PubMed (OMIM) for id: 761234

Year	Number of Results
1994	1
1995	3
1997	1
1998	5
1999	6
2000	5
2001	3
2002	3
2003	6
2004	2
2005	2
2024	0

1

Pendrin is a novel in vivo downstream target gene of the TTF-1/Nkx-2.1 homeodomain transcription factor in differentiated thyroid cells.

Dentice M, Luongo C, Elefante A, Ambrosio R, Salzano S, Zannini M, Nitsch R, Di Lauro R, Rossi G, Fenzi G, Salvatore D. Dentice M, et al. Mol Cell Biol. 2005 Nov;25(22):10171-82. doi: 10.1128/MCB.25.22.10171-10182.2005. Mol Cell Biol. 2005. PMID: 16260629 Free PMC article.

2

SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities.

Pryor SP, Madeo AC, Reynolds JC, Sarlis NJ, Arnos KS, Nance WE, Yang Y, Zalewski CK, Brewer CC, Butman JA, Griffith AJ. Pryor SP, et al. J Med Genet. 2005 Feb;42(2):159-65. doi: 10.1136/jmg.2004.024208. J Med Genet. 2005. PMID: 15689455 Free PMC article. No abstract available.

3

Intrafamilial variability of the deafness and goiter phenotype in Pendred syndrome caused by a T416P mutation in the SLC26A4 gene.

Napiontek U, Borck G, Müller-Forell W, Pfarr N, Bohnert A, Keilmann A, Pohlenz J. Napiontek U, et al. J Clin Endocrinol Metab. 2004 Nov;89(11):5347-51. doi: 10.1210/jc.2004-1013. J Clin Endocrinol Metab. 2004. PMID: 15531480

4

Distal renal tubular acidosis in mice that lack the forkhead transcription factor Foxi1.

Blomqvist SR, Vidarsson H, Fitzgerald S, Johansson BR, Ollerstam A, Brown R, Persson AE, Bergström G Gö, Enerbäck S. Blomqvist SR, et al. J Clin Invest. 2004 Jun;113(11):1560-70. doi: 10.1172/JCI20665. J Clin Invest. 2004. PMID: 15173882 Free PMC article.

5

Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese.

Tsukamoto K, Suzuki H, Harada D, Namba A, Abe S, Usami S. Tsukamoto K, et al. Eur J Hum Genet. 2003 Dec;11(12):916-22. doi: 10.1038/sj.ejhg.5201073. Eur J Hum Genet. 2003. PMID: 14508505

6

Screening the SLC26A4 gene in probands with deafness and goiter (Pendred syndrome) ascertained from a large group of students of the schools for the deaf in Turkey.

Tekin M, Akçayöz D, Comak E, Boğoçlu G, Duman T, Fitoz S, Ilhan I, Akar N. Tekin M, et al. Clin Genet. 2003 Oct;64(4):371-4. doi: 10.1034/j.1399-0004.2003.00144.x. Clin Genet. 2003. PMID: 12974744 No abstract available.

7

Solitary thyroid nodule as presenting symptom of Pendred syndrome caused by a novel splice-site mutation in intron 8 of the SLC26A4 gene.

Massa G, Jaenen N, de Varebeke SJ, Peeters N, Wuyts W. Massa G, et al. Eur J Pediatr. 2003 Oct;162(10):674-7. doi: 10.1007/s00431-003-1281-0. Epub 2003 Aug 15. Eur J Pediatr. 2003. PMID: 12920581

8

Mutations in the PDS gene in German families with Pendred's syndrome: V138F is a founder mutation.

Borck G, Roth C, Martiné U, Wildhardt G, Pohlenz J. Borck G, et al. J Clin Endocrinol Metab. 2003 Jun;88(6):2916-21. doi: 10.1210/jc.2002-021334. J Clin Endocrinol Metab. 2003. PMID: 12788906

9

PDS is a new susceptibility gene to autoimmune thyroid diseases: association and linkage study.

Hadj Kacem H, Rebai A, Kaffel N, Masmoudi S, Abid M, Ayadi H. Hadj Kacem H, et al. J Clin Endocrinol Metab. 2003 May;88(5):2274-80. doi: 10.1210/jc.2002-021460. J Clin Endocrinol Metab. 2003. PMID: 12727986

10

Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness.

Park HJ, Shaukat S, Liu XZ, Hahn SH, Naz S, Ghosh M, Kim HN, Moon SK, Abe S, Tukamoto K, Riazuddin S, Kabra M, Erdenetungalag R, Radnaabazar J, Khan S, Pandya A, Usami SI, Nance WE, Wilcox ER, Riazuddin S, Griffith AJ. Park HJ, et al. J Med Genet. 2003 Apr;40(4):242-8. doi: 10.1136/jmg.40.4.242. J Med Genet. 2003. PMID: 12676893 Free PMC article.

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