نتایج جستجو برای: ژن ctns

تعداد نتایج: 15923  

Journal: :Journal of bacteriology 2000
Q Cheng B J Paszkiet N B Shoemaker J F Gardner A A Salyers

Bacteroides conjugative transposons (CTns) are thought to transfer by first excising themselves from the chromosome to form a nonreplicating circle, which is then transferred by conjugation to a recipient. Earlier studies showed that transfer of most Bacteroides CTns is stimulated by tetracycline, but it was not known which step in transfer is regulated. We have cloned and sequenced both ends o...

Journal: :Journal of the American Society of Nephrology : JASN 2014
Robert L Chevalier

Although rare, nephropathic cystinosis is a devastating monogenic disorder leading to renal failure in the second decade of life. Fanconi syndrome, the initial renal manifestation of cystinosis in the young child, established the proximal tubule as a primary target of injury now recognized as the result of mutations in cystinosin (CTNS), the lysosomal cystine-proton cotransporter.1 A major chal...

Journal: : 2023

Nephropathic cystinosis is a rare inherited disease characterized by cristallization of cystine in lyzosomes. Cystine accumulation caused the mutations CTNS gene encoding for cystinosine, transporter. Cystinosis commonly affects kidneys leading to renal Fanconi sysnrome during first year life, followed progressive kidney failure that necessitates initiation replacement therapy childhood or adol...

Journal: :Journal of Entomological Society of Iran 2023

وراثت مقاومت سفیدبالک گلخانه، Trialeurodes vaporariorum Westwood (Hemiptera: Aleyrodidae)، به دو ترکیب ایمیداکلوپرید و کلرپایریفوس مورد مطالعه قرار گرفت. در این پژوهش، از جمعیت فیلستان ورامین (FL) عنوان والد مقاوم فردیس کرج (FR) حساس استفاده شد. مقدار ترتیب حدودا 62/13 91/14 برابر بود. عدم وجود اختلاف معنی‌دار LC50 روی تلاقی‌های F1 (R♂×S♀) Fʹ1 (R♀×S♂) نشان داد که T. نوع اتوزومی (غیرجنسی) است. ه...

Journal: :Kidney international 2016
Craig B Langman Bruce A Barshop Georges Deschênes Francesco Emma Paul Goodyer Graham Lipkin Julian P Midgley Chris Ottolenghi Aude Servais Neveen A Soliman Jess G Thoene Elena N Levtchenko

Nephropathic cystinosis is an autosomal recessive metabolic, lifelong disease characterized by lysosomal cystine accumulation throughout the body that commonly presents in infancy with a renal Fanconi syndrome and, if untreated, leads to end-stage kidney disease (ESKD) in the later childhood years. The molecular basis is due to mutations in CTNS, the gene encoding for the lysosomal cystine-prot...

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