نتایج جستجو برای: y chromosomal microdeletions

تعداد نتایج: 539215  

2013
Mohammad Hasan Sheikhha Mohammad Ali Zaimy Saeede Soleimanian Seyed Mehdi Kalantar Azam Rasti Maryam Golzade Hamid Hoseini Fahraji

BACKGROUND It has been hypothesized that Y-q microdeletion can account for significant proportion of infertility in men. There are three nonoverlapping regions referred to as the "azoozpermia factors" AZFa, AZFb, and AZFc from proximal to distal part of Y-q. These have been defined as spermatogenesis loci, this region deletions have been shown to be involved in male azoospermic or severe oligoo...

Journal: :Asian journal of andrology 2012
Annelien Massart Willy Lissens Herman Tournaye Katrien Stouffs

Approximately 10%-15% of couples are infertile, and a male factor is involved in almost half of these cases. This observation is due in part to defects in spermatogenesis, and the underlying causes, including genetic abnormalities, remain largely unknown. Until recently, the only genetic tests used in the diagnosis of male infertility were aimed at detecting the presence of microdeletions of th...

2014
Xiao-Bin Zhu Zi-Jue Zhu Er-Lei Zhi Zheng Li

Objective: Microdeletions of azoospermia factor (AZF) regions in Y chromosome were a genetic risk factor of spermatogenic failure and male infertility. Most laboratories carried out the AZF microdeletion testing by using peripheral intravenous blood, and AZF microdeletion in spermatozoa of infertile patients was sometimes not identical to that of peripheral intravenous blood due to the existenc...

Journal: :Genetics and molecular research : GMR 2015
Y Dong Y Pan R Wang Z Zhang Q Xi R-Z Liu

Male infertility is mostly caused by spermatogenic failure. Currently, routine genetic analyses of unexplained azoospermia or oligozoospermia are limited to the investigation of Y chromosomal microdeletions and chromosome karyotype analyses. The aim of this study was to find spermatogenic failure genes in patients with chromosomal abnormalities and unexplained azoospermia caused by copy number ...

2018
Dominik S. Westphal Stephanie Andres Christine Makowski Thomas Meitinger Julia Hoefele

Introduction: Microdeletions in the chromosomal region 2q34 and its neighboring regions lead to a phenotypic spectrum including autism, intellectual disability, and epilepsy. Up to now, only few affected patients have been reported. Therefore, the genetic pathogenesis is not completely understood. One of the most discussed candidate genes in this context is MAP2, a gene responsible for microtub...

2013
Don Kyung Choi In Hyuck Gong Jin Ho Hwang Jong Jin Oh Jae Yup Hong

PURPOSE We evaluated clinical characteristics, sperm retrieval rates, and birth rates in a relatively large number of infertile patients with Y chromosome microdeletions. MATERIALS AND METHODS We retrospectively reviewed clinical data from 213 patients with nonobstructive azoospermia (NOA) and 76 patients with oligoasthenoteratozoospermia (OATS) who were tested for Y chromosome microdeletion ...

Journal: :Human reproduction 2013
Heike Cappallo-Obermann Caroline Feig Wolfgang Schulze Andrej-Nikolai Spiess

STUDY QUESTION What are the reference values for delineating altered somatic cell gene expression from transcript enrichment/dilution in gene expression studies of human spermatogenesis? SUMMARY ANSWER We have designed a crosstable and rule-of-thumb values for different stages of spermatogenic impairment that define the reference cut-off values for altered gene expression in Sertoli and Leydi...

2013
P. N. Barbhuiya R. Mahanta

Specific genetic marker based molecular study of the azfa & azfd region microdeletion in infertile cases of northeast india. a b c d e Introduction: The first cases of Y chromosome microdeletions and male infertility were reported in 1992 and many case series have subsequently been reported from various parts of the world. A very few studies have been done involving the patients of NorthEast In...

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