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 *

50 related articles for article (PubMed ID: 9758716)

  • 21. ACTH resistance syndromes.
    Huebner A; Elias LL; Clark AJ
    J Pediatr Endocrinol Metab; 1999 Apr; 12 Suppl 1():277-93. PubMed ID: 10698592
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Adrenocorticotropin receptor in familial glucocorticoid deficiency].
    Takayanagi R; Sakai Y; Nawata H; Nishiyama S; Ito T; Kodama M; Matsuda I; Matsuda H
    Nihon Rinsho; 1993 Oct; 51(10):2643-8. PubMed ID: 8254933
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Familial glucocorticoid deficiency due to the ACTH receptor gene mutations].
    Katsumata N
    Nihon Rinsho; 2002 Feb; 60(2):260-4. PubMed ID: 11857911
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [ACTH receptor, ACTH receptor anomaly, and familial glucocorticoid deficiency].
    Fukata J; Li CL; Saibara T; Onishi S
    Nihon Rinsho; 1998 Jul; 56(7):1836-42. PubMed ID: 9702062
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Isolated glucocorticoid deficiency and ACTH receptor mutations.
    Tsigos C
    Arch Med Res; 1999; 30(6):475-80. PubMed ID: 10714360
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The molecular basis of adrenocorticotrophin resistance syndrome.
    Elias LL; Clark AL
    Prog Mol Biol Transl Sci; 2009; 88():155-71. PubMed ID: 20374727
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Familial glucocorticoid deficiency].
    Mazur A; Ostański M; Kalina M
    Pediatr Endocrinol Diabetes Metab; 2007; 13(2):91-4. PubMed ID: 17880814
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The molecular pathogenesis of ACTH insensitivity syndromes.
    Clark AJ; Metherell L; Swords FM; Elias LL
    Ann Endocrinol (Paris); 2001 Apr; 62(2):207-11. PubMed ID: 11353896
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Inherited ACTH insensitivity illuminates the mechanisms of ACTH action.
    Clark AJ; Metherell LA; Cheetham ME; Huebner A
    Trends Endocrinol Metab; 2005 Dec; 16(10):451-7. PubMed ID: 16271481
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Advances in the understanding of the genetic basis of adrenal insufficiency.
    Storr HL; Savage MO; Clark AJ
    J Pediatr Endocrinol Metab; 2002 Dec; 15 Suppl 5():1323-8. PubMed ID: 12510986
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mechanisms of disease: the adrenocorticotropin receptor and disease.
    Clark AJ; Metherell LA
    Nat Clin Pract Endocrinol Metab; 2006 May; 2(5):282-90. PubMed ID: 16932299
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [ACTH resistance syndromes].
    Naville D; Penhoat A; Bégeot M
    Ann Endocrinol (Paris); 2000 Nov; 61(5):428-39. PubMed ID: 11084394
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Adrenocorticotropin receptor and adrenal disorders.
    Allolio B; Reincke M
    Horm Res; 1997; 47(4-6):273-8. PubMed ID: 9167964
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The genetics of ACTH resistance syndromes.
    Metherell LA; Chan LF; Clark AJ
    Best Pract Res Clin Endocrinol Metab; 2006 Dec; 20(4):547-60. PubMed ID: 17161331
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Familial glucocorticoid deficiency: one syndrome, but more than one gene.
    Clark AJ; Cammas FM; Watt A; Kapas S; Weber A
    J Mol Med (Berl); 1997 Jun; 75(6):394-9. PubMed ID: 9231879
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Isolated glucocorticoid deficiency: Genetic causes and animal models.
    Maharaj A; Maudhoo A; Chan LF; Novoselova T; Prasad R; Metherell LA; Guasti L
    J Steroid Biochem Mol Biol; 2019 May; 189():73-80. PubMed ID: 30817990
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A novel homozygous insertion and review of published mutations in the NNT gene causing familial glucocorticoid deficiency (FGD).
    Jazayeri O; Liu X; van Diemen CC; Bakker-van Waarde WM; Sikkema-Raddatz B; Sinke RJ; Zhang J; van Ravenswaaij-Arts CM
    Eur J Med Genet; 2015 Dec; 58(12):642-9. PubMed ID: 26548497
    [TBL] [Abstract][Full Text] [Related]  

  • 38. ACTH Receptor (MC2R) Specificity: What Do We Know About Underlying Molecular Mechanisms?
    Fridmanis D; Roga A; Klovins J
    Front Endocrinol (Lausanne); 2017; 8():13. PubMed ID: 28220105
    [TBL] [Abstract][Full Text] [Related]  

  • 39. ACTH resistance: genes and mechanisms.
    Meimaridou E; Hughes CR; Kowalczyk J; Chan LF; Clark AJ; Metherell LA
    Endocr Dev; 2013; 24():57-66. PubMed ID: 23392095
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Disorders of adrenal development.
    Ferraz-de-Souza B; Achermann JC
    Endocr Dev; 2008; 13():19-32. PubMed ID: 18493131
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 3.