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Full text of "Datormagazin 1990" - Internet Archive

The frequency of the CTSS-25A allele was 0.457 in Caucasians and 0.431 in Canadian Inuit. Because of the importance of the CTSS gene product in vascular matrix remodeling, this polymorphism may be useful in the study of associations with atherosclerosis and related phenotypes. To examine the functional ramifications associated with greater Ctss expression, the Ctss gene was deleted in the mdx genetic background, resulting in protection from muscular dystrophy pathogenesis that included reduced myofiber turnover and histopathology, reduced fibrosis, and improved running capacity. CTSS has 5,430 functional associations with biological entities spanning 8 categories (molecular profile, organism, chemical, functional term, phrase or reference, disease, phenotype or trait, structural feature, cell line, cell type or tissue, gene, protein or microRNA) extracted from 78 datasets. CTSS (cathepsin S) is a protein-coding gene. Diseases associated with CTSS include cercarial dermatitis, and abdominal aortic aneurysm. GO annotations related to this gene include cysteine-type endopeptidase activity.

Ctss gene

If you continue, we'll assume that you are happy to receive all cookies. Biological context of CTSS. The frequency of the CTSS-25A allele was 0.457 in Caucasians and 0.431 in Canadian Inuit. Because of the importance of the CTSS gene product in vascular matrix remodeling, this polymorphism may be useful in the study of associations with atherosclerosis and related phenotypes.

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Om noen skulle ha IC-12N med DTMF och CTSS i nyskick. Anders 08-984419.

Full text of "Datormagazin 1990" - Internet Archive

CTSS has 5,430 functional associations with biological entities spanning 8 categories (molecular profile, organism, chemical, functional term, phrase or reference, disease, phenotype or trait, structural feature, cell line, cell type or tissue, gene, protein or microRNA) extracted from 78 datasets. CTSS (cathepsin S) is a protein-coding gene. Diseases associated with CTSS include cercarial dermatitis, and abdominal aortic aneurysm. GO annotations related to this gene include cysteine-type endopeptidase activity. An important paralog of this gene is CTSF. 2021-03-09 ctss breaks up proteins into small pieces that may be used to degrade parts of a pathogen.

GO annotations related to this gene include cysteine-type endopeptidase activity.
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Inbygd VOX. 1750 hz CTSS or children's therapeutic services and supports are a great tool for helping for mitochondrial diseases are being done in the U.K. Germ line gene editing, CTSS Japan, som uppgavs syssla med säkerhetsfrågor.

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Graviditetsdiabetes omprogrammerar stamceller - Life

2006).To investigate whether there are additive effects of simultaneously deleting these tumor-promoting cathepsins, we generated CtsB by Gene › CTSS Antibodies; CTSS Antibodies . The protein CTSS, a member of the peptidase C1 family, is a lysosomal cysteine proteinase that may participate in the degradation of antigenic proteins to peptides for presentation on MHC class II molecules. Conclusion: The single nucleotide polymorphisms (SNPs) of rs774320676 and rs928508030 of CTSS gene were related with risk for acute atherosclerotic cerebral infarction. The T allele at rs774320676 locus and G allele at rs928508030 locus of CTSS were genetic susceptibility genes of acute atherosclerotic cerebral infarction.

sp A0A183 LCE6A_HUMAN Late cornified envelope protein

Diseases associated with CTSS include cercarial dermatitis, and abdominal aortic aneurysm. GO annotations related to this gene include cysteine-type endopeptidase activity. An important paralog of this gene is CTSF.

Gene: Ctss - ENSMUSG00000038642 - Mus musculus (mouse) General information. Ensembl ID: ENSMUSG00000038642: Name: Ctss: Description CTSS gene expression is highest in BR300 TNBC subtype and associated with DNA damage/cell cycle pathways. CTSS gene expression was evaluated using an in house dataset containing 300 breast cancer patients. Analysis revealed (a) CTSS expression to be highest in TNBC. It is notable that CTSS is a differentially expressed gene in the kidney of IgAN patients and associated with the pathogenesis of IgAN (31, 32). In this study, we found significantly up-regulated CTSS expression in the kidney tissues, particularly in the glomerular mesangium and tubular epithelial cells from human IgAN patients, and higher CTSC (Cathepsin C) is a Protein Coding gene. Diseases associated with CTSC include Papillon-Lefevre Syndrome and Haim-Munk Syndrome.