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kw.\*:("Gène SLC26A4")

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The expression of wild-type pendrin (SLC26A4) in human embryonic kidney (HEK 293 Phoenix) cells leads to the activation of cationic currentsDOSSENA, Silvia; MACCAGNI, Antonella; ZOROWKA, Patrick et al.European journal of endocrinology. 2005, Vol 153, Num 5, pp 693-699, issn 0804-4643, 7 p.Article

Goitrous congenital hypothyroidism and hearing impairment associated with mutations in the TPO and SLC26A4/PDS genesPFARR, Nicole; BORCK, Guntram; TURK, Andrew et al.The Journal of clinical endocrinology and metabolism. 2006, Vol 91, Num 7, pp 2678-2681, issn 0021-972X, 4 p.Article

Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairmentKAHRIZI, Kimia; MOHSENI, Marzieh; AZIZI, Fereydoun et al.European journal of pediatrics. 2009, Vol 168, Num 6, pp 651-653, issn 0340-6199, 3 p.Article

Intrafamilial variability of the deafness and goiter phenotype in pendred syndrome caused by a T416P mutation in the SLC26A4 geneNAPIONTEK, Ulrike; BORCK, Guntram; MÜLLER-FORELL, Wiebke et al.The Journal of clinical endocrinology and metabolism. 2004, Vol 89, Num 11, pp 5347-5351, issn 0021-972X, 5 p.Article

High phenotypic intrafamilial variability in patients with Pendred syndrome and a novel duplication in the SLC26A4 gene : clinical characterization and functional studies of the mutated SLC26A4 proteinFUGAZZOLA, Laura; CIRELLO, Valentina; PAULMICHL, Markus et al.European journal of endocrinology. 2007, Vol 157, Num 3, pp 331-338, issn 0804-4643, 8 p.Article

Pendred syndrome among patients with congenital hypothyroidism detected by neonatal screening : identification of two novel PDS/SLC26A4 mutationsBANGHOVA, Karolina; AL TAJI, Eva; CINEK, Ondrej et al.European journal of pediatrics. 2008, Vol 167, Num 7, pp 777-783, issn 0340-6199, 7 p.Article

Hypermethylation of the Pendred syndrome gene SLC26A4 is an early event in thyroid tumorigenesisXING, Mingzhao; TOKUMARU, Yutaka; WU, Guojun et al.Cancer research (Baltimore). 2003, Vol 63, Num 9, pp 2312-2315, issn 0008-5472, 4 p.Article

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