Green ED - Search Results

1

The PDS gene, Pendred syndrome and non-syndromic deafness DFNB4.

Wilcox ER, Everett LA, Li XC, Lalwani AK, Green ED. Wilcox ER, et al. Among authors: green ed. Adv Otorhinolaryngol. 2000;56:145-51. doi: 10.1159/000059088. Adv Otorhinolaryngol. 2000. PMID: 10868226 Review. No abstract available.

2

Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear.

Everett LA, Morsli H, Wu DK, Green ED. Everett LA, et al. Among authors: green ed. Proc Natl Acad Sci U S A. 1999 Aug 17;96(17):9727-32. doi: 10.1073/pnas.96.17.9727. Proc Natl Acad Sci U S A. 1999. PMID: 10449762 Free PMC article.

3

Expression of PDS/Pds, the Pendred syndrome gene, in endometrium.

Suzuki K, Royaux IE, Everett LA, Mori-Aoki A, Suzuki S, Nakamura K, Sakai T, Katoh R, Toda S, Green ED, Kohn LD. Suzuki K, et al. Among authors: green ed. J Clin Endocrinol Metab. 2002 Feb;87(2):938. doi: 10.1210/jcem.87.2.8390. J Clin Endocrinol Metab. 2002. PMID: 11836344

4

Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome.

Royaux IE, Belyantseva IA, Wu T, Kachar B, Everett LA, Marcus DC, Green ED. Royaux IE, et al. Among authors: green ed. J Assoc Res Otolaryngol. 2003 Sep;4(3):394-404. doi: 10.1007/s10162-002-3052-4. J Assoc Res Otolaryngol. 2003. PMID: 14690057 Free PMC article.

5

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS).

Everett LA, Glaser B, Beck JC, Idol JR, Buchs A, Heyman M, Adawi F, Hazani E, Nassir E, Baxevanis AD, Sheffield VC, Green ED. Everett LA, et al. Among authors: green ed. Nat Genet. 1997 Dec;17(4):411-22. doi: 10.1038/ng1297-411. Nat Genet. 1997. PMID: 9398842

6

A mutation in PDS causes non-syndromic recessive deafness.

Li XC, Everett LA, Lalwani AK, Desmukh D, Friedman TB, Green ED, Wilcox ER. Li XC, et al. Among authors: green ed. Nat Genet. 1998 Mar;18(3):215-7. doi: 10.1038/ng0398-215. Nat Genet. 1998. PMID: 9500541 No abstract available.

7

A family of mammalian anion transporters and their involvement in human genetic diseases.

Everett LA, Green ED. Everett LA, et al. Among authors: green ed. Hum Mol Genet. 1999;8(10):1883-91. doi: 10.1093/hmg/8.10.1883. Hum Mol Genet. 1999. PMID: 10469841 Review.

8

Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome.

Coucke PJ, Van Hauwe P, Everett LA, Demirhan O, Kabakkaya Y, Dietrich NL, Smith RJ, Coyle E, Reardon W, Trembath R, Willems PJ, Green ED, Van Camp G. Coucke PJ, et al. Among authors: green ed. J Med Genet. 1999 Jun;36(6):475-7. J Med Genet. 1999. PMID: 10874637 Free PMC article.

9

Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome.

Everett LA, Belyantseva IA, Noben-Trauth K, Cantos R, Chen A, Thakkar SI, Hoogstraten-Miller SL, Kachar B, Wu DK, Green ED. Everett LA, et al. Among authors: green ed. Hum Mol Genet. 2001 Jan 15;10(2):153-61. doi: 10.1093/hmg/10.2.153. Hum Mol Genet. 2001. PMID: 11152663

10

Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion.

Royaux IE, Wall SM, Karniski LP, Everett LA, Suzuki K, Knepper MA, Green ED. Royaux IE, et al. Among authors: green ed. Proc Natl Acad Sci U S A. 2001 Mar 27;98(7):4221-6. doi: 10.1073/pnas.071516798. Proc Natl Acad Sci U S A. 2001. PMID: 11274445 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

339 results

Search Page

Filters