Seymour AB - Search Results

1

Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma.

Caldas C, Hahn SA, da Costa LT, Redston MS, Schutte M, Seymour AB, Weinstein CL, Hruban RH, Yeo CJ, Kern SE. Caldas C, et al. Among authors: seymour ab. Nat Genet. 1994 Sep;8(1):27-32. doi: 10.1038/ng0994-27. Nat Genet. 1994. PMID: 7726912

2

Allelotype of pancreatic adenocarcinoma using xenograft enrichment.

Hahn SA, Seymour AB, Hoque AT, Schutte M, da Costa LT, Redston MS, Caldas C, Weinstein CL, Fischer A, Yeo CJ, et al. Hahn SA, et al. Among authors: seymour ab. Cancer Res. 1995 Oct 15;55(20):4670-5. Cancer Res. 1995. PMID: 7553647

3

Allelotype of pancreatic adenocarcinoma.

Seymour AB, Hruban RH, Redston M, Caldas C, Powell SM, Kinzler KW, Yeo CJ, Kern SE. Seymour AB, et al. Cancer Res. 1994 May 15;54(10):2761-4. Cancer Res. 1994. PMID: 8168108

4

p53 mutations in pancreatic carcinoma and evidence of common involvement of homocopolymer tracts in DNA microdeletions.

Redston MS, Caldas C, Seymour AB, Hruban RH, da Costa L, Yeo CJ, Kern SE. Redston MS, et al. Among authors: seymour ab. Cancer Res. 1994 Jun 1;54(11):3025-33. Cancer Res. 1994. PMID: 8187092

5

Homozygous deletion map at 18q21.1 in pancreatic cancer.

Hahn SA, Hoque AT, Moskaluk CA, da Costa LT, Schutte M, Rozenblum E, Seymour AB, Weinstein CL, Yeo CJ, Hruban RH, Kern SE. Hahn SA, et al. Among authors: seymour ab. Cancer Res. 1996 Feb 1;56(3):490-4. Cancer Res. 1996. PMID: 8564959

6

Molecular genetic profiles of colitis-associated neoplasms.

Kern SE, Redston M, Seymour AB, Caldas C, Powell SM, Kornacki S, Kinzler KW. Kern SE, et al. Among authors: seymour ab. Gastroenterology. 1994 Aug;107(2):420-8. doi: 10.1016/0016-5085(94)90167-8. Gastroenterology. 1994. PMID: 8039618 Free article.

7

Oncogenic forms of p53 inhibit p53-regulated gene expression.

Kern SE, Pietenpol JA, Thiagalingam S, Seymour A, Kinzler KW, Vogelstein B. Kern SE, et al. Science. 1992 May 8;256(5058):827-30. doi: 10.1126/science.1589764. Science. 1992. PMID: 1589764

8

An integrated genetic map of the pearl locus of mouse chromosome 13.

Seymour AB, Yanak BL, O'Brien EP, Rusiniak ME, Novak EK, Pinto LH, Swank RT, Gorin MB. Seymour AB, et al. Genome Res. 1996 Jun;6(6):538-44. doi: 10.1101/gr.6.6.538. Genome Res. 1996. PMID: 8828042 Free article.

9

Linkage analysis of X-linked cone-rod dystrophy: localization to Xp11.4 and definition of a locus distinct from RP2 and RP3.

Seymour AB, Dash-Modi A, O'Connell JR, Shaffer-Gordon M, Mah TS, Stefko ST, Nagaraja R, Brown J, Kimura AE, Ferrell RE, Gorin MB. Seymour AB, et al. Am J Hum Genet. 1998 Jan;62(1):122-9. doi: 10.1086/301667. Am J Hum Genet. 1998. PMID: 9443860 Free PMC article.

10

The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness.

Feng L, Seymour AB, Jiang S, To A, Peden AA, Novak EK, Zhen L, Rusiniak ME, Eicher EM, Robinson MS, Gorin MB, Swank RT. Feng L, et al. Among authors: seymour ab. Hum Mol Genet. 1999 Feb;8(2):323-30. doi: 10.1093/hmg/8.2.323. Hum Mol Genet. 1999. PMID: 9931340

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