نتایج جستجو برای: cyp1b1 gene mutation

تعداد نتایج: 1285161  

Farhud, Daryoush, Pourkalhor , Hanieh ,

Neurofibromatosis is a genetic disorder that causes tumors in nerve tissue. These tumors can grow in any part of the nervous system, including the brain, spinal cord and nerves. The disease gene can be passed from a parent to a child through marked autosomal dominant inheritance or it can happen due to a spontaneous mutation of a gene. A parent with neurofibromatosis has a 50% chance of passing...

Journal: :مجله دانشگاه علوم پزشکی کرمانشاه 0
rahim golmohamadi department of anatomical medicine, sabzevar university of medical sciences mehdi nikbakht department of anatomical medicine, isfahan university of medical sciences

introduction: colorectal cancer (crc) is one of the most prevalent cancers in the world. genetic disorders and dietary habits play a part in crc. the most important cancer suppressor gene is p53. different mutations rates in 7th exon of p53 gene are reported in different areas  which may have a relationship with prognosis of crc. this study examines the relationship between mutation in 7th exon...

Journal: :Human molecular genetics 1997
I Stoilov A N Akarsu M Sarfarazi

Primary congenital glaucoma (Buphthalmos) is an autosomal recessive eye disorder, postulated to result from developmental defects in the anterior eye segment. Previously, we reported two chromosomal locations for this condition on 2p21 (GLC3A) and 1p36 (GLC3B) respectively. In this study, heritable mutations of human cytochrome P4501B1 gene (CYP1B1) in affected individuals of five well-characte...

Journal: :iranian journal of child neurology 0
mohammad mehdi heidari* 1. department of biology, school of sciences, yazd university, yazd, iran mehri khatami 1. department of biology, school of sciences, yazd university, yazd, iran jafar pourakrami 2. department of biology, faculty of sciences, science and research branch of the islamic azad university, tehran, iran.

how to cite this article: heidari mm , khatami m, pourakrami j. novel point mutations in frataxin gene in iranian patients with friedreich’s ataxia. iran j child neurol. 2014 winter; 8(1):32-36.   objective friedreich’s ataxia is the most common form of hereditary ataxia with autosomal recessive pattern. more than 96% of patients are homozygous for gaa repeat extension on both alleles in the fi...

Journal: :international journal of reproductive biomedicine 0
mir davood omrani agneta nordenskhold

background: for screening sequence variations in genes, rapid turnover time is of fundamental importance. while, many of the current methods are unfortunately time consuming and technically difficult to implement. denaturing high-performance liquid chromatography (dhplc) method had been shown to be a high-throughput, time saving, and economical tool for mutation screening. objective: in the pre...

Journal: :Molecular pharmacology 2002
Eleni Aklillu Mikael Oscarson Mats Hidestrand Brith Leidvik Charlotta Otter Magnus Ingelman-Sundberg

Cytochrome P450 1B1 (CYP1B1) is an extrahepatic enzyme of potential importance for the metabolism of estrogen and for metabolic activation of environmental carcinogens. We investigated an Ethiopian population for functional polymorphisms in the CYP1B1 gene using genomic DNA sequencing and detected three novel single nucleotide polymorphisms (SNPs). One of these (4360C-->G in exon 3) is present ...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2007
Wanqing Wen Zefang Ren Xiao Ou Shu Qiuyin Cai Chuanzhong Ye Yu-Tang Gao Wei Zheng

Cytochrome P450 1B1 (CYP1B1) and catechol-O-methyltransferase (COMT) are important estrogen-metabolizing enzymes that may affect breast cancer risk. Few studies have directly measured the expression of CYP1B1 and COMT genes in breast tissue samples. The subjects in this study were a subgroup of participants of the Shanghai Breast Cancer Study including 64 patients diagnosed with breast cancer a...

2009
Mukesh Tanwar Tanuj Dada Ramanjit Sihota Rima Dada

PURPOSE Primary congenital glaucoma (PCG) is an autosomal recessive eye disorder that is postulated to result from developmental defects in the anterior eye segment. Mutations in the cytochrome P4501B1 (CYP1B1) gene are a predominant cause of congenital glaucoma. In this study we identify CYP1B1 mutations in PCG patients. METHODS Twenty-three unrelated PCG patients and 50 healthy controls wer...

Journal: :Cancer research 2006
Yuki Tsuchiya Miki Nakajima Shingo Takagi Takao Taniya Tsuyoshi Yokoi

MicroRNAs (miRNA) are small noncoding RNAs that regulate gene expression through translational repression or mRNA cleavage. Here, we found that cytochrome P450 (CYP), a superfamily of drug-metabolizing enzymes, is a target of miRNA. Human CYP1B1, which is highly expressed in estrogen target tissues, catalyzes the metabolic activation of various procarcinogens and the 4-hydroxylation of 17beta-e...

Journal: :Clinical chemistry 1998
C Dassi S Signorini P Gerthoux M Cazzaniga P Brambilla

Cytochrome P450 (CYP) 1B1 activates polycyclic aromatic hydrocarbons and aryl aromatic hydrocarbons to carcinogens. We describe a competitive reverse transcription-PCR (RT-PCR) assay for the quantification of CYP1B1 mRNA in blood mononuclear cells (BMCs) by simultaneous RT and PCR amplification of cellular RNA with decreasing amounts of an internal standard. The concentration of CYP1B1 mRNA is ...

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