D. Smith

发表

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

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

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

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

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.

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.

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

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

A molecular cytogenetic analysis of 7q31 in prostate cancer.

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

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.

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

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

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.

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

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

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.

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

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

Macrophage-stimulating protein and its receptor in non-small-cell lung tumors: induction of receptor tyrosine phosphorylation and cell migration.

D. Sugarbaker, C. Willett, M. H. Wang, 1998, American journal of respiratory cell and molecular biology.

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.

Activation of p73 silent allele in lung cancer.

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

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.

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.

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.

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.

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

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

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.

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.

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

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

The human loci DNF15S2 and D3S94 have a high degree of sequence similarity to acyl-peptide hydrolase and are located at 3p21.3.

A. Baldini, D. Ginzinger, V. Shridhar, 1992, American journal of human genetics.

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.

Cloning of a putative human voltage-gated chloride channel (CIC-2) cDNA widely expressed in human tissues.

G. Cutting, C. Montrose‐Rafizadeh, W. Guggino, 1995, Human molecular genetics.

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

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

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.

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

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

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.

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.

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.

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.

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.

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

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

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.

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.

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.

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

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

Gene Expression Pattern Associated with Radiotherapy Sensitivity in Cervical Cancer

D. Sahota, T. Cheung, S. Yim, 2006, Cancer journal.

Molecular characterization of a novel human gene, SEC13R, related to the yeast secretory pathway gene SEC13, and mapping to a conserved linkage group on human chromosome 3p24-p25 and mouse chromosome 6.

A. Swaroop, M. Meisler, W. Liu, 1994, Human molecular genetics.

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.

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.

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.

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

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