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Items: 30

1.

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

Gotoh L, Mitsuyasu H, Kobayashi Y, Oribe N, Takata A, Ninomiya H, Stanton VP Jr, Springett GM, Kawasaki H, Kanba S.

Psychiatr Genet. 2009 Dec;19(6):328-35. doi: 10.1097/YPG.0b013e3283328e26.

PMID:
19820430
2.

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

Mitsuyasu H, Kawasaki H, Ninomiya H, Kinukawa N, Yamanaka T, Tahira T, Stanton VP Jr, Springett GM, Hayashi K, Tashiro N, Kanba S.

J Psychiatr Res. 2007 Nov;41(9):763-75. Epub 2006 Aug 2.

PMID:
16887146
3.

Pharmacogenetic study of statin therapy and cholesterol reduction.

Chasman DI, Posada D, Subrahmanyan L, Cook NR, Stanton VP Jr, Ridker PM.

JAMA. 2004 Jun 16;291(23):2821-7.

PMID:
15199031
4.

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

Zhu AX, Puchalski TA, Stanton VP Jr, Ryan DP, Clark JW, Nesbitt S, Charlat O, Kelly P, Kreconus E, Chabner BA, Supko JG.

Clin Colorectal Cancer. 2004 Feb;3(4):225-34.

PMID:
15025795
5.

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

Orzack SH, Gusfield D, Olson J, Nesbitt S, Subrahmanyan L, Stanton VP Jr.

Genetics. 2003 Oct;165(2):915-28.

6.

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

Wolfe JL, Wang BH, Kawate T, Stanton VP Jr.

J Am Chem Soc. 2003 Sep 3;125(35):10500-1.

PMID:
12940715
7.

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

Wolfe JL, Kawate T, Sarracino DA, Zillmann M, Olson J, Stanton VP Jr, Verdine GL.

Proc Natl Acad Sci U S A. 2002 Aug 20;99(17):11073-8. Epub 2002 Aug 8.

8.

Navajo neuropathy: relation to MDR3 mRNA deficiency.

Ortiz D, Arias IM, McKellar L, Stanton VP Jr.

Hepatology. 2002 Jun;35(6):1548. No abstract available.

PMID:
12029645
9.

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

Basilion JP, Schievella AR, Burns E, Rioux P, Olson JC, Monia BP, Lemonidis KM, Stanton VP Jr, Housman DE.

Mol Pharmacol. 1999 Aug;56(2):359-69.

PMID:
10419555
10.

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

Shen LX, Basilion JP, Stanton VP Jr.

Proc Natl Acad Sci U S A. 1999 Jul 6;96(14):7871-6.

11.

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

Borrow J, Stanton VP Jr, Andresen JM, Becher R, Behm FG, Chaganti RS, Civin CI, Disteche C, Dubé I, Frischauf AM, Horsman D, Mitelman F, Volinia S, Watmore AE, Housman DE.

Nat Genet. 1996 Sep;14(1):33-41.

PMID:
8782817
13.

The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9.

Borrow J, Shearman AM, Stanton VP Jr, Becher R, Collins T, Williams AJ, Dubé I, Katz F, Kwong YL, Morris C, Ohyashiki K, Toyama K, Rowley J, Housman DE.

Nat Genet. 1996 Feb;12(2):159-67.

PMID:
8563754
14.

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

Cai W, Aburatani H, Stanton VP Jr, Housman DE, Wang YK, Schwartz DC.

Proc Natl Acad Sci U S A. 1995 May 23;92(11):5164-8.

15.

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

Liu J, Stanton VP Jr, Fujiwara TM, Wang JX, Rezonzew R, Crumley MJ, Morgan K, Gros P, Housman D, Schurr E.

Genomics. 1995 Mar 20;26(2):178-91.

PMID:
7601441
16.

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.

Hunter KW, Ontiveros SD, Watson ML, Stanton VP Jr, Gutierrez P, Bhat D, Rochelle J, Graw S, Ton C, Schalling M, et al.

Mamm Genome. 1994 Oct;5(10):597-607.

PMID:
7849394
17.

YAC contigs for 4q35 in the region of the facioscapulohumeral muscular dystrophy (FSHD) gene.

Weiffenbach B, Dubois J, Manning S, Ma NS, Schutte BC, Winokur ST, Altherr MR, Jacobsen SJ, Stanton VP Jr, Yokoyama K, et al.

Genomics. 1994 Feb;19(3):532-41.

PMID:
8188296
18.

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

Moir DT, Dorman TE, Xue F, Ma NS, Stanton VP Jr, Housman D, Bowden DW, Noll WW, Mao J.

Gene. 1993 Dec 22;136(1-2):177-83.

PMID:
7904972
19.

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

Haas M, Aburatani H, Stanton VP Jr, Bhatt M, Housman D, Ward DC.

Genomics. 1993 Apr;16(1):90-6.

PMID:
8486389
20.

Clinical and genetic studies of renal cell carcinomas in a family with a constitutional chromosome 3;8 translocation. Genetics of familial renal carcinoma.

Li FP, Decker HJ, Zbar B, Stanton VP Jr, Kovacs G, Seizinger BR, Aburatani H, Sandberg AA, Berg S, Hosoe S, Brown RS.

Ann Intern Med. 1993 Jan 15;118(2):106-11.

PMID:
8416305
21.

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

Valentijn LJ, Bolhuis PA, Zorn I, Hoogendijk JE, van den Bosch N, Hensels GW, Stanton VP Jr, Housman DE, Fischbeck KH, Ross DA, et al.

Nat Genet. 1992 Jun;1(3):166-70.

PMID:
1303229
22.

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

Brook JD, McCurrach ME, Harley HG, Buckler AJ, Church D, Aburatani H, Hunter K, Stanton VP, Thirion JP, Hudson T, et al.

Cell. 1992 Apr 17;69(2):385. No abstract available.

PMID:
1568252
23.

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

Hubert R, Stanton VP Jr, Aburatani H, Warren J, Li H, Housman DE, Arnheim N.

Genomics. 1992 Apr;12(4):683-7.

PMID:
1349296
24.

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

Brook JD, McCurrach ME, Harley HG, Buckler AJ, Church D, Aburatani H, Hunter K, Stanton VP, Thirion JP, Hudson T, et al.

Cell. 1992 Feb 21;68(4):799-808. Erratum in: Cell. 1992 Apr 17;69(2):385.

PMID:
1310900
25.

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

McGrew BR, Nichols DW, Stanton VP Jr, Cai H, Whorf RC, Patel V, Cooper GM, Laudano AP.

Oncogene. 1992 Jan;7(1):33-42.

PMID:
1741164
26.

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

Abrams ES, Stanton VP Jr.

Methods Enzymol. 1992;212:71-104. No abstract available.

PMID:
1325604
27.

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

Schwartz CE, Haber DA, Stanton VP, Strong LC, Skolnick MH, Housman DE.

Genomics. 1991 Aug;10(4):927-30.

PMID:
1655633
28.

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

Goradia TM, Stanton VP Jr, Cui XF, Aburatani H, Li HH, Lange K, Housman DE, Arnheim N.

Genomics. 1991 Jul;10(3):748-55.

PMID:
1679751
29.

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

Stanton VP Jr, Nichols DW, Laudano AP, Cooper GM.

Mol Cell Biol. 1989 Feb;9(2):639-47.

30.

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