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 *

156 related articles for article (PubMed ID: 1906047)

  • 1. Sequence of the variant thyroxine-binding globulin (TBG) in a Montreal family with partial TBG deficiency.
    Janssen OE; Takeda K; Refetoff S
    Hum Genet; 1991 Jun; 87(2):119-22. PubMed ID: 1906047
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sequencing of the variant thyroxine-binding globulin (TBG)-Quebec reveals two nucleotide substitutions.
    Bertenshaw R; Takeda K; Refetoff S
    Am J Hum Genet; 1991 Apr; 48(4):741-4. PubMed ID: 1901689
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Complete thyroxine-binding globulin (TBG) deficiency caused by a single nucleotide deletion in the TBG gene.
    Li P; Janssen OE; Takeda K; Bertenshaw RH; Refetoff S
    Metabolism; 1991 Nov; 40(11):1231-4. PubMed ID: 1943753
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Sequencing of the variant thyroxine-binding globulin (TBG)-San Diego reveals two nucleotide substitutions.
    Bertenshaw R; Sarne D; Tornari J; Weinberg M; Refetoff S
    Biochim Biophys Acta; 1992 Aug; 1139(4):307-10. PubMed ID: 1515456
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular basis for the properties of the thyroxine-binding globulin-slow variant in American blacks.
    Waltz MR; Pullman TN; Takeda K; Sobieszczyk P; Refetoff S
    J Endocrinol Invest; 1990 Apr; 13(4):343-9. PubMed ID: 2115061
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. A novel mutation causing complete deficiency of thyroxine binding globulin.
    Ueta Y; Mitani Y; Yoshida A; Taniguchi S; Mori A; Hattori K; Hisatome I; Manabe I; Takeda K; Sato R; Ahmmed GU; Tsuboi M; Ohtahara A; Hiroe K; Tanaka Y; Shigemasa C
    Clin Endocrinol (Oxf); 1997 Jul; 47(1):1-5. PubMed ID: 9302363
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Replacement of Leu227 by Pro in thyroxine-binding globulin (TBG) is associated with complete TBG deficiency in three of eight families with this inherited defect.
    Mori Y; Takeda K; Charbonneau M; Refetoff S
    J Clin Endocrinol Metab; 1990 Mar; 70(3):804-9. PubMed ID: 2155256
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Two novel mutations in the gene encoding thyroxine-binding globulin (TBG) as a cause of complete TBG deficiency in Taiwan.
    Su CC; Wu YC; Chiu CY; Won JG; Jap TS
    Clin Endocrinol (Oxf); 2003 Apr; 58(4):409-14. PubMed ID: 12641622
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Two new inherited defects of the thyroxine-binding globulin (TBG) molecule presenting as partial TBG deficiency.
    Takamatsu J; Refetoff S; Charbonneau M; Dussault JH
    J Clin Invest; 1987 Mar; 79(3):833-40. PubMed ID: 3102557
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sequence of the variant thyroxine-binding globulin of Australian aborigines. Only one of two amino acid replacements is responsible for its altered properties.
    Takeda K; Mori Y; Sobieszczyk S; Seo H; Dick M; Watson F; Flink IL; Seino S; Bell GI; Refetoff S
    J Clin Invest; 1989 Apr; 83(4):1344-8. PubMed ID: 2495303
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.