Glynn MW - Search Results

1

Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome.

Fang J, Dagenais SL, Erickson RP, Arlt MF, Glynn MW, Gorski JL, Seaver LH, Glover TW. Fang J, et al. Among authors: glynn mw. Am J Hum Genet. 2000 Dec;67(6):1382-8. doi: 10.1086/316915. Epub 2000 Nov 8. Am J Hum Genet. 2000. PMID: 11078474 Free PMC article.

2

Mutation of the FOXC2 gene in familial distichiasis.

Brooks BP, Dagenais SL, Nelson CC, Glynn MW, Caulder MS, Downs CA, Glover TW. Brooks BP, et al. Among authors: glynn mw. J AAPOS. 2003 Oct;7(5):354-7. doi: 10.1016/s1091-8531(03)00144-7. J AAPOS. 2003. PMID: 14566319

3

Incomplete processing of mutant lamin A in Hutchinson-Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition.

Glynn MW, Glover TW. Glynn MW, et al. Hum Mol Genet. 2005 Oct 15;14(20):2959-69. doi: 10.1093/hmg/ddi326. Epub 2005 Aug 26. Hum Mol Genet. 2005. PMID: 16126733

4

Stably transfected common fragile site sequences exhibit instability at ectopic sites.

Ragland RL, Glynn MW, Arlt MF, Glover TW. Ragland RL, et al. Among authors: glynn mw. Genes Chromosomes Cancer. 2008 Oct;47(10):860-72. doi: 10.1002/gcc.20591. Genes Chromosomes Cancer. 2008. PMID: 18615677 Free article.

5

Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.

Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P, Dutra A, Pak E, Durkin S, Csoka AB, Boehnke M, Glover TW, Collins FS. Eriksson M, et al. Among authors: glynn mw. Nature. 2003 May 15;423(6937):293-8. doi: 10.1038/nature01629. Epub 2003 Apr 25. Nature. 2003. PMID: 12714972 Free PMC article.

6

Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model.

Innis JW, Mortlock D, Chen Z, Ludwig M, Williams ME, Williams TM, Doyle CD, Shao Z, Glynn M, Mikulic D, Lehmann K, Mundlos S, Utsch B. Innis JW, et al. Hum Mol Genet. 2004 Nov 15;13(22):2841-51. doi: 10.1093/hmg/ddh306. Epub 2004 Sep 22. Hum Mol Genet. 2004. PMID: 15385446

7

Direct molecular diagnosis of multiple endocrine neoplasia type 1.

Petty EM, Glynn M, Bale AE. Petty EM, et al. Methods Mol Med. 2001;49:227-42. doi: 10.1385/1-59259-081-0:227. Methods Mol Med. 2001. PMID: 21370144

8

The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency.

Maestri NE, Lord C, Glynn M, Bale A, Brusilow SW. Maestri NE, et al. Medicine (Baltimore). 1998 Nov;77(6):389-97. Medicine (Baltimore). 1998. PMID: 9854602 Free article.

9

The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas.

Gailani MR, Ståhle-Bäckdahl M, Leffell DJ, Glynn M, Zaphiropoulos PG, Pressman C, Undén AB, Dean M, Brash DE, Bale AE, Toftgård R. Gailani MR, et al. Nat Genet. 1996 Sep;14(1):78-81. doi: 10.1038/ng0996-78. Nat Genet. 1996. PMID: 8782823

10

Uniform amplification of a mixture of deoxyribonucleic acids with varying GC content.

Baskaran N, Kandpal RP, Bhargava AK, Glynn MW, Bale A, Weissman SM. Baskaran N, et al. Among authors: glynn mw. Genome Res. 1996 Jul;6(7):633-8. doi: 10.1101/gr.6.7.633. Genome Res. 1996. PMID: 8796351 Free article.

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