نتایج جستجو برای: x gene mutations

تعداد نتایج: 1789763  

Asadi F, Hashemian E Mirfakhrai R

Background: Mayer - Rokitansky - Kuster - Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part of the vagina in women showing normal development of secondary sexual characteristics and a normal 46, XX karyotype. Congenital anomaly of the female genital tract, estimated to occur in approximately 1 in every 5,000 females. It is caused by a failure of deve...

Journal: :iranian journal of parasitology 0
soudabeh heidari parasitology and mycology dept. shahid beheshti university of medical sciences, tehran, iran. mojgan bandehpour cellular and molecular biology research center, shahid beheshti university of medical sciences, tehran, iran and biotechnology dept. shahid beheshti university of medical sciences, tehran, iran. seyyed-javad seyyed-tabaei parasitology and mycology dept. shahid beheshti university of medical sciences, tehran, iran. zarintaj valadkhani parasitology dept. pasteur institute of iran, tehran, iran. ali haghighi parasitology and mycology dept. shahid beheshti university of medical sciences, tehran, iran. alireza abadi social medicine dept. shahid beheshti university of medical sciences, tehran, iran.

background: trichomonas vaginalis causes trichomoniasis and metronidazole is its chosen drug for treatment. ferredoxin has role in electron transport and carbohydrate metabolism and the conversion of an inactive form of metronidazole (co) to its active form (cpr). ferredoxin gene mutations reduce gene expression and increase its resistance to metronidazole. in this study, the frequency of ferre...

Nuclear genetic mutations have been extensively investigated in solid tumors. However, the role of the mitochondrial genome remains uncertain. Since the metabolism of solid tumors is associated with aerobic glycolysis and high lactate production, tumors may have mitochondrial dysfunctions. Familial adenomatous polyposis (FAP) is a rare form‌ of colorectal cancer and an autosomal dominant inheri...

Hamid Tebyanian, Hamze farhadian Mehdi Behdani Mohamad Reza Imen Shahidi,

Objective: The Rifampicin resistance and susceptibility of Mycobacterium tuberculosis are caused by mutations in the 81-base pair region of the rpoB gene encoding the b-subunit of RNA polymerase. Methods: Isoniazid resistance of M. tuberculosis is related to mutations in inha , oxyR and ahpC genes which 30 to 90 percent of Isoniazid resistance is occurred in 3015 codons of kat...

2017
Dinesh Rakheja Kenneth S. Chen Yangjian Liu Abhay A. Shukla Vanessa Schmid Tsung-Cheng Chang Shama Khokhar Jonathan E. Wickiser Nitin J. Karandikar James S. Malter Joshua T. Mendell James F. Amatruda

Farzaneh Ghasemi, Mehri Khatami, Mohammad Mehdi Heidari, Reyhane Chamani,

Background: CDKN2A, encoding two important tumor suppressor proteins p16 and p14, is a tumor suppressor gene. Mutations in this gene and subsequently the defect in p16 and p14 proteins lead to the downregulation of RB1/p53 and cancer malignancy. To identify the structural and functional effects of mutations, various powerful bioinformatics tools are available. The aim of this study is the ident...

Introduction: Pseudomonas aeruginosa is an opportunistic pathogen of clinical importance, particularly in immunocompromised and burn patients. This bacterium is becoming resistant to many antibiotics via intrinsic or acquired mechanisms. Mutations in anti-mutator genes, such as pfpI, can be a potential intrinsic mechanism of antibiotic resistance. This study aimed to evaluate the possible effec...

Background: Phenylketonuria (PKU), the most common inborn error of aminoacid metabolism, is an autosomal recessive disorder caused by more than 600 mutations in Phenylalanine Hydroxylase gene (PAH). Distribution pattern of mutations in the PAH gene are specific to each population. The aim of this study was to identify mutations in exons 10 and 11 of the PAH gene in patients with PKU from Golest...

Journal: :international journal of advanced biological and biomedical research 2014
hamid tebyanian hamze farhadian mohamad reza imen shahidi mehdi behdani

objective: the rifampicin resistance and susceptibility of mycobacterium tuberculosis are caused by mutations in the 81-base pair region of the rpob gene encoding the b-subunit of rna polymerase. methods: isoniazid resistance of m. tuberculosis is related to mutations in inha , oxyr and ahpc genes which 30 to 90 percent of isoniazid resistance is occurred in 3015 codons of katg gene. the rpob a...

Journal: :پژوهش های علوم دامی ایران 0
زینب محمدی هدایت الله روشنفکر محمد تقی بیگی نصیری حمید رجبی معماری

the aim of the current study is to amplification the regularity region encompassed the mutations changing the myostatin gene express and also to determine sequential analysis. the blood samples taken from 12 najdi cattles in najdi cattle station in shushtar city, khuzestan province. then the dna extracted to amplification 730bp and 561bp fragments. sequencing was performed after the precision i...

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