King MC - Search Results

1

Germline variants drive myelodysplastic syndrome in young adults.

Feurstein S, Churpek JE, Walsh T, Keel S, Hakkarainen M, Schroeder T, Germing U, Geyh S, Heuser M, Thol F, Pohlkamp C, Haferlach T, Gao J, Owen C, Goehring G, Schlegelberger B, Verma D, Krause DS, Gao G, Cronin T, Gulsuner S, Lee M, Pritchard CC, Subramanian HP, Del Gaudio D, Li Z, Das S, Kilpivaara O, Wartiovaara-Kautto U, Wang ES, Griffiths EA, Döhner K, Döhner H, King MC, Godley LA. Feurstein S, et al. Among authors: king mc. Leukemia. 2021 Aug;35(8):2439-2444. doi: 10.1038/s41375-021-01137-0. Epub 2021 Jan 28. Leukemia. 2021. PMID: 33510405 Free PMC article. No abstract available.

2

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. Among authors: king mc. 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

3

SeqHelp: a program to analyze molecular sequences utilizing common computational resources.

Lee MK, Lynch ED, King MC. Lee MK, et al. Among authors: king mc. Genome Res. 1998 Mar;8(3):306-12. doi: 10.1101/gr.8.3.306. Genome Res. 1998. PMID: 9521933 Free PMC article.

4

Single nucleotide polymorphisms (SNPs) in the estrogen receptor gene and breast cancer susceptibility.

Schubert EL, Lee MK, Newman B, King MC. Schubert EL, et al. Among authors: king mc. J Steroid Biochem Mol Biol. 1999 Nov;71(1-2):21-7. doi: 10.1016/s0960-0760(99)00126-0. J Steroid Biochem Mol Biol. 1999. PMID: 10619354

5

A novel sodium bicarbonate cotransporter-like gene in an ancient duplicated region: SLC4A9 at 5q31.

Lipovich L, Lynch ED, Lee MK, King MC. Lipovich L, et al. Among authors: king mc. Genome Biol. 2001;2(4):RESEARCH0011. doi: 10.1186/gb-2001-2-4-research0011. Epub 2001 Mar 22. Genome Biol. 2001. PMID: 11305939 Free PMC article.

6

From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30.

Walsh T, Walsh V, Vreugde S, Hertzano R, Shahin H, Haika S, Lee MK, Kanaan M, King MC, Avraham KB. Walsh T, et al. Among authors: king mc. Proc Natl Acad Sci U S A. 2002 May 28;99(11):7518-23. doi: 10.1073/pnas.102091699. Proc Natl Acad Sci U S A. 2002. PMID: 12032315 Free PMC article.

7

Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population.

Shaag A, Walsh T, Renbaum P, Kirchhoff T, Nafa K, Shiovitz S, Mandell JB, Welcsh P, Lee MK, Ellis N, Offit K, Levy-Lahad E, King MC. Shaag A, et al. Among authors: king mc. Hum Mol Genet. 2005 Feb 15;14(4):555-63. doi: 10.1093/hmg/ddi052. Epub 2005 Jan 13. Hum Mol Genet. 2005. PMID: 15649950

8

Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population.

Walsh T, Abu Rayan A, Abu Sa'ed J, Shahin H, Shepshelovich J, Lee MK, Hirschberg K, Tekin M, Salhab W, Avraham KB, King MC, Kanaan M. Walsh T, et al. Among authors: king mc. Hum Genomics. 2006 Jan;2(4):203-11. doi: 10.1186/1479-7364-2-4-203. Hum Genomics. 2006. PMID: 16460646 Free PMC article.

9

Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer.

Walsh T, Casadei S, Coats KH, Swisher E, Stray SM, Higgins J, Roach KC, Mandell J, Lee MK, Ciernikova S, Foretova L, Soucek P, King MC. Walsh T, et al. Among authors: king mc. JAMA. 2006 Mar 22;295(12):1379-88. doi: 10.1001/jama.295.12.1379. JAMA. 2006. PMID: 16551709

10

Ten genes for inherited breast cancer.

Walsh T, King MC. Walsh T, et al. Among authors: king mc. Cancer Cell. 2007 Feb;11(2):103-5. doi: 10.1016/j.ccr.2007.01.010. Cancer Cell. 2007. PMID: 17292821 Free article.

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