Lee MK - Search Results

1

Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity.

Zhang MY, Keel SB, Walsh T, Lee MK, Gulsuner S, Watts AC, Pritchard CC, Salipante SJ, Jeng MR, Hofmann I, Williams DA, Fleming MD, Abkowitz JL, King MC, Shimamura A. Zhang MY, et al. Among authors: lee mk. Haematologica. 2015 Jan;100(1):42-8. doi: 10.3324/haematol.2014.113456. Epub 2014 Sep 19. Haematologica. 2015. PMID: 25239263 Free PMC article.

2

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.

3

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.

4

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

5

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.

6

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

7

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

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

8

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: lee mk. 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

9

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: lee mk. 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.

10

Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1.

Young TL, Ives E, Lynch E, Person R, Snook S, MacLaren L, Cater T, Griffin A, Fernandez B, Lee MK, King MC. Young TL, et al. Among authors: lee mk. Hum Mol Genet. 2001 Oct 15;10(22):2509-14. doi: 10.1093/hmg/10.22.2509. Hum Mol Genet. 2001. PMID: 11709538

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