Isolation of the defective gene in X linked agammaglobulinaemia.
作者信息
Vetrie D
出版信息
J Med Genet. 1993 Jun;30(6):452-3. doi: 10.1136/jmg.30.6.452.
Abstract
摘要
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本文引用的文献
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Agammaglobulinemia.无丙种球蛋白血症
Pediatrics. 1952 Jun;9(6):722-8.
2
Cloning of the X-linked glycerol kinase deficiency gene and its identification by sequence comparison to the Bacillus subtilis homologue.
Hum Mol Genet. 1993 Feb;2(2):97-106. doi: 10.1093/hmg/2.2.97.
3
Genetic linkage analysis identifies new proximal and distal flanking markers for the X-linked agammaglobulinemia gene locus, refining its localization in Xq22.遗传连锁分析确定了X连锁无丙种球蛋白血症基因座新的近端和远端侧翼标记，将其定位精确到Xq22。
Hum Mol Genet. 1993 Feb;2(2):139-41. doi: 10.1093/hmg/2.2.139.
4
Isolation of the human Xp21 glycerol kinase gene by positional cloning.通过定位克隆分离人类Xp21甘油激酶基因。
Hum Mol Genet. 1993 Feb;2(2):107-14. doi: 10.1093/hmg/2.2.107.
5
Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase.门克斯病候选基因的分离及其编码铜转运ATP酶的证据。
Nat Genet. 1993 Jan;3(1):7-13. doi: 10.1038/ng0193-7.
6
Isolation of a partial candidate gene for Menkes disease by positional cloning.通过定位克隆分离门克斯病的部分候选基因。
Nat Genet. 1993 Jan;3(1):20-5. doi: 10.1038/ng0193-20.
7
Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein.分离出一种门克斯病的候选基因，该基因编码一种潜在的重金属结合蛋白。
Nat Genet. 1993 Jan;3(1):14-9. doi: 10.1038/ng0193-14.
8
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters.推测的X连锁肾上腺脑白质营养不良基因与ABC转运蛋白具有意外的同源性。
Nature. 1993 Feb 25;361(6414):726-30. doi: 10.1038/361726a0.
9
Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia.人类X连锁无丙种球蛋白血症中B细胞胞质酪氨酸激酶的表达缺陷
Cell. 1993 Jan 29;72(2):279-90. doi: 10.1016/0092-8674(93)90667-f.
10
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.
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