The murine form of TXK, a novel TEC kinase expressed in thymus maps to chromosome 5.

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作者信息

Haire R N, Litman G W

机构信息

Department of Pediatrics, University of South Florida, All Children's Hospital, St. Petersburg 33701, USA.

出版信息

Mamm Genome. 1995 Jul;6(7):476-80. doi: 10.1007/BF00360659.

DOI:10.1007/BF00360659

PMID:7579892

Abstract

摘要

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The murine form of TXK, a novel TEC kinase expressed in thymus maps to chromosome 5.

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J Exp Med. 1999 Nov 15;190(10):1427-38. doi: 10.1084/jem.190.10.1427.

Molecular cloning of a docking protein, BRDG1, that acts downstream of the Tec tyrosine kinase.对接蛋白BRDG1的分子克隆，该蛋白在Tec酪氨酸激酶下游发挥作用。

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Cell. 1993 Jan 29;72(2):279-90. doi: 10.1016/0092-8674(93)90667-f.

Developmental regulation of a murine T-cell-specific tyrosine kinase gene, Tsk.小鼠T细胞特异性酪氨酸激酶基因Tsk的发育调控

Proc Natl Acad Sci U S A. 1993 Jan 15;90(2):669-73. doi: 10.1073/pnas.90.2.669.

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases.与X连锁无丙种球蛋白血症相关的基因是蛋白质酪氨酸激酶src家族的成员。

Nature. 1993 Jan 21;361(6409):226-33. doi: 10.1038/361226a0.

Identification, cloning, and characterization of a novel human T-cell-specific tyrosine kinase located at the hematopoietin complex on chromosome 5q.位于5号染色体q臂造血因子复合体上的一种新型人类T细胞特异性酪氨酸激酶的鉴定、克隆及特性分析。

Blood. 1993 Sep 1;82(5):1561-72.

Mutation of unique region of Bruton's tyrosine kinase in immunodeficient XID mice.免疫缺陷XID小鼠中布鲁顿酪氨酸激酶独特区域的突变

Science. 1993 Jul 16;261(5119):358-61. doi: 10.1126/science.8332901.

Colocalization of X-linked agammaglobulinemia and X-linked immunodeficiency genes.X连锁无丙种球蛋白血症与X连锁免疫缺陷基因的共定位。

Science. 1993 Jul 16;261(5119):355-8. doi: 10.1126/science.8332900.

Paralysis and early death in cysteine string protein mutants of Drosophila.果蝇半胱氨酸串珠蛋白突变体中的麻痹和早期死亡

Science. 1994 Feb 18;263(5149):977-80. doi: 10.1126/science.8310297.

Cloning and expression of a human CDC42 GTPase-activating protein reveals a functional SH3-binding domain.一种人类CDC42 GTP酶激活蛋白的克隆与表达揭示了一个功能性SH3结合结构域。

J Biol Chem. 1993 Dec 15;268(35):26059-62.

ZAP-70 deficiency in an autosomal recessive form of severe combined immunodeficiency.ZAP-70缺乏症以常染色体隐性形式表现为严重联合免疫缺陷。

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