Yang Gao

发表

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

Yunxia Cao, Siyu Liu, Jintao Zhang, 2021, Human molecular genetics.

Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia

Yunxia Cao, Xiaojin He, Junqiang Zhang, 2021, Reproductive Biology and Endocrinology.

Mechanisms of indigo naturalis on treating ulcerative colitis explored by GEO gene chips combined with network pharmacology and molecular docking

Yang Gao, Kanjun Chen, Hui Zhu, 2020, Scientific Reports.

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

F. Tao, Xiaoyu Chen, Yunxia Cao, 2022, Cells.

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

Kuokuo Li, Yunxia Cao, Xiaojin He, 2022, Reproductive Biology and Endocrinology.

Homozygous mutations in DZIP1 can induce asthenoteratospermia with severe MMAF

Chuanmao Zhang, L. Jin, H. Saiyin, 2020, Journal of Medical Genetics.

Novel bi-allelic variants in DNAH2 cause severe asthenoteratozoospermia with multiple morphological abnormalities of the flagella.

P. Zhou, Yunxia Cao, Huan Wu, 2021, Reproductive biomedicine online.

Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility.

M. Ikawa, P. Ray, L. Jin, 2020, American journal of human genetics.

Patients with severe asthenoteratospermia carrying SPAG6 or RSPH3 mutations have a positive pregnancy outcome following intracytoplasmic sperm injection

P. Zhou, Yunxia Cao, Huan Wu, 2020, Journal of Assisted Reproduction and Genetics.

Biallelic mutations in CFAP65 cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and mice

P. Ray, L. Jin, Yunxia Cao, 2019, Journal of Medical Genetics.

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

Kuokuo Li, F. Tao, P. Zhou, 2021, Frontiers in Genetics.

Loss of function mutation in DNAH7 induces male infertility associated with abnormalities of the sperm flagella and mitochondria in human

Kuokuo Li, F. Tao, P. Zhou, 2022, Clinical genetics.

Kui Jie Tong Ameliorates Ulcerative Colitis by Regulating Gut Microbiota and NLRP3/Caspase-1 Classical Pyroptosis Signaling Pathway

Yang Gao, Ping Zhang, Sizhen Gu, 2022, Disease markers.

Identification of Novel Biallelic TLE6 Variants in Female Infertility With Preimplantation Embryonic Lethality

P. Zhou, Yunxia Cao, Huan Wu, 2021, Frontiers in Genetics.

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

Kuokuo Li, Yunxia Cao, Xiaojin He, 2021, Reproductive Biology and Endocrinology.

Novel Variants in HFM1 Lead to Male Infertility Due to Non-obstructive Azoospermia

Kuokuo Li, Yunxia Cao, Xiaojin He, 2021 .

A novel homozygous mutation in WDR19 induces disorganization of microtubules in sperm flagella and nonsyndromic asthenoteratospermia

P. Zhou, Yunxia Cao, Huan Wu, 2020, Journal of Assisted Reproduction and Genetics.

A novel homozygous mutation in the meiotic gene MSH4 leading to male infertility due to non-obstructive azoospermia.

Yunxia Cao, Xiaojin He, Huiru Cheng, 2020, American journal of translational research.

A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens

P. Zhou, Yunxia Cao, Huan Wu, 2020, Journal of Assisted Reproduction and Genetics.

Novel Biallelic TLE6 Variants Induce Preimplantation Embryonic Lethality That Cannot be Rescued by IVF or ICSI

P. Zhou, Yunxia Cao, Huan Wu, 2021 .

Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models.

Y. Li, Yong-Gang Yao, Zhixi Su, 2023, American journal of human genetics.

Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF

Kuokuo Li, Yunxia Cao, Huan Wu, 2021, Reproductive Biology and Endocrinology.

Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA

L. Jin, Yunxia Cao, Huan Wu, 2023, Journal of Medical Genetics.

Novel FSIP2 Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans

Kuokuo Li, Yu-xia Cao, P. Zhou, 2023, International journal of biological sciences.

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

Kuokuo Li, Yunxia Cao, Huan Wu, 2022, Reproductive Biology and Endocrinology.

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

L. Jin, Yunxia Cao, Huan Wu, 2019, American journal of human genetics.

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

L. Jin, H. Saiyin, P. Zhou, 2020, American journal of human genetics.

DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath

Kuokuo Li, Yu-xia Cao, P. Zhou, 2023, Cell Death & Disease.

Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice.

Yunxia Cao, Huan Wu, Xiaojin He, 2021, American journal of human genetics.

Biallelic loss‐of‐function mutations in SEPTIN4 (C17ORF47), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humans

Kuokuo Li, F. Tao, P. Zhou, 2022, Human mutation.

Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease

Kuokuo Li, P. Zhou, Yunxia Cao, 2021, Human mutation.

A homozygous loss‐of‐function mutation in FBXO43 causes human non‐obstructive azoospermia

F. Tao, P. Zhou, Yiyuan Liu, 2021, Clinical genetics.

Novel HYDIN variants associated with male infertility in two Chinese families

Kuokuo Li, Yu-xia Cao, P. Zhou, 2023, Frontiers in Endocrinology.

Novel deleterious splicing variant in HFM1 causes gametogenesis defect and recurrent implantation failure: concerning the risk of chromosomal abnormalities in embryos

Kuokuo Li, P. Zhou, Yunxia Cao, 2023, Journal of Assisted Reproduction and Genetics.

Sperm DNA integrity status is associated with DNA methylation signatures of imprinted genes and non-imprinted genes

P. Zhou, Yunxia Cao, Huan Wu, 2021, Journal of Assisted Reproduction and Genetics.

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

Kuokuo Li, F. Tao, P. Zhou, 2022, Reproductive Biology and Endocrinology.

Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humans

Kuokuo Li, Yiyuan Liu, Yunxia Cao, 2022, Human Genetics.

Differences in the Gut Microbiome of Women With and Without Hypoactive Sexual Desire Disorder: Case Control Study

P. Zhou, Yunxia Cao, Huan Wu, 2021, Journal of medical Internet research.

Differences in the Gut Microbiome of Women With and Without Hypoactive Sexual Desire Disorder: Case Control Study (Preprint)

P. Zhou, Yunxia Cao, Huan Wu, 2020 .

Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility

Kuokuo Li, F. Tao, P. Zhou, 2021, Journal of Assisted Reproduction and Genetics.

Bi-allelic human TEKT3 mutations cause male infertility with oligoasthenoteratozoospermia due to acrosomal hypoplasia and reduced progressive motility.

Kuokuo Li, P. Zhou, Yiyuan Liu, 2023, Human molecular genetics.

Novel compound heterozygous variants in dynein axonemal heavy chain 17 cause asthenoteratospermia with sperm flagellar defects.

P. Zhou, Yunxia Cao, Xiaojin He, 2020, Journal of genetics and genomics = Yi chuan xue bao.

Differences in the Gut Microbiome of Women With and Without Hypoactive Sexual Desire Disorder: Case Control Study (Preprint)

P. Zhou, Yunxia Cao, Huan Wu, 2020 .

ACROSIN deficiency causes total fertilization failure in humans by preventing the sperm from penetrating the zona pellucida.

Kuokuo Li, Yiyuan Liu, Yunxia Cao, 2023, Human reproduction.

LRRC23 deficiency causes male infertility with idiopathic asthenozoospermia by disrupting the assembly of radial spokes

Yu-xia Cao, P. Zhou, Huan Wu, 2023, Clinical genetics.

Bi-allelic variants in chromatoid body protein TDRD6 cause spermiogenesis defects and severe oligoasthenoteratozoospermia in humans

Huan Wu, Xiaojin He, Yang Gao, 2024, Journal of Medical Genetics.