2024年12月25日 · FANCC (FA Complementation Group C) is a Protein Coding gene. Diseases associated with FANCC include Fanconi Anemia, Complementation Group C and Fanconi …

The FANCC gene provides instructions for making a protein that is involved in a process known as the Fanconi anemia (FA) pathway. The FA pathway turns on (activates) when the process …

Fanconi anemia, complementation group C (FANCC) is a gene that encodes a protein that is a member of the Fanconi anemia complementation group. The protein complex functions in the …

范科尼贫血（fanconi anemia，FA）是最常见的遗传性骨髓衰竭性疾病，是染色体不稳定综合征的主要类型之一。 在不同种族、不同地区发病率有所不同。 在亚洲人群中发病率为1/160 000， …

Fanconi anemia group C protein is a protein that in humans is encoded by the FANCC gene. [5][6] This protein delays the onset of apoptosis and promotes homologous recombination repair of …

FANCC was the first gene causal for FA to be identified, and consequently has been the most intensively studied. Loss of function studies have demonstrated an important role for FANCC …

Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and …

2025年2月17日 · Fanconi Anemia (FA) is an autosomal recessive disorder characterized by diverse clinical manifestations such as aplastic anemia, cancer predisposition, and …

范可尼贫血是一种遗传异质性隐性疾病，其特征是细胞遗传学不稳定、对 DNA 交联剂过敏、染色体断裂增加和 DNA 修复缺陷。 Fanconi 贫血互补组的成员不具有序列相似性；它们通过组装 …

FANCC gene encodes the Fanconi anemia group C protein which functions in apoptosis, redox regulation, cytokine signaling and other cellular processes. Fanconi anemia (FA) is an …