نتایج جستجو برای: gene deletion

تعداد نتایج: 1179434  

Journal: : 2021

Objective: Dystrophinopathies are the most frequently researched neuromuscular disease group due to their characteristic and diverse clinical genetic spectrum. This study aims evaluate deletion duplication profile of dystrophin gene in Turkey by investigating data from a tertiary center. Material Methods: Dystrophin MLPA microarray results 53 patients, 49 with dystrophinopathy 4 neurogenetic sy...

Journal: :acta medica iranica 0
a nikzamir department of biochemistry, school of medicine, ahwaz jondi shapour university of medical sciences, m nakhjavani endocrinology and metabolism research center (emrc), vali-e-asr hospital, tehran university of medic t golmohammadi department of biochemistry, school of medicine, tehran university of medical sciences, tehran, iran l dibai endocrinology and metabolism research center (emrc), vali-e-asr hospital, tehran university of medic r saffary endocrinology and metabolism research center (emrc), vali-e-asr hospital, tehran university of medic

diabetes mellitus is a multifactorial disease. it has recently been shown that an insertion (i)/deletion (d) polymorphism exists in the angiotensin-converting enzyme (ace) gene that can affect the serum ace level. there are three genotypes: dd, di, and ii, with the ace level being highest in dd, intermediate in di, and lowest in ii. in the present investigation, 170 patients with type 2 diabete...

تقوی, سیداسداله, رستگار لاری, قاسم, رسول زادگان, مریم, علا, فریدون, کاظمی, احمد,

    Background & Aim: Bernard-Soulier syndrome (B.S.S) is a rare hereditary bleeding disorder due to molecular defects of platelet GPIb–IX–V. The GPIb-IX-V complex is composed of four chains of GPIbα, GPIbβ, GPIX and GPV.  The largest chain of this complex is GPIbα and is responsible for binding to ligand and most of identified mutations belong to this glycoprotein.  The aim of  this  study was...

Autumn sowing of sugar beet is a suitable way in sustainable agriculture. Bolting is an undesirable phenomenon which reduces sugar beet yield and it is the most important limiting factor in autumn sowing of sugar beet. Identification and comparison of the sequence of flowering genes in various genotypes can help to understand the molecular mechanisms controlling bolting. In the previous studies...

Khazaei Koohpar, Zeinab, Ranji, Najmeh, Rezaei, Omid,

Introduction: Mutation in SLC26A4 gene is one of reason of syndromic and non-syndomic hearing loss. Mutation in this gene is reported to be the second most common cause of deafness in the worldwide, after GJB2 gene. The aim of this study was to evaluate mutations in exon 10 of SLC26A4 gene in individuals with hearing loss in Guilan province. Materials and Methods: In this descriptive cross-sect...

Journal: :Wellcome open research 2023

We present the genome sequence of Leishmania mexicana MNYC/BZ/62/M379 modified to express Cas9 and T7 RNA-polymerase, revealing high similarity reference (MHOM/GT2001/U1103). Through RNAseq-based annotation coding sequences untranslated regions, we provide primer for construct sgRNA template generation CRISPR-assisted gene deletion endogenous tagging.

Journal: :iranian journal of veterinary research 2013
a. s. bagheri sarvestani a. niazi m. j. zamiri m. dadpasand taromsari

the induction and regulation of broodiness is of the most important role of prolactin in avian species.the promoter region of the prolactin gene is an appropriate model for studying tissue-specific andhormonally-regulated activation of gene transcription. in this study, the association between prolactinpromoter region alleles and egg production in fars native chickens was investigated. in total...

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