نتایج جستجو برای: polymorphism carrier detection

تعداد نتایج: 735034  

Azim Adibmanesh, Hamid Yaghooti, Mehrnoosh Zakerkish, Narges Mohammad Taghvaei,

Background: Nitric oxide (NO) produced by endothelial NO synthase (eNOS) mediates a large range of processes, and abnormality in the production of NO has been implicated in diabetic complications including diabetic nephropathy (DN). G894T polymorphism in the eNOS gene has been shown to decreased activity the NO levels of plasma. The association between eNOS Glu298Asp gene polymorphism and DN ri...

Journal: :Light: Science & Applications 2020

Journal: :Antimicrobial agents and chemotherapy 1999
A S Lee I H Lim L L Tang A Telenti S Y Wong

Genotypic analysis of resistance to isoniazid (INH) in Mycobacterium tuberculosis is complex due to the various genes potentially involved. Mutations in ketoacyl acyl carrier protein synthase (encoded by kasA) were present in 16 of 160 (10%) INH-resistant isolates (R121K [n = 1], G269S [n = 3], G312S [n = 11], G387D [n = 1]). However, G312S was also present in 6 of 32 (19%) susceptible strains....

Journal: :The British journal of ophthalmology 1995
A A Bergen J B ten Brink M J van Schooneveld

Juvenile retinoschisis is a rare, X linked hereditary vitroretinal degeneration. Female carriers of the disease do not develop any ocular abnormalities. Therefore, carrier detection by DNA analysis is extremely useful for these females. In order to evaluate the usefulness of a new class of DNA markers for carrier detection in X linked juvenile retinoschisis, DNA carrier detection or carrier exc...

Journal: :Journal of Clinical Investigation 1990

Journal: :American Journal of Clinical Pathology 2008

To prevent distribution of recessive alleles in dairy herds all bulls used for AI (Artificial Insemination) haveto be tested. In this study 26 blood and 4 semen samples were supplied from Iranian Holstein bulls used forAI. Genomic DNA was extracted from 100 μl of blood and 200 μl of semen. Samples were tested by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR...

Journal: :Journal of medical genetics 1989
A Figus R Lampis M Devoto M S Ristaldi A Ideo S de Virgilis A M Nurchi A Corrias R Corda M E Lai

Wilson's disease, a rare autosomal recessive disorder, has been recently mapped to the long arm of chromosome 13 (q14.1). In this study, we carried out linkage analysis between three chromosome 13 DNA markers, D13S1, D13S10, D13S2, the locus for the red cell enzyme esterase D (ESD), and the Wilson's disease locus (WND) in 17 Wilson's disease families of Italian descent, mostly from Sardinia. We...

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