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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.


Attitudes of Ghanaian women toward genetic testing for sickle cell trait.

Ross PT, Lypson ML, Ursu DC, Everett LA, Rodrigues O, Campbell AD.

Int J Gynaecol Obstet. 2011 Dec;115(3):264-8. doi: 10.1016/j.ijgo.2011.08.004. Epub 2011 Oct 8.


Reduced ENaC protein abundance contributes to the lower blood pressure observed in pendrin-null mice.

Kim YH, Pech V, Spencer KB, Beierwaltes WH, Everett LA, Green ED, Shin W, Verlander JW, Sutliff RL, Wall SM.

Am J Physiol Renal Physiol. 2007 Oct;293(4):F1314-24. Epub 2007 Aug 8.


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.


New insights into the role of pendrin (SLC26A4) in inner ear fluid homeostasis.

Everett LA.

Novartis Found Symp. 2006;273:213-25; discussion 225-30, 261-4.


Angiotensin II increases chloride absorption in the cortical collecting duct in mice through a pendrin-dependent mechanism.

Pech V, Kim YH, Weinstein AM, Everett LA, Pham TD, Wall SM.

Am J Physiol Renal Physiol. 2007 Mar;292(3):F914-20. Epub 2006 Oct 31.


Intercalated cell H+/OH- transporter expression is reduced in Slc26a4 null mice.

Kim YH, Verlander JW, Matthews SW, Kurtz I, Shin W, Weiner ID, Everett LA, Green ED, Nielsen S, Wall SM.

Am J Physiol Renal Physiol. 2005 Dec;289(6):F1262-72. Epub 2005 Sep 6.


NaCl restriction upregulates renal Slc26a4 through subcellular redistribution: role in Cl- conservation.

Wall SM, Kim YH, Stanley L, Glapion DM, Everett LA, Green ED, Verlander JW.

Hypertension. 2004 Dec;44(6):982-7. Epub 2004 Oct 11.


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.


Deoxycorticosterone upregulates PDS (Slc26a4) in mouse kidney: role of pendrin in mineralocorticoid-induced hypertension.

Verlander JW, Hassell KA, Royaux IE, Glapion DM, Wang ME, Everett LA, Green ED, Wall SM.

Hypertension. 2003 Sep;42(3):356-62. Epub 2003 Aug 18.


Formate-stimulated NaCl absorption in the proximal tubule is independent of the pendrin protein.

Karniski LP, Wang T, Everett LA, Green ED, Giebisch G, Aronson PS.

Am J Physiol Renal Physiol. 2002 Nov;283(5):F952-6.


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.

J Clin Endocrinol Metab. 2002 Feb;87(2):938.


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.


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.

Hum Mol Genet. 2001 Jan 15;10(2):153-61.


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.


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

Wilcox ER, Everett LA, Li XC, Lalwani AK, Green ED.

Adv Otorhinolaryngol. 2000;56:145-51. Review. No abstract available.


Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells.

Royaux IE, Suzuki K, Mori A, Katoh R, Everett LA, Kohn LD, Green ED.

Endocrinology. 2000 Feb;141(2):839-45.


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

Everett LA, Green ED.

Hum Mol Genet. 1999;8(10):1883-91. Review.


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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