79 related articles for article (PubMed ID: 11857914)
1. [Congenital central hypothyroidism due to the mutations of the thyrotropin-releasing hormone receptor gene].
Yamada M; Mori M
Nihon Rinsho; 2002 Feb; 60(2):277-83. PubMed ID: 11857914
[TBL] [Abstract][Full Text] [Related]
2. [TRH receptor].
Yamada M; Mori M
Nihon Rinsho; 1998 Jul; 56(7):1931-7. PubMed ID: 9702078
[TBL] [Abstract][Full Text] [Related]
3. A novel mechanism for isolated central hypothyroidism: inactivating mutations in the thyrotropin-releasing hormone receptor gene.
Collu R; Tang J; Castagné J; Lagacé G; Masson N; Huot C; Deal C; Delvin E; Faccenda E; Eidne KA; Van Vliet G
J Clin Endocrinol Metab; 1997 May; 82(5):1561-5. PubMed ID: 9141550
[TBL] [Abstract][Full Text] [Related]
4. The gene for the thyrotropin receptor (TSHR) as a candidate gene for congenital hypothyroidism with thyroid dysgenesis.
Krude H; Biebermann H; Göpel W; Grüters A
Exp Clin Endocrinol Diabetes; 1996; 104 Suppl 4():117-20. PubMed ID: 8981017
[TBL] [Abstract][Full Text] [Related]
5. Generation of thyrotropin-releasing hormone receptor 1-deficient mice as an animal model of central hypothyroidism.
Rabeler R; Mittag J; Geffers L; Rüther U; Leitges M; Parlow AF; Visser TJ; Bauer K
Mol Endocrinol; 2004 Jun; 18(6):1450-60. PubMed ID: 14988432
[TBL] [Abstract][Full Text] [Related]
6. Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes.
Camilot M; Teofoli F; Gandini A; Franceschi R; Rapa A; Corrias A; Bona G; Radetti G; Tatò L
Clin Endocrinol (Oxf); 2005 Aug; 63(2):146-51. PubMed ID: 16060907
[TBL] [Abstract][Full Text] [Related]
7. Central Hypothyroidism Due to a TRHR Mutation Causing Impaired Ligand Affinity and Transactivation of Gq.
García M; González de Buitrago J; Jiménez-Rosés M; Pardo L; Hinkle PM; Moreno JC
J Clin Endocrinol Metab; 2017 Jul; 102(7):2433-2442. PubMed ID: 28419241
[TBL] [Abstract][Full Text] [Related]
8. [Familial congenital hypothyroidism due to loss of function mutation of the thyrotropin receptor (resistance to thyrotropin)].
Matsushita A; Nakamura H
Nihon Rinsho; 2002 Feb; 60(2):284-90. PubMed ID: 11857915
[TBL] [Abstract][Full Text] [Related]
9. [Congenital TSH * PRL combined deficiency (TRH receptor gene mutation)].
Hashimoto K; Yamada M
Nihon Rinsho; 2006 May; Suppl 1():81-4. PubMed ID: 16776099
[No Abstract] [Full Text] [Related]
10. Central hypothyroidism: consequences in adult life.
Asteria C; Persani L; Beck-Peccoz P
J Pediatr Endocrinol Metab; 2001; 14 Suppl 5():1263-9; discussion 1297-8. PubMed ID: 11964021
[TBL] [Abstract][Full Text] [Related]
11. Familial Central Hypothyroidism Caused by a Novel IGSF1 Gene Mutation.
Tenenbaum-Rakover Y; Turgeon MO; London S; Hermanns P; Pohlenz J; Bernard DJ; Bercovich D
Thyroid; 2016 Dec; 26(12):1693-1700. PubMed ID: 27310681
[TBL] [Abstract][Full Text] [Related]
12. Transcription of the human thyrotropin-releasing hormone receptor gene-analysis of basal promoter elements and glucocorticoid response elements.
Høvring PI; Matre V; Fjeldheim AK; Loseth OP; Gautvik KM
Biochem Biophys Res Commun; 1999 Apr; 257(3):829-34. PubMed ID: 10208868
[TBL] [Abstract][Full Text] [Related]
13. Pituitary adenomas of patients with acromegaly express thyrotropin-releasing hormone receptor messenger RNA: cloning and functional expression of the human thyrotropin-releasing hormone receptor gene.
Yamada M; Monden T; Satoh T; Satoh N; Murakami M; Iriuchijima T; Kakegawa T; Mori M
Biochem Biophys Res Commun; 1993 Sep; 195(2):737-45. PubMed ID: 8396925
[TBL] [Abstract][Full Text] [Related]
14. Initially elevated TSH and congenital central hypothyroidism due to a homozygous mutation of the TSH beta subunit gene: case report and review of the literature.
Partsch CJ; Riepe FG; Krone N; Sippell WG; Pohlenz J
Exp Clin Endocrinol Diabetes; 2006 May; 114(5):227-34. PubMed ID: 16804796
[TBL] [Abstract][Full Text] [Related]
15. Congenital secondary hypothyroidism due to a mutation C105Vfs114X thyrotropin-beta mutation: genetic study of five unrelated families from Switzerland and Argentina.
Deladoëy J; Vuissoz JM; Domené HM; Malik N; Gruneiro-Papendieck L; Chiesa A; Heinrich JJ; Mullis PE
Thyroid; 2003 Jun; 13(6):553-9. PubMed ID: 12930599
[TBL] [Abstract][Full Text] [Related]
16. Congenital central hypothyroidism due to a homozygous mutation in the thyrotropin beta-subunit gene follows an autosomal recessive inheritance.
Doeker BM; Pfäffle RW; Pohlenz J; Andler W
J Clin Endocrinol Metab; 1998 May; 83(5):1762-5. PubMed ID: 9589689
[TBL] [Abstract][Full Text] [Related]
17. A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism.
Koulouri O; Nicholas AK; Schoenmakers E; Mokrosinski J; Lane F; Cole T; Kirk J; Farooqi IS; Chatterjee VK; Gurnell M; Schoenmakers N
J Clin Endocrinol Metab; 2016 Mar; 101(3):847-51. PubMed ID: 26735259
[TBL] [Abstract][Full Text] [Related]
18. [Cloning and characterization of the human thyrotropin-releasing hormone receptor: regulation of thyrotropin-releasing hormone receptor mRNA levels by thyroid hormone].
Yamada M; Mori M
Nihon Rinsho; 1994 Apr; 52(4):1001-6. PubMed ID: 8196161
[TBL] [Abstract][Full Text] [Related]
19. Screening for mutations of the human thyroid peroxidase gene in patients with congenital hypothyroidism.
Grüters A; Köhler B; Wolf A; Söling A; de Vijlder L; Krude H; Biebermann H
Exp Clin Endocrinol Diabetes; 1996; 104 Suppl 4():121-3. PubMed ID: 8981018
[TBL] [Abstract][Full Text] [Related]
20. Syndromes of hormone resistance in the hypothalamic-pituitary-thyroid axis.
Beck-Peccoz P; Persani L; Calebiro D; Bonomi M; Mannavola D; Campi I
Best Pract Res Clin Endocrinol Metab; 2006 Dec; 20(4):529-46. PubMed ID: 17161330
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
