King MC - Search Results

1

Mapping the functional domains of BRCA1. Interaction of the ring finger domains of BRCA1 and BARD1.

Meza JE, Brzovic PS, King MC, Klevit RE. Meza JE, et al. Among authors: king mc. J Biol Chem. 1999 Feb 26;274(9):5659-65. doi: 10.1074/jbc.274.9.5659. J Biol Chem. 1999. PMID: 10026184 Free article.

2

Human, canine and murine BRCA1 genes: sequence comparison among species.

Szabo CI, Wagner LA, Francisco LV, Roach JC, Argonza R, King MC, Ostrander EA. Szabo CI, et al. Among authors: king mc. Hum Mol Genet. 1996 Sep;5(9):1289-98. doi: 10.1093/hmg/5.9.1289. Hum Mol Genet. 1996. PMID: 8872468

3

The cancer-predisposing mutation C61G disrupts homodimer formation in the NH2-terminal BRCA1 RING finger domain.

Brzovic PS, Meza J, King MC, Klevit RE. Brzovic PS, et al. Among authors: king mc. J Biol Chem. 1998 Apr 3;273(14):7795-9. doi: 10.1074/jbc.273.14.7795. J Biol Chem. 1998. PMID: 9525870 Free article.

4

Insights into the functions of BRCA1 and BRCA2.

Welcsh PL, Owens KN, King MC. Welcsh PL, et al. Among authors: king mc. Trends Genet. 2000 Feb;16(2):69-74. doi: 10.1016/s0168-9525(99)01930-7. Trends Genet. 2000. PMID: 10652533 Review.

5

BRCA1 RING domain cancer-predisposing mutations. Structural consequences and effects on protein-protein interactions.

Brzovic PS, Meza JE, King MC, Klevit RE. Brzovic PS, et al. Among authors: king mc. J Biol Chem. 2001 Nov 2;276(44):41399-406. doi: 10.1074/jbc.M106551200. Epub 2001 Aug 28. J Biol Chem. 2001. PMID: 11526114 Free article.

6

Structure of a BRCA1-BARD1 heterodimeric RING-RING complex.

Brzovic PS, Rajagopal P, Hoyt DW, King MC, Klevit RE. Brzovic PS, et al. Among authors: king mc. Nat Struct Biol. 2001 Oct;8(10):833-7. doi: 10.1038/nsb1001-833. Nat Struct Biol. 2001. PMID: 11573085

7

Functional characterization of a novel BRCA1-null ovarian cancer cell line in response to ionizing radiation.

DelloRusso C, Welcsh PL, Wang W, Garcia RL, King MC, Swisher EM. DelloRusso C, et al. Among authors: king mc. Mol Cancer Res. 2007 Jan;5(1):35-45. doi: 10.1158/1541-7786.MCR-06-0234. Mol Cancer Res. 2007. PMID: 17259345 Free article.

8

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: king mc. 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.

9

Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome.

Pierce SB, Chisholm KM, Lynch ED, Lee MK, Walsh T, Opitz JM, Li W, Klevit RE, King MC. Pierce SB, et al. Among authors: king mc. Proc Natl Acad Sci U S A. 2011 Apr 19;108(16):6543-8. doi: 10.1073/pnas.1103471108. Epub 2011 Apr 4. Proc Natl Acad Sci U S A. 2011. PMID: 21464306 Free PMC article.

10

Mutations in LARS2, encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome.

Pierce SB, Gersak K, Michaelson-Cohen R, Walsh T, Lee MK, Malach D, Klevit RE, King MC, Levy-Lahad E. Pierce SB, et al. Among authors: king mc. Am J Hum Genet. 2013 Apr 4;92(4):614-20. doi: 10.1016/j.ajhg.2013.03.007. Epub 2013 Mar 28. Am J Hum Genet. 2013. PMID: 23541342 Free PMC article.

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