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Items: 7


Murine coagulation factor VIII is synthesized in endothelial cells.

Everett LA, Cleuren AC, Khoriaty RN, Ginsburg D.

Blood. 2014 Jun 12;123(24):3697-705. doi: 10.1182/blood-2014-02-554501. Epub 2014 Apr 9.


Macrophage invasion contributes to degeneration of stria vascularis in Pendred syndrome mouse model.

Jabba SV, Oelke A, Singh R, Maganti RJ, Fleming S, Wall SM, Everett LA, Green ED, Wangemann P.

BMC Med. 2006 Dec 22;4:37.


Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model.

Wangemann P, Itza EM, Albrecht B, Wu T, Jabba SV, Maganti RJ, Lee JH, Everett LA, Wall SM, Royaux IE, Green ED, Marcus DC.

BMC Med. 2004 Aug 20;2:30.


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.

J Assoc Res Otolaryngol. 2003 Sep;4(3):394-404.


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.

Proc Natl Acad Sci U S A. 2001 Mar 27;98(7):4221-6.


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.

J Med Genet. 1999 Jun;36(6):475-7.


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.

Proc Natl Acad Sci U S A. 1999 Aug 17;96(17):9727-32.

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