نتایج جستجو برای: globozoospermic

تعداد نتایج: 52  

Kamran Ghaedi, Marziyeh Tavalaee Mohammad Hossein Nasr-Esfahani, Mohammad Reza Deemeh Parastoo Modarres Somayeh Tanhaei

Objective Globozoospermia is a rare syndrome with an incidence of less than 0.1% among infertile men. Researchers have recently identified a large deletion, about 200 kbp, encompassing the whole length of DPY19L2 or mutations in SPATA16 and PICK1 genes associated with globozoospermia. The aim of this study was to analyze the DPY19L2 gene deletion using polymerase chain reaction technique for th...

Journal: :Human reproduction 2010
Chizuru Ito Kenji Yamatoya Keiichi Yoshida Koichi Kyono Ryoji Yao Tetsuo Noda Kiyotaka Toshimori

BACKGROUND Recently we reported that an oocyte activation ability in human and mouse sperm is associated with head flatness or the presence of perinuclear theca (PT) substance, MN13, which is an oocyte activation-related protein localized on the post-acrosomal sheath (PAS). As such, we hypothesize that the appearance of oocyte activation ability is stage-specifically regulated and depends on th...

2015
Sandra Yassine Jessica Escoffier Roland Abi Nahed Virginie Pierre Thomas Karaouzene Pierre F. Ray Christophe Arnoult

The acrosome is an organelle that is central to sperm physiology and a defective acrosome biogenesis leads to globozoospermia, a severe male infertility. The identification of the actors involved in acrosome biogenesis is therefore particularly important to decipher the molecular pathogeny of globozoospermia. We recently showed that a defect in the DPY19L2 gene is present in more than 70% of gl...

Journal: :international journal of fertility and sterility 0
parastoo modarres somayeh tanhaei marziyeh tavalaee kamran ghaedi mohammad reza deemeh mohammad hossein nasr-esfahani

objective: globozoospermia is a rare syndrome with an incidence of less than 0.1% among infertile men. researchers have recently identified a large deletion, about 200 kbp, encompassing the whole length of dpy19l2 or mutations in spata16 and pick1 genes associated with globozoospermia. the aim of this study was to analyze the dpy19l2 gene deletion using polymerase chain reaction technique for t...

2014
Sanam MORADAN Behpour YOUSEFI

Globozoospermia syndrome is a rare teratozoospermia with an incidence below 0.1%. Presence of 100% round sperm heads, absence of acrosome, and messy sperm body and tail are the main characteristics of this syndrome. The activation ability of oocytes and consequently the fertilization rate decrease due to the absence of acrosome. The pathogenesis of this syndrome is not clear [1-2]. Globozoosper...

Journal: :Fertility and Sterility 2021

In men with ART failure, sperm DNA sequencing ultrastructural analysis can identify specific defects and guide treatment. the past 2 years, 22 consenting who failed IVF cycles due to severe astheno-/teratozoospermia were recruited; specimens from 3 fertile used as controls. To assess ultrastructure by transmission electron microscopy (TEM), pelleted spermatozoa fixed, embedded, sectioned 100-nm...

Farzaneh Rabiee, Kamran Ghaedi, Marziyeh Tavalaee, Mohammad Hossein Nasr-Esfahani, Mohammad Reza Deemeh Soudabeh Javadian-Elyaderani

Objective(s): Phospholipase C ζ (PLCζ) is considered as a nominee for sperm associated oocyte activating factors and is located back-to-back with CAPZA3, an actin-capping protein controlling actin polymerization during spermiogenesis. They contain a common bidirectional promoter. The objective of this study was to identify individuals with parallel low expression of PLCζ and CAPZA3 mRNA, in hop...

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