نتایج جستجو برای: 89 mutation

تعداد نتایج: 345254  

Journal: :College & Research Libraries 1989

Journal: :Journal of the South African Veterinary Association 2018

Journal: :Journal of the Royal Statistical Society: Series A (Statistics in Society) 1991

Journal: :Proteins 2021

Proteins: Structure, Function, and BioinformaticsVolume 89, Issue 4 p. C1-C1 ISSUE INFORMATION - COVER IMAGEFree Access Cover Image, Volume First published: 02 March 2021 https://doi.org/10.1002/prot.25916AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text full-text accessPlease review our Terms Conditions of Use check box below sh...

2017
Kasper Aalbæk Kjærgaard Morten Krogh Christiansen Morten Schmidt Morten Smærup Olsen Henrik Kjærulf Jensen

BACKGROUND Heterozygous familial hypercholesterolemia increases the risk of adverse cardiovascular events. Whether affected relatives of probands are at increased risk remains unknown. We aimed to evaluate the long-term cardiovascular risk in heterozygous familial hypercholesterolemia relatives with a low-density lipoprotein receptor (LDLR) mutation who were all recommended statin therapy. ME...

Journal: :iranian journal of otorhinolaryngology 0
shahin abdollahi-fakhim department of pediatric otorhinolaryngology, children’s hospital, tabriz university of medical sciences, tabriz, iran. mehrdad asghari estiar department of medical genetics, school of medicine, tehran university of medical sciences, tehran, iran. parizad varghaei faculty of medicine, tabriz university of medical sciences, tabriz, iran mahdi alizadeh sharafi tabriz genetic analysis center (tgac), tabriz university of medical sciences, tabriz, iran. masoud sakhinia faculty of medicine, university of liverpool, liverpool, united kingdom. ebrahim sakhinia tuberculosis and lung disease research center, tabriz university of medical sciences, tabriz, iran.

introduction: cleft lips and cleft palates are common congenital abnormalities in children. various chromosomal loci have been suggested to be responsible the development of these abnormalities. the present study was carried out to investigate the association between the suspected genes (methylenetetrahydrofolate reductase [mthfr] a1298c and c677t) that might contribute into the etiology of the...

Journal: :Haematologica 2010
Hoi Soo Yoon Hee-Jin Kim Keon-Hee Yoo Ki-Woong Sung Hong-Hoe Koo Hyoung Jin Kang Hee Young Shin Hyo Seop Ahn Ji-Yoon Kim Young-Tak Lim Keun-Wook Bae Ki-O Lee Ji-Sook Shin Seung-Tae Lee Hae-Sun Chung Sun-Hee Kim Chan-Jeoung Park Hyun-Sook Chi Ho-Joon Im Jong Jin Seo

BACKGROUND Familial hemophagocytic lymphohistiocytosis is a fatal disease characterized by immune dysregulation from defective function of cytotoxic lymphocytes. Three causative genes have been identified for this autosomal recessive disorder (PRF1, UNC13D, and STX11). We investigated the molecular genetics of familial hemophagocytic lymphohistiocytosis in Korea. DESIGN AND METHODS Pediatric ...

Hassan Dastsooz, Majid Fardaei, Nazanin Vahedi

Objective(s):  Denaturing high performance liquid chromatography (DHPLC) is a high throughput approach for screening DNA sequence variations. To assess oven calibration, cartridge performance, buffer composition and stability, the WAVE Low and High Range Mutation Standards are employed to ensure reproducibility and accuracy of the chromatographic analysis. The purpose of this study was to provi...

Journal: :Jundishapur journal of microbiology 2016
Zahra Eghbali Ali Mojtahedi Malek Moien Ansar Saba Fakhrieh Asl Keyvan Aminian

BACKGROUND Helicobacter pylori is curved Gram negative and microaerophilic bacilli that have infected half of the world's population. It is recognized as the causative agent of duodenal ulcer, gastritis peptic ulcer, mucosa-associated lymphoid tissue (MALT) lymphoma and is associated with gastric adenocarcinoma. Resistance to clarithromycin is related to point mutations in 23SrRNA gene on nt 21...

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