Clstn2 heart
WebApr 4, 2024 · Clinical resource with information about CLSTN2, A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population., A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus., Genome-wide association for … WebExpression of CLSTN2 (CDHR13, CS2, CSTN2, FLJ39113) in breast tissue. Antibody staining with HPA031342 in immunohistochemistry.
Clstn2 heart
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WebMar 21, 2024 · GeneCards Summary for CLSTN2 Gene. CLSTN2 (Calsyntenin 2) is a Protein Coding gene. Diseases associated with CLSTN2 include Astigmatism and … AKT1 is one of 3 closely related serine/threonine-protein kinases (AKT1, … HOMER1 (Homer Scaffold Protein 1) is a Protein Coding gene. Diseases … JUN (Jun Proto-Oncogene, AP-1 Transcription Factor Subunit) is a … FAT1 (FAT Atypical Cadherin 1) is a Protein Coding gene. Diseases associated with … Complete information for MET gene (Protein Coding), MET Proto-Oncogene, … APP (Amyloid Beta Precursor Protein) is a Protein Coding gene. Diseases … SMAD4 (SMAD Family Member 4) is a Protein Coding gene. Diseases … CDH13 (Cadherin 13) is a Protein Coding gene. Diseases associated with CDH13 … LAMA1 (Laminin Subunit Alpha 1) is a Protein Coding gene. Diseases … MBP (Myelin Basic Protein) is a Protein Coding gene. Diseases associated with … WebNational Center for Biotechnology Information
WebRead Free Manual Of Neonatal Care John P Cloherty Free Download Pdf direct primary care johns hopkins community physicians dr john p carey md baltimore md ent ... WebKIBRA and CLSTN2 polymorphisms exert interactive effects on human episodic memory. 27: 20691427: 2010: Genetic associations of brain structural networks in schizophrenia: a preliminary study. 17: 19058786: 2009: Allelic variation of calsyntenin 2 (CLSTN2) modulates the impact of developmental tobacco smoke exposure on mnemonic …
Web开馆时间：周一至周日7:00-22:30 周五 7:00-12:00; 我的图书馆 WebCLSTN2 shares 58% amino acid identity with CLSTN1 and 94% identity with its mouse homolog. Northern blot analysis of human tissues detected a 5-kb transcript expressed exclusively in brain. In situ hybridization showed nonuniform Clstn2 expression in the majority of adult mouse brain regions. In cerebral cortex, Clstn2 was found in the somas ...
WebJun 24, 2024 · LongevityMap variant Entry Details Longevity Association Significant Population American (Caucasian) Study Design Genome-wide association study using 1,471 genotyped participants from the Framingham Heart Study, of which 1,173 individuals had known lifespans, plus 517 individuals from the Offspring cohort for validating …
WebAug 18, 2024 · CLSTN2 gene, collected tissues including heart, liver, spleen, lung, kidney, muscle, fat, ovary, and fallopian tube were obtained from the female kids when they orbs bookshop huntlyWebNov 3, 2024 · Study explored the in vivo effects of calsyntenin-2 deficiency on emotional and social behavioral endophenotypes in a mouse, found a striking effect of sex on expression of social behavior and emotionality in Clstn2-knock-out mice, but hyperactivity coupled with pronounced repetitive behavior was observed in Clstn2-knock-out mice of both sexes. orbs breastWebMar 12, 2024 · Generation of calsyntenin (Clstn) triple knockout (TKO) mice.a Representation of calsyntenin (CLSTN) domains and target regions of single-guide RNAs (sgRNAs). Each CLSTN has two cadherin domains (blue box), one LG/LNS domain (red box), and one or two kinesin-binding sites (blue line). The target region is designed to be … ippf africa regional officeWebMar 1, 2024 · HDL-C and triglycerides are the main biochemical determinants of cholesterol efflux capacity each explaining >11% of variance. • In a GWAS, 2 novel genetic loci (KLKB1 & CLSTN2) and the known APOE/C1 locus are associated with cholesterol efflux capacity.The KLKB1 locus is significant irrespective of adjustment for kidney function, … orbs block islandWebSuppression of tumorigenicity 2 (ST2) is a member of the interleukin (IL)-1 receptor family, whose role was originally established in the context of inflammatory and autoimmune … ippf annual performance report 2021WebCLSTN2. 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. orbs bookshopWebCLN2 disease is a rare genetic disorder that affects children. 1,2 Through ongoing research, doctors have made important discoveries that are helping us understand why this … ippf arab world