نتایج جستجو برای: y chromosome

تعداد نتایج: 603865  

It has been established that the Y chromosome carries genes required for spermatogenesis and male fertility. For many decades worldwide screening for gene identification has been conducted in research laboratories. However, it has been a difficult process in identifying such genes (i.e. causative mutations) which could explain the phenotypic variation and could be potentially used as markers fo...

Journal: :international journal of reproductive biomedicine 0
rubina tabassum siddiqui nosheen mujtaba mamoona naz

background: microdeletions of the azoospermia factor locus of the long arm of y chromosome are an etiological factor of severe oligozoospermia or azoospermia. objective: the aim of this study was to investigate the prevalence of y-chromosome microdeletions in azf region and their role in infertility in pakistani population. materials and methods: the type of deletions in azf locus were detected...

Dissanayake Vajira HW Jayasekara RW Wetthasinghe TK

Background: Many advances have been made in reproductive medicine yet the spontaneous loss of a pregnancy remains the most common complication of pregnancy. The aetiology of spontaneous recurrent pregnancy loss (RPL) is multifactorial. Y chromosome microdeletions are found in approximately 7% of men with low sperm counts and, compared to the general population, a higher frequency of spontaneous...

Journal: :international journal of reproductive biomedicine 0
fadlalla elfateh ruixue wang zhihong zhang yuting jiang shuang chen ruizhi liu

background: wide range of disorders ranging from genetic disorders to coital difficulties can influence male fertility. in this regard, genetic factors are highlighted as the most frequent, contributed to 10-15%, of male infertility causes. objective: to investigate the influence of genetic abnormalities on semen quality and reproductive hormone levels of infertile men from northeast china. mat...

Y chromosome microdeletions are the second genetic cause of male infertility. The incidence of Y chromosome microdeletions can vary considerably depending on several factors, including patient selection criteria, population composition, and diagnostic protocols. They are associated with spermatogenic failure and lead to azoospermia or oligozoospermia. The advance in assisted reproductive techno...

Background and Aim: The Y-chromosome azoospermic factor (AZF) regions consist of genes whose specific roles and functions in spermatogenesis and fertility have not been completely clarified. Hence, recognition of the association between AZF microdeletions and male infertility has suggestions for the diagnosis, treatment, and genetic counseling. The main objective of the present study was invest...

Journal: :jentashapir journal of health research 0
sahar baheri physiology research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran ghasem saki physiology research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran; physiology research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran. tel/fax: +98-6113332036 javad mohammadi asl department of genetics, faculty of medicine, ahvaz jundishapur university of medical sciences, ahvaz, ir iran ali khodadadi department of immunology, faculty of medicine, ahvaz jundishapur university of medical sciences, ahvaz, ir iran

conclusions albumin gradient method is the enrichment of y-bearing chromosome sperms. separation of spermatozoa by albumin gradient method, introduced by ericsson, is a suitable method for sex selection of male offspring. this technique is safe, because it neither requires toxic materials during sperm separation, nor involves embryo manipulation. objectives the study aimed to assess the separat...

Journal: :journal of paramedical sciences 0
farhad shaveisi-zadeh department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran kimia davarian department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran abolfazl movafagh department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran reza mirfakhraie molecular pathology research center, imam reza hospital, kermanshah university of medical sciences, kermanshah, iran zahra rostami-far department of biochemistry, school of medicine, kermanshah university of medical sciences, kermanshah, iran reza alibakhshi department of biochemistry, school of medicine, kermanshah university of medical sciences, kermanshah, iran.

about 15% of couples have infertility problems, half of which are related to male factors. cytogenetic and genetic disorders account for about 10% of the male infertility problems. the aim of this study was to determine the frequency and types of both cytogenetic abnormalities and azf microdeletions of y chromosome in idiopathic azoospermic and oligospermic infertile men in west of iran. in thi...

Journal: :iranian journal of cancer prevention 0
pegah khosravi 1. dept. of bioinformatics, institute of biochemistry and biophysics (ibb), university of tehran, tehran, iran 2. school of biological sciences, institute for research in fundamental sciences (ipm), tehran, iran javad zahiri 1. faculty of mathematics, k. n. toosi university of technology, tehran, iran 2. dept. of bioinformatics, institute of biochemistry and biophysics (ibb), university of tehran, tehran, iran vahid h. gazestani institute of parasitology, mcgill university, montreal, quebec, canada samira mirkhalaf dept. of bioinformatics, institute of biochemistry and biophysics (ibb), university of tehran, tehran, iran mohammad akbarzadeh dept. of bioinformatics, institute of biochemistry and biophysics (ibb), university of tehran, tehran, iran mehdi sadeghi 1.national institute of genetic engineering and biotechnology, tehran, iran 2.school of biological sciences, institute for research in fundamental sciences (ipm), tehran, iran

background prostate cancer is a serious genetic disease known as the first widespread cancer in men, yet the molecular changes required for the cancer progression is not fully understood. availability of high-throughput gene expression data has led to the development of various computational methods for the identification of critical genes involved in the cancer. methods in this paper, we show ...

2003
Leonor Gusmão Angel Carracedo

The Y chromosome is one of the smallest human chromosomes with an average size of 60 million base pairs (Mb). Between X and Y chromosomes, exchange is limited to small pseudoautosomal regions (PAR) of the X-Y pair (see Figure 1). During male meiosis, recombination only takes place at the most distal short arm (PAR 1) and at the tip of the Y chromosome long arm (PAR 2). For most of its length (t...

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