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 *

155 related articles for article (PubMed ID: 21423243)

  • 1. Autoimmunity: acquired versus inherited pituitary deficiency - same difference?
    Drouin J; Takayasu S
    Nat Rev Endocrinol; 2011 May; 7(5):255-6. PubMed ID: 21423243
    [No Abstract]   [Full Text] [Related]  

  • 2. Anti-PIT-1 antibody syndrome; a novel clinical entity leading to hypopituitarism.
    Bando H; Iguchi G; Yamamoto M; Hidaka-Takeno R; Takahashi Y
    Pediatr Endocrinol Rev; 2015 Mar; 12(3):290-6. PubMed ID: 25962206
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. Congenital hypopituitarism due to POU1F1 gene mutation.
    Lee NC; Tsai WY; Peng SF; Tung YC; Chien YH; Hwu WL
    J Formos Med Assoc; 2011 Jan; 110(1):58-61. PubMed ID: 21316014
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel mechanism of pituitary hormone deficiency: genetic variants shift splicing to produce a dominant negative transcription factor isoform.
    Brue T; Camper SA
    Eur J Endocrinol; 2021 Nov; 185(6):C19-C25. PubMed ID: 34597272
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Disorders of pituitary gland development].
    Migita O; Umezawa A
    Nihon Rinsho; 2006 May; Suppl 1():206-11. PubMed ID: 16776128
    [No Abstract]   [Full Text] [Related]  

  • 7. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. MECHANISMS IN ENDOCRINOLOGY: An update in the genetic aetiologies of combined pituitary hormone deficiency.
    Castinetti F; Reynaud R; Saveanu A; Jullien N; Quentien MH; Rochette C; Barlier A; Enjalbert A; Brue T
    Eur J Endocrinol; 2016 Jun; 174(6):R239-47. PubMed ID: 26733480
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic disorders of the pituitary.
    Cohen LE
    Curr Opin Endocrinol Diabetes Obes; 2012 Feb; 19(1):33-9. PubMed ID: 22157402
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The role of CBP/p300 interactions and Pit-1 dimerization in the pathophysiological mechanism of combined pituitary hormone deficiency.
    Cohen RN; Brue T; Naik K; Houlihan CA; Wondisford FE; Radovick S
    J Clin Endocrinol Metab; 2006 Jan; 91(1):239-47. PubMed ID: 16263824
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Lessons from monogenic causes of growth hormone deficiency.
    Brue T; Saveanu A; Jullien N; Fauquier T; Castinetti F; Enjalbert A; Barlier A; Reynaud R
    Ann Endocrinol (Paris); 2017 Jun; 78(2):77-79. PubMed ID: 28483366
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Clinical and genetic analysis of an infant with combined pituitary hormone deficiency due to POU1F1 gene variants].
    Li Q; Li J; Chang G; Ding Y; Wang Y; Shen Y; Wang J; Wang X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Sep; 37(9):1018-1020. PubMed ID: 32820520
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The molecular basis of hypopituitarism.
    Radovick S; Cohen LE; Wondisford FE
    Horm Res; 1998; 49 Suppl 1():30-6. PubMed ID: 9554467
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prospective investigation of pituitary functions in patients with acute infectious meningitis: is acute meningitis induced pituitary dysfunction associated with autoimmunity?
    Tanriverdi F; De Bellis A; Teksahin H; Alp E; Bizzarro A; Sinisi AA; Bellastella G; Paglionico VA; Bellastella A; Unluhizarci K; Doganay M; Kelestimur F
    Pituitary; 2012 Dec; 15(4):579-88. PubMed ID: 22228382
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification and functional analysis of the novel S179R POU1F1 mutation associated with combined pituitary hormone deficiency.
    Miyata I; Vallette-Kasic S; Saveanu A; Takeuchi M; Yoshikawa H; Tajima A; Tojo K; Reynaud R; Gueydan M; Enjalbert A; Tajima N; Eto Y; Brue T
    J Clin Endocrinol Metab; 2006 Dec; 91(12):4981-7. PubMed ID: 16968807
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel heterozygous intronic mutation in POU1F1 is associated with combined pituitary hormone deficiency.
    Takagi M; Kamasaki H; Yagi H; Fukuzawa R; Narumi S; Hasegawa T
    Endocr J; 2017 Feb; 64(2):229-234. PubMed ID: 27885216
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel germline mutation, IVS4+1G>A, of the POU1F1 gene underlying combined pituitary hormone deficiency.
    Snabboon T; Plengpanich W; Buranasupkajorn P; Khwanjaipanich R; Vasinanukorn P; Suwanwalaikorn S; Khovidhunkit W; Shotelersuk V
    Horm Res; 2008; 69(1):60-4. PubMed ID: 18059085
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular basis of pituitary development defects.
    Turki ZM; Hamaoui RB; Ben Slama C
    Tunis Med; 2007 Dec; 85(12):999-1003. PubMed ID: 19170376
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pituitary autoimmunity is associated with hypopituitarism in patients with primary empty sella.
    Lupi I; Manetti L; Raffaelli V; Grasso L; Sardella C; Cosottini M; Iannelli A; Gasperi M; Bogazzi F; Caturegli P; Martino E
    J Endocrinol Invest; 2011 Sep; 34(8):e240-4. PubMed ID: 21623153
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.