نتایج جستجو برای: protein sequencing

تعداد نتایج: 1336591  

The flowering process in plants proceeds through the induction of an inflorescence meristem triggered by several pathways. Many of the genes associated with these pathways encode transcription factors of the MADS domain family. The MADS-domain transcription factor APETALA1 (AP1) is a key regulator of flower development. The first step to understand the molecular mechanisms under the function of...

Journal: :iranian biomedical journal 0
نیره نوری nayereh nouri نرگس نوری narges nouri امید آریانی omid aryani بهنام کمالی دهقان behnam kamalidehghan مریم صدقی maryam sedghi مسعود هوشمند massoud houshmand

background: ataxia with oculomotor apraxia type 1 (aoa1) shows early onset with autosomal recessive inheritance and is caused by a mutation in the aprataxin (aptx) gene encoding for the aptx protein. methods: in this study, a 7-year-old girl born of a first-cousin consanguineous marriage was described with early-onset progressive ataxia and aoa, with increased cholesterol concentration and decr...

Journal: :iranian journal of parasitology 0
m niyyati department of parasitology and mycology, school of public health, tehran university of medical sciences, tehran, iran s rezaie department of parasitology and mycology, school of public health, tehran university of medical sciences, tehran, iran z babaei department of parasitology and mycology, school of public health, tehran university of medical sciences, tehran, iran m rezaeian department of parasitology and mycology, school of public health, tehran university of medical sciences, tehran, iran

background: acanthamoeba keratitis develops by pathogenic acanthamoeba such as a. pal­es­tinen­sis . indeed this species is one of the known causative agents of amoebic keratitis in iran. mannose binding protein (mbp) is the main pathogenicity factors for developing this sight threatening disease. we aimed to characterize mbp gene in pathogenic acanthamoeba isolates such as a. palestinensis . m...

   Background & Objective:  Peroxisome biogenesis disorders (PBDs) are a group of diseases with peroxisomal dysfunction. Wide range of symptoms are associated with the disease which are due to mutations in the PEX genes. The PEX1 mutation occurs in Zellweger syndrome (ZS), a severe autosomal recessive condition with hypotonia, intellectual disability, and hepatic enlargement. The present study ...

Journal: :Current Opinion in Structural Biology 2017

Fatemeh Shenavar Mahboobeh Khodadad, Mohammad-Reza Fattahi Nasrollah Erfani, Reza Hajhosseini Samaneh Bina Seyed Younes Hosseini, Shahin Ahmadian,

Objective(s): Up to now, many researches have been performed to improve the antitumoral effect of melanoma differentiation-associated gene-7 (mda-7) protein. The purpose of our research was to construct 3 expression vectors producing mda-7 in fusion with RGD (Arginine-Glycine-Aspartic acid) peptide and evaluate their expression.     Materials and Methods: mda-7 gene with two different RGD sequ...

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