نتایج جستجو برای: azf region

تعداد نتایج: 538164  

2015
Majid Motovali-Bashi Zahra Rezaei Fariba Dehghanian Halimeh Rezaei

Received: 22 December 2014 Revised: 26 April 2015 Accepted: 12 May 2015 Abstract Background: Infertility is a health problem which affects about 10-20% of married couples. Male factor infertility is involved approximately 50% of infertile couples. Most of male infertility is regarding to deletions in the male-specific region of the Y chromosome. Objective: In this study, the occurrence of delet...

Journal: :Genetics and molecular research : GMR 2013
H-G Zhang Z-B Zhang R-X Wang Y Yu X-W Yu E Fadlalla R-Z Liu

The prevalence of microdeletions of azoospermia factor (AZF) among azoospermic Klinefelter's syndrome (KFS) patients shows conflicting data. We aimed to detect this frequency in a Northeast Chinese population, and to investigate the possible association between AZF microdeletions and KFS by comparison with previous conflicting reports. Eighty men affected with KFS and a random healthy control g...

Journal: :International Journal of Andrology 2008

2016
Wooi F. Lim Jon Burdach Alister P.W. Funnell Richard C.M. Pearson Kate G.R. Quinlan Merlin Crossley

Transcription factors are often regarded as having two separable components: a DNA-binding domain (DBD) and a functional domain (FD), with the DBD thought to determine target gene recognition. While this holds true for DNA bindingin vitro, it appears thatin vivoFDs can also influence genomic targeting. We fused the FD from the well-characterized transcription factor Krüppel-like Factor 3 (KLF3)...

2010
Paulo Navarro-Costa Carlos E. Plancha João Gonçalves

The azoospermia factor (AZF) regions consist of three genetic domains in the long arm of the human Y chromosome referred to as AZFa, AZFb and AZFc. These are of importance for male fertility since they are home to genes required for spermatogenesis. In this paper a comprehensive analysis of AZF structure and gene content will be undertaken. Particular care will be given to the molecular mechani...

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...

Background The human Y chromosome is essential for human sex determination and male germ cell development and maintenance. In 1996, Vogt et al. identified three recurrently deleted regions in Yq11 termed the azoospermia factor (AZF). The AZF region is subdivided into three non-overlapping sub-regions called AZFa, AZFb and AZFc and microdeletion in these regions is the most important etiology of...

Journal: :Human reproduction 1997
J A Kremer J H Tuerlings E J Meuleman F Schoute E Mariman D F Smeets L H Hoefsloot D D Braat H M Merkus

Intracytoplasmic sperm injection (ICSI) is a successful treatment option for severe male infertility, although the aetiology of the disorder remains unclear in most cases. Recently, microdeletions in the AZF region of the Y chromosome have been detected in men with azoospermia or severe oligozoospermia. In this study we investigated the prevalence of microdeletions in the AZF region of the Y ch...

2013
Ramaswamy Suganthi VV Vijesh Sanjay Jayachandran Jahangir Ali Fathima Benazir

BACKGROUND Y chromosomal microdeletion is an important genetic disorder, which may arise due to intrachromosomal recombination between homologous sequences in the male specific region of the human Y chromosome. It is frequently associated with the quantitative reduction of sperm. The screening for Y chromosomal microdeletions has a great clinical value. OBJECTIVE To develop a sequence tagged ...

Journal: :Asian journal of andrology 2007
Jin Ho Choe Jong Woo Kim Joong Shik Lee Ju Tae Seo

AIM To evaluate the occurrence of classical azoospermia factor (AZF) deletions of the Y chromosome as a routine examination in azoospermic subjects with Klinefelter syndrome (KS). METHODS Blood samples were collected from 95 azoospermic subjects with KS (91 subjects had a 47,XXY karyotype and four subjects had a mosaic 47,XXY/46,XY karyotype) and a control group of 93 fertile men. The values ...

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