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Cloning of the bovine and rat Fanconi anemia group C cDNA.

作者信息

Ching Ying Wong J, Alon N, Buchwald M

机构信息

Department of Genetics, Research Institute, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada.

出版信息

Mamm Genome. 1997 Jul;8(7):522-5. doi: 10.1007/s003359900490.

DOI:10.1007/s003359900490
PMID:9196001
Abstract
摘要

相似文献

1
Cloning of the bovine and rat Fanconi anemia group C cDNA.
Mamm Genome. 1997 Jul;8(7):522-5. doi: 10.1007/s003359900490.
2
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.
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3
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.范可尼贫血主要基因FAA的cDNA的表达克隆
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The delta327 mutation in the Fanconi anemia group C gene generates a novel transcript lacking the first two coding exons.范可尼贫血C组基因中的delta327突变产生了一种缺少前两个编码外显子的新转录本。
Hum Mutat. 1998;Suppl 1:S275-7. doi: 10.1002/humu.1380110187.
5
Cloning and analysis of the murine Fanconi anemia group C cDNA.小鼠范可尼贫血C组cDNA的克隆与分析
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6
A Leu554-to-Pro substitution completely abolishes the functional complementing activity of the Fanconi anemia (FACC) protein.亮氨酸554突变为脯氨酸会完全消除范可尼贫血(FACC)蛋白的功能互补活性。
Hum Mol Genet. 1993 Feb;2(2):123-6. doi: 10.1093/hmg/2.2.123.
7
Strong FANCA/FANCG but weak FANCA/FANCC interaction in the yeast 2-hybrid system.在酵母双杂交系统中,FANCA与FANCG相互作用强烈,但FANCA与FANCC相互作用较弱。
Blood. 2000 Jan 15;95(2):719-20.
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Clinical variability of Fanconi anemia (type C) results from expression of an amino terminal truncated Fanconi anemia complementation group C polypeptide with partial activity.范可尼贫血(C型)的临床变异性源于氨基末端截短的具有部分活性的范可尼贫血互补组C多肽的表达。
Blood. 1996 May 15;87(10):4424-32.
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A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews.FACC基因的一种常见突变会导致德系犹太人患范科尼贫血。
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Characterization of the 5' region of the Fanconi anaemia group C (FACC) gene.
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引用本文的文献

1
FANCC interacts with Hsp70 to protect hematopoietic cells from IFN-gamma/TNF-alpha-mediated cytotoxicity.FANCC与热休克蛋白70(Hsp70)相互作用,以保护造血细胞免受干扰素-γ/肿瘤坏死因子-α介导的细胞毒性作用。
EMBO J. 2001 Aug 15;20(16):4478-89. doi: 10.1093/emboj/20.16.4478.

本文引用的文献

1
Exon 6 skipping in the Fanconi anemia C gene associated with a nonsense/missense mutation (775C-->T) in exon 5: the first example of a nonsense mutation in one exon causing skipping of another downstream.范可尼贫血C基因第6外显子跳跃与第5外显子的无义/错义突变(775C→T)相关:一个外显子中的无义突变导致下游另一个外显子跳跃的首例。
Hum Mutat. 1998;Suppl 1:S25-7. doi: 10.1002/humu.1380110109.
2
p53 activates Fanconi anemia group C gene expression.p53激活范可尼贫血C组基因的表达。
Hum Mol Genet. 1997 Feb;6(2):277-83. doi: 10.1093/hmg/6.2.277.
3
Novel mutations and polymorphisms in the Fanconi anemia group C gene.
范可尼贫血C组基因中的新型突变和多态性
Hum Mutat. 1996;8(2):140-8. doi: 10.1002/(SICI)1098-1004(1996)8:2<140::AID-HUMU6>3.0.CO;2-F.
4
An essential gene, ESR1, is required for mitotic cell growth, DNA repair and meiotic recombination in Saccharomyces cerevisiae.在酿酒酵母中,一个必需基因ESR1对于有丝分裂细胞生长、DNA修复和减数分裂重组是必需的。
Nucleic Acids Res. 1994 Aug 11;22(15):3104-12. doi: 10.1093/nar/22.15.3104.
5
Mitotic checkpoint genes in budding yeast and the dependence of mitosis on DNA replication and repair.芽殖酵母中的有丝分裂检查点基因以及有丝分裂对DNA复制和修复的依赖性。
Genes Dev. 1994 Mar 15;8(6):652-65. doi: 10.1101/gad.8.6.652.
6
Cloning and analysis of the murine Fanconi anemia group C cDNA.小鼠范可尼贫血C组cDNA的克隆与分析
Hum Mol Genet. 1993 Jun;2(6):655-62. doi: 10.1093/hmg/2.6.655.
7
Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype.通过互补分析对范可尼贫血患者进行分类:第五种遗传亚型的证据。
Blood. 1995 Sep 15;86(6):2156-60.
8
Characterization of the 5' region of the Fanconi anaemia group C (FACC) gene.
Hum Mol Genet. 1995 Aug;4(8):1321-6. doi: 10.1093/hmg/4.8.1321.
9
Estrogen-dependent expression of the cystic fibrosis transmembrane regulator gene in a novel uterine epithelial cell line.新型子宫上皮细胞系中囊性纤维化跨膜调节基因的雌激素依赖性表达。
J Cell Sci. 1994 Sep;107 ( Pt 9):2439-48. doi: 10.1242/jcs.107.9.2439.
10
Prototype sequence clues within the Fanconi anaemia group C gene.范可尼贫血C组基因内的原型序列线索。
J Med Genet. 1995 Aug;32(8):669-70. doi: 10.1136/jmg.32.8.669-a.