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10. PROP1, HESX1, POU1F1, LHX3 and LHX4 mutation and deletion screening and GH1 P89L and IVS3+1/+2 mutation screening in a Dutch nationwide cohort of patients with combined pituitary hormone deficiency. de Graaff LC; Argente J; Veenma DC; Drent ML; Uitterlinden AG; Hokken-Koelega AC Horm Res Paediatr; 2010; 73(5):363-71. PubMed ID: 20389107 [TBL] [Abstract][Full Text] [Related]
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12. W194XProp1 and S156insTProp1, both of which have intact DNA-binding domain, show a different DNA-binding activity to the Prop1-binding element in human Pit-1 gene. Shibahara H; Ikeshita N; Sugiyama Y; Toda K; Yamamoto D; Herningtyas EH; Maki T; Kubota E; Iguchi G; Iida K; Takahashi Y; Kaji H; Chihara K; Okimura Y Mol Cell Endocrinol; 2010 Jul; 323(2):167-71. PubMed ID: 20381582 [TBL] [Abstract][Full Text] [Related]
13. Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study. Baş F; Uyguner ZO; Darendeliler F; Aycan Z; Çetinkaya E; Berberoğlu M; Şiklar Z; Öcal G; Darcan Ş; Gökşen D; Topaloğlu AK; Yüksel B; Özbek MN; Ercan O; Evliyaoğlu O; Çetinkaya S; Şen Y; Atabek E; Toksoy G; Aydin BK; Bundak R Endocrine; 2015 Jun; 49(2):479-91. PubMed ID: 25500790 [TBL] [Abstract][Full Text] [Related]
14. Hearing impairment in hypothyroid dwarf mice caused by mutations of the thyroid peroxidase gene. Johnson KR; Gagnon LH; Longo-Guess CM; Harris BS; Chang B J Assoc Res Otolaryngol; 2014 Feb; 15(1):45-55. PubMed ID: 24297261 [TBL] [Abstract][Full Text] [Related]
15. Restoration of ion channel function in deafness-causing KCNQ4 mutants by synthetic channel openers. Leitner MG; Feuer A; Ebers O; Schreiber DN; Halaszovich CR; Oliver D Br J Pharmacol; 2012 Apr; 165(7):2244-59. PubMed ID: 21951272 [TBL] [Abstract][Full Text] [Related]
17. [From gene to disease; POU1F1- and PROP1-mutations in pituitary hormone deficiency]. Wit JM; Vulsma T; de Vijlder JJ Ned Tijdschr Geneeskd; 2001 Dec; 145(50):2425-7. PubMed ID: 11776668 [TBL] [Abstract][Full Text] [Related]
18. Inner Hair Cell and Neuron Degeneration Contribute to Hearing Loss in a DFNA2-Like Mouse Model. Carignano C; Barila EP; Rías EI; Dionisio L; Aztiria E; Spitzmaul G Neuroscience; 2019 Jul; 410():202-216. PubMed ID: 31102762 [TBL] [Abstract][Full Text] [Related]
19. Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency. Vieira TC; Boldarine VT; Abucham J Arq Bras Endocrinol Metabol; 2007 Oct; 51(7):1097-103. PubMed ID: 18157385 [TBL] [Abstract][Full Text] [Related]
20. Prestin-Dependence of Outer Hair Cell Survival and Partial Rescue of Outer Hair Cell Loss in PrestinV499G/Y501H Knockin Mice. Cheatham MA; Edge RM; Homma K; Leserman EL; Dallos P; Zheng J PLoS One; 2015; 10(12):e0145428. PubMed ID: 26682723 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]