123 related articles for article (PubMed ID: 8077354)
1. Impaired intracellular transport contributes to partial thyroxine-binding globulin deficiency in a Japanese family.
Miura Y; Mori Y; Kambe F; Tani Y; Oiso Y; Seo H
J Clin Endocrinol Metab; 1994 Sep; 79(3):740-4. PubMed ID: 8077354
[TBL] [Abstract][Full Text] [Related]
2. A truncated thyroxine-binding globulin due to a frameshift mutation is retained within the rough endoplasmic reticulum: a possible mechanism of complete thyroxine-binding globulin deficiency in Japanese.
Miura Y; Kambe F; Yamamori I; Mori Y; Tani Y; Murata Y; Oiso Y; Seo H
J Clin Endocrinol Metab; 1994 Feb; 78(2):283-7. PubMed ID: 8106612
[TBL] [Abstract][Full Text] [Related]
3. Sequence of a variant thyroxine-binding globulin (TBG) in a family with partial TBG deficiency in Japanese (TBG-PDJ).
Miura Y; Mori Y; Yamamori I; Tani Y; Murata Y; Yoshimoto M; Kinoshita E; Matsumoto T; Oiso Y; Seo H
Endocr J; 1993 Feb; 40(1):127-32. PubMed ID: 7951486
[TBL] [Abstract][Full Text] [Related]
4. Gene screening of thyroxine-binding globulin (TBG) deficiencies in the Japanese: only two mutations account for TBG deficiencies in the Japanese.
Inagaki A; Miura Y; Mori Y; Saito H; Seo H; Oiso Y
J Clin Endocrinol Metab; 1996 Feb; 81(2):580-5. PubMed ID: 8636271
[TBL] [Abstract][Full Text] [Related]
5. Molecular analysis of females manifesting thyroxine-binding globulin (TBG) deficiency: selective X-chromosome inactivation responsible for the difference between phenotype and genotype in TBG-deficient females.
Okamoto H; Mori Y; Tani Y; Nakagomi Y; Sano T; Ohyama K; Saito H; Oiso Y
J Clin Endocrinol Metab; 1996 Jun; 81(6):2204-8. PubMed ID: 8964852
[TBL] [Abstract][Full Text] [Related]
6. An additional carbohydrate chain in the variant thyroxine-binding globulin-Gary (TBGAsn-96) impairs its secretion.
Kambe F; Seo H; Mori Y; Murata Y; Janssen OE; Refetoff S; Matsui N
Mol Endocrinol; 1992 Mar; 6(3):443-9. PubMed ID: 1584218
[TBL] [Abstract][Full Text] [Related]
7. [Inherited abnormality of thyroxine-binding globulin: its gene abnormality and pathogenesis].
Murata Y; Mori Y; Miura Y
Nihon Rinsho; 1994 Apr; 52(4):880-5. PubMed ID: 8196174
[TBL] [Abstract][Full Text] [Related]
8. Partial deficiency of thyroxine-binding globulin-Allentown is due to a mutation in the signal peptide.
Fingerhut A; Reutrakul S; Knuedeler SD; Moeller LC; Greenlee C; Refetoff S; Janssen OE
J Clin Endocrinol Metab; 2004 May; 89(5):2477-83. PubMed ID: 15126580
[TBL] [Abstract][Full Text] [Related]
9. Gene amplification as a cause of inherited thyroxine-binding globulin excess in two Japanese families.
Mori Y; Miura Y; Takeuchi H; Igarashi Y; Sugiura J; Saito H; Oiso Y
J Clin Endocrinol Metab; 1995 Dec; 80(12):3758-62. PubMed ID: 8530630
[TBL] [Abstract][Full Text] [Related]
10. Identification of thyroxine-binding globulin-San Diego in a family from Houston and its characterization by in vitro expression using Xenopus oocytes.
Janssen OE; Astner ST; Grasberger H; Gunn SK; Refetoff S
J Clin Endocrinol Metab; 2000 Jan; 85(1):368-72. PubMed ID: 10634412
[TBL] [Abstract][Full Text] [Related]
11. Effect of tunicamycin and monensin on secretion of thyroxine-binding globulin by cultured human hepatoma (Hep G2) cells.
Bartalena L; Robbins J
J Biol Chem; 1984 Nov; 259(21):13610-4. PubMed ID: 6092384
[TBL] [Abstract][Full Text] [Related]
12. The role of glycosylation in the molecular conformation and secretion of thyroxine-binding globulin.
Murata Y; Magner JA; Refetoff S
Endocrinology; 1986 Apr; 118(4):1614-21. PubMed ID: 3081330
[TBL] [Abstract][Full Text] [Related]
13. Gene screening in Japanese families with complete deficiency of thyroxine-binding globulin demonstrates that a nucleotide deletion at codon 352 may be a race specific mutation.
Takeda K; Iyota K; Mori Y; Tamura Y; Suehiro T; Kubo Y; Refetoff S; Hashimoto K
Clin Endocrinol (Oxf); 1994 Feb; 40(2):221-6. PubMed ID: 8137521
[TBL] [Abstract][Full Text] [Related]
14. C-terminal amino acid alteration rather than late termination causes complete deficiency of thyroxine-binding globulin CD-NeuIsenburg.
Moeller LC; Fingerhut A; Lahner H; Grasberger H; Weimer B; Happ J; Mann K; Janssen OE
J Clin Endocrinol Metab; 2006 Aug; 91(8):3215-8. PubMed ID: 16735497
[TBL] [Abstract][Full Text] [Related]
15. Thyroxine-binding globulin variant (TBG-Kumamoto): identification of a point mutation and genotype analysis of its family.
Shirotani T; Kishikawa H; Wake N; Miyamura N; Hashimoto Y; Motoyoshi S; Yamaguchi K; Shichiri M
Endocrinol Jpn; 1992 Dec; 39(6):577-84. PubMed ID: 1294376
[TBL] [Abstract][Full Text] [Related]
16. A mutation causing reduced biological activity and stability of thyroxine-binding globulin probably as a result of abnormal glycosylation of the molecule.
Mori Y; Seino S; Takeda K; Flink IL; Murata Y; Bell GI; Refetoff S
Mol Endocrinol; 1989 Mar; 3(3):575-9. PubMed ID: 2501669
[TBL] [Abstract][Full Text] [Related]
17. Complete thyroxine-binding globulin (TBG) deficiency in two families without mutations in coding or promoter regions of the TBG genes: in vitro demonstration of exon skipping.
Reutrakul S; Dumitrescu A; Macchia PE; Moll GW; Vierhapper H; Refetoff S
J Clin Endocrinol Metab; 2002 Mar; 87(3):1045-51. PubMed ID: 11889160
[TBL] [Abstract][Full Text] [Related]
18. Complete deficiency of thyroxine-binding globulin (TBG-CD Buffalo) caused by a new nonsense mutation in the thyroxine-binding globulin gene.
Carvalho GA; Weiss RE; Vladutiu AO; Refetoff S
Thyroid; 1998 Feb; 8(2):161-5. PubMed ID: 9510125
[TBL] [Abstract][Full Text] [Related]
19. Nucleotide deletion resulting in frameshift as a possible cause of complete thyroxine-binding globulin deficiency in six Japanese families.
Yamamori I; Mori Y; Seo H; Hirooka Y; Imamura S; Miura Y; Matsui N; Oiso Y
J Clin Endocrinol Metab; 1991 Aug; 73(2):262-7. PubMed ID: 1906892
[TBL] [Abstract][Full Text] [Related]
20. Down-regulation of thyroxine-binding globulin messenger ribonucleic acid by 3,5,3'-triiodothyronine in human hepatoblastoma cells.
Crowe TC; Cowen NL; Loidl NM; Topliss DJ; Stockigt JR; Barlow JW
J Clin Endocrinol Metab; 1995 Jul; 80(7):2233-7. PubMed ID: 7608285
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
