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DNAH1 gene mutations and their potential association with dysplasia of the sperm fibrous sheath and infertility in the Han Chinese population

Fertility and sterility, 2017-06, Vol.107 (6), p.1312-1318.e2

2017

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Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice

American journal of human genetics, 2019-04, Vol.104 (4), p.738-748

2019

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Editorial: Genetic factors in male infertility

Frontiers in genetics, 2023-04, Vol.14, p.1187445-1187445

2023

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Loss of DRC1 function leads to multiple morphological abnormalities of the sperm flagella and male infertility in human and mouse

Human molecular genetics, 2021-10, Vol.30 (21), p.1996-2011

2021

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Clinical detection, diagnosis and treatment of morphological abnormalities of sperm flagella: A review of literature

Frontiers in genetics, 2022-11, Vol.13, p.1034951-1034951

2022

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Biallelic mutations of CFAP251 cause sperm flagellar defects and human male infertility

Journal of human genetics, 2019-01, Vol.64 (1), p.49-54

2019

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Successful Results of Intracytoplasmic Sperm Injection of a Chinese Patient With Multiple Morphological Abnormalities of Sperm Flagella Caused by a Novel Splicing Mutation in CFAP251

Frontiers in genetics, 2022-01, Vol.12, p.783790-783790

2022

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Bi-allelic variants in human WDR63 cause male infertility via abnormal inner dynein arms assembly

Cell discovery, 2021-11, Vol.7 (1), p.110-110, Article 110

2021

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Effect of Prednisolone Administration on Patients with Unexplained Recurrent Miscarriage and in Routine Intracytoplasmic Sperm Injection: A Meta-Analysis

American journal of reproductive immunology (1989), 2015-07, Vol.74 (1), p.89-97

2015

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Reactive Oxygen Species Secreted by Leukocytes in Semen Induce Self-Expression of Interleukin-6 and Affect Sperm Quality

American journal of men's health, 2020-09, Vol.14 (5), p.1557988320970053-1557988320970053

2020

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Genetic analysis and intracytoplasmic sperm injection outcomes of Chinese patients with congenital bilateral absence of vas deferens

Journal of assisted reproduction and genetics, 2022-03, Vol.39 (3), p.719-728

2022

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Patient with CATSPER3 mutations‐related failure of sperm acrosome reaction with successful pregnancy outcome from intracytoplasmic sperm injection (ICSI)

Molecular genetics & genomic medicine, 2021-02, Vol.9 (2), p.e1579-n/a

2021

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Computational Portable Microscopes for Point-of-Care-Test and Tele-Diagnosis

Cells (Basel, Switzerland), 2022-11, Vol.11 (22), p.3670

2022

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Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella

American journal of human genetics, 2017-06, Vol.100 (6), p.854-864

2017

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Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and Mice

American journal of human genetics, 2019-12, Vol.105 (6), p.1168-1181

2019

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Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella

Journal of medical genetics, 2019-02, Vol.56 (2), p.96-103

2019

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Homozygous mutations in DZIP1 can induce asthenoteratospermia with severe MMAF

Journal of medical genetics, 2020-07, Vol.57 (7), p.445-453

2020

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Patient with multiple morphological abnormalities of sperm flagella caused by a novel ARMC2 mutation has a favorable pregnancy outcome from intracytoplasmic sperm injection

Journal of assisted reproduction and genetics, 2022-07, Vol.39 (7), p.1673-1681

2022

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Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility

American journal of human genetics, 2021-02, Vol.108 (2), p.309-323

2021

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Deep learning colorful ptychographic iterative engine lens-less diffraction microscopy

Optics and lasers in engineering, 2022-03, Vol.150, p.106843, Article 106843

2022

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CFAP43-mediated intra-manchette transport is required for sperm head shaping and flagella formation

Zygote (Cambridge), 2021-02, Vol.29 (1), p.75-81

2021

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BMI1 promotes steroidogenesis through maintaining redox homeostasis in mouse MLTC-1 and primary Leydig cells

Cell cycle (Georgetown, Tex.), 2020-08, Vol.19 (15), p.1884-1898

2020

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Myotubularin related protein 7 is essential for the spermatogonial stem cell homeostasis via PI3K/AKT signaling

Cell cycle (Georgetown, Tex.), 2019-10, Vol.18 (20), p.2800-2813

2019

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Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice

Journal of medical genetics, 2022-07, Vol.59 (7), p.710-718

2022

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Homozygous loss-of-function mutations in FSIP2 cause male infertility with asthenoteratospermia

Journal of genetics and genomics, 2019-01, Vol.46 (1), p.53-56

2019

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DNAH1 gene mutations and their potential association with dysplasia of the sperm fibrous sheath and infertility in the Han Chinese population

Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice

Editorial: Genetic factors in male infertility

Loss of DRC1 function leads to multiple morphological abnormalities of the sperm flagella and male infertility in human and mouse

Clinical detection, diagnosis and treatment of morphological abnormalities of sperm flagella: A review of literature

Biallelic mutations of CFAP251 cause sperm flagellar defects and human male infertility

Successful Results of Intracytoplasmic Sperm Injection of a Chinese Patient With Multiple Morphological Abnormalities of Sperm Flagella Caused by a Novel Splicing Mutation in CFAP251

Bi-allelic variants in human WDR63 cause male infertility via abnormal inner dynein arms assembly

Effect of Prednisolone Administration on Patients with Unexplained Recurrent Miscarriage and in Routine Intracytoplasmic Sperm Injection: A Meta-Analysis

Reactive Oxygen Species Secreted by Leukocytes in Semen Induce Self-Expression of Interleukin-6 and Affect Sperm Quality

Genetic analysis and intracytoplasmic sperm injection outcomes of Chinese patients with congenital bilateral absence of vas deferens

Patient with CATSPER3 mutations‐related failure of sperm acrosome reaction with successful pregnancy outcome from intracytoplasmic sperm injection (ICSI)

Computational Portable Microscopes for Point-of-Care-Test and Tele-Diagnosis

Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella

Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and Mice

Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella

Homozygous mutations in DZIP1 can induce asthenoteratospermia with severe MMAF

Patient with multiple morphological abnormalities of sperm flagella caused by a novel ARMC2 mutation has a favorable pregnancy outcome from intracytoplasmic sperm injection

Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility

Deep learning colorful ptychographic iterative engine lens-less diffraction microscopy

CFAP43-mediated intra-manchette transport is required for sperm head shaping and flagella formation

BMI1 promotes steroidogenesis through maintaining redox homeostasis in mouse MLTC-1 and primary Leydig cells

Myotubularin related protein 7 is essential for the spermatogonial stem cell homeostasis via PI3K/AKT signaling

Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice

Homozygous loss-of-function mutations in FSIP2 cause male infertility with asthenoteratospermia

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