Meyn MS - Search Results

1

Gene for topoisomerase III maps within the Smith-Magenis syndrome critical region: analysis of cell-cycle distribution and radiation sensitivity.

Elsea SH, Fritz E, Schoener-Scott R, Meyn MS, Patel PI. Elsea SH, et al. Among authors: meyn ms. Am J Med Genet. 1998 Jan 6;75(1):104-8. Am J Med Genet. 1998. PMID: 9450867

2

Overexpression of a truncated human topoisomerase III partially corrects multiple aspects of the ataxia-telangiectasia phenotype.

Fritz E, Elsea SH, Patel PI, Meyn MS. Fritz E, et al. Among authors: meyn ms. Proc Natl Acad Sci U S A. 1997 Apr 29;94(9):4538-42. doi: 10.1073/pnas.94.9.4538. Proc Natl Acad Sci U S A. 1997. PMID: 9114025 Free PMC article.

3

TEL1 from Saccharomyces cerevisiae suppresses chromosome aberrations induced by ionizing radiation in ataxia-telangiectasia cells without affecting cell cycle checkpoints.

Cao JP, Meyn MS, Eckardt-Schupp F, Fritz E. Cao JP, et al. Among authors: meyn ms. Radiat Environ Biophys. 2001 Dec;40(4):309-15. doi: 10.1007/s00411-001-0125-4. Radiat Environ Biophys. 2001. PMID: 11820740

4

Human fibroblasts transfected with an ATM antisense vector respond abnormally to ionizing radiation.

Uhrhammer N, Fritz E, Boyden L, Meyn MS. Uhrhammer N, et al. Among authors: meyn ms. Int J Mol Med. 1999 Jul;4(1):43-7. doi: 10.3892/ijmm.4.1.43. Int J Mol Med. 1999. PMID: 10373636

5

The yeast TEL1 gene partially substitutes for human ATM in suppressing hyperrecombination, radiation-induced apoptosis and telomere shortening in A-T cells.

Fritz E, Friedl AA, Zwacka RM, Eckardt-Schupp F, Meyn MS. Fritz E, et al. Among authors: meyn ms. Mol Biol Cell. 2000 Aug;11(8):2605-16. doi: 10.1091/mbc.11.8.2605. Mol Biol Cell. 2000. PMID: 10930457 Free PMC article.

6

Recommendations for the integration of genomics into clinical practice.

Bowdin S, Gilbert A, Bedoukian E, Carew C, Adam MP, Belmont J, Bernhardt B, Biesecker L, Bjornsson HT, Blitzer M, D'Alessandro LC, Deardorff MA, Demmer L, Elliott A, Feldman GL, Glass IA, Herman G, Hindorff L, Hisama F, Hudgins L, Innes AM, Jackson L, Jarvik G, Kim R, Korf B, Ledbetter DH, Li M, Liston E, Marshall C, Medne L, Meyn MS, Monfared N, Morton C, Mulvihill JJ, Plon SE, Rehm H, Roberts A, Shuman C, Spinner NB, Stavropoulos DJ, Valverde K, Waggoner DJ, Wilkens A, Cohn RD, Krantz ID. Bowdin S, et al. Among authors: meyn ms. Genet Med. 2016 Nov;18(11):1075-1084. doi: 10.1038/gim.2016.17. Epub 2016 May 12. Genet Med. 2016. PMID: 27171546 Free PMC article. Review.

7

Velo-facio-skeletal syndrome in a mother and daughter.

Teebi AS, Qumsiyeh MB, Meyers-Seifer CH, Meyn MS. Teebi AS, et al. Among authors: meyn ms. Am J Med Genet. 1995 Jul 31;58(1):8-12. doi: 10.1002/ajmg.1320580103. Am J Med Genet. 1995. PMID: 7573161

8

Molecular and cytogenetic characterization of 9p- abnormalities.

Teebi AS, Gibson L, McGrath J, Meyn MS, Breg WR, Yang-Feng TL. Teebi AS, et al. Among authors: meyn ms. Am J Med Genet. 1993 May 15;46(3):288-92. doi: 10.1002/ajmg.1320460310. Am J Med Genet. 1993. PMID: 8488873

9

Molecular definition of the smallest region of deletion overlap in the Wolf-Hirschhorn syndrome.

Gandelman KY, Gibson L, Meyn MS, Yang-Feng TL. Gandelman KY, et al. Among authors: meyn ms. Am J Hum Genet. 1992 Sep;51(3):571-8. Am J Hum Genet. 1992. PMID: 1379774 Free PMC article.

10

Pseudo-trisomy 13 syndrome with upper limb shortness and radial hypoplasia.

Boles RG, Teebi AS, Neilson KA, Meyn MS. Boles RG, et al. Among authors: meyn ms. Am J Med Genet. 1992 Nov 15;44(5):638-40. doi: 10.1002/ajmg.1320440522. Am J Med Genet. 1992. PMID: 1481825

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