نتایج جستجو برای: NLRP7

تعداد نتایج: 82  

Journal: :European journal of obstetrics, gynecology, and reproductive biology 2012
Ebtesam M Abdalla Bruce E Hayward Ahmed Shamseddin Mona M Nawar

OBJECTIVES Hydatidiform mole is an aberrant pregnancy with hyperproliferative vesicular trophoblast and defective fetal development. In 2006, mutations in NLRP7 were found to be responsible for recurrent hydatidiform moles (RHM), but genetic heterogeneity has been demonstrated and mutations of C6orf221 were later reported in several families. Here we report a new Egyptian family in which two si...

2017
Jyun-Yuan Huang Pei-Hsiu Yu Yueh-Chun Li Pao-Lin Kuo

BACKGROUND Nucleotide-binding oligomerization domain (NACHT), leucine rich repeat (LRR) and pyrin domain (PYD) 7 containing protein, NLRP7, is a member of the NLR family which serves as innate immune sensors. Mutations and genetic variants of NLRP7 have been found in women with infertility associated conditions, such as recurrent hydatidiform mole, recurrent miscarriage, and preeclampsia. Decid...

Journal: :Human molecular genetics 2014
Sangeetha Mahadevan Shu Wen Ying-Wooi Wan Hsiu-Huei Peng Subhendu Otta Zhandong Liu Michelina Iacovino Elisabeth M Mahen Michael Kyba Bekim Sadikovic Ignatia B Van den Veyver

Maternal-effect mutations in NLRP7 cause rare biparentally inherited hydatidiform moles (BiHMs), abnormal pregnancies containing hypertrophic vesicular trophoblast but no embryo. BiHM trophoblasts display abnormal DNA methylation patterns affecting maternally methylated germline differentially methylated regions (gDMRs), suggesting that NLRP7 plays an important role in reprogramming imprinted g...

Journal: :Human reproduction 2015
Elie Akoury Li Zhang Asangla Ao Rima Slim

STUDY QUESTION What is the subcellular localization in human oocytes and preimplantation embryos, of the two maternal-effect proteins, NLRP7 and KHDC3L, responsible for recurrent hydatidiform moles (RHMs)? SUMMARY ANSWER NLRP7 and KHDC3L localize to the oocyte cytoskeleton and are polar and absent from the cell-to-cell contact region in early preimplantation embryos. WHAT IS KNOWN ALREADY N...

Journal: :Molecular human reproduction 2013
I Manokhina C W Hanna M D Stephenson D E McFadden W P Robinson

Maternal effect genes control early events of embryogenesis. Maternal homozygous and compound mutations in two such genes, NLRP7 and c6orf221, have been detected in the majority of women experiencing recurrent biparental hydatidiform moles. It was suggested that other forms of reproductive wastage, including diploid androgenetic moles, partial moles, polyploidy, recurrent spontaneous abortions ...

2015
Heike Singer Arijit Biswas Nicole Nuesgen Johannes Oldenburg Osman El-Maarri Cees Oudejans

Mutations in the maternal effect gene NLRP7 cause biparental hydatidiform mole (HYDM1). HYDM1 is characterized by abnormal growth of placenta and lack of proper embryonic development. The molar tissues are characterized by abnormal methylation patterns at differentially methylated regions (DMRs) of imprinted genes. It is not known whether this occurs before or after fertilization, but the high ...

Journal: :Molecular human reproduction 2012
Rima Slim Philippe Coullin Ange-Lucien Diatta Wafaa Chebaro David Courtin Sonia Abdelhak Andre Garcia

Gestational choriocarcinomas are malignant tumors of trophoblastic cells that affect 5-25% of women with sporadic hydatidiform moles (HMs) depending on countries and studies. Nucleotide binding and oligomerization domain-like receptor protein 7 (NLRP7) is a major gene responsible for recurrent HMs and recently mutations in this gene have also been shown in 13% of women with sporadic, non-recurr...

Journal: :Molecular human reproduction 2012
L Andreasen L Bolund I Niemann E S Hansen L Sunde

Hydatidiform moles (HMs) most often occur sporadically and are either diploid androgenetic or triploid. The very rare familial recurrent HMs (FRHMs) have been related to NLRP7 and C6orf221 mutations in the mother. FRHMs are most often diploid with both maternal and paternal origin of the molar genome. We have screened a cohort of 11 women with diploid HMs with biparental contributions to the mo...

Journal: :Journal of medical genetics 2011
Christiane Messaed Wafaa Chebaro Raphael B Di Roberto Cecile Rittore Annie Cheung Jocelyne Arseneau Ariel Schneider Moy Fong Chen Kurt Bernishke Urvashi Surti Lori Hoffner Philippe Sauthier William Buckett JianHua Qian Nga Man Lau Rashmi Bagga James C Engert Philippe Coullin Isabelle Touitou Rima Slim

BACKGROUND NLRP7 mutations are responsible for recurrent molar pregnancies and associated reproductive wastage. To investigate the role of NLRP7 in sporadic moles and other forms of reproductive wastage, the authors sequenced this gene in a cohort of 135 patients with at least one hydatidiform mole or three spontaneous abortions; 115 of these were new patients. METHODS/RESULTS All mutations w...

Journal: :Molecular human reproduction 2014
Heike Singer Arijit Biswas Nicole Zimmer Christiane Messaed Johannes Oldenburg Rima Slim Osman El-Maarri

Mutations in NLRP7 (NOD-like-receptor family, pyrin domain containing 7) are responsible for a type of recurrent pregnancy loss known as recurrent hydatidiform mole (HYDM1). This condition is characterized by abnormal growth of the placenta, a lack of proper embryonic development and abnormal methylation patterns at multiple imprinted loci in diploid biparental molar tissues. The role of NLRP7 ...

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