Cyp27a1

WebHuman Gene CYP27A1 (ENST00000258415.9) Description:Homo sapiens cytochrome P450 family 27 subfamily A member 1 (CYP27A1), mRNA; nuclear gene for mitochondrial product. (from RefSeq NM_000784) RefSeq Summary (NM_000784):This gene encodes a member of the cytochrome P450 superfamily of enzymes. Web本发明提供有效改善代谢的油脂组合物及其应用。本发明的油脂组合物,中,Sn‑2C16:0的含量为25~50wt%,Sn‑2C16:0占比为55~65wt%。本发明还提供该油脂组合物在制备用于调节对象胆汁酸代谢及肠道菌群等中的应用。在婴幼儿的配方奶粉和辅食中使用本发明的油脂组合物,有助于增加婴幼儿肠道菌 ...

PXR induces CYP27A1 and regulates cholesterol metabolism in …

WebOther symptoms may include brittle bones that are prone to fracture (osteoporosis) and an increased risk of developing heart or lung failure because of lipid buildup. It is caused by … WebJul 1, 2024 · BackgroundCerebrotendinous xanthomatosis (CTX) is an autosomal recessive disorder of bile acid synthesis caused by mutations in the CYP27A1 gene. CTX is an underdiagnosed and potentially treatable disease, thus a detailed appreciation of the phenotypic spectrum and genetic characteristics are crucial for early diagnosis and … how to smoke without a lighter https://newlakestechnologies.com

CYP27A1 Loss Dysregulates Cholesterol Homeostasis in …

WebNM_000784.4(CYP27A1):c.578G>A (p.Arg193Gln) AND Cholestanol storage disease Clinical significance: Conflicting interpretations of pathogenicity, Uncertain significance(1); Likely benign(1) (Last evaluated: Oct 26, 2024) WebDec 4, 2024 · Analysis of CYP27A1 mutations in Han Chinese women with intrahepatic cholestasis of pregnancy. Xin S, Liu X, Liu H, Zeng X, Xiong Y, Zhou M, Zou Y, Zeng Y, Zheng J, Lai HXin S, et al. J Matern Fetal Neonatal Med, 2024 Dec. PMID 34930075; CYP27A1-dependent anti-melanoma activity of limonoid natural products targets … WebCYP27A1 deficiency causes hypertriglyceridemia and hepatomegaly in mice, indicating that CYP27A1 function affects other metabolic processes in this species (J.J. Repa, 2000). Anomalous expression of the genes encoding the two other known hydroxylases that facilitate the entry of cholesterol into the bile acid biosynthetic pathway does not ... novant orthopedics charlotte nc

Frontiers Downregulation of Cyp7a1 by Cholic Acid and ...

Category:CYP2R1 - Wikipedia

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Cyp27a1

CYP27A1 Loss Dysregulates Cholesterol Homeostasis in Prostate …

WebOct 28, 2024 · Sterol 27-hydroxylase (CYP27A1) is a key enzyme in bile acids (BAs) biosynthesis and a regulator of cholesterol metabolism. Cyp27a1/Apolipoprotein E double knockout (DKO) mice fed with western diet (WD) are protected from atherosclerosis via up-regulation of hepatic Cyp7a1 and Cyp3a11. WebOct 6, 2024 · To verify the vitamin D activation disorder in BA, we detected the expression of CYP2R1 and CYP27A1, which are important hydroxylases that convert vitamin D to 25 (OH)D in the liver. qPCR showed...

Cyp27a1

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WebJul 11, 2024 · Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive genetic disorder caused by an abnormality in the CYP27A1 gene, resulting in a deficiency of the mitochondrial enzyme sterol 27-hydroxylase. The lack of this enzyme prevents cholesterol from being converted into a bile acid called chenodeoxycholic acid. WebOther symptoms may include brittle bones that are prone to fracture (osteoporosis) and an increased risk of developing heart or lung failure because of lipid buildup. It is caused by genetic changes in the CYP27A1 gene. Resource (s) for Medical Professionals and Scientists on This Disease:

WebSep 23, 2024 · 27-hydroxycholesterol (27HC), synthesized from cholesterol by the enzyme CYP27A1, differentially impacts estrogen receptor positive (ER+) breast cancer (BC) cell … WebJan 7, 2009 · The defect in cerebrotendinous xanthomatosis was shown by Cali et al. (1991) to reside in the CYP27A1 gene; see 606530.0001-606530.0002. In a 53-year-old man …

WebNov 29, 2016 · Description: single nucleotide variant Variant details Conditions Gene (s) Help NM_000784.4 (CYP27A1):c.1151C>T (p.Pro384Leu) Allele ID 76739 Variant type single nucleotide variant Variant length 1 bp Cytogenetic location 2q35 Genomic location 2: 218814154 (GRCh38) GRCh38 UCSC 2: 219678877 (GRCh37) GRCh37 UCSC HGVS … WebThe CYP27A1 gene is a member of the cytochrome P450 gene family. Enzymes produced from the cytochrome P450 genes are involved in the formation and breakdown of various …

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WebDec 19, 2013 · Guyant-Marechal et al. (2005) described a 53-year-old man with an unusual CTX phenotype, involving no mental retardation and a progressive neuropsychiatric … how to smoke without a lighter or matchesWebCYP27A1 Polyclonal Antibody detects CYP27A1 protein at cytoplasm in human endometrial carcinoma by immunohistochemical analysis. Sample: Paraffin-embedded human endometrial carcinoma. CYP27A1 Polyclonal … novant orthopedics in kernersvilleWebCYP27A1 is considered a potential therapeutic target in breast cancer and age-related neurodegenerative diseases; however, CYP27A1 inhibition should be ≤50%. Herein, 131 … how to smoke without a wraphow to smoke without a vapeWebSep 23, 2024 · Considering that CYP27A1 is responsible for regulating 27HC levels, it is reasonable to assume that the differential CYP27A1 expression may serve as a surrogate biomarker for 27HC levels in the... how to smoke without getting addictedWebApr 1, 2024 · The 2 most common genetic mutations in Chinese adult CTX patients were c.1263+1G>A and c.379C>T. Exon 2 of the CYP27A1 gene was identified as a mutation hot spot. Conclusions: Chinese adult patients with CTX have complex clinical characteristics, a long diagnostic cycle, and various CYP27A1 gene mutations. Early diagnosis and … how to smoke without weedWebApr 2, 2024 · CYP27A1 is lost in prostate cancer and predictive of progression. A, TCGA was queried for mRNA levels of CYP27A1 in tumor samples and Gleason score at the time of diagnosis. Patients whose tumors have a Gleason score >7 have significantly lower levels of expression of CYP27A1 than how to smoke without hurting your lungs