V. Stanton

发表

Analysis and exploration of the use of rule-based algorithms and consensus methods for the inferral of haplotypes.

D. Gusfield, S. Orzack, Jeffrey Olson, 2003, Genetics.

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

Manish S. Shah, A. Poustka, D. Church, 1993, Cell.

Ordered restriction endonuclease maps of yeast artificial chromosomes created by optical mapping on surfaces.

H. Aburatani, D. Schwartz, D. Housman, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Screening Large‐Insert Libraries by Hybridization

V. Stanton, Mark T. Ross (gridding: YAC, BAC, and PAC colony hybridiza, Sam LaBrie (BAC/PAC colony hybridization and analysis), 1999 .

The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding protein

C. Disteche, F. Behm, D. Horsman, 1996, Nature Genetics.

Definition of the human raf amino-terminal regulatory region by deletion mutagenesis

V. Stanton, G. Cooper, D. W. Nichols, 1989, Molecular and cellular biology.

Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member

David E. Housman, Russell G. Snell, Hiroyuki Aburatani, 1992, Cell.

Activation of human raf transforming genes by deletion of normal amino-terminal coding sequences

V. Stanton, G. Cooper, 1987, Molecular and cellular biology.

Tolerogenic nanoparticles suppress central nervous system inflammation

V. Stanton, F. Quintana, D. Sherr, 2020, Proceedings of the National Academy of Sciences.

Rapid identification of overlapping YACs in the MEN2 region of human chromosome 10 by hybridization with Alu element-mediated PCR products.

D. Housman, D. Bowden, V. Stanton, 1993, Gene.

Use of denaturing gradient gel electrophoresis to study conformational transitions in nucleic acids.

V. Stanton, E. S. Abrams, E. Abrams, 1992, Methods in enzymology.

Selective killing of cancer cells based on loss of heterozygosity and normal variation in the human genome: a new paradigm for anticancer drug therapy.

D. Housman, J. Basilion, V. Stanton, 1999, Molecular pharmacology.

Re: CYP2D6 genotype and tamoxifen response in postmenopausal women with endocrine-responsive breast cancer: the Breast International Group 1-98 trial.

V. Stanton, 2012, Journal of the National Cancer Institute.

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

H. Aburatani, D. Church, V. Stanton, 1992, Cell.

Synthesis and polymerase incorporation of 5'-amino-2',5'-dideoxy-5'-N-triphosphate nucleotides.

V. Stanton, J. L. Wolfe, T. Kawate, 2002, Nucleic acids research.

Sequence-specific dinucleotide cleavage promoted by synergistic interactions between neighboring modified nucleotides in DNA.

B. Wang, V. Stanton, J. L. Wolfe, 2003, Journal of the American Chemical Society.

Single-nucleotide polymorphisms can cause different structural folds of mRNA.

J. Basilion, V. Stanton, J P Basilion, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Sperm typing allows accurate measurement of the recombination fraction between D3S2 and D3S3 on the short arm of human chromosome 3.

H. Aburatani, R. Hubert, D. Housman, 1992, Genomics.

Ordering three DNA polymorphisms on human chromosome 3 by sperm typing.

K. Lange, H. Aburatani, T. Goradia, 1991, Genomics.

Large-scale cloning of human chromosome 2-specific yeast artificial chromosomes (YACs) using an interspersed repetitive sequences (IRS)-PCR approach.

D. Housman, V. Stanton, P. Gros, 1995, Genomics.

Clinical and Genetic Studies of Renal Cell Carcinomas in a Family with a Constitutional Chromosome 3; 8 Translocation: Genetics of Familial Renal Carcinoma

H. Aburatani, B. Zbar, V. Stanton, 1993, Annals of Internal Medicine.

The peripheral myelin gene PMP–22/GAS–3 is duplicated in Charcot–Marie–Tooth disease type 1A

D. Housman, F. Baas, V. Stanton, 1992, Nature Genetics.

Genetic variation in mRNA coding sequences of highly conserved genes.

D. Housman, F. Baas, V. Stanton, 2001, Physiological genomics.

High-resolution physical mapping by combined Alu-hybridization/PCR screening: construction of a yeast artificial chromosome map covering 31 centimorgans in 3p21-p14.

H. Aburatani, D. Housman, V. Stanton, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Pharmacogenetic Study of Statin Therapy and Cholesterol Reduction

David Posada, Paul M. Ridker, Nancy R. Cook, 2004 .

Familial predisposition to Wilms tumor does not segregate with the WT1 gene.

M. Skolnick, D. Housman, L. Strong, 1991, Genomics.

Genetic structure of the dopamine receptor D4 gene (DRD4) and lack of association with schizophrenia in Japanese patients.

S. Kanba, N. Kinukawa, V. Stanton, 2007, Journal of psychiatric research.

Rapid and efficient construction of yeast artificial chromosome contigs in the mouse genome with interspersed repetitive sequence PCR (IRS-PCR): Generation of a 5-cM, >5 megabase contig on mouse Chromosome 1

H. Aburatani, D. Housman, K. Hunter, 1994, Mammalian Genome.

A genotyping strategy based on incorporation and cleavage of chemically modified nucleotides

Jeffrey Olson, V. Stanton, G. Verdine, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Phosphorylation occurs in the amino terminus of the Raf-1 protein.

V. Stanton, G. Cooper, H. Cai, 1992, Oncogene.

Dihydropyrimidine dehydrogenase and thymidylate synthase polymorphisms and their association with 5-fluorouracil/leucovorin chemotherapy in colorectal cancer.

Jeffrey W. Clark, A. Zhu, S. Nesbitt, 2004, Clinical colorectal cancer.

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.

Isolation and FISH mapping of 80 cosmid clones on the short arm of human chromosome 3.

H. Aburatani, D. Housman, D. Ward, 1993, Genomics.

High-frequency DNA sequence polymorphisms in the insulin receptor gene detected by denaturing gradient gel blots.

D. Housman, V. Stanton, B. Krolewski, 1992, Genomics.

Association analysis of adenosine A1 receptor gene (ADORA1) polymorphisms with schizophrenia in a Japanese population

N. Oribe, S. Kanba, A. Takata, 2009, Psychiatric genetics.

The region surrounding the PKD1 gene: a 700-kb P1 contig from a YAC-deficient interval.

K. Klinger, G. Landes, D. Housman, 1996, Genome research.

Mapping 638 STSs to regions of human chromosome 3.

P. O'Connell, S. Naylor, V. Stanton, 1996, Cytogenetics and cell genetics.

Loss of heterozygosity of methylenetetrahydrofolate reductase in colon carcinomas.

W. Foulkes, R. Rozen, I. Tomlinson, 1999, Oncology reports.

Navajo neuropathy: Relation to MDR3 mRNA deficiency

V. Stanton, J. Gorski, S. Hall, 2002, Hepatology.