C. Morris

发表

Assignment1 of the murine kinectin gene (Ktn1) to mouse chromosome 14C2 by fluorescence in situ hybridization

C. Morris, M. McDonald, E. Leung, 1998, Cytogenetic and Genome Research.

Double complex mutations involving F8 and FUNDC2 caused by distinct break‐induced replication

C. Morris, C. Férec, Jian-Min Chen, 2007, Human mutation.

Association of chromosome band 8q22 copy number gain with high grade invasive breast carcinomas by assessment of core needle biopsies

C. Morris, L. Walker, G. Harris, 2008, Genes, chromosomes & cancer.

Constitutional t(5;7)(q11;p15) rearranged to acquire monosomy 7q and trisomy 1q in a patient with myelodysplastic syndrome transforming to acute myelocytic leukemia.

P. Ganly, C. Morris, M. McDonald, 2004, Cancer genetics and cytogenetics.

Spontaneous germline amplification and translocation of a transgene array.

C. Morris, E. Whitelaw, M. Kearns, 2001, Mutation research.

Ph-positive leukemia: a transgenic mouse model.

V. Kaartinen, J. Voncken, N. Heisterkamp, 1993, Leukemia & lymphoma.

Isolation and chromosomal localization of CRKL, a human crk-like gene.

N. Heisterkamp, J. Groffen, J. ten Hoeve, 1993, Oncogene.

Chromosomal localization of the human glycoasparaginase gene to 4q32–q33

N. Heisterkamp, J. Groffen, C. Morris, 2004, Human Genetics.

Philadelphia-positive leukemia Entire ABL gene is joined with 5'-BCR in some patients with

N. Heisterkamp, J. Groffen, C. Morris, 2011 .

Human Herpesvirus 6 Latently Infects Early Bone Marrow Progenitors In Vivo

C. Morris, R. Marasca, M. Luppi, 1999, Journal of Virology.

Telomeric association of chromosomes in B-cell lymphoid leukemia

C. Morris, P. H. Fitzgerald, 2004, Human Genetics.

Entire ABL gene is joined with 5'-BCR in some patients with Philadelphia-positive leukemia.

N. Heisterkamp, J. Groffen, C. Morris, 1991, Blood.

Familial Mutations of the Transcription Factor RUNX1 (AML1, CBFA2) Predispose to Acute Myeloid Leukemia

P. Ganly, C. Morris, L. Walker, 2004, Leukemia & lymphoma.

leukemias involving the chromosome breakpoint 9q34 Basophils (Bsp-1+) derive from the leukemic clone in human myeloid

C. Morris, P. H. Fitzgerald, M. Bodger, 2011 .

Basophils (Bsp-1+) derive from the leukemic clone in human myeloid leukemias involving the chromosome breakpoint 9q34.

C. Morris, P. H. Fitzgerald, M. Bodger, 1989, Blood.

neoplasia . Monocyte esterase deficiency in malignant

C. Morris, J. McCormick, M. Mccaigue, 2022 .

HRAS1 and INS genes are relocated but not structurally altered as a result of the t(7;11) (p15;p15) in a clone from a patient with acute myeloid leukaemia (M4)

C. Morris, P. H. Fitzgerald, G. Corbett, 1989, British journal of haematology.

A cytogenetic and molecular analysis of five variant Philadelphia translocations in chronic myeloid leukemia.

C. Morris, P. H. Fitzgerald, I. Rosman, 1988, Cancer genetics and cytogenetics.

Essential thrombocythaemia and the Philadelphia chromosome

C. Morris, M. Beard, D. Heaton, 1988, British journal of haematology.

Complexity of an apparently simple variant Ph translocation in chronic myeloid leukemia.

C. Morris, P. H. Fitzgerald, Peter H. Fitzgerald, 1987, Leukemia research.

Molecular Definition of Interstitial Deletions of Chromosome 13 in Leukemic Cells

C. Morris, P. H. Fitzgerald, P. Crossen, 1991, Genes, chromosomes & cancer.

CRK proto-oncogene maps to human chromosome band 17p13.

T. Fioretos, N. Heisterkamp, J. Groffen, 1993, Oncogene.

Localization of human c-mos to chromosome band 8q11 in leukemic cells with the t(8;21) (q22;q22)

C. Morris, P. H. Fitzgerald, J. Bowen, 1989, Human Genetics.

The variable hematologic expression of the BCR-ABL genomic mutation and its possible determinants.

C. Morris, P. H. Fitzgerald, 1989, Cancer genetics and cytogenetics.

The oncogene ETS1 is distant from the chromosome 11 breakpoint in leukaemic cells with the t(11;19)(q23;p13).

C. Morris, P. H. Fitzgerald, M. Kennedy, 1989, Leukemia research.

Fine mapping of an apparently targeted latent human herpesvirus type 6 integration site in chromosome band 17p13.3

C. Morris, M. McDonald, M. Luppi, 1999, Journal of medical virology.

Spatial organization of ABR and CRK genes on human chromosome band 17p13.3.

D. Ledbetter, N. Heisterkamp, J. Groffen, 1995, Oncogene.

Curative-dose Chemoradiotherapy Versus Total Laryngectomy For Stage T3-T4 Squamous Cell Carcinoma of the Larynx

W. Mendenhall, C. Morris, B.J. Boyce, 2019, American journal of clinical oncology.

Genomic diversity correlates with clinical variation in Ph′-negative chronic myeloid leukaemia

A. Reeve, C. Morris, P. H. Fitzgerald, 1986, Nature.

A novel inherited mutation of the transcription factor RUNX1 causes thrombocytopenia and may predispose to acute myeloid leukaemia

P. Ganly, C. Morris, L. Walker, 2002, British journal of haematology.

Rearrangement of the human ABL oncogene in a glioblastoma.

N. Heisterkamp, J. Groffen, C. Morris, 1990, Cancer research.

Genotyping the factor VIII intron 22 inversion locus using fluorescent in situ hybridization.

C. Morris, M. McDonald, C. Sheen, 2011, Blood cells, molecules & diseases.

Blood Cells, Molecules, and Diseases

C. Morris, M. McDonald, C. Sheen, 2011 .

Nonrandom distribution of interspersed repeat elements in the BCR and ABL1 genes and its relation to breakpoint cluster regions

C. Morris, E. Wells, A. Jeffs, 2001, Genes, chromosomes & cancer.

The BCR gene recombines preferentially with Alu elements in complex BCR-ABL translocations of chronic myeloid leukaemia.

S. Sowerby, C. Morris, T. Smith, 1998, Human molecular genetics.

Clonal development and karyotype evolution during leukemogenesis of BCR/ABL transgenic mice.

J. Voncken, N. Heisterkamp, J. Groffen, 1992, Blood.

Translocation (5;10)(q22;q24) in a case of acute lymphoblastic leukemia.

P. Ganly, C. Morris, M. McDonald, 2006, Cancer genetics and cytogenetics.

Refined physical map of the human PAX2/HOX11/NFKB2 cancer gene region at 10q24 and relocalization of the HPV6AI1 viral integration site to 14q13.3-q21.1

J. Korenberg, M. Eccles, A. Neri, 2003, BMC Genomics.

The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP96 and class I homeoprotein HOXA9

Keisuke Toyama, Reinhard Becher, Christine Morris, 1996, Nature Genetics.

Polyploidy in myelofibrosis: analysis by cytogenetic and SNP array indicates association with advancing disease

C. Morris, M. Koleth, W. Stevenson, 2013, Molecular Cytogenetics.

A full-length and potentially active LINE element is integrated polymorphically within the IGL locus in a genomically unstable region of chromosome 22

C. Morris, S. Benjes, 2001, Human Genetics.

A complex chromosome rearrangement forms the BCR‐ABL fusion gene in leukemic cells with a normal karyotype

N. Heisterkamp, J. Groffen, C. Morris, 1991, Genes, chromosomes & cancer.

Cytokeratin KRT8/18 expression differentiates distinct subtypes of grade 3 invasive ductal carcinoma of the breast.

C. Morris, L. Walker, G. Harris, 2007, Cancer genetics and cytogenetics.

Comparative genomic hybridization reveals previously undescribed amplifications and deletions in the chronic myeloid leukemia‐derived K‐562 cell line

C. Morris, M. McDonald, Philip Rodley, 1997, Genes, chromosomes & cancer.

The small GTPase RAC3 gene is located within chromosome band 17q25.3 outside and telomeric of a region commonly deleted in breast and ovarian tumours

N. Heisterkamp, J. Groffen, C. Morris, 2000, Cytogenetic and Genome Research.

Identification of multiple forms of 180-kDa ribosome receptor in human cells.

R. Gentz, D. Parry, C. Morris, 1998, DNA and cell biology.

Chronic myeloid leukemia: cytogenetic methods and applications for diagnosis and treatment.

C. Morris, 2011, Methods in molecular biology.

Urinary tract infection in infants and young children presenting with fever without a focus in Port Moresby.

C. Morris, J. Vince, N. Tefuarani, 2007, Papua and New Guinea medical journal.

Evidence for the repeated primary non-disjunction of chromosome 21 as a result of premature centromere division (PCD)

C. Morris, P. H. Fitzgerald, S. Archer, 2004, Human Genetics.

The integrin α10 subunit: expression pattern, partial gene structure, and chromosomal localization

C. Morris, E. Leung, G. Krissansen, 2000, Cytogenetic and Genome Research.

Dual-Color Fluorescence In Situ Hybridization Reveals an Association of Chromosome 8q22 but Not 8p21 Imbalance with High Grade Invasive Breast Carcinoma

C. Morris, M. McDonald, L. Walker, 2013, PloS one.

Direct versus cultured preparation of bone marrow cells from 22 patients with acute myeloid leukemia

C. Morris, P. H. Fitzgerald, L. M. Giles, 2004, Human Genetics.

An evaluation of high resolution chromosome banding of hematologic cells by methotrexate synchronization and thymidine release.

C. Morris, P. H. Fitzgerald, 1985, Cancer genetics and cytogenetics.

Karyotypic evolution in patients with acute myeloid leukemia.

C. Morris, P. H. Fitzgerald, 1984, Cancer genetics and cytogenetics.

Cytogenetic studies of acute promyelocytic leukemia.

C. Morris, P. H. Fitzgerald, M. Beard, 1982, Cancer genetics and cytogenetics.

Does multisomy of chromosome 1q confer a proliferative advantage in B‐cell acute lymphoblastic leukemia

C. Morris, P. Wyld, P. H. Fitzgerald, 1984, Cancer.

Localization of the SRC oncogene to chromosome band 20q11.2 and loss of this gene with deletion (20q) in two leukemic patients.

C. Morris, P. H. Fitzgerald, P. Hollings, 1989, Blood.

SRC Oncogene to Chromosome Band 20q1 1.2 and Loss of This Gene With Deletion (20q) in Two Leukemic Patients

C. Morris, P. H. Fitzgerald, P. Hollings, 2016 .

Identification of amplified genes in a patient with acute myeloid leukemia and double minute chromosomes.

C. Morris, P. Rodley, M. Morrison, 1999, Cancer genetics and cytogenetics.

Complex chromosomal translocations in the Philadelphia chromosome leukemias. Serial translocations or a concerted genomic rearrangement?

C. Morris, P. H. Fitzgerald, Peter H. Fitzgerald, 1991, Cancer genetics and cytogenetics.

Donor Leukocyte Infusions In The Treatment Of Chronic Myeloid Leukemia In Relapse Post Bone Marrow Transplantation

C. Morris, G. Hill, D. Hart, 1996, Pathology.

cDNA cloning of human DEC-205, a putative antigen-uptake receptor on dendritic cells

Masato Kato, C. Morris, G. Clark, 1998, Immunogenetics.

Reactivation of heritably silenced gene expression in mice

David I. K. Martin, C. Morris, E. Whitelaw, 2000, Mammalian Genome.

Localization of the TRK proto-oncogene to human chromosome bands 1q23-1q24.

N. Heisterkamp, J. Groffen, C. Morris, 1991, Oncogene.

Ph-negative chronic myeloid leukemia: molecular analysis of ABL insertion into M-BCR on chromosome 22.

N. Heisterkamp, J. Groffen, C. Morris, 1990, Blood.

DNA sequence analysis of the major breakpoint cluster region of the BCR gene rearranged in Philadelphia-positive human leukemias.

S. Sowerby, C. Morris, P. H. Fitzgerald, 1993, Oncogene.

Cloning and Characterization of a Novel β Integrin-Related cDNA Coding for the Protein TIED (“Ten β Integrin EGF-like Repeat Domains”) That Maps to Chromosome Band 13q33: A Divergent Stand-Alone Integrin Stalk Structure

C. Morris, E. Leung, G. Krissansen, 1999 .

TheCG-1 gene, a member of the kinectin and ES/130 family, maps to human chromosome band 14q22

C. Print, C. Morris, G. Krissansen, 2004, Immunogenetics.

Isolation of NotI sites from chromosome 22q11.

A. Poustka, N. Heisterkamp, J. Groffen, 1993, Genomics.

Human coproantibody secretory immunoglobulin A response to Yersinia species

C. Morris, M. Noble, K. Fletcher, 1988, Journal of clinical microbiology.

Ph-Negative Chronic Myeloid Leukemia: The Nature of the Breakpoint Junctions and Mechanism of ABL Transposition

C. Morris, P. H. Fitzgerald, 1992 .

Nonrandom cytogenetic changes in New Zealand patients with acute myeloid leukemia.

C. Morris, P. H. Fitzgerald, M. Beard, 1983, Cancer genetics and cytogenetics.

Ph‐negative chronic myeloid leukaemia

A. Reeve, C. Morris, P. H. Fitzgerald, 1987, British journal of haematology.

Cloning, sequence analysis, and chromosomal localization of the novel human integrin α11 subunit (ITGA11)

C. Morris, E. Leung, A. Weaver, 1999 .

A greater incidence of complex translocations in myeloid leukemias than in lymphomas and lymphoid leukemias associated with IGH rearrangement.

C. Morris, P. H. Fitzgerald, 1996, Cancer genetics and cytogenetics.

The human tyrosine kinase gene (FER) maps to chromosome 5 and is deleted in myeloid leukemias with a del(5q).

N. Heisterkamp, J. Groffen, J. Testa, 1990, Cytogenetics and cell genetics.

The integrin alpha10 subunit: expression pattern, partial gene structure, and chromosomal localization.

C. Morris, E. Leung, G. Krissansen, 1999, Cytogenetics and cell genetics.

Comparative genomic hybridization reveals previously undescribed amplifications and deletions in the chronic myeloid leukemia‐derived K‐562 cell line

C. Morris, Brent Price, M. Mcdonald, 1997, Genes, chromosomes & cancer.

ABR, an active BCR-related gene.

N. Heisterkamp, J. Groffen, C. Morris, 1989, Nucleic acids research.

Localization of a gamma-glutamyl-transferase-related gene family on chromosome 22

N. Heisterkamp, J. Groffen, C. Morris, 1993, Human Genetics.

A second hypervariable RFLP within the ABR gene.

N. Heisterkamp, J. Groffen, C. Morris, 1990, Nucleic acids research.

A hypervariable RFLP within the ABR gene.

N. Heisterkamp, J. Groffen, C. Morris, 1990, Nucleic acids research.

3′ BCR recombines with IGL locus in BCR‐ABL–positive Philadelphia‐negative chronic myeloid leukemia

S. Sowerby, A. Reeve, C. Morris, 1999, Genes, Chromosomes and Cancer.