Goldberg YP - Search Results

1

Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations.

Goldberg YP, MacFarlane J, MacDonald ML, Thompson J, Dube MP, Mattice M, Fraser R, Young C, Hossain S, Pape T, Payne B, Radomski C, Donaldson G, Ives E, Cox J, Younghusband HB, Green R, Duff A, Boltshauser E, Grinspan GA, Dimon JH, Sibley BG, Andria G, Toscano E, Kerdraon J, Bowsher D, Pimstone SN, Samuels ME, Sherrington R, Hayden MR. Goldberg YP, et al. Clin Genet. 2007 Apr;71(4):311-9. doi: 10.1111/j.1399-0004.2007.00790.x. Clin Genet. 2007. PMID: 17470132

2

Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes.

Kremer B, Almqvist E, Theilmann J, Spence N, Telenius H, Goldberg YP, Hayden MR. Kremer B, et al. Among authors: goldberg yp. Am J Hum Genet. 1995 Aug;57(2):343-50. Am J Hum Genet. 1995. PMID: 7668260 Free PMC article.

3

Structural analysis of the 5' region of mouse and human Huntington disease genes reveals conservation of putative promoter region and di- and trinucleotide polymorphisms.

Lin B, Nasir J, Kalchman MA, McDonald H, Zeisler J, Goldberg YP, Hayden MR. Lin B, et al. Among authors: goldberg yp. Genomics. 1995 Feb 10;25(3):707-15. doi: 10.1016/0888-7543(95)80014-d. Genomics. 1995. PMID: 7759106

4

Genomic organization of the human alpha-adducin gene and its alternately spliced isoforms.

Lin B, Nasir J, McDonald H, Graham R, Rommens JM, Goldberg YP, Hayden MR. Lin B, et al. Among authors: goldberg yp. Genomics. 1995 Jan 1;25(1):93-9. doi: 10.1016/0888-7543(95)80113-z. Genomics. 1995. PMID: 7774961

5

Differential 3' polyadenylation of the Huntington disease gene results in two mRNA species with variable tissue expression.

Lin B, Rommens JM, Graham RK, Kalchman M, MacDonald H, Nasir J, Delaney A, Goldberg YP, Hayden MR. Lin B, et al. Among authors: goldberg yp. Hum Mol Genet. 1993 Oct;2(10):1541-5. doi: 10.1093/hmg/2.10.1541. Hum Mol Genet. 1993. PMID: 7903579

6

The molecular genetics of Huntington's disease.

Goldberg YP, Telenius H, Hayden MR. Goldberg YP, et al. Curr Opin Neurol. 1994 Aug;7(4):325-32. doi: 10.1097/00019052-199408000-00009. Curr Opin Neurol. 1994. PMID: 7952241 Review.

7

Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm.

Telenius H, Kremer B, Goldberg YP, Theilmann J, Andrew SE, Zeisler J, Adam S, Greenberg C, Ives EJ, Clarke LA, et al. Telenius H, et al. Among authors: goldberg yp. Nat Genet. 1994 Apr;6(4):409-14. doi: 10.1038/ng0494-409. Nat Genet. 1994. PMID: 8054984

8

Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic cases.

Goldberg YP, Andrew SE, Theilmann J, Kremer B, Squitieri F, Telenius H, Brown JD, Hayden MR. Goldberg YP, et al. J Med Genet. 1993 Dec;30(12):987-90. doi: 10.1136/jmg.30.12.987. J Med Genet. 1993. PMID: 8133509 Free PMC article.

9

Molecular analysis of late onset Huntington's disease.

Kremer B, Squitieri F, Telenius H, Andrew SE, Theilmann J, Spence N, Goldberg YP, Hayden MR. Kremer B, et al. Among authors: goldberg yp. J Med Genet. 1993 Dec;30(12):991-5. doi: 10.1136/jmg.30.12.991. J Med Genet. 1993. PMID: 8133510 Free PMC article.

10

A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing.

Andrew SE, Goldberg YP, Theilmann J, Zeisler J, Hayden MR. Andrew SE, et al. Among authors: goldberg yp. Hum Mol Genet. 1994 Jan;3(1):65-7. doi: 10.1093/hmg/3.1.65. Hum Mol Genet. 1994. PMID: 8162053

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