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Journal Abstract Search

279 related items for PubMed ID: 14561704

  • 21.
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  • 22. Novel Mutations in HESX1 and PROP1 Genes in Combined Pituitary Hormone Deficiency.
    Avbelj Stefanija M, Kotnik P, Bratanič N, Žerjav Tanšek M, Bertok S, Bratina N, Battelino T, Trebušak Podkrajšek K.
    Horm Res Paediatr; 2015; 84(3):153-8. PubMed ID: 26111865
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  • 23.
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  • 24. 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
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  • 26. Growth without growth hormone and similar dysmorphic features in three patients with sporadic combined pituitary hormone deficiencies.
    Gat-Yablonski G, Lazar L, Bar M, de Vries L, Weintrob N, Phillip M.
    Horm Res; 2009 Oct; 72(5):302-9. PubMed ID: 19844116
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  • 27. Alu-element insertion in the homeodomain of HESX1 and aplasia of the anterior pituitary.
    Sobrier ML, Netchine I, Heinrichs C, Thibaud N, Vié-Luton MP, Van Vliet G, Amselem S.
    Hum Mutat; 2005 May; 25(5):503. PubMed ID: 15841484
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  • 28. Growth hormone deficiency and combined pituitary hormone deficiency: does the genotype matter?
    Dattani MT.
    Clin Endocrinol (Oxf); 2005 Aug; 63(2):121-30. PubMed ID: 16060904
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  • 30. [Clinical and genetic aspects of combined pituitary hormone deficiencies].
    Castinetti F, Reynaud R, Saveanu A, Quentien MH, Albarel F, Barlier A, Enjalbert A, Brue T.
    Ann Endocrinol (Paris); 2008 Feb; 69(1):7-17. PubMed ID: 18291347
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  • 31.
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  • 32. Genetic defects in the development and function of the anterior pituitary gland.
    Cushman LJ, Showalter AD, Rhodes SJ.
    Ann Med; 2002 Feb; 34(3):179-91. PubMed ID: 12173688
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  • 33.
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  • 34. A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency.
    Diaczok D, Romero C, Zunich J, Marshall I, Radovick S.
    J Clin Endocrinol Metab; 2008 Nov; 93(11):4351-9. PubMed ID: 18728160
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  • 35. LHX3 and LHX4 transcription factors in pituitary development and disease.
    Colvin SC, Mullen RD, Pfaeffle RW, Rhodes SJ.
    Pediatr Endocrinol Rev; 2009 Jan; 6 Suppl 2():283-90. PubMed ID: 19337183
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  • 36.
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  • 37. HESX1- and TCF3-mediated repression of Wnt/β-catenin targets is required for normal development of the anterior forebrain.
    Andoniadou CL, Signore M, Young RM, Gaston-Massuet C, Wilson SW, Fuchs E, Martinez-Barbera JP.
    Development; 2011 Nov; 138(22):4931-42. PubMed ID: 22007134
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  • 38. Combined Pituitary Hormone Deficiency Caused by a Synonymous HESX1 Gene Mutation.
    Coutinho E, Brandão CM, Lemos MC.
    J Clin Endocrinol Metab; 2019 Jul 01; 104(7):2851-2854. PubMed ID: 30888394
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  • 39. Inhibition of cortical neuron differentiation by Groucho/TLE1 requires interaction with WRPW, but not Eh1, repressor peptides.
    Buscarlet M, Perin A, Laing A, Brickman JM, Stifani S.
    J Biol Chem; 2008 Sep 05; 283(36):24881-8. PubMed ID: 18611861
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  • 40. Pituitary hormone deficiencies due to transcription factor gene alterations.
    Reynaud R, Saveanu A, Barlier A, Enjalbert A, Brue T.
    Growth Horm IGF Res; 2004 Dec 05; 14(6):442-8. PubMed ID: 15519252
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