Nephrocystin 3
Web当前位置：上海岚派生物科技有限公司>>elisa试剂盒>>人elisa试剂盒>>人*转移酶6抗体（igm）elisa检测试剂盒 WebOct 18, 2024 · Renal–hepatic–pancreatic dysplasia type 1 (RHPD1) is a rare sporadic and autosomal recessive disorder with unknown incidence. RHPD1 is caused by biallelic …
Nephrocystin 3
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WebJul 1, 2010 · Nephrocystin-3 is localized at primary cilia in renal epithelial cells. To further define the role of nephrocystin-3 in the ciliary function, we characterized the subcellular … Web(b) Nephrocystin-3, the product of the NPHP3 gene, contains a coiled-coil domain (CC), a tubulin tyrosine ligase domain (TTL), and a tetratricopeptide-repeat domain (TPR). Most …
WebReference Title: Reference Citation: 1. Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic … WebLoss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia. Bergmann C, Fliegauf M, Brüchle NO, Frank V, Olbrich H, Kirschner J, et al. Am J Hum Genet. 2008 Apr;82(4):959–70. PubMed Europe PMC Scholia; Glomerulocystic kidney disease.
WebK19360 NPHP3; nephrocystin-3 Chromosome and associated proteins [BR:ko03036] Eukaryotic type Centrosome formation and ciliogenesis proteins Other centriole … WebDescription: Homo sapiens nephrocystin 1 (NPHP1), transcript variant 4, mRNA. (from RefSeq NM_001128179) RefSeq Summary (NM_001128179): This gene encodes a protein with src homology domain 3 (SH3) patterns. This protein interacts with Crk-associated substrate, and it appears to function in the control of cell division, as well as in cell-cell …
WebMar 16, 2024 · Mutations in the NPHP3 gene (which encodes nephrocystin-3, another nephrocystin-1 and inversin–interacting protein) result in a variety of human …
WebDescription: Homo sapiens nephrocystin 1 (NPHP1), transcript variant 4, mRNA. (from RefSeq NM_001128179) RefSeq Summary (NM_001128179): This gene encodes a … cite them right kentWebMar 16, 2024 · Medullary cystic kidney disease (MCKD) and nephronophthisis (NPH) refer to 2 inherited diseases with similar renal morphology characterized by bilateral small … diane reay miseducation reviewWebNephrocystin-1 is a protein that in humans is encoded by the NPHP1 gene. Function. This gene encodes a protein with src homology domain 3 (SH3) patterns. Mutations in this … cite them right middlesexhttp://citations.perkinelmer.com/search.php?sqlQuery=SELECT%20author%2C%20title%2C%20type%2C%20year%2C%20publication%2C%20abbrev_journal%2C%20volume%2C%20issue%2C%20page_from%2C%20page_to%2C%20pages%2C%20keywords%2C%20abstract%2C%20url%2C%20call_number%2C%20serial%20FROM%20refs%20WHERE%20%28title%20RLIKE%20%22Volocity%22%20OR%20abstract%20RLIKE%20%22Volocity%22%20OR%20keywords%20RLIKE%20%22Volocity%22%20OR%20pages%20RLIKE%20%22Volocity%22%20OR%20publication%20RLIKE%20%22Volocity%22%20OR%20area%20RLIKE%20%22Volocity%22%29%20ORDER%20BY%20year%20DESC&submit=Display&citeStyle=APA&orderBy=year%20DESC&showQuery=0&formType=sqlSearch&showRows=10&rowOffset=900&client=&viewType=Web cite them right login inWebfragment,FC)，糖结合在FC 上。 公司专业供应的抗体，是用于化学反应、分析化验、研究实验、教学实验、化学配方使用的纯净化学品，品质卓越，价格实惠，多种规格供应，售后完善。 产品名称 英文名称 型号 KDEL Receptor抗体 KDEL Receptor GOY-0 cite them right mybibWebSe ha demostrado que una dieta rica en frutas, verduras, cereales integrales, pescado y frutos secos puede disminuir la presión arterial. Esto se debe a que estos alimentos contienen nutrientes como potasio, calcio y magnesio, que ayudan a regular la presión arterial. Por otro lado, es importante evitar el consumo excesivo de sodio, ya que ... cite them right mhraWebNephrocystin-3; Required for normal ciliary development and function. Inhibits disheveled-1-induced canonical Wnt-signaling activity and may also play a role in the control of non-canonical Wnt signaling which regulates planar cell polarity. Probably acts as a molecular switch between different Wnt signaling pathways. diane reay working class