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Mumps Orchitis: Clinical Aspects and Mechanisms

Frontiers in immunology, 2021-03, Vol.12, p.582946-582946

2021

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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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Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice

American journal of human genetics, 2020-09, Vol.107 (3), p.514-526

2020

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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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Geometric Quality Assessment of Prefabricated Steel Box Girder Components Using 3D Laser Scanning and Building Information Model

Remote sensing (Basel, Switzerland), 2023-02, Vol.15 (3), p.556

2023

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Altered miRNA profile in testis of post-cryptorchidopexy patients with non-obstructive azoospermia

Reproductive biology and endocrinology, 2018-08, Vol.16 (1), p.78-78, Article 78

2018

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Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF

Reproductive biology and endocrinology, 2022-03, Vol.20 (1), p.41-41, Article 41

2022

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Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia

Reproductive biology and endocrinology, 2022-04, Vol.20 (1), p.63-63, Article 63

2022

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Diverse phenotypes and fertility outcomes of patients with androgen insensitivity syndrome in a Chinese family harboring identical AR gene variant

BMC medical genomics, 2024-10, Vol.17 (1), p.249-8, Article 249

2024

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Sequence characterization and expression pattern analysis of six kinds of IL-17 family genes in the Asian swamp eel (Monopterus albus)

Fish & shellfish immunology, 2019-06, Vol.89, p.257-270

2019

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Recognition of Glycometabolism-Associated lncRNAs as Prognosis Markers for Bladder Cancer by an Innovative Prediction Model

Frontiers in genetics, 2022-07, Vol.13, p.918705-918705

2022

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Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia

Reproductive biology and endocrinology, 2021-02, Vol.19 (1), p.27-27, Article 27

2021

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Targeting TIGIT Inhibits Bladder Cancer Metastasis Through Suppressing IL-32

Frontiers in pharmacology, 2022-01, Vol.12, p.801493-801493

2022

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AIM2 inflammasome activation benefits the therapeutic effect of BCG in bladder carcinoma

Frontiers in pharmacology, 2022-10, Vol.13, p.1050774-1050774

2022

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A mitochondrial-targeted peptide ameliorated podocyte apoptosis through a HOCl-alb-enhanced and mitochondria-dependent signalling pathway in diabetic rats and in vitro

Journal of enzyme inhibition and medicinal chemistry, 2019-01, Vol.34 (1), p.394-404

2019

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Novel variants in helicase for meiosis 1 lead to male infertility due to non-obstructive azoospermia

Reproductive biology and endocrinology, 2021-08, Vol.19 (1), p.129-129, Article 129

2021

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Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility

Journal of assisted reproduction and genetics, 2022-01, Vol.39 (1), p.251-259

2022

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A homozygous nonsense mutation of PLCZ1 cause male infertility with oocyte activation deficiency

Journal of assisted reproduction and genetics, 2020-04, Vol.37 (4), p.821-828

2020

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Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations

Reproductive biology and endocrinology, 2022-01, Vol.20 (1), p.5-5, Article 5

2022

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miR-34c disrupts spermatogonial stem cell homeostasis in cryptorchid testes by targeting Nanos2

Reproductive biology and endocrinology, 2018-10, Vol.16 (1), p.97-97, Article 97

2018

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Correction: Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia

Reproductive biology and endocrinology, 2022-05, Vol.20 (1), p.79-79, Article 79

2022

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Case Report: Novel Biallelic Mutations in ARMC4 Cause Primary Ciliary Dyskinesia and Male Infertility in a Chinese Family

Frontiers in genetics, 2021-07, Vol.12

2021

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Correction to: Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF

Reproductive biology and endocrinology, 2022-04, Vol.20 (1), p.74-74, Article 74

2022

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The microbiota continuum along the upper reproductive tract of male rat and its relation to semen parameters

Heliyon, 2024-06, Vol.10 (12), p.e32556, Article e32556

2024

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Activation of MT1/MT2 to Protect Testes and Leydig Cells against Cisplatin-Induced Oxidative Stress through the SIRT1/Nrf2 Signaling Pathway

Cells (Basel, Switzerland), 2022-05, Vol.11 (10), p.1690

2022

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Mumps Orchitis: Clinical Aspects and Mechanisms

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

Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice

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

Geometric Quality Assessment of Prefabricated Steel Box Girder Components Using 3D Laser Scanning and Building Information Model

Altered miRNA profile in testis of post-cryptorchidopexy patients with non-obstructive azoospermia

Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF

Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia

Diverse phenotypes and fertility outcomes of patients with androgen insensitivity syndrome in a Chinese family harboring identical AR gene variant

Sequence characterization and expression pattern analysis of six kinds of IL-17 family genes in the Asian swamp eel (Monopterus albus)

Recognition of Glycometabolism-Associated lncRNAs as Prognosis Markers for Bladder Cancer by an Innovative Prediction Model

Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia

Targeting TIGIT Inhibits Bladder Cancer Metastasis Through Suppressing IL-32

AIM2 inflammasome activation benefits the therapeutic effect of BCG in bladder carcinoma

A mitochondrial-targeted peptide ameliorated podocyte apoptosis through a HOCl-alb-enhanced and mitochondria-dependent signalling pathway in diabetic rats and in vitro

Novel variants in helicase for meiosis 1 lead to male infertility due to non-obstructive azoospermia

Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility

A homozygous nonsense mutation of PLCZ1 cause male infertility with oocyte activation deficiency

Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations

miR-34c disrupts spermatogonial stem cell homeostasis in cryptorchid testes by targeting Nanos2

Correction: Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia

Case Report: Novel Biallelic Mutations in ARMC4 Cause Primary Ciliary Dyskinesia and Male Infertility in a Chinese Family

Correction to: Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF

The microbiota continuum along the upper reproductive tract of male rat and its relation to semen parameters

Activation of MT1/MT2 to Protect Testes and Leydig Cells against Cisplatin-Induced Oxidative Stress through the SIRT1/Nrf2 Signaling Pathway

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