WebSep 4, 2024 · Here, we reveal that, in Neurospora crassa, NC2 activates catalase-3 (cat-3) gene transcription in the form of heterodimer mediated by histone fold (HF) domains of two subunits. Deletion of HF domain in either of two subunits disrupts the NC2α-NC2β interaction and the binding of intact NC2 heterodimer to cat-3 locus. Loss of NC2 … WebC2D is caused by mutations in the C2 gene and is inherited in an autosomal recessive fashion. Complement component 2 deficiency (C2D) is a genetic condition that affects the immune system. Signs and symptoms include recurrent bacterial infections and risk for a variety of autoimmune conditions. Infections can be very serious and are common in ...
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WebHPO (Human Phenotype Ontology, 5405 gene sets) C6 (oncogenic gene sets, 189 gene sets) C7 (immunologic gene sets, 5219 gene sets) IMMUNESIGDB (ImmuneSigDB gene sets, 4872 gene sets) VAX (vaccine response gene sets, 347 gene sets) C8 (cell type signature gene sets, 830 gene sets) Click on a gene set name to view its gene set page. WebC2. General description of the gene and the encoded protein (s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas project. Official gene symbol, which is typically a short form of the gene name, according to HGNC. Full gene name according to HGNC. Assigned HPA protein class (es) for the encoded ... bank statement in japanese
Molecular cloning, characterization and expression of the …
WebC2D is caused by genetic changes in the C2 gene and is inherited in an autosomal recessive fashion. Resource(s) for Medical Professionals and Scientists on This Disease: … WebFOXC2. Forkhead box protein C2 (FOXC2) also known as forkhead-related protein FKHL14 (FKHL14), transcription factor FKH-14, or mesenchyme fork head protein 1 (MFH1) is a … WebThe che-2 gene encodes a new member of the WD40 protein family, suggesting that it acts in protein-protein interaction. Analysis of mutation sites showed that both the amino … pollution in russia