These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

181 related articles for article (PubMed ID: 22143287)

  • 1. Genetic background of Prop1(df) mutants provides remarkable protection against hypothyroidism-induced hearing impairment.
    Fang Q; Giordimaina AM; Dolan DF; Camper SA; Mustapha M
    J Assoc Res Otolaryngol; 2012 Apr; 13(2):173-184. PubMed ID: 22143287
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants.
    Mustapha M; Fang Q; Gong TW; Dolan DF; Raphael Y; Camper SA; Duncan RK
    J Neurosci; 2009 Jan; 29(4):1212-23. PubMed ID: 19176829
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic variation in thyroid folliculogenesis influences susceptibility to hypothyroidism-induced hearing impairment.
    Mortensen AH; Fang Q; Fleming MT; Jones TJ; Daly AZ; Johnson KR; Camper SA
    Mamm Genome; 2019 Feb; 30(1-2):5-22. PubMed ID: 30778664
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Candidate genes for panhypopituitarism identified by gene expression profiling.
    Mortensen AH; MacDonald JW; Ghosh D; Camper SA
    Physiol Genomics; 2011 Oct; 43(19):1105-16. PubMed ID: 21828248
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice.
    Karolyi IJ; Dootz GA; Halsey K; Beyer L; Probst FJ; Johnson KR; Parlow AF; Raphael Y; Dolan DF; Camper SA
    Mamm Genome; 2007 Aug; 18(8):596-608. PubMed ID: 17899304
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A modifier gene alleviates hypothyroidism-induced hearing impairment in Pou1f1dw dwarf mice.
    Fang Q; Longo-Guess C; Gagnon LH; Mortensen AH; Dolan DF; Camper SA; Johnson KR
    Genetics; 2011 Oct; 189(2):665-73. PubMed ID: 21840860
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Thyroid hormone receptors TRalpha1 and TRbeta differentially regulate gene expression of Kcnq4 and prestin during final differentiation of outer hair cells.
    Winter H; Braig C; Zimmermann U; Geisler HS; Fränzer JT; Weber T; Ley M; Engel J; Knirsch M; Bauer K; Christ S; Walsh EJ; McGee J; Köpschall I; Rohbock K; Knipper M
    J Cell Sci; 2006 Jul; 119(Pt 14):2975-84. PubMed ID: 16803873
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Genetic background of inherited multiple pituitary hormone deficiency. Mutations of PROP1 gene in Hungary].
    Halász Z
    Orv Hetil; 2011 Feb; 152(6):221-32. PubMed ID: 21278027
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations in PROP1 cause familial combined pituitary hormone deficiency.
    Wu W; Cogan JD; Pfäffle RW; Dasen JS; Frisch H; O'Connell SM; Flynn SE; Brown MR; Mullis PE; Parks JS; Phillips JA; Rosenfeld MG
    Nat Genet; 1998 Feb; 18(2):147-9. PubMed ID: 9462743
    [TBL] [Abstract][Full Text] [Related]  

  • 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]  

  • 11. Identification of Novel PROP1 and POU1F1 Mutations in Patients with Combined Pituitary Hormone Deficiency.
    Birla S; Khadgawat R; Jyotsna VP; Jain V; Garg MK; Bhalla AS; Sharma A
    Horm Metab Res; 2016 Dec; 48(12):822-827. PubMed ID: 27756091
    [TBL] [Abstract][Full Text] [Related]  

  • 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]  

  • 16. Persistent Prop1 expression delays gonadotrope differentiation and enhances pituitary tumor susceptibility.
    Cushman LJ; Watkins-Chow DE; Brinkmeier ML; Raetzman LT; Radak AL; Lloyd RV; Camper SA
    Hum Mol Genet; 2001 May; 10(11):1141-53. PubMed ID: 11371507
    [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]
    of 10.