نتایج جستجو برای: microdeletions

تعداد نتایج: 900  

Journal: :Central European Journal of Immunology 2020

2012
D Plaseska-Karanfilska P Noveski T Plaseski I Maleva S Madjunkova Z Moneva

Infertility is a major health problem today, affecting about 15.0% of couples trying to have a child. Impaired fertility of the male is causative in 20.0% of infertile couples and contributory in up to another 30.0-40.0%. Infertility already affects about 5.0-7.0% of the general male population and may further increase in the future, considering the apparent trend of declining sperm count in in...

Journal: :Journal of Experimental & Clinical Assisted Reproduction 2005
Paul E Kihaile Atsushi Yasui Yoshihiro Shuto

BACKGROUND To compare the frequency of Y-chromosome microdeletions in Japanese and African azoospermic and oligozoospermic men and describe embryo characteristics and reproductive outcome following in vitro fertilization (IVF) with intracytoplasmic sperm injection (ICSI). METHODS Our study was performed prospectively at two centers, a private IVF clinic and a university hospital. Japanese and...

Journal: :Human reproduction 2002
C M Luetjens J Gromoll M Engelhardt S Von Eckardstein M Bergmann E Nieschlag M Simoni

BACKGROUND Deletions of the AZF (azoospermia factor) subregions on the Y chromosome are accompanied by a diverse spectrum of spermatogenic disturbances ranging from hypospermatogenesis to total depletion of germ cells causing infertility. The AZF region encodes gene products which are candidates for the genetic control of spermatogenesis. Although it is known which genes are involved, a general...

2012
Caio Robledo D'Angioli Costa Quaio Tatiana Ferreira de Almeida Lilian Maria José Albano Israel Gomy Debora Romeo Bertola Monica Castro Varela Celia P Koiffmann Chong Ae Kim

OBJECTIVE Prader-Willi Syndrome is a common etiology of syndromic obesity that is typically caused by either a paternal microdeletion of a region in chromosome 15 (microdeletions) or a maternal uniparental disomy of this chromosome. The purpose of this study was to describe the most significant clinical features of 35 Brazilian patients with molecularly confirmed Prader-Willi syndrome and to de...

Journal: :The Indian journal of medical research 2010
Reza Mirfakhraie Farzaneh Mirzajani Sayed Mahdi Kalantar Maryam Montazeri Nasser Salsabili Gholam Reza Pourmand Massoud Houshmand

BACKGROUND & OBJECTIVES Genetic factors contribute about 10 per cent of male infertility. Among these, genes in azoospermia factor (AZF) region including AZFa, AZFb, AZFc and AZFd on the long arm of Y chromosome are considered most important for spermatogenesis. Deletions in these regions are thought to be involved in some cases of male infertility associated with azoospermia or oligozoospermia...

Journal: :American Journal of Human Genetics 2009
Paweł Stankiewicz Partha Sen Samarth S. Bhatt Mekayla Storer Zhilian Xia Bassem A. Bejjani Zhishuo Ou Joanna Wiszniewska Daniel J. Driscoll Juan Bolivar Mislen Bauer Elaine H. Zackai Donna McDonald-McGinn Małgorzata M.J. Nowaczyk Mitzi Murray Tamim H. Shaikh Vicki Martin Matthew Tyreman Ingrid Simonic Lionel Willatt Joan Paterson Sarju Mehta Diana Rajan Tomas Fitzgerald Susan Gribble Elena Prigmore Ankita Patel Lisa G. Shaffer Nigel P. Carter Sau Wai Cheung Claire Langston Charles Shaw-Smith

Alveolar capillary dysplasia with misalignment of pulmonary veins (ACD/MPV) is a rare, neonatally lethal developmental disorder of the lung with defining histologic abnormalities typically associated with multiple congenital anomalies (MCA). Using array CGH analysis, we have identified six overlapping microdeletions encompassing the FOX transcription factor gene cluster in chromosome 16q24.1q24...

Journal: :Croatian medical journal 2001
J Sertić P Cvitković A Myers R K Saiki A Stavljenić Rukavina

Today, approximately 15% of couples have reduced fertility. In most cases the reason is male infertility, usually of genetic origin. Thus, in the context of research in genes involved in reproduction and sex determination, genetic defects in gametogenesis are being extensively studied. The most frequent pathogenic causes of male infertility are Y chromosomal microdeletions and obstructive azoos...

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: :Proceedings of the National Academy of Sciences of the United States of America 2013
De-Chen Lin Liang Xu Ling-Wen Ding Arjun Sharma Li-Zhen Liu Henry Yang Patrick Tan Jay Vadgama Beth Y Karlan Jenny Lester Nicole Urban Michèl Schummer Ngan Doan Jonathan W Said Hongmao Sun Martin Walsh Craig J Thomas Paresma Patel Dong Yin Daniel Chan H Phillip Koeffler

Discovery of cancer genes through interrogation of genomic dosage is one of the major approaches in cancer research. In this study, we report that phosphodiesterase subtype 4D (PDE4D) gene was homozygously deleted in 198 cases of 5,569 primary solid tumors (3.56%), with most being internal microdeletions. Unexpectedly, the microdeletions did not result in loss of their gene products. Screening ...

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