J. Cowell, M. Ren, 2011, Blood.

Genomic analysis of CD8+ NK/T cell line, 'SRIK-NKL', with array-based CGH (aCGH), SKY/FISH and molecular mapping.

S. Matsui, J. Cowell, M. Rossi, 2008, Leukemia research.

Direct isolation of human transcribed sequences from yeast artificial chromosomes through the application of RNA fingerprinting.

J. Cowell, I. Still, P. Vince, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Evaluating human cancer cell metastasis in zebrafish

Xiayang Xie, J. Cowell, Yong Teng, 2013, BMC Cancer.

EagI andNotI linking clones from human chromosomes 11 and Xp

K. Davies, D. Porteous, B. Harding, 1996, Human Genetics.

Genomic profiling of myeloid sarcoma by array comparative genomic hybridization

R. Cheney, N. Nowak, J. Conroy, 2005, Genes, chromosomes & cancer.

Application of bacterial artificial chromosome array-based comparative genomic hybridization and spectral karyotyping to the analysis of glioblastoma multiforme.

N. Nowak, J. Conroy, S. Matsui, 2004, Cancer genetics and cytogenetics.

Identification and characterisation of constitutional chromosome abnormalities using arrays of bacterial artificial chromosomes

N. Nowak, J. Conroy, J. Cowell, 2004, British Journal of Cancer.

Characterization of the 1p/19q Chromosomal Loss in Oligodendrogliomas Using Comparative Genomic Hybridization Arrays (CGHa)

G. Barnett, N. Nowak, J. Cowell, 2004, Journal of neuropathology and experimental neurology.

High-resolution analysis of genetic events in cancer cells using bacterial artificial chromosome arrays and comparative genome hybridization.

N. Nowak, J. Cowell, 2003, Advances in cancer research.

Candidate glioblastoma development gene identification using concordance between copy number abnormalities and gene expression level changes

Michael R Rossi, Y. Turpaz, L. Hawthorn, 2007, Genes, chromosomes & cancer.

Double minutes and homogeneously staining regions: gene amplification in mammalian cells.

J. Cowell, J K Cowell, 1982, Annual review of genetics.

Pediatric primary intramedullary spinal cord glioblastoma

J. Cowell, Suash J Sharma, R. Lober, 2010, Rare tumors.

Identification of a novel gene (ADPRTL1) encoding a potential Poly(ADP-ribosyl)transferase protein.

J. Cowell, I. Still, P. Vince, 1999, Genomics.

Array CGH analysis of pediatric medulloblastomas

J. Rutka, N. Nowak, J. Conroy, 2006, Genes, chromosomes & cancer.

A transcription map of the minimally deleted region from 13q14 in B-cell chronic lymphocytic leukemia as defined by large scale sequencing of the 650 kb critical region

B. Roe, L. Hawthorn, H. Pan, 2000, Oncogene.

Wasf3 deficiency reveals involvement in metastasis in a mouse model of breast cancer.

M. Thangaraju, J. Cowell, H. Qin, 2019, The American journal of pathology.

The WASF3-NCKAP1-CYFIP1 Complex Is Essential for Breast Cancer Metastasis.

E. Kennedy, J. Cowell, H. Qin, 2016, Cancer research.

Mitochondrial ATAD3A combines with GRP78 to regulate the WASF3 metastasis-promoting protein

J. Cowell, Yong Teng, Austin Shull, 2015, Oncogene.

WASF3 regulates miR-200 inactivation by ZEB1 through suppression of KISS1 leading to increased invasiveness in breast cancer cells

L. Hawthorn, J. Cowell, Y. Teng, 2013, Oncogene.

Critical role of the WASF3 gene in JAK2/STAT3 regulation of cancer cell motility.

J. Cowell, Yong Teng, Pushpankur Ghoshal, 2013, Carcinogenesis.

HSP90 and HSP70 Proteins Are Essential for Stabilization and Activation of WASF3 Metastasis-promoting Protein*

J. Cowell, Yong Teng, L. Ngoka, 2012, The Journal of Biological Chemistry.

c-Abl-mediated Phosphorylation of WAVE3 Is Required for Lamellipodia Formation and Cell Migration*

K. Sossey-Alaoui, Xiurong Li, J. Cowell, 2007, Journal of Biological Chemistry.

Primary tumor-induced immunity eradicates disseminated tumor cells in syngeneic mouse model

M. Wicha, A. Arbab, J. Cowell, 2019, Nature Communications.

Loss of ATF3 Promotes Hormone-induced Prostate Carcinogenesis and the Emergence of CK5+CK8+ Epithelial Cells

Tsonwin Hai, H. Ding, Ziyan Wang, 2015, Oncogene.

NB4S, a member of the TBC1 domain family of genes, is truncated as a result of a constitutional t(1;10)(p22;q21) chromosome translocation in a patient with stage 4S neuroblastoma.

T. Roberts, J. Cowell, O. Chernova, 1998, Human molecular genetics.

Chromosome 13 ZNF198 Gene and Lack of Evidence for Multiple Genes Disrupted on The t(8;13) Atypical Myeloproliferative Disorder: Further Analysis of the

J. Cowell, I. Still, 2011 .

Induction of the plasminogen activator inhibitor-2 in cells expressing the ZNF198/FGFR1 fusion kinase that is involved in atypical myeloproliferative disease.

L. Hawthorn, J. Cowell, P. Kunapuli, 2006, Blood.

ZNF198 protein, involved in rearrangement in myeloproliferative disease, forms complexes with the DNA repair-associated HHR6A/6B and RAD18 proteins

J. Cowell, R. Somerville, I. Still, 2003, Oncogene.

Molecular definition of chromosome translocations involving 10q24 and 19q13 in human malignant glioma cells.

J. Cowell, O. Chernova, 1998, Cancer genetics and cytogenetics.

Assignment of four sequence-tagged sites to three subregions of 13q12 using a somatic cell hybrid mapping panel.

J. Cowell, A. Michalski, 1993, Genomics.

The consistent 13q14 translocation breakpoint seen in chronic B-cell leukaemia (BCLL) involves deletion of the D13S25 locus which lies distal to the retinoblastoma predisposition gene.

L. Hawthorn, D. Oscier, J. Cowell, 1993, Oncogene.

Recessive Oncogenes and Anti-Oncogenes

J. Cowell, 1990 .

Mechanisms of oncogenesis in patients with familial retinoblastoma.

A. Hogg, J. Cowell, Z. Onadim, 1993, British Journal of Cancer.

Genetics and cytogenetics of retinoblastoma.

A. Hogg, J. Cowell, 1992, Cancer Genetics and Cytogenetics.

HOXC9 directly regulates distinct sets of genes to coordinate diverse cellular processes during neuronal differentiation

Shuang Huang, Huidong Shi, Jeong-Hyeon Choi, 2013, BMC Genomics.

Identification of consistent novel submegabase deletions in low‐grade oligodendrogliomas using array‐based comparative genomic hybridization

Michael R Rossi, Daniel Gaile, R. Eddy, 2005, Genes, chromosomes & cancer.

Long tandem repeats as a form of genomic copy number variation: structure and length polymorphism of a chromosome 5p repeat in control and schizophrenia populations

V. Willour, L. DeLisi, C. Ross, 2009, Psychiatric genetics.

The third member of the transforming acidic coiled coil-containing gene family, TACC3, maps in 4p16, close to translocation breakpoints in multiple myeloma, and is upregulated in various cancer cell lines.

J. Cowell, I. Still, J K Cowell, 1999, Genomics.

The TACC proteins are coregulators of the Retinoid X Receptor

J. Cowell, I. Still, B. Lauffart, 2008 .

The TACC domain identifies a family of centrosomal proteins that can interact with microtubules.

F. Gergely, J. Raff, J. Kilmartin, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Cloning of TACC1, an embryonically expressed, potentially transforming coiled coil containing gene, from the 8p11 breast cancer amplicon

Alan Wolfman, Ivan H Still, A. Wolfman, 1999, Oncogene.

COP1 and GSK3β cooperate to promote c-Jun degradation and inhibit breast cancer cell tumorigenesis.

Jiahuai Han, Shuang Huang, H. Ding, 2013, Neoplasia.

Monocytic and granulocytic myeloid derived suppressor cells differentially regulate spatiotemporal tumour plasticity during metastatic cascade

M. Thangaraju, A. Arbab, R. Kolhe, 2017, Nature Communications.

Interaction of the transforming acidic coiled-coil 1 (TACC1) protein with ch-TOG and GAS41/NuBI1 suggests multiple TACC1-containing protein complexes in human cells.

J. Cowell, S. Howell, I. Still, 2002, The Biochemical journal.

A novel member of the WD-repeat gene family, WDR11, maps to the 10q26 region and is disrupted by a chromosome translocation in human glioblastoma cells

B. Roe, E. Malaj, J. Cowell, 2001, Oncogene.

Evaluation of phosphatidylinositol-3-kinase catalytic subunit (PIK3CA) and epidermal growth factor receptor (EGFR) gene mutations in pancreaticobiliary adenocarcinoma.

J. Cowell, J. Gibbs, M. Rossi, 2013, Journal of gastrointestinal oncology.

Mutation in the FGFR1 tyrosine kinase domain or inactivation of PTEN is associated with acquired resistance to FGFR inhibitors in FGFR1‐driven leukemia/lymphomas

J. Cowell, H. Qin, M. Ren, 2017, International journal of cancer.

Sepantronium is a DNA damaging agent that synergizes with PLK1 inhibitor volasertib.

J. Cowell, Justin Choi, Jeane Silva, 2014, American journal of cancer research.

Defined genetic events associated with the spontaneous in vitro transformation of ElA/Ras-expressing human IMR90 fibroblasts.

S. Lowe, G. Hannon, S. Matsui, 2006, Carcinogenesis.

Novel FGFR inhibitor ponatinib suppresses the growth of non-small cell lung cancer cells overexpressing FGFR1.

John Cowell, Gentao Liu, J. Cowell, 2013, Oncology reports.

2-5A antisense directed against telomerase RNA produces apoptosis in ovarian cancer cells.

R. Silverman, J. Cowell, J. Paranjape, 2000, Gynecologic oncology.

Molecular characterization of a consistent 4.5-megabase deletion at 4q28 in prostate cancer cells.

N. Nowak, S. Matsui, J. Cowell, 2005, Cancer genetics and cytogenetics.

Analysis of Wilms Tumors Using SNP Mapping Array-Based Comparative Genomic Hybridization

L. Hawthorn, J. Cowell, 2011, PloS one.

Frequent homozygous deletions of the D13S25 locus in chromosome region 13q14 defines the location of a gene critical in leukaemogenesis in chronic B-cell lymphocytic leukaemia.

L. Hawthorn, D. Oscier, M. Corcoran, 1994, Oncogene.

Construction of a bacterial artificial chromosome (BAC) contig across the minimally deleted region in 13q14.3 in B‐cell chronic lymphocytic leukemia

L. Hawthorn, J. Cowell, J. Cowell, 1998, Annals of human genetics.

A novel gene, LGI1, from 10q24 is rearranged and downregulated in malignant brain tumors

J. Cowell, R. Somerville, O. Chernova, 1998, Oncogene.

A Deletion Hybrid Breakpoint Map of the Chromosomal Region 13q14–q21 Orders 19 Genetic Markers in 10 Intervals

L. Hawthorn, H. Scheffer, R. Kooy, 1994, European journal of human genetics : EJHG.

The application of microarray technology to the analysis of the cancer genome.

L. Hawthorn, J. Cowell, 2007, Current molecular medicine.

The involvement of JAK-STAT3 in cell motility, invasion, and metastasis

J. Cowell, Y. Teng, James L Ross, 2014, JAK-STAT.

The molecular genetics of retinoblastoma and Wilms' tumor.

J. Cowell, J. Pritchard, 1987, Critical reviews in oncology/hematology.

Genetic analysis of Down syndrome-associated heart defects in mice

Li Zhang, Antonio Baldini, N. Nowak, 2011, Human Genetics.

Manipulation of nonsense mediated decay identifies gene mutations in colon cancer Cells with microsatellite instability

S. Markowitz, N. Nowak, Y. Ionov, 2004, Oncogene.

A novel mutation in the promotor region in a family with a mild form of retinoblastoma indicates the location of a new regulatory domain for the RB1 gene.

J. Cowell, B. Bia, A. Akoulitchev, 1996, Oncogene.

Identification of mutations in the WT1 gene in tumours from patients with the WAGR syndrome.

D. Housman, D. Haber, J. Cowell, 1992, Oncogene.

Expression of oligodendrocyte progenitor cell antigens by gliomas: implications for the histogenesis of brain tumors.

Y. Shoshan, G. Barnett, B. Trapp, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Development of Autoimmunity in IL-14α-Transgenic Mice1

J. Cowell, Vijay Kumar, Y. Lin-Lee, 2006, The Journal of Immunology.

Reexpression of LGI1 in glioma cells results in dysregulation of genes implicated in the canonical axon guidance pathway.

L. Hawthorn, J. Cowell, K. Lo, 2010, Genomics.

Regional localization of 192 genic markers on human chromosome 1.

C. Auffray, T. Roberts, J. Cowell, 1996, Genomics.

Targeting FGFR1 to suppress leukemogenesis in syndromic and de novo AML in murine models

S. Malek, J. Karp, J. Cowell, 2016, Oncotarget.

Gain of 1q Is a Potential Univariate Negative Prognostic Marker for Survival in Medulloblastoma

S. Pomeroy, C. Eberhart, J. Cowell, 2007, Clinical Cancer Research.

Targeting the WASF3 Complex to Suppress Metastasis.

E. Kennedy, J. Cowell, Ameya J. Limaye, 2022, Pharmacological research.

Suppression of Breast Cancer Metastasis Using Stapled Peptides Targeting the WASF Regulatory Complex

E. Kennedy, A. Arbab, J. Cowell, 2017, Cancer growth and metastasis.

Src activation plays an important key role in lymphomagenesis induced by FGFR1 fusion kinases.

J. Cowell, H. Qin, M. Ren, 2011, Cancer research.

WAVE3, an actin-polymerization gene, is truncated and inactivated as a result of a constitutional t(1;13)(q21;q12) chromosome translocation in a patient with ganglioneuroblastoma

B. Roe, E. Malaj, K. Sossey-Alaoui, 2002, Oncogene.

Chromosome analysis of human neuroblastoma cell line TR14 showing double minutes and an aberration involving chromosome 1.

J. Cowell, H. Rupniak, 1983, Cancer genetics and cytogenetics.

M. Jay, J. Cowell, J. Hungerford, 1988, Eye.

Application of PCR amplification of DNA from paraffin embedded tissue sections to linkage analysis in familial retinoblastoma.

J. Cowell, Z. Onadim, 1991, Journal of medical genetics.

Genetic counselling in retinoblastoma: importance of ocular fundus examination of first degree relatives and linkage analysis.

J. Cowell, Z. Onadim, J. Hungerford, 1991, The British journal of ophthalmology.

The genetics of retinoblastoma.

J. Cowell, 1991, British Journal of Cancer.

One hundred years of retinoblastoma research. From the clinic to the gene and back again.

J. Cowell, 1989, Ophthalmic paediatrics and genetics.

Retinoblastoma – Clinical and Genetic Aspects: A Review

M. Jay, J. Cowell, J. Hungerford, 1988, Journal of the Royal Society of Medicine.

Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumour.

P. Scambler, J. Cowell, R. Grundy, 1998, British Journal of Cancer.

Differential expression of the LGI and SLIT families of genes in human cancer cells.

Michael R Rossi, K. Huntoon, J. Cowell, 2005, Gene.

Chromosome abnormalities associated with salivary gland epithelial cell lines transformed in vitro and in vivo with evidence of a role for genetic imbalance in transformation.

J. Cowell, John K. Cowell, 1981, Cancer research.

Consistent chromosome abnormalities associated with mouse bladder epithelial cell lines transformed in vitro.

J. Cowell, 1980, Journal of the National Cancer Institute.

Cytogenetic changes in Wilms' tumors.

J. Cowell, J. Pritchard, J. Pritchard, 1988, Cancer genetics and cytogenetics.

TTC4, a novel candidate tumor suppressor gene at 1p31 is often mutated in malignant melanoma of the skin

M. Poetsch, J. Cowell, T. Dittberner, 2000, Oncogene.

The promise of zebrafish as a chemical screening tool in cancer therapy.

Xiayang Xie, J. Cowell, Yong Teng, 2015, Future medicinal chemistry.

Mass spectroscopy identifies the splicing-associated proteins, PSF, hnRNP H3, hnRNP A2/B1, and TLS/FUS as interacting partners of the ZNF198 protein associated with rearrangement in myeloproliferative disease.

J. Cowell, John K Cowell, Chitta S Kasyapa, 2005, Experimental cell research.

Molecular genetic analysis of chromosome 11p in familial Wilms tumour.

J. Cowell, P. Baird, J. Pritchard, 1994, British Journal of Cancer.

Novel amplicons on the short arm of chromosome 7 identified using high resolution array CGH contain over expressed genes in addition to EGFR in glioblastoma multiforme

L. Hawthorn, N. Nowak, S. Matsui, 2005, Genes, chromosomes & cancer.

Inactivation of the WASF3 gene in prostate cancer cells leads to suppression of tumorigenicity and metastases

J. Cowell, Y. Teng, S. Sharma, 2010, British Journal of Cancer.

Identifying candidate colon cancer tumor suppressor genes using inhibition of nonsense-mediated mRNA decay in colon cancer cells

L. Hawthorn, Y. Ionov, J. Cowell, 2007, Oncogene.

CLCA2 tumour suppressor gene in 1p31 is epigenetically regulated in breast cancer

K. Sossey-Alaoui, Xiurong Li, J. Cowell, 2004, Oncogene.

Array comparative genome hybridization analysis of acute lymphoblastic leukaemia and acute megakaryoblastic leukaemia in patients with Down syndrome

L. Kearney, S. Izraeli, J. Cowell, 2008, British journal of haematology.

A role for p300/CREB binding protein genes in promoting cancer progression in colon cancer cell lines with microsatellite instability.

Y. Ionov, S. Matsui, J. Cowell, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Preferential loss of maternal alleles in sporadic Wilms' tumour.

J. Cowell, R. Wadey, J. Pritchard, 1990, Oncogene.

The use of SCID mice for the growth of retinoblastoma cell lines and for the establishment of xenografts from primary tumours.

J. Cowell, G. Morgan, Y. Song, 1997, European journal of cancer.

Demonstration of bias in series of retinoblastoma.

M. Jay, J. Cowell, J. Hungerford, 1989, Ophthalmic paediatrics and genetics.

PRENATAL EXCLUSION OF HEREDITARY RETINOBLASTOMA

K. Nicolaides, M. Jay, J. Cowell, 1988, The Lancet.

Functional interrelationship between the WASF3 and KISS1 metastasis‐associated genes in breast cancer cells

Mingyao Liu, J. Cowell, Yong Teng, 2011, International journal of cancer.

The temporal and spatial expression pattern of the LGI1 epilepsy predisposition gene during mouse embryonic cranial development

J. Cowell, Jeane Silva, Guanghu Wang, 2011, BMC Neuroscience.

Molecular characterization of a 7p15–21 homozygous deletion in a Wilms tumor

K. Sossey-Alaoui, J. Cowell, D. David, 2003, Genes, chromosomes & cancer.

Interpreting aCGH-defined karyotypic changes in gliomas using copy number status, loss of heterozygosity and allelic ratios.

L. Hawthorn, J. Cowell, K. Lo, 2010, Experimental and molecular pathology.

EVI5 is a novel centrosomal protein that binds to α- and γ-tubulin

T. Ranalli, J. Cowell, S. Faitar, 2005 .

TTC4, a novel human gene containing the tetratricopeptide repeat and mapping to the region of chromosome 1p31 that is frequently deleted in sporadic breast cancer.

T. Roberts, J. Cowell, G. Su, 1999, Genomics.

Genetic fingerprinting of the development and progression of T-cell lymphoma in a murine model of atypical myeloproliferative disorder initiated by the ZNF198-fibroblast growth factor receptor-1 chimeric tyrosine kinase.

Xiurong Li, J. Cowell, M. Ren, 2009, Blood.

Contrasting response of euchromatin and heterochromatin to translocation in polytene chromosomes of Drosophila melanogaster

J. Cowell, I. Hartmann-Goldstein, 1980, Chromosoma.

Appearance of double minute chromosomes in somatic cell hybridisation experiments involving the HAT selection system.

J. Cowell, 1982, Cell biology international reports.

STAINING REGIONS: Gene Amplification in Mammalian Cellsl

J. Cowell, 1982 .

The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11

J. Cowell, R. Wadey, J. Pritchard, 1989, Human Genetics.

A new chromosome region possibly derived from double minutes in an in vitro transformed epithelial cell line.

J. Cowell, 1980, Cytogenetics and cell genetics.

Modification of the DNA content in translocated regions of Drosophila polytene chromosomes

J. Cowell, I. Hartmann-Goldstein, 1980, Chromosoma.

The EVI5 TBC domain provides the GTPase-activating protein motif for RAB11

J. Cowell, C. Dufresne, S. Faitar, 2007, Oncogene.

miR-339 Promotes Development of Stem Cell Leukemia/Lymphoma Syndrome via Downregulation of the BCL2L11 and BAX Proapoptotic Genes.

L. Hawthorn, E. Kitamura, J. Cowell, 2018, Cancer research.

Mechanisms of resistance to FGFR1 inhibitors in FGFR1-driven leukemias and lymphomas: implications for optimized treatment

J. Cowell, Tianxiang Hu, 2021, Cancer drug resistance.

Genome-wide aberrations in pancreatic adenocarcinoma.

R. Hruban, A. Maitra, M. Goggins, 2005, Cancer genetics and cytogenetics.

Primary tumor-induced immunity eradicates disseminated tumor cells in syngeneic mouse model

M. Wicha, A. Arbab, J. Cowell, 2019, Nature Communications.

The miR-17/92 cluster is involved in the molecular etiology of the SCLL syndrome driven by the BCR-FGFR1 chimeric kinase

E. Kitamura, J. Cowell, H. Qin, 2017, Oncogene.

The co-chaperone UNC45A is essential for the expression of mitotic kinase NEK7 and tumorigenesis

Huidong Shi, J. Roig, J. Cowell, 2019, The Journal of Biological Chemistry.

FGFR1 fusion kinase regulation of MYC expression drives development of stem cell leukemia/lymphoma syndrome

J. Cowell, H. Qin, Jan van Riggelen, 2018, Leukemia.

Application of intragenic DNA probes in prenatal screening for retinoblastoma gene carriers in the United Kingdom.

M. Jay, J. Cowell, Z. Onadim, 1990, Archives of disease in childhood.

Follow-up of retinoblastoma patients having prenatal and perinatal predictions for mutant gene carrier status using intragenic polymorphic probes from the RB1 gene.

J. Cowell, Z. Onadim, J. Hungerford, 1992, British Journal of Cancer.

The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletions.

J. Cowell, P. Rutland, E. Thompson, 1987, Archives of disease in childhood.

deletions . submicroscopic chromosome esterase D activity : detection of retinoblastoma patients for The need to screen all

J. Cowell, P. Rutland, E. Thompson, 2022 .

Insertional inactivation of the WT1 gene in tumour cells from a patient with WAGR syndrome

J. Cowell, P. Baird, M. Boavida, 1993, Human Genetics.

Germline mutations in the RB1 gene in patients with hereditary retinoblastoma

J. Cowell, B. Bia, Yue-Zhang Song, 1995, Genes, chromosomes & cancer.

Development of autoimmunity in IL-14alpha-transgenic mice.

J. Cowell, Vijay Kumar, Y. Lin-Lee, 2006, Journal of Immunology.

The neural progenitor-restricted isoform of the MARK4 gene in 19q13.2 is upregulated in human gliomas and overexpressed in a subset of glioblastoma cell lines

R. Moroni, G. Finocchiaro, B. Pollo, 2003, Oncogene.

IRAK1-regulated IFN-γ signaling induces MDSC to facilitate immune evasion in FGFR1-driven hematological malignancies

J. Cowell, R. Pacholczyk, Yun Liu, 2021, Molecular Cancer.

Down-regulation of WAVE3, a metastasis promoter gene, inhibits invasion and metastasis of breast cancer cells.

Andrei V Bakin, K. Sossey-Alaoui, Xiurong Li, 2007, The American journal of pathology.

Application of oligonucleotides arrays for coincident comparative genomic hybridization, ploidy status and loss of heterozygosity studies in human cancers.

J. Cowell, K. Lo, 2009, Methods in molecular biology.

Loss of the BCR-FGFR1 GEF Domain Suppresses RHOA Activation and Enhances B-Lymphomagenesis in Mice.

J. Cowell, H. Qin, N. Savage, 2018, Cancer research.

Incorporation of 35 novel gene transcripts into the physical and genetic map of human chromosome 13.

C. Auffray, L. Hawthorn, T. Roberts, 1996, Genomics.

Comprehensive analysis of loss of heterozygosity events in glioblastoma using the 100K SNP mapping arrays and comparison with copy number abnormalities defined by BAC array comparative genomic hybridization

Paul Gardina, Y. Turpaz, D. Bailey, 2008, Genes, chromosomes & cancer.

A model of BCR‐FGFR1 driven human AML in immunocompromised mice

E. Kitamura, J. Cowell, H. Qin, 2016, British journal of haematology.

Copy number and gene expression alterations in radiation-induced papillary thyroid carcinoma from chernobyl pediatric patients.

L. Hawthorn, J. Cowell, Leighton Stein, 2010, Thyroid : official journal of the American Thyroid Association.

Comparative genomic hybridization and its application to Wilms’ tumorigenesis

G. Landes, T. Houseal, J. Cowell, 1998, Cytogenetic and Genome Research.

Molecular characterization of the breakpoint region associated with a constitutional t(2;15)(q34;q26) in a patient with multiple myeloma.

E. Kitamura, J. Cowell, O. Chernova, 2001, Cancer genetics and cytogenetics.

Rac1/2 activation promotes FGFR1 driven leukemogenesis in stem cell leukemia/lymphoma syndrome

David A. Williams, J. Cowell, Meaghan K McGuinness, 2020, Haematologica.

Constitutional nonsense germline mutations in the RB1 gene detected in patients with early onset unilateral retinoblastoma.

J. Cowell, H. Cragg, 1996, European journal of cancer.

Molecular Genetics of Retinoblastoma

J. Cowell, 1994 .

Retinoblastoma: the paradigm for a genetically inherited cancer syndrome

J. Cowell, 1996 .

Genetic and cytogenetic analysis of patients showing reduced esterase-D levels and mental retardation from a survey of 500 individuals with retinoblastoma.

M. Jay, J. Cowell, J. Hungerford, 1989, Ophthalmic paediatrics and genetics.

DNA methyltransferase 1–mediated CpG methylation of the miR-150-5p promoter contributes to fibroblast growth factor receptor 1–driven leukemogenesis

J. Cowell, Yun Liu, Sumin Lu, 2019, The Journal of Biological Chemistry.

Retinoblastoma: a possible link with low level radiation.

C. Stiller, J. Cowell, J. Morris, 1993, Journal of medical genetics.

Celecoxib Ameliorates Seizure Susceptibility in Autosomal Dominant Lateral Temporal Epilepsy

J. Cowell, Ya-Jun Xie, Liang Zhou, 2018, The Journal of Neuroscience.

Inactivation of Lgi1 in murine neuronal precursor cells leads to dysregulation of axon guidance pathways.

L. Hawthorn, J. Cowell, Jeane Silva, 2020, Genomics.

Defining the expression pattern of the LGI1 gene in BAC transgenic mice

Shiaoching Gong, N. Heintz, S. Matsui, 2007, Mammalian Genome.

EVI5 protein associates with the INCENP-aurora B kinase-survivin chromosomal passenger complex and is involved in the completion of cytokinesis.

K. Sossey-Alaoui, T. Ranalli, J. Cowell, 2006, Experimental cell research.

Knockdown of zebrafish Lgi1a results in abnormal development, brain defects and a seizure-like behavioral phenotype.

Xiayang Xie, J. Cowell, Yong Teng, 2010, Human molecular genetics.

-Transgenic Mice α Development of Autoimmunity in IL-14

J. Cowell, Y. Lin-Lee, Tao Wang, 2013 .

Truncating mutations in the ACVR2 gene attenuates activin signaling in prostate cancer cells.

Y. Ionov, Andrei V Bakin, J. Cowell, 2005, Cancer genetics and cytogenetics.

Development of ZMYM2‐FGFR1 driven AML in human CD34+ cells in immunocompromised mice

T. George, J. Cowell, H. Qin, 2016, International journal of cancer.

Identification of inactivating mutations in the JAK1, SYNJ2, and CLPTM1 genes in prostate cancer cells using inhibition of nonsense-mediated decay and microarray analysis.

L. Hawthorn, Y. Ionov, J. Cowell, 2005, Cancer genetics and cytogenetics.

Independent constitutional germline mutations occurring in the RB1 gene in cousins with bilateral retinoblastoma.

J. Cowell, B. Bia, 1995, Oncogene.

Overlay Tool© for aCGHViewer©: An Analysis Module Built for aCGHViewer© used to Perform Comparisons of Data Derived from Different Microarray Platforms

Y. Turpaz, D. Bailey, J. Cowell, 2007, Cancer informatics.

FGFR1OP2-FGFR1 induced myeloid leukemia and T-cell lymphoma in a mouse model

J. Cowell, H. Qin, M. Ren, 2016, Haematologica.

Characterization of the breakpoints in unbalanced t(5;11)(p15;p15) constitutional chromosome translocations in two patients with beckwith-wiedemann syndrome using fluorescence in situ hybridisation.

R. Aledo, J. Cowell, R. Grundy, 1998, International journal of molecular medicine.

The nuclear oncoproteins: RB and p53.

J. Cowell, 1990, Seminars in cancer biology.

LGI 1 , a Putative Tumor Metastasis Suppressor Gene , Controls in Vitro Invasiveness and Expression of Matrix Metalloproteinases in Glioma Cells through the ERK 1 / 2 Pathway *

L. Hawthorn, J. Cowell, P. Kunapuli, 2004 .

A novel missense mutation in patients from a retinoblastoma pedigree showing only mild expression of the tumor phenotype

J. Cowell, B. Bia, 1998, Oncogene.

Reexpression of LGI1 in glioma cells results in dysregulation of genes implicated in the canonical axon guidance pathway.

L. Hawthorn, J. Cowell, K. Lo, 2010, Genomics.

Critical role of the WASF3 gene in JAK2/STAT3 regulation of cancer cell motility.

J. Cowell, Yong Teng, Pushpankur Ghoshal, 2013, Carcinogenesis.

LGI1: from zebrafish to human epilepsy.

J. Cowell, 2014, Progress in brain research.

Deletion of chromosome region 13q14 is transmissible and does not always predispose to retinoblastoma

M. Jay, J. Cowell, J. Hungerford, 1988, Human Genetics.

Hoechst 33258 as a quantitative fluorochrome. A rapid method for accurate DNA measurements in single cells in situ using a simple microfluorimeter and

J. Cowell, L. M. Franks, 2011 .

Evolution of a normal karyotype in a mouse bladder epithelial cell line transformed in vitro.

J. Cowell, 1981, Cancer genetics and cytogenetics.

The WASF3-NCKAP1-CYFIP1 Complex Is Essential for Breast Cancer Metastasis.

E. Kennedy, J. Cowell, H. Qin, 2016, Cancer research.

Carrier detection and prenatal screening of the retinoblastoma gene

J. Cowell, Z. Onadim, 1990, The Journal of pathology.

A chromosomal breakpoint that separates the esterase D and retinoblastoma predisposition loci in a patient with del(13)(q14q31).

M. Jay, J. Cowell, J. Hungerford, 1987, Cancer genetics and cytogenetics.

Molecular characterization of a (1;10)(p22;q21) constitutional translocation from a patient with neuroblastoma.

R. S. Mead, J. Cowell, 1995, Cancer genetics and cytogenetics.

Src activation plays an important key role in lymphomagenesis induced by FGFR1 fusion kinases.

J. Cowell, H. Qin, M. Ren, 2011, Cancer research.

Constitutive Notch pathway activation in murine ZMYM2-FGFR1-induced T-cell lymphomas associated with atypical myeloproliferative disease.

J. Cowell, M. Ren, 2011, Blood.