نتایج جستجو برای: ژن ctsk

تعداد نتایج: 15893  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2013
Wei Chen Guochun Zhu Liang Hao Mengrui Wu Hongliang Ci Yi-Ping Li

Despite recent insights gained from the effects of targeted deletion of the Finkel-Biskis-Jinkins osteosarcoma oncogene (c-fos), Spleen focus-forming virus (SFFV) proviral integration 1 (PU.1), microphthalmia-associated transcription factor, NF-κB, and nuclear factor of activated cells cytoplasmic 1 (NFATc1) transcription factor genes, the mechanism underlying transcription factors specifying o...

2016
Bruna Benso Marcelo Franchin Adna Prado Massarioli Jonas Augusto Rizzato Paschoal Severino Matias Alencar Gilson Cesar Nobre Franco Pedro Luiz Rosalen

Given their medical importance, natural products represent a tremendous source of drug discovery. The aim of this study was to investigate Malva sylvestris L. extract and fractions and their pharmacological activities followed by chemical identification. The aqueous fraction (AF) was identified as the bioactive fraction in the in vitro and in vivo assays. The AF controlled the neutrophil migrat...

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: :American journal of medical genetics. Part A 2011
Debora Bertola Meire Aguena Guilherme Yamamoto Chong Ae Kim Maria Rita Passos-Bueno

Pycnodysostosis is a rare autosomal recessive bone disorder that results from loss-of-function mutations in the CTSK gene. This gene is located at chromosome band 1q21 and codes for a lysosomal cysteine protease that functions in bone resorption and remodeling [Gelb et al., 1996]. In the last 40 years, an atypical mode of inheritance (uniparental disomy—UPD) has been recognized as a mechanism r...

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