Goldstein A - Search Results

1

Characterization of a YAC contig containing the NBCCS locus and a novel Kruppel-type zinc finger sequence on chromosome segment 9q22.3.

Chidambaram A, Gailani M, Gerrard B, Stewart C, Goldstein A, Chumakov I, Bale AE, Dean M. Chidambaram A, et al. Among authors: goldstein a. Genes Chromosomes Cancer. 1997 Mar;18(3):212-8. doi: 10.1002/(sici)1098-2264(199703)18:3<212::aid-gcc7>3.0.co;2-4. Genes Chromosomes Cancer. 1997. PMID: 9071574

2

Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients.

Shimkets R, Gailani MR, Siu VM, Yang-Feng T, Pressman CL, Levanat S, Goldstein A, Dean M, Bale AE. Shimkets R, et al. Among authors: goldstein a. Am J Hum Genet. 1996 Aug;59(2):417-22. Am J Hum Genet. 1996. PMID: 8755929 Free PMC article.

3

National Cancer Institute Workshop Report: the phakomatoses revisited.

Tucker M, Goldstein A, Dean M, Knudson A. Tucker M, et al. Among authors: goldstein a. J Natl Cancer Inst. 2000 Apr 5;92(7):530-3. doi: 10.1093/jnci/92.7.530. J Natl Cancer Inst. 2000. PMID: 10749907 No abstract available.

4

Identification of somatic mutations of the RNF6 gene in human esophageal squamous cell carcinoma.

Lo HS, Hu N, Gere S, Lu N, Su H, Goldstein AM, Taylor PR, Lee MP. Lo HS, et al. Cancer Res. 2002 Aug 1;62(15):4191-3. Cancer Res. 2002. PMID: 12154016

5

High frequency of CDKN2A alterations in esophageal squamous cell carcinoma from a high-risk Chinese population.

Hu N, Wang C, Su H, Li WJ, Emmert-Buck MR, Li G, Roth MJ, Tang ZZ, Lu N, Giffen C, Albert PS, Taylor PR, Goldstein AM. Hu N, et al. Genes Chromosomes Cancer. 2004 Mar;39(3):205-16. doi: 10.1002/gcc.10315. Genes Chromosomes Cancer. 2004. PMID: 14732922

6

Retrospective family study of childhood medulloblastoma.

Ng D, Stavrou T, Liu L, Taylor MD, Gold B, Dean M, Kelley MJ, Dubovsky EC, Vezina G, Nicholson HS, Byrne J, Rutka JT, Hogg D, Reaman GH, Goldstein AM. Ng D, et al. Am J Med Genet A. 2005 May 1;134(4):399-403. doi: 10.1002/ajmg.a.30653. Am J Med Genet A. 2005. PMID: 15759260

7

Allelotyping of esophageal squamous-cell carcinoma on chromosome 13 defines deletions related to family history.

Hu N, Su H, Li WJ, Giffen C, Goldstein AM, Hu Y, Wang C, Roth MJ, Li G, Dawsey SM, Xu Y, Taylor PR, Emmert-Buck MR. Hu N, et al. Genes Chromosomes Cancer. 2005 Nov;44(3):271-8. doi: 10.1002/gcc.20242. Genes Chromosomes Cancer. 2005. PMID: 16015646

8

Whole-exome sequencing of nevoid basal cell carcinoma syndrome families and review of Human Gene Mutation Database PTCH1 mutation data.

Gianferante DM, Rotunno M, Dean M, Zhou W, Hicks BD, Wyatt K, Jones K, Wang M, Zhu B, Goldstein AM, Mirabello L. Gianferante DM, et al. Mol Genet Genomic Med. 2018 Nov;6(6):1168-1180. doi: 10.1002/mgg3.498. Epub 2018 Nov 8. Mol Genet Genomic Med. 2018. PMID: 30411536 Free PMC article.

9

Infrequent mutation in the BRCA2 gene in esophageal squamous cell carcinoma.

Hu N, Li G, Li WJ, Wang C, Goldstein AM, Tang ZZ, Roth MJ, Dawsey SM, Huang J, Wang QH, Ding T, Giffen C, Taylor PR, Emmert-Buck MR. Hu N, et al. Clin Cancer Res. 2002 Apr;8(4):1121-6. Clin Cancer Res. 2002. PMID: 11948123

10

Evidence for a familial esophageal cancer susceptibility gene on chromosome 13.

Hu N, Goldstein AM, Albert PS, Giffen C, Tang ZZ, Ding T, Taylor PR, Emmert-Buck MR. Hu N, et al. Cancer Epidemiol Biomarkers Prev. 2003 Oct;12(10):1112-5. Cancer Epidemiol Biomarkers Prev. 2003. PMID: 14578153

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