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Biallelic mutations in MOS cause female infertility characterized by human early embryonic arrest and fragmentation

EMBO molecular medicine, 2021-12, Vol.13 (12), p.e14887-n/a

2021

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Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility

Human mutation, 2021-01, Vol.42 (1), p.31-36

2021

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A newly discovered mutation in PICK1 in a human with globozoospermia

Asian journal of andrology, 2010-07, Vol.12 (4), p.556-560

2010

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Histological endometrial dating: a reliable tool for personalized frozen-thawed embryo transfer in patients with repeated implantation failure in natural cycles

BMC pregnancy and childbirth, 2023-03, Vol.23 (1), p.199-199, Article 199

2023

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Trophectoderm Biopsy Differentially Influences the Level of Serum β-Human Chorionic Gonadotropin With Different Embryonic Trophectoderm Scores in Early Pregnancy From 7847 Single-Blastocyst Transfer Cycles

Frontiers in endocrinology (Lausanne), 2022-02, Vol.13, p.794720-794720

2022

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Abnormalities in centrosome number in human embryos and embryonic stem cells

Molecular reproduction and development, 2016-05, Vol.83 (5), p.392-404

2016

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Mosaic variegated aneuploidy syndrome with tetraploid, and predisposition to male infertility triggered by mutant CEP192

HGG advances, 2024-01, Vol.5 (1), p.100256-100256, Article 100256

2024

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Tumor progression of culture-adapted human embryonic stem cells during long-term culture

Genes chromosomes & cancer, 2008-08, Vol.47 (8), p.665-679

2008

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Telomerase insufficiency induced telomere erosion accumulation in successive generations in dyskeratosis congenita family

Molecular genetics & genomic medicine, 2019-07, Vol.7 (7), p.e00709-n/a

2019

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A rare polypyrimidine tract mutation in the androgen receptor gene results in complete androgen insensitivity syndrome

Asian journal of andrology, 2018-05, Vol.20 (3), p.308-310

2018

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Biallelic variants in IQCN cause sperm flagellar assembly defects and male infertility

Human reproduction (Oxford), 2023-07, Vol.38 (7), p.1390-1398

2023

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Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency

BMC medical genetics, 2018-01, Vol.19 (1), p.15-15, Article 15

2018

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Over-expression of miR375 reduces glucose-induced insulin secretion in Nit-1 cells

Molecular biology reports, 2011-06, Vol.38 (5), p.3061-3065

2011

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Immune profiling and RNA-seq uncover the cause of partial unexplained recurrent implantation failure

International immunopharmacology, 2023-08, Vol.121, p.110513-110513, Article 110513

2023

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Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia

Journal of medical genetics, 2023-02, Vol.60 (2), p.144-153

2023

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Transcriptional Activation of Human CDCA8 Gene Regulated by Transcription Factor NF-Y in Embryonic Stem Cells and Cancer Cells

The Journal of biological chemistry, 2015-09, Vol.290 (37), p.22423-22434

2015

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Identification of biparental and diploid blastocysts from monopronuclear zygotes with the use of a single-nucleotide polymorphism array

Fertility and sterility, 2018-08, Vol.110 (3), p.545-554.e5

2018

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Analysis of the first mitotic spindles in human in vitro fertilized tripronuclear zygotes after pronuclear removal

Reproductive biomedicine online, 2009-11, Vol.19 (5), p.745-754

2009

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Rapid quantification of semen hepatitis B virus DNA by real-time polymerase chain reaction

World journal of gastroenterology : WJG, 2005-09, Vol.11 (34), p.5385

2005

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A DMD case caused by X chromosome rearrangement

Yíchuán, 2023-01, Vol.45 (1), p.88

2023

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Angiogenic potential difference between two types of endothelial progenitor cells from human umbilical cord blood

Cell biology international, 2006-12, Vol.30 (12), p.1018-1027

2006

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Non-invasive prenatal molecular detection of a fetal point mutation for congenital adrenal hyperplasia using co-amplification at lower denaturation temperature PCR

Chinese medical journal, 2010-11, Vol.123 (22), p.3343-3346

2010

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Adherent and non-adherent dendritic cells are equivalently qualified in GM-CSF, IL-4 and TNF-α culture system

Cellular immunology, 2012-05, Vol.277 (1-2), p.44-48

2012

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Effect of thyroid autoimmunity per se on assisted reproduction treatment outcomes: A meta-analysis

Taiwanese journal of obstetrics & gynecology, 2016-04, Vol.55 (2), p.159-165

2016

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Cloning of a full-length cDNA of human testis-specific spermatogenic cell apoptosis inhibitor TSARG2 as a candidate oncogene

Biochemical and biophysical research communications, 2004-06, Vol.319 (1), p.32-40

2004

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Biallelic mutations in MOS cause female infertility characterized by human early embryonic arrest and fragmentation

Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility

A newly discovered mutation in PICK1 in a human with globozoospermia

Histological endometrial dating: a reliable tool for personalized frozen-thawed embryo transfer in patients with repeated implantation failure in natural cycles

Trophectoderm Biopsy Differentially Influences the Level of Serum β-Human Chorionic Gonadotropin With Different Embryonic Trophectoderm Scores in Early Pregnancy From 7847 Single-Blastocyst Transfer Cycles

Abnormalities in centrosome number in human embryos and embryonic stem cells

Mosaic variegated aneuploidy syndrome with tetraploid, and predisposition to male infertility triggered by mutant CEP192

Tumor progression of culture-adapted human embryonic stem cells during long-term culture

Telomerase insufficiency induced telomere erosion accumulation in successive generations in dyskeratosis congenita family

A rare polypyrimidine tract mutation in the androgen receptor gene results in complete androgen insensitivity syndrome

Biallelic variants in IQCN cause sperm flagellar assembly defects and male infertility

Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency

Over-expression of miR375 reduces glucose-induced insulin secretion in Nit-1 cells

Immune profiling and RNA-seq uncover the cause of partial unexplained recurrent implantation failure

Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia

Transcriptional Activation of Human CDCA8 Gene Regulated by Transcription Factor NF-Y in Embryonic Stem Cells and Cancer Cells

Identification of biparental and diploid blastocysts from monopronuclear zygotes with the use of a single-nucleotide polymorphism array

Analysis of the first mitotic spindles in human in vitro fertilized tripronuclear zygotes after pronuclear removal

Rapid quantification of semen hepatitis B virus DNA by real-time polymerase chain reaction

A DMD case caused by X chromosome rearrangement

Angiogenic potential difference between two types of endothelial progenitor cells from human umbilical cord blood

Non-invasive prenatal molecular detection of a fetal point mutation for congenital adrenal hyperplasia using co-amplification at lower denaturation temperature PCR

Adherent and non-adherent dendritic cells are equivalently qualified in GM-CSF, IL-4 and TNF-α culture system

Effect of thyroid autoimmunity per se on assisted reproduction treatment outcomes: A meta-analysis

Cloning of a full-length cDNA of human testis-specific spermatogenic cell apoptosis inhibitor TSARG2 as a candidate oncogene

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