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A hemizygous loss‐of‐function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia

Clinical genetics, 2024-07, Vol.106 (1), p.27-36

2024

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XRCC2 mutation causes premature ovarian insufficiency as well as non‐obstructive azoospermia in humans

Clinical genetics, 2019-03, Vol.95 (3), p.442-443

2019

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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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Mutant ZP1 in Familial Infertility

The New England journal of medicine, 2014-03, Vol.370 (13), p.1220-1226

2014

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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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X‐chromosome inactivation pattern of amniocytes predicts the risk of dystrophinopathy in fetal carriers of DMD mutations

Prenatal diagnosis, 2019-07, Vol.39 (8), p.603-608

2019

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The clinical and neonatal outcomes after stimulation of immotile spermatozoa using SperMagic medium

Andrologia, 2018-09, Vol.50 (7), p.e13056-n/a

2018

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Novel loss‐of‐function mutation in MCM8 causes premature ovarian insufficiency

Molecular genetics & genomic medicine, 2020-04, Vol.8 (4), p.e1165-n/a

2020

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miR-200a-3p promotes β-Amyloid-induced neuronal apoptosis through down-regulation of SIRT1 in Alzheimer’s disease

Journal of biosciences, 2017-09, Vol.42 (3), p.397-404

2017

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Next‐generation sequence‐based preimplantation genetic testing for monogenic disease resulting from maternal mosaicism

Molecular genetics & genomic medicine, 2021-05, Vol.9 (5), p.e1662-n/a

2021

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

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

2023

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Novel FOXL2 mutations cause blepharophimosis‐ptosis‐epicanthus inversus syndrome with premature ovarian insufficiency

Molecular genetics & genomic medicine, 2018-03, Vol.6 (2), p.261-267

2018

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Pronuclear removal of tripronuclear zygotes can establish heteroparental normal karyotypic human embryonic stem cells

Journal of assisted reproduction and genetics, 2016-01, Vol.33 (2), p.255-263

2016

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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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Novel inactivating mutations in the FSH receptor cause premature ovarian insufficiency with resistant ovary syndrome

Reproductive biomedicine online, 2019-03, Vol.38 (3), p.397-406

2019

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A case of megalencephalic leukoencephalopathy with subcortical cysts type 1 was identified with a novel compound heterozygous alteration (c.135delC; c.423+2dupT) in China

Clinical case reports, 2017-06, Vol.5 (6), p.961-967

2017

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Two missense STK11 gene variations impaired LKB1/adenosine monophosphate-activated protein kinase signaling in Peutz-Jeghers syndrome

World journal of gastrointestinal oncology, 2024-04, Vol.16 (4), p.1532-1546

2024

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A single low dose of dendritic cells modified with lentivirus containing a truncated neu gene can effectively suppress neu-overexpressing tumors

The journal of gene medicine, 2010-07, Vol.12 (7), p.604-612

2010

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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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Polar body transfer restores the developmental potential of oocytes to blastocyst stage in a case of repeated embryo fragmentation

Journal of assisted reproduction and genetics, 2017-05, Vol.34 (5), p.563-571

2017

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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 hemizygous loss‐of‐function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia

XRCC2 mutation causes premature ovarian insufficiency as well as non‐obstructive azoospermia in humans

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

Mutant ZP1 in Familial Infertility

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

X‐chromosome inactivation pattern of amniocytes predicts the risk of dystrophinopathy in fetal carriers of DMD mutations

The clinical and neonatal outcomes after stimulation of immotile spermatozoa using SperMagic medium

Novel loss‐of‐function mutation in MCM8 causes premature ovarian insufficiency

miR-200a-3p promotes β-Amyloid-induced neuronal apoptosis through down-regulation of SIRT1 in Alzheimer’s disease

Next‐generation sequence‐based preimplantation genetic testing for monogenic disease resulting from maternal mosaicism

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

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

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

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

Novel FOXL2 mutations cause blepharophimosis‐ptosis‐epicanthus inversus syndrome with premature ovarian insufficiency

Pronuclear removal of tripronuclear zygotes can establish heteroparental normal karyotypic human embryonic stem cells

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

Novel inactivating mutations in the FSH receptor cause premature ovarian insufficiency with resistant ovary syndrome

A case of megalencephalic leukoencephalopathy with subcortical cysts type 1 was identified with a novel compound heterozygous alteration (c.135delC; c.423+2dupT) in China

Two missense STK11 gene variations impaired LKB1/adenosine monophosphate-activated protein kinase signaling in Peutz-Jeghers syndrome

A single low dose of dendritic cells modified with lentivirus containing a truncated neu gene can effectively suppress neu-overexpressing tumors

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

Polar body transfer restores the developmental potential of oocytes to blastocyst stage in a case of repeated embryo fragmentation

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

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