نتایج جستجو برای: single mutation

تعداد نتایج: 1124173  

B.Y. Cao, G.Q. Zhu Q.I. Wang Y.G. Kang Y.Z. Lv

In this study, we investigated the relationship between the genetic polymorphism of growth differentiation factor 9 (GDF9) genes and the litter size in 384 individuals of five breeds of black goats. Four pairs of primers were designed to detect single nucleotide polymorphism of GDF9 gene in goats by PCR-SSCP. The least square was used to analyze the relation between different genotypes and the ...

Journal: :iranian journal of basic medical sciences 0
abdolvahab moradi infectious diseases research center, department of microbiology, school of medicine, golestan university of medical sciences, gorgan, iran sareh zhand infectious diseases research center, department of microbiology, school of medicine, golestan university of medical sciences, gorgan, iran amir ghaemi infectious diseases research center, department of microbiology, school of medicine, golestan university of medical sciences, gorgan, iran naeme javid infectious diseases research center, department of microbiology, school of medicine, golestan university of medical sciences, gorgan, iran masoud bazouri infectious diseases research center, department of microbiology, school of medicine, golestan university of medical sciences, gorgan, iran alijan tabarraei infectious diseases research center, department of microbiology, school of medicine, golestan university of medical sciences, gorgan, iran

objective(s): it has been reported that the mutation of the pre-core (pc) and basal-core promoter (bcp) may play an important role in the development of hbv-related hepatocellular carcinoma (hcc). in this study the pc and bcp mutations were investigated in chronic hbv patients. materials and methods:in this study, 120 chronic hbv patients from golestan, northeast of iran who were not vaccinated...

Journal: :iranian journal of public health 0
m hashemzadeh chaleshtori dd farhud r taylor v hadavi ma patton ar afzal

mutations in the gjb2 gene at the dfnb1 locus on chromosome 13q12 are associated with autosomal recessive non syndromic hearing loss (arnshl) in many populations. a single mutation, at position 35 (35delg) accounts for approximately 30-63% of mutations in white populations with a carrier frequency of 1.5-2.5% in most european, north american and mediterranean populations. in this study we have ...

Journal: :Theoretical Computer Science 2023

Two mechanisms have recently been proposed that can significantly speed up finding distant improving solutions via mutation, namely using a random mutation rate drawn from heavy-tailed distribution (“fast mutation”, Doerr et al. (2017) [2]) and increasing the strength based on stagnation detection mechanism (Rajabi Witt (2020) [3]). Whereas latter obtain asymptotically best probability of singl...

Journal: :iranian biomedical journal 0
ایثار نصیری issar nassiri مهری فقیهی mehri faghihi منوچهر توسلی manoochehr tavassoli

background: pharmacogenomics is the study of genetic variations among individuals to predict the probability that a patient will respond to single or multidrug chemotherapy. breast cancer is one of the most common cancers among women worldwide. treatment of breast cancer by application of biological rationales gives us the ability to match the correct pharmacology to individual tumour genetic p...

Journal: :iranian journal of applied animal science 2013
g.q. zhu q.i. wang y.g. kang y.z. lv b.y. cao

in this study, we investigated the relationship between the genetic polymorphism of growth differentiation factor 9 (gdf9) genes and the litter size in 384 individuals of five breeds of black goats. four pairs of primers were designed to detect single nucleotide polymorphism of gdf9 gene in goats by pcr-sscp. the least square was used to analyze the relation between different genotypes and the ...

Journal: :iranian journal of medical sciences 0
z. rahimi a. vaisi raygani a. merat m. haghshenass n. gerard r.l. nagel

background: approximately 180 mutations have been described in β-thalassemia worldwide with specific spectrum in each ethnic population. this study determines the spectrum and the frequency of β-thalassemia mutations in patients with β-thalassemia trait and sickle cell-β-thalassemia.   methods: fifteen compound heterozygous sickle cell thalassemia (sct) and 23 β-thalassemia trait patients were ...

اکرمی پور, رضا, خالقی, سمیه, علی بخشی, رضا, بیدکی, سید کاظم ,

  Background: Alpha thalassemia is a single gene disorder, inherited in an autosomal recessive manner. The thalassemia occurs mostly in peoples from the Mediterranean to Southeast Asia. The present study was aimed to identify the prevalence of nondeletional Alpha thalassemia mutations in our samples in the Kermanshah province.   Methods : This study included Alpha thalassemia individuals who ha...

Members the DNA Methyltransferases (DNMT) gene family have been shown to play fundamental roles in regulating embryonic growth and development from embryonic fertilization to postnatal life; through regulating the establishment and/or maintenance of specific epigenetic marks. The present study was conducted to identify potential reported mutations within the exon 33 of DNMT-1, intron 4 of DNMT-...

Ali Ghorashi Hossein Hayatgheybi, Mahzad Akbarpour Masoud Houshmand

Background Ghezel sheep are highly prolific and one of the local sheep breeds in Iran and Turkey. Growth differentiation factor-9 (GDF9) gene has been found to be essential for growth and differentiation of early ovarian follicles. Novel mutations in GDF9 have been associated with increased ovulation rates and high litter sizes in heterozygous carriers. Therefore, fecundity gene for GDF9 (FecGH...

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