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Assignment of the gene for a ubiquitin-conjugating enzyme (UBE2I) to human chromosome band 16p13.3 by in situ hybridization.

作者信息

Tachibana M, Iwata N, Watanabe A, Nobukuni Y, Ploplis B, Kajigaya S

机构信息

Laboratory of Molecular Genetics, National Institute of Deafness and Other Communications Disorders, NIH, Rockville, MD 20850, USA.

出版信息

Cytogenet Cell Genet. 1996;75(4):222-3. doi: 10.1159/000134487.

DOI:10.1159/000134487
PMID:9067428
Abstract
摘要

相似文献

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Assignment of the gene for a ubiquitin-conjugating enzyme (UBE2I) to human chromosome band 16p13.3 by in situ hybridization.通过原位杂交将泛素结合酶(UBE2I)基因定位于人类染色体16p13.3带。
Cytogenet Cell Genet. 1996;75(4):222-3. doi: 10.1159/000134487.
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Cloning, expression, and mapping of UBE2I, a novel gene encoding a human homologue of yeast ubiquitin-conjugating enzymes which are critical for regulating the cell cycle.
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Molecular cloning of the cDNA and chromosome localization of the gene for human ubiquitin-conjugating enzyme 9.人泛素缀合酶9基因的cDNA分子克隆及染色体定位
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SOLH, a human homologue of the Drosophila melanogaster small optic lobes gene is a member of the calpain and zinc-finger gene families and maps to human chromosome 16p13.3 near CATM (cataract with microphthalmia).SOLH是果蝇小眼叶基因的人类同源物,是钙蛋白酶和锌指基因家族的成员,定位于人类16号染色体p13.3区域,靠近CATM(伴有小眼症的白内障)基因。
Genomics. 1998 Jul 15;51(2):197-206. doi: 10.1006/geno.1998.5395.
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Assignment of a human cold shock domain protein A intronless pseudogene (CSDAP1) to human chromosome 16 band p11.2 by in situ hybridization.
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Assignment1 of the ubiquitin conjugating enzyme gene, UBE2G2, to human chromosome band 21q22.3 by in situ hybridization.
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cDNA cloning, characterization, and chromosome mapping of UBE2E2 encoding a human ubiquitin-conjugating E2 enzyme.编码人泛素结合E2酶的UBE2E2的cDNA克隆、特性分析及染色体定位
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Assignment of UBE2D1 to human chromosome bands 10q11.2-->q21 by in situ hybridization.通过原位杂交将泛素结合酶E2D1定位于人类染色体带10q11.2→q21。
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Autosomal dominant congenital cataract and microphthalmia associated with a familial t(2;16) translocation.常染色体显性遗传性先天性白内障和小眼症与家族性t(2;16)易位相关。
Hum Genet. 1992 Sep-Oct;90(1-2):177-8. doi: 10.1007/BF00210770.

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Localization of a target region of allelic loss to a 1-cM interval on chromosome 16p.13.13 in hepatocellular carcinoma.肝细胞癌中等位基因缺失目标区域定位于16号染色体短臂13.13区的一个1厘摩区间。
Jpn J Cancer Res. 1999 Sep;90(9):951-6. doi: 10.1111/j.1349-7006.1999.tb00840.x.