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 *

183 related articles for article (PubMed ID: 14974930)

  • 21. Hereditary complete thyroxine-binding globulin deficiency: identification by T3 resin uptake test and DNA analysis.
    Noguchi T; Yamamori I; Takamatsu J; Nakajima T; Mori Y; Kumahara Y
    Intern Med; 1993 Jan; 32(1):6-9. PubMed ID: 8495048
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Thyroxine-binding globulin gene and variants].
    Seo H
    Nihon Rinsho; 2006 May; Suppl 1():508-12. PubMed ID: 16776202
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. [Thyroxine-binding globulin abnormalities].
    Kambe F; Seo H
    Nihon Rinsho; 2005 Oct; 63 Suppl 10():133-6. PubMed ID: 16279617
    [No Abstract]   [Full Text] [Related]  

  • 25. Familial thyroxine-binding globulin deficiency associated with hyperthyroidism.
    Tojo K; Miura Y; Mori Y; Yano M; Tanaka H; Hosoya T; Sakai O
    Intern Med; 1995 May; 34(5):413-7. PubMed ID: 7647413
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Inherited X chromosome linked thyroxine-binding globulin (TBG) deficiency in a homozygous female.
    Bigazzi M; Ronga R; Olivotti AL; Scarselli G; Refetoff S
    J Endocrinol Invest; 1980; 3(4):349-52. PubMed ID: 6162876
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Graves' disease and thyroxine-binding globulin deficiency.
    Dall'Aglio E; Robuschi G; Minelli R; Guerra M; Bentivoglio M; Roti E
    Arch Intern Med; 1988 Jun; 148(6):1445-6. PubMed ID: 3132126
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. [Partial thyroxine binding globulin deficiency in test tube infants: report of cases and literature review].
    Fang YL; Wang CL; Liang L
    Zhonghua Er Ke Za Zhi; 2016 Jun; 54(6):428-32. PubMed ID: 27256229
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Partial deficiency of thyroxine-binding globulin: an HLA study.
    Hníková O; Ivasková E; Kracmar P; Kupková L; Sajdlová H; Zikmund J
    Horm Res; 1993; 40(5-6):201-3. PubMed ID: 8112720
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. TBG deficiency: description of two novel mutations associated with complete TBG deficiency and review of the literature.
    Mannavola D; Vannucchi G; Fugazzola L; Cirello V; Campi I; Radetti G; Persani L; Refetoff S; Beck-Peccoz P
    J Mol Med (Berl); 2006 Oct; 84(10):864-71. PubMed ID: 16947003
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. A novel mutation (del 1711 G) in the TBG gene as a cause of complete TBG deficiency.
    Lacka K; Nizankowska T; Ogrodowicz A; Lacki JK
    Thyroid; 2007 Nov; 17(11):1143-6. PubMed ID: 17887925
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. [Inborn defect of thyroxine binding globulin (TBG) diagnosed during screening for congenital hypothyroidism].
    Hníková O; Kracmar P
    Cesk Pediatr; 1983 Jul; 38(7):416-8. PubMed ID: 6413079
    [No Abstract]   [Full Text] [Related]  

  • 38. Familial thyroxine-binding globulin deficiency in association with non-toxic goitre.
    Bratusch-Marrain P; Haydl H; Waldhäusl W; Dudczak R; Graninger W
    Acta Endocrinol (Copenh); 1979 May; 91(1):70-6. PubMed ID: 110022
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Congenital thyroxine binding globulin deficiency: incidence and inheritance.
    Jenkins MB; Steffes MW
    Hum Genet; 1987 Sep; 77(1):80-4. PubMed ID: 3114125
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 10.