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Times Cited: 99
Times Cited: 99
Times Cited
Times Co-cited
Similarity
Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest.
Yao Xu, Yingli Shi, Jing Fu, Min Yu, Ruizhi Feng, Qing Sang, Bo Liang, Biaobang Chen, Ronggui Qu, Bin Li,[...]. Am J Hum Genet 2016
Yao Xu, Yingli Shi, Jing Fu, Min Yu, Ruizhi Feng, Qing Sang, Bo Liang, Biaobang Chen, Ronggui Qu, Bin Li,[...]. Am J Hum Genet 2016
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Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility.
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Mutations in NLRP2 and NLRP5 cause female infertility characterised by early embryonic arrest.
Jian Mu, Wenjing Wang, Biaobang Chen, Ling Wu, Bin Li, Xiaoyan Mao, Zhihua Zhang, Jing Fu, Yanping Kuang, Xiaoxi Sun,[...]. J Med Genet 2019
Jian Mu, Wenjing Wang, Biaobang Chen, Ling Wu, Bin Li, Xiaoyan Mao, Zhihua Zhang, Jing Fu, Yanping Kuang, Xiaoxi Sun,[...]. J Med Genet 2019
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Mutations in TUBB8 and Human Oocyte Meiotic Arrest.
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A subcortical maternal complex essential for preimplantation mouse embryogenesis.
Lei Li, Boris Baibakov, Jurrien Dean. Dev Cell 2008
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Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest.
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Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte.
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Identification of a human subcortical maternal complex.
Kai Zhu, Liying Yan, Xiaoxin Zhang, Xukun Lu, Tianren Wang, Jie Yan, Xinqi Liu, Jie Qiao, Lei Li. Mol Hum Reprod 2015
Kai Zhu, Liying Yan, Xiaoxin Zhang, Xukun Lu, Tianren Wang, Jie Yan, Xinqi Liu, Jie Qiao, Lei Li. Mol Hum Reprod 2015
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Mater, a maternal effect gene required for early embryonic development in mice.
Z B Tong, L Gold, K E Pfeifer, H Dorward, E Lee, C A Bondy, J Dean, L M Nelson. Nat Genet 2000
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Novel mutations in genes encoding subcortical maternal complex proteins may cause human embryonic developmental arrest.
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Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans.
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The subcortical maternal complex controls symmetric division of mouse zygotes by regulating F-actin dynamics.
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Role for PADI6 and the cytoplasmic lattices in ribosomal storage in oocytes and translational control in the early mouse embryo.
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Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
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Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos.
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A Maternal Functional Module in the Mammalian Oocyte-To-Embryo Transition.
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Maternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming.
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Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles.
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The subcortical maternal complex: multiple functions for one biological structure?
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The human knockout phenotype of PADI6 is female sterility caused by cleavage failure of their fertilized eggs.
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Novel mutations and structural deletions in TUBB8: expanding mutational and phenotypic spectrum of patients with arrest in oocyte maturation, fertilization or early embryonic development.
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Maternal variants in NLRP and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring.
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Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).
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Peptidylarginine deiminase (PAD) 6 is essential for oocyte cytoskeletal sheet formation and female fertility.
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12
Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP.
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17
Restarting life: fertilization and the transition from meiosis to mitosis.
Dean Clift, Melina Schuh. Nat Rev Mol Cell Biol 2013
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12
Transducin-like enhancer of split-6 (TLE6) is a substrate of protein kinase A activity during mouse oocyte maturation.
Francesca E Duncan, Elizabeth Padilla-Banks, Miranda L Bernhardt, Teri S Ord, Wendy N Jefferson, Stuart B Moss, Carmen J Williams. Biol Reprod 2014
Francesca E Duncan, Elizabeth Padilla-Banks, Miranda L Bernhardt, Teri S Ord, Wendy N Jefferson, Stuart B Moss, Carmen J Williams. Biol Reprod 2014
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The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility.
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A genomics approach to females with infertility and recurrent pregnancy loss.
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Sateesh Maddirevula, Khalid Awartani, Serdar Coskun, Latifa F AlNaim, Niema Ibrahim, Firdous Abdulwahab, Mais Hashem, Saad Alhassan, Fowzan S Alkuraya. Hum Genet 2020
60
Maternal-effect gene Ces5/Ooep/Moep19/Floped is essential for oocyte cytoplasmic lattice formation and embryonic development at the maternal-zygotic stage transition.
Fumi Tashiro, Masami Kanai-Azuma, Satsuki Miyazaki, Masahiro Kato, Tomofumi Tanaka, Shuichi Toyoda, Eiji Yamato, Hayato Kawakami, Tatsushi Miyazaki, Jun-Ichi Miyazaki. Genes Cells 2010
Fumi Tashiro, Masami Kanai-Azuma, Satsuki Miyazaki, Masahiro Kato, Tomofumi Tanaka, Shuichi Toyoda, Eiji Yamato, Hayato Kawakami, Tatsushi Miyazaki, Jun-Ichi Miyazaki. Genes Cells 2010
23
Protein tyrosine kinase Wee1B is essential for metaphase II exit in mouse oocytes.
Jeong Su Oh, Andrej Susor, Marco Conti. Science 2011
Jeong Su Oh, Andrej Susor, Marco Conti. Science 2011
15
New biallelic mutations in WEE2: expanding the spectrum of mutations that cause fertilization failure or poor fertilization.
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Jing Dai, Wei Zheng, Can Dai, Jing Guo, Changfu Lu, Fei Gong, Yan Li, Qinwei Zhou, Guangxiu Lu, Ge Lin. Fertil Steril 2019
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A novel homozygous variant in NLRP5 is associate with human early embryonic arrest in a consanguineous Chinese family.
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Bi-allelic Missense Pathogenic Variants in TRIP13 Cause Female Infertility Characterized by Oocyte Maturation Arrest.
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BTG4 is a meiotic cell cycle-coupled maternal-zygotic-transition licensing factor in oocytes.
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10
Zygotic genome activation during the maternal-to-zygotic transition.
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Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
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10
PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice.
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37
Homozygous missense mutation Arg207Cys in the WEE2 gene causes female infertility and fertilization failure.
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Novel mutations in WEE2: Expanding the spectrum of mutations responsible for human fertilization failure.
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Expanding the genetic and phenotypic spectrum of female infertility caused by TLE6 mutations.
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Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific Imprinting.
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16
Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families.
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14
Culture and selection of viable blastocysts: a feasible proposition for human IVF?
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Mutation analysis of the TUBB8 gene in nine infertile women with oocyte maturation arrest.
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A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility.
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Mutant ZP1 in familial infertility.
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14
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.