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C2orf37

WebDescription. C2orf37 antibody LS-C186957 is an unconjugated rabbit polyclonal antibody to human C2orf37 (DCAF17) (aa68-117). Validated for WB. WebDec 15, 2011 · Woodhouse–Sakati Syndrome (WSS) is a rare autosomal recessive multisystemic disorder that is marked by hypogonadism, alopecia, intellectual disability, deafness, diabetes mellitus and progressive extrapyramidal defects.Mutations in the gene C2orf37 are the cause of Woodhouse–Sakati syndrome. In the present study, a four …

Mutations in C2orf37, Encoding a Nucleolar Protein

WebView detailed information about property W10402 E 7th St, Black River Falls, WI 54615 including listing details, property photos, school and neighborhood data, and much more. WebC2orf37 antibody LS-C186957 is an unconjugated rabbit polyclonal antibody to human C2orf37 (DCAF17) (aa68-117). Validated for WB. Products. Research Areas. COVID-19. Resources. Contact Us. Distributors Login. Quick Order. Cart . Login. Registration enables users to use special features of this website, such as past combi beko b1rcne364w https://clustersf.com

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WebC7237 2.92F to 2.4F Adapter Centric RF. 800-399-6891. Login or Sign Up. 1130 Junction Dr. Suite 121 Allen, TX 75013 800-399-6891 [email protected]. 0. About Centric RF. … WebNovel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse-Sakati syndrome J Genet. 2015 Sep;94(3):489-92. doi: 10.1007/s12041-015-0544-7. Authors Mansoor C Abdulla 1 , Anas M Alazami, Jemshad Alungal, Jassim M Koya, Mohthash Musambil. Affiliation 1 Department of ... WebDec 1, 2008 · C2orf37 mutations were reported to be responsible for WSS in 2008 [5]. Nuclear C2orf37 overexpression was determined, compatibly with the disease … drug discovery scientist

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Category:C2orf37 mutational spectrum in Woodhouse-Sakati …

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C2orf37

3037 NW 92nd Ave, Coral Springs, FL 33065 Zillow

WebWoodhouse-Sakati syndrome (WSS) is a rare autosomal recessive disorder that encompasses hypogonadism, deafness, alopecia, mental retardation, diabetes mellitus … WebDec 1, 2010 · C2orf37 mutational spectrum in Woodhouse–Sakati syndrome patients. Woodhouse–Sakati syndrome (WSS) is a rare autosomal recessive disorder that encompasses hypogonadism, deafness, alopecia ...

C2orf37

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Proteintech Anti-C2orf37 Polyclonal, Catalog # 26033-1-AP. Tested in Western Blot (WB) and Immunohistochemistry (Paraffin) (IHC (P)) applications. This antibody reacts with Human, Mouse samples. Supplied as 150 µL purified antibody (0.3 mg/mL). WebMay 18, 2012 · Immunohistochemical analysis showed nearly ubiquitous nucleolar expression of C2orf37 in mouse embryos, with enhanced staining in brain, liver, and …

WebNov 2, 2010 · C2orf37 mutational spectrum in Woodhouse–Sakati syndrome patients. Woodhouse–Sakati syndrome (WSS) is a rare autosomal recessive disorder that encompasses hypogonadism, deafness, alopecia, mental retardation, diabetes mellitus and progressive extrapyramidal defects. The syndrome is caused by mutation of the C2orf37 … WebDec 15, 2011 · The C2orf37 shows high level expression in brain, liver and skin tissues that is consistent with the disease phenotype observed in these organs (Alazami et al., 2008). …

WebNov 20, 2008 · Our data revealed a common founder mutation in C2orf37 as the cause of WSS in all the Saudi families we examined, including the ones originally described by Woodhouse and Sakati. Subsequent …

WebAug 23, 2015 · A mutation in the C2orf37 gene was described as the cause of WSS in 2008 in the Saudi families including the ones originally described by Woodhouse and Sakati …

WebBioz Stars score, Techniques, Protocol Conditions and more for C2orf37 Rabbit Polyclonal Antibody, supplied by WuXi AppTec. Data for C2orf37 Rabbit Polyclonal Antibody gathered from related PubMed articles. drug discovery postdocWebNov 2, 2010 · C2orf37 mutational spectrum in Woodhouse–Sakati syndrome patients. Woodhouse–Sakati syndrome (WSS) is a rare autosomal recessive disorder that … combi baby seatsWebDec 1, 2010 · Direct sequencing of the C2orf37 gene revealed that the c.436delC (p.Ala147Hisfs*9) mutation was present in a homozygous state in all affected siblings and in a heterozygous state in the parents ... combi bathWebC2orf37 antibody LS-C477171 is an HRP-conjugated rabbit polyclonal antibody to C2orf37 (DCAF17) (aa68-117) from human. It is reactive with human and chimpanzee. Validated for WB. combi benchWebDec 15, 2011 · Linkage in the family was established to the gene C2orf37, mapped on chromosome 2q22.3–2q35. DNA sequence analysis revealed a novel splice site mutation involving a homozygous G → A transition in the splice donor site of intron 3 (c.321 + 1 G > A) of C2orf37. This study presents a first report of Woodhouse–Sakati syndrome … drug discovery services marketWebDec 12, 2008 · C2orf37 Mutations Are Responsible for Woodhouse-Sakati Syndrome (A) WSS patient with dystonia and alopecia. (B) One illustrative WSS pedigree showing multiple consanguinity loops. (C) Haplotype analysis of Saudi WSS patients. Each column represents one of the 18 patients studied, and each row represents one of the SNPs … drug discovery today 2003 8 1128WebJun 9, 2014 · (Beaches MLS) 4 beds, 2.5 baths, 3265 sq. ft. house located at 10237 NW 2nd St, Coral Springs, FL 33071 sold for $349,500 on Jun 9, 2014. MLS# F1258600. … combi blocks 試薬