Lee MK - Search Results

1

Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome.

Pierce SB, Walsh T, Chisholm KM, Lee MK, Thornton AM, Fiumara A, Opitz JM, Levy-Lahad E, Klevit RE, King MC. Pierce SB, et al. Among authors: lee mk. Am J Hum Genet. 2010 Aug 13;87(2):282-8. doi: 10.1016/j.ajhg.2010.07.007. Epub 2010 Jul 30. Am J Hum Genet. 2010. PMID: 20673864 Free PMC article.

2

Closing in on a breast cancer gene on chromosome 17q.

Hall JM, Friedman L, Guenther C, Lee MK, Weber JL, Black DM, King MC. Hall JM, et al. Among authors: lee mk. Am J Hum Genet. 1992 Jun;50(6):1235-42. Am J Hum Genet. 1992. PMID: 1598904 Free PMC article.

3

Complex segregation analysis of primary hepatocellular carcinoma in Chinese families: interaction of inherited susceptibility and hepatitis B viral infection.

Shen FM, Lee MK, Gong HM, Cai XQ, King MC. Shen FM, et al. Among authors: lee mk. Am J Hum Genet. 1991 Jul;49(1):88-93. Am J Hum Genet. 1991. PMID: 1648308 Free PMC article.

4

Possible linkage of the estrogen receptor gene to breast cancer in a family with late-onset disease.

Zuppan P, Hall JM, Lee MK, Ponglikitmongkol M, King MC. Zuppan P, et al. Among authors: lee mk. Am J Hum Genet. 1991 Jun;48(6):1065-8. Am J Hum Genet. 1991. PMID: 2035527 Free PMC article.

5

Novel inherited mutations and variable expressivity of BRCA1 alleles, including the founder mutation 185delAG in Ashkenazi Jewish families.

Friedman LS, Szabo CI, Ostermeyer EA, Dowd P, Butler L, Park T, Lee MK, Goode EL, Rowell SE, King MC. Friedman LS, et al. Among authors: lee mk. Am J Hum Genet. 1995 Dec;57(6):1284-97. Am J Hum Genet. 1995. PMID: 8533757 Free PMC article.

6

Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1.

Smith TM, Lee MK, Szabo CI, Jerome N, McEuen M, Taylor M, Hood L, King MC. Smith TM, et al. Among authors: lee mk. Genome Res. 1996 Nov;6(11):1029-49. doi: 10.1101/gr.6.11.1029. Genome Res. 1996. PMID: 8938427 Free article.

7

BRCA2 in American families with four or more cases of breast or ovarian cancer: recurrent and novel mutations, variable expression, penetrance, and the possibility of families whose cancer is not attributable to BRCA1 or BRCA2.

Schubert EL, Lee MK, Mefford HC, Argonza RH, Morrow JE, Hull J, Dann JL, King MC. Schubert EL, et al. Among authors: lee mk. Am J Hum Genet. 1997 May;60(5):1031-40. Am J Hum Genet. 1997. PMID: 9150150 Free PMC article.

8

Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous.

Lynch ED, Lee MK, Morrow JE, Welcsh PL, León PE, King MC. Lynch ED, et al. Among authors: lee mk. Science. 1997 Nov 14;278(5341):1315-8. Science. 1997. PMID: 9360932

9

Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis.

Lynch ED, Ostermeyer EA, Lee MK, Arena JF, Ji H, Dann J, Swisshelm K, Suchard D, MacLeod PM, Kvinnsland S, Gjertsen BT, Heimdal K, Lubs H, Møller P, King MC. Lynch ED, et al. Among authors: lee mk. Am J Hum Genet. 1997 Dec;61(6):1254-60. doi: 10.1086/301639. Am J Hum Genet. 1997. PMID: 9399897 Free PMC article.

10

Long terminal repeat and nef gene variants of human immunodeficiency virus type 1 in perinatally infected long-term survivors and rapid progressors.

Rousseau C, Abrams E, Lee M, Urbano R, King MC. Rousseau C, et al. AIDS Res Hum Retroviruses. 1997 Dec 10;13(18):1611-23. doi: 10.1089/aid.1997.13.1611. AIDS Res Hum Retroviruses. 1997. PMID: 9430253

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