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Items: 1 to 20 of 101

1.

The structure of the human thyroxine binding globulin (TBG) gene.

Akbari MT, Kapadi A, Farmer MJ, Fitch NJ, McCann KP, Kordestani S, Flink IL, Sheppard MC, Ramsden DB.

Biochim Biophys Acta. 1993 Dec 14;1216(3):446-54.

PMID:
8268226
2.

Molecular cloning and primary structure of rat thyroxine-binding globulin.

Imamura S, Mori Y, Murata Y, Yamamori I, Miura Y, Oiso Y, Seo H, Matsui N, Refetoff S.

Biochemistry. 1991 Jun 4;30(22):5406-11.

PMID:
1903654
3.

Localization of the human thyroxine-binding globulin gene to the long arm of the X chromosome (Xq21-22).

Trent JM, Flink IL, Morkin E, van Tuinen P, Ledbetter DH.

Am J Hum Genet. 1987 Sep;41(3):428-35.

4.

Structure of the human gene for the neural phosphoprotein B-50 (GAP-43).

Nielander HB, De Groen PC, Eggen BJ, Schrama LH, Gispen WH, Schotman P.

Brain Res Mol Brain Res. 1993 Sep;19(4):293-302.

PMID:
8231732
5.

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.

6.

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.

PMID:
1906892
7.

Human thyroxine-binding globulin gene: complete sequence and transcriptional regulation.

Hayashi Y, Mori Y, Janssen OE, Sunthornthepvarakul T, Weiss RE, Takeda K, Weinberg M, Seo H, Bell GI, Refetoff S.

Mol Endocrinol. 1993 Aug;7(8):1049-60.

PMID:
8232304
8.

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.

PMID:
8530630
9.

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.

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11.
12.

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.

13.
14.

Autosomally transmitted low concentration of thyroxine-binding globulin.

Kobayashi H, Sakurai A, Katai M, Hashizume K.

Thyroid. 1999 Feb;9(2):159-63.

PMID:
10090316
15.
16.

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.

PMID:
9302363
17.

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.

PMID:
12641622
18.

Characterization of the human bone sialoprotein (BSP) gene and its promoter sequence.

Kim RH, Shapiro HS, Li JJ, Wrana JL, Sodek J.

Matrix Biol. 1994 Jan;14(1):31-40.

PMID:
8061918
19.

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 Jr, Vierhapper H, Refetoff S.

J Clin Endocrinol Metab. 2002 Mar;87(3):1045-51.

PMID:
11889160
20.

[Cloning of human thyroxine-binding globulin cDNA, isolation of the gene, and its transcriptional regulation].

Kambe F, Seo H.

Nihon Rinsho. 1994 Apr;52(4):875-9. Review. Japanese.

PMID:
8196173
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