D. Smith

发表

Role of PI3K signaling in survival and progression of LNCaP prostate cancer cells to the androgen refractory state.

D. Tindall, Haojie Huang, H. Huang, 2001, Endocrinology.

Cloning and characterization of the human t(3;6)(p14;p11) translocation breakpoint associated with hematologic malignancies.

S. Knuutila, R. Gemmill, H. Drabkin, 1993, Cancer genetics and cytogenetics.

The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched-related gene, TRC8.

F. Li, Frederick P. Li, N. Tanaka, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction.

R. Espinosa, M. L. Le Beau, T. Glover, 1998, Human molecular genetics.

Carboxypeptidase A3 (CPA3): a novel gene highly induced by histone deacetylase inhibitors during differentiation of prostate epithelial cancer cells.

H. Huang, Haojie Huang, D. Smith, 1999, Cancer research.

Human acid ceramidase is overexpressed but not mutated in prostate cancer

D. Bostwick, W. Liu, A. Yokomizo, 2000, Genes, chromosomes & cancer.

Involvement of H-cadherin (CDH13) on 16q in the region of frequent deletion in ovarian cancer.

L. Hartmann, W. Cliby, D. Smith, 1999, International journal of oncology.

Overabundance of rare-cutting restriction endonuclease sites in the human genome.

D. Smith, O. Miller, W. Golembieski, 1987, Nucleic acids research.

Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.

B. Mcgillivray, C. Venditti, D. Smith, 1996, Journal of medical genetics.

A molecular cytogenetic analysis of 7q31 in prostate cancer.

D. Bostwick, W. Liu, H. Huang, 1997, Cancer research.

Activation of p73 silent allele in lung cancer.

D. Tindall, W. Liu, A. Yokomizo, 1998, Cancer research.

Differential expression and allelotyping of the p73 gene in neuroblastoma.

D. Tindall, S. Thibodeau, W. Liu, 2000, International journal of oncology.

Saturation of human chromosome 3 with unique sequence hybridization probes.

R. Geist, H. Drabkin, D. Smith, 1989, Genomics.

Allele-specific late replication and fragility of the most active common fragile site, FRA3B.

W. Liu, H. Huang, D. Smith, 1999, Human molecular genetics.

A gene from human chromosomal band 3p21.1 encodes a highly conserved arginine-rich protein and is mutated in renal cell carcinomas.

D. Grignon, W. Sakr, R. Shridhar, 1996, Oncogene.

Mutations in the arginine-rich protein gene, in lung, breast, and prostate cancers, and in squamous cell carcinoma of the head and neck.

D. Grignon, J. Siegfried, W. Sakr, 1996, Cancer research.

Construction of a consistent YAC contig for human chromosome region 3p14.1.

R. Siebert, D. Smith, W. Bardenheuer, 1996, Genome research.

Characterization of a microdissection library from human chromosome region 3p14.

D. Smith, B. Horsthemke, W. Bardenheuer, 1994, Genomics.

Localization of 616 human chromosome 3-specific cosmids using a somatic cell hybrid deletion mapping panel.

P. Green, D. Ginzinger, W. Liu, 1991, Genomics.

Regional localization of chromosome 3-specific DNA fragments by using a hybrid cell deletion mapping panel.

H. Drabkin, D. Smith, C. Scoggin, 1988, American journal of human genetics.

Precise localization of aphidicolin-induced breakpoints on the short arm of human chromosome 3.

T. Glover, D. Smith, B. Opalka, 1995, Genomics.

Identification and chromosomal localization of CTNNAL1, a novel protein homologous to alpha-catenin.

W. Liu, D. Smith, R. Urrutia, 1998, Genomics.

Mapping of the gene for human cysteine proteinase inhibitor stefin A, STF1, to chromosome 3cen-q21.

Bonnie F. Sloane, D. Smith, W. Hsieh, 1991, Genomics.

A cloned major Schistosoma mansoni egg antigen with homologies to small heat shock proteins elicits Th1 responsiveness

D. Smith, D. Boros, Y. Cai, 1996, Infection and immunity.

A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints.

R. Shridhar, T. Glover, D. Smith, 1996, Genomics.

Exon skipping in IVD RNA processing in isovaleric acidemia caused by point mutations in the coding region of the IVD gene.

J. Vockley, W. Liu, P. Rogan, 2000, American journal of human genetics.

Von HippelLindau disease maps to the region of chromosome 3 associated with renal cell carcinoma

J. Haines, C. Mathew, J. Halperin, 1988, Nature.

Isolation of large numbers of chromosome 3-specific cosmids containing clusters of rare restriction-endonuclease sites.

A. Judge, H. Drabkin, D. Smith, 1991, American journal of human genetics.

MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME 2 AND CONFINED PLACENTAL MOSAICISM FOR TRISOMY 2 IN A FETUS WITH INTRAUTERINE GROWTH RESTRICTION, HYPOSPADIAS, AND OLIGOHYDRAMNIOS

S. Langlois, A. Aylsworth, D. Smith, 1997, Prenatal diagnosis.

A 2.5-Mb physical map within 3p21.1 spans the breakpoint associated with Greig cephalopolysyndactyly syndrome.

N. Tommerup, R. Gemmill, H. Drabkin, 1991, Genomics.

Identification of two cosmids derived from within chromosomal band 3p21.1 that contain clusters of rare restriction sites and evolutionarily conserved sequences.

H. Drabkin, D. Smith, W. Golembieski, 1989, American journal of human genetics.

FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites.

T. Glover, D. Smith, B. Hall, 1996, Human molecular genetics.

GBAS, a novel gene encoding a protein with tyrosine phosphorylation sites and a transmembrane domain, is co-amplified with EGFR.

C. James, W. Liu, D. Smith, 1998, Genomics.

Human AML cells in NOD/SCID mice: engraftment potential and gene expression

P. Meltzer, S. Gore, D. Small, 2002, Leukemia.

RORA, a large common fragile site gene, is involved in cellular stress response

R. Kuhn, Yuan-Xiao Zhu, D. Smith, 2006, Oncogene.

Differential screening of a human chromosome 3 library identifies hepatocyte growth factor-like/macrophage-stimulating protein and its receptor in injured lung. Possible implications for neuroendocrine cell survival.

D. Sugarbaker, C. Willett, D. Smith, 1997, The Journal of clinical investigation.

Cloning of the human homolog of conductin (AXIN2), a gene mapping to chromosome 17q23-q24.

W. Liu, A. Yokomizo, D. Smith, 1999, Genomics.

Denaturing high performance liquid chromatography (DHPLC) used in the detection of germline and somatic mutations.

S N Thibodeau, C. James, S. Thibodeau, 1998, Nucleic acids research.

Identification of molecular markers and signaling pathway in endometrial cancer in Hong Kong Chinese women by genome-wide gene expression profiling

Michael J. Birrer, Tak-Hong Cheung, So Fan Yim, 2007, Oncogene.

A human alphoid DNA clone from the EcoRI dimeric family: genomic and internal organization and chromosomal assignment.

M. Rocchi, D. Miller, A. Baldini, 1989, Genomics.

Common fragile sites and cancer (review).

H. Huang, D. Smith, D I Smith, 1998, International journal of oncology.

The characterization of the common fragile site FRA16D and its involvement in multiple myeloma translocations.

L. Roberts, T. Glover, K. Krummel, 2000, Genomics.

Genetic analysis of early- versus late-stage ovarian tumors.

G. Mills, F. Couch, S. Iturria, 2001, Cancer research.

Aphidicolin-induced FRA3B breakpoints cluster in two distinct regions.

R. Shridhar, T. Glover, D. Smith, 1997, Genomics.

Mutation analysis of the putative tumor suppressor PTEN/MMAC1 in human ovarian cancer.

D. Tindall, L. Hartmann, W. Liu, 1998, International journal of oncology.

Frequent breakpoints in the 3p14.2 fragile site, FRA3B, in pancreatic tumors.

F. Sarkar, R. Shridhar, T. Glover, 1996, Cancer research.

Isolation and characterization of a 1 Mb region of 5q23.3-q31.2 surrounding the human lysyl oxidase gene.

D. Smith, S. Krawetz, S. Smith, 1995, Journal of molecular and cellular cardiology.

Determination of the specificity of aphidicolin-induced breakage of the human 3p14.2 fragile site.

J. Testa, D. Smith, N. Wang, 1993, Genomics.

Genetic instability of microsatellite sequences in many non-small cell lung carcinomas.

J. Siegfried, J. Hunt, D. Smith, 1994, Cancer research.

Genome composition and tandemly repetitive sequence at some centromeres in the lizard Podarcis s. sicula Raf.

E. Olmo, D. Smith, G. Odierna, 2004, Genetica.

Cloning of tumor suppressor genes involved in solid tumor development.

D. Smith, M. del Mar Alonso, D. Smith, 1993, Archives of otolaryngology--head & neck surgery.

FHIT and TSG101 in thyroid tumours: aberrant transcripts reflect rare abnormal RNA processing events of uncertain pathogenetic or clinical significance.

N. Eberhardt, A. Yokomizo, D. Smith, 2000, Clinical endocrinology.

Genomic organization and mutation analysis of p73 in oligodendrogliomas with chromosome 1 p-arm deletions.

W. Liu, H. Huang, D. Smith, 1998, Genomics.

Integrations of the hepatitis B virus (HBV) and human papillomavirus (HPV) into the human telomerase reverse transcriptase (hTERT) gene in liver and cervical cancers

B. McMahon, E. Thorland, J. Bruix, 2003, Oncogene.

Loss of expression of a new member of the DNAJ protein family confers resistance to chemotherapeutic agents used in the treatment of ovarian cancer.

L. Hartmann, S. Kaufmann, H. Huang, 2001, Cancer research.

Altered expression of tumor suppressor PHF20 in myeloproliferative neoplasms

A. Tefferi, D. Smith, T. Lasho, 2014, Leukemia.

Assignment of the human serotonin 1F receptor gene (HTR1F) to the short arm of chromosome 3 (3p13-p14.1).

M. Nöthen, J. Erdmann, P. Propping, 1997, Molecular membrane biology.