نتایج جستجو برای: azf microdeletions

تعداد نتایج: 1042  

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: :medical journal of islamic republic of iran 0
h najmabadi from the welfare science and rehabilitation university (hn), tehran, iran; karimi-nejad pathology & genetic center (hn, ss, fs), tehran, iran; division of endocrinology, metabolism, and molecularmedicine (kk. wt, lr, an, mg, sb) and department of obstetrics and gynecology (bs), charles r.drew university of medicine and science, los angeles, ca, usa; department of obstetrics andgynecology, university of melbourne, australia; institute of reproduction and development (dmdk,rim. kal), monash university, melbourne, australia, and prince henry:s medical research institute (rimc), and karolinska institute, stokholm, sweden (s a). dm de kretser s arver w taylor c mallidis hw gorden baker

it is now agreed that 10-25% of infertile men with azoospermia have submicroscopic deletions of the y chromosome long ann (yq), consistent with the proposed location of the azoospermia locus (azf) in yq 11.23. however, it is not known whether yq microdeletions are unique to men with azoospermia or whether they are also observed in infertile men with less severe defects of spermatogenesis (oligo...

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...

2016
Raheleh Masoudi Liusa Mazaheri-Asadi Shahryar Khorasani

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...

A NIEVA, B SUH, C MALLIDIS, DM De KRETSER, F SAHEBJAM, H NAJMABADI, HW GORDEN BAKER, KA LOVELAND, L RAMIREZ, M GUTIERREZ, RI McLACHLAN, S ARVER, S BHASIN, S SAHEBJAM, W TAYLOR,

It is now agreed that 10-25% of infertile men with azoospermia have submicroscopic deletions of the Y chromosome long ann (yq), consistent with the proposed location of the azoospermia locus (AZF) in Yq 11.23. However, it is not known whether Yq microdeletions are unique to men with azoospermia or whether they are also observed in infertile men with less severe defects of spermatogenesis (o...

2016
Virginie Riou Debany Fonseca-Batista Arnout Roukaerts Isabelle C. Biegala Shree Ram Prakya Clara Magalhães Loureiro Mariana Santos Angel E. Muniz-Piniella Mara Schmiing Marc Elskens Natacha Brion M. Ana Martins Frank Dehairs

To understand the impact of the northwestern Azores Current Front (NW-AzC/AzF) system on HCO3--and N2-fixation activities and unicellular diazotrophic cyanobacteria (UCYN) distribution, we combined geochemical and biological approaches from the oligotrophic surface to upper mesopelagic waters. N2-fixation was observed to sustain 45-85% of the HCO3--fixation in the picoplanktonic fraction perfor...

2017
Fahimeh Asadi Mohammad Ali Sadighi Gilani Azadeh Ghaheri Javad Roodgar Saffari Mohammadreza Zamanian

OBJECTIVE Microdeletions of the Y chromosome long arm are the most common molecular genetic causes of severe infertility in men. They affect three regions including azoospermia factors (AZFa, AZFb and AZFc), which contain various genes involved in spermatogenesis. The aim of the present study was to reveal the patterns of Y chromosome microdeletions in Iranian infertile men referred to Royan In...

Journal: :Reports of biochemistry & molecular biology 2017
Zeeba Kamaliyan Sara Pouriamanesh Mona Amin-Beidokhti Amir Rezagholizadeh Reza Mirfakhraie

BACKGROUND The PIWI-interacting RNA (piRNA) pathway has an essential role in transposon silencing, meiosis progression, spermatogenesis, and germline maintenance. HIWI genes are critical for piRNA biogenesis and function. Therefore, polymorphisms in HIWI genes contribute to spermatogenesis defects and can be considered as risk factors for male infertility. The aim of the present study was to in...

Journal: :Journal of andrology 2003
Kumarasamy Thangaraj Nalini J Gupta Kadupu Pavani Alla G Reddy Subbaya Subramainan Deepa Selvi Rani Bibaswan Ghosh Baidyanath Chakravarty Lalji Singh

Genetic factors cause about 10% of male infertility. Azoospermia factors (AZFa, AZFb, AZFc) are considered to be the most important for spermatogenesis. We therefore made an attempt to evaluate the genetic cause of azoospermia, Y chromosome deletion in particular, in Indian men. We have analyzed a total of 570 men, including 340 azoospermic men and 230 normal control subjects. DNA samples were ...

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