نتایج جستجو برای: azfa

تعداد نتایج: 158  

Journal: :Actas urologicas espanolas 2014
A Gallego R Rogel S Luján B Plaza F Delgado F Boronat

OBJECTIVE Aproximately 10% of patients with non-obstructive azoospermia and 5% with non-obstructive severe oligozoospermia carry AZF region microdeletions (AZoospermic Factor) in the Y chromosome. The aim of this study is to analize the clinical and pathological findings in this group of patients and compare them with the previous evidence. MATERIAL AND METHODS Retrospective study of 11 patie...

ژورنال: ارمغان دانش 2013
بردبار, مریم , حجتی, زهره , رضایی, زهرا, متولی باشی, مجید , محمودی, رضا,

چکیده زمینه و هدف: حذف ها در کرومزوم Y یکی از دلایل عمده ژنتیکی ناباروری است. هدف این مطالعه تعیین فراوانی حذف‌های کوچک ناحیه AZF کروموزم Y مردان نابارور در جمعیت اصفهان بود. روش بررسی: در این مطالعه موردـ شاهدی به طور تصادفی تعداد 100 مرد نابارور مراجعه کننده به مرکز ناباروری اصفهان به عنوان گروه مورد و 100 مرد بارور سالم به عنوان گروه شاهد انتخاب شدند. DNAخون افراد هر دو گروه استخراج ...

Journal: :Human reproduction 2012
Craig Niederberger

BACKGROUND DDX3Y (DBY), located within AZoospermia Factor a (AZFa) region of the human Y chromosome (Yq11), encodes a conserved DEAD-box RNA helicase expressed only in germ cells and with a putative function at G1-S phase of the cell cycle. Deletion of AZFa results most often in germ cell aplasia, i.e. Sertoli-cell-only syndrome. To investigate the function of DDX3Y during human spermatogenesis...

Journal: :Asian journal of andrology 2011
Qing Wu Guo-Wu Chen Tao-Fei Yan Hui Wang Yu-Ling Liu Zheng Li Shi-Wei Duan Fei Sun Yun Feng Hui-Juan Shi

Multiplex polymerase chain reaction (PCR) has been widely used to detect Y-chromosome microdeletions, which is one of the major causes of male infertility. Both the European Academy of Andrology (EAA) and the European Molecular Genetics Quality Network (EMQN) have recommended the use of sY84 and sY86 markers for the detection of azoospermia factor a (AZFa) microdeletion during DNA testing for m...

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...

2017
Carolina Gonçalves Mariana Cunha Eduardo Rocha Susana Fernandes Joaquina Silva Luís Ferraz Cristiano Oliveira Alberto Barros Mário Sousa

The aim of the present work was to present the outcomes of the patients with Y-chromosome microdeletions treated by intracytoplasmic sperm injection (ICSI), either using fresh (TESE) or frozen-thawed (TESE-C) testicular sperm and ejaculated sperm (EJAC). The originality of this work resides in the comparisons between the different types of Y-microdeletions (AZFa, AZFb, and AZFc) and treatments,...

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: :Actas urologicas espanolas 2013
C R Bonarriba J P Burgués V Vidaña X Ruiz P Pizá

INTRODUCTION Testicular sperm extraction with intracytoplasmic sperm injection is the standard treatment for azoospermia. The objective of this study is to identify predictive factors of successful sperm retrieval. MATERIALS AND METHODS Between June 2003 and May 2011, we tried testicular sperm extraction (TESE) in 74 azoospermic patients in the Reproductive Medicine Unit of Son Espases Hospit...

2014
Qiu-Yue Wu Na Li Wei-Wei Li Tian-Fu Li Cui Zhang Ying-Xia Cui Xin-Yi Xia Jin-Sheng Zhai

BACKGROUND To review the possible mechanisms proposed to explain the etiology of 46, XX sex reversal by investigating the clinical characteristics and their relationships with chromosomal karyotype and the SRY(sex-determining region Y)gene. METHODS Five untreated 46, XX patients with SRY-positive were referred for infertility. Clinical data were collected, and Karyotype analysis of G-banding ...

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