Mingrong Lv

发表

Performance evaluation of differential splicing analysis methods and splicing analytics platform construction

K. Xia, Kuokuo Li, Guihu Zhao, 2022, Nucleic acids research.

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.

Predict Value of Relative Telomere Length, TERT, and Follicular Fluid Anti-mullerian Hormone Levels for IVF Outcome in Infertile Women

P. Zhou, Yunxia Cao, Zhiguo Zhang, 2021 .

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 Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice.

Shimin Zhao, P. Ray, L. Jin, 2019, American journal of human genetics.

Melatonin alleviates deoxynivalenol-induced apoptosis of human granulosa cells by reducing mutually accentuated FOXO1 and ER stress

P. Zhou, Yunxia Cao, Zhiguo Zhang, 2021, Biology of Reproduction.

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.

lethal, autosomal recessive neurodegenerative disease and leads to progressive impairment of movement and cognition. A couple with a proband child with calcium-independent group VI phospholipase A2 (PLA2G6)-associated INAD and a previous affected pregnancy sought pre-implantation genetic diagnosis

P. Zhou, Yunxia Cao, Huan Wu, 2019 .

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

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

Altered mRNAs Profiles in the Testis of Patients With “Secondary Idiopathic Non-Obstructive Azoospermia”

Kuokuo Li, Yunxia Cao, Xiaojin He, 2022, Frontiers in Cell and Developmental Biology.

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 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 .

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

J. Veltman, M. O’Bryan, P. Ray, 2021, American journal of human genetics.

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.

miR-323-3p regulates the steroidogenesis and cell apoptosis in polycystic ovary syndrome (PCOS) by targeting IGF-1.

Yunxia Cao, Xiaojin He, Zhiguo Zhang, 2019, Gene.

Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF

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

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

Jingze Tan, Hongyan Wang, L. Jin, 2018, Journal of Human Genetics.

Gene expression profiling of human blastocysts from in vivo and ‘rescue IVM’ with or without melatonin treatment

P. Zhou, Yunxia Cao, Zhiguo Zhang, 2017, Molecular medicine reports.

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.

Homozygous mutations in SPEF2 induce multiple morphological abnormalities of the sperm flagella and male infertility

Yong Zhu, L. Jin, Yunxia Cao, 2019, Journal of Medical Genetics.

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

Jian Wang, Jingze Tan, Hongyan Wang, 2018, Journal of Medical Genetics.

Artificial oocyte activation to improve reproductive outcomes in couples with various causes of infertility: a retrospective cohort study.

P. Zhou, Yunxia Cao, Xiaojin He, 2020, Reproductive biomedicine online.

Successful preimplantation genetic diagnosis by targeted next-generation sequencing on an ion torrent personal genome machine platform

P. Zhou, Yunxia Cao, Xiaojin He, 2018, Oncology letters.

Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice.

Yunxia Cao, Xiaojin He, G. Lin, 2021, 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.

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

Jingze Tan, Hongyan Wang, L. Jin, 2018, Journal of Human Genetics.

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.

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 truncating variants in CFAP206 cause male infertility in human and mouse

N. Thierry-Mieg, Kuokuo Li, F. Tao, 2021, Human 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.

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.

Prioritizing de novo potential non-canonical splicing variants in neurodevelopmental disorders

Kuokuo Li, Xiaomeng Wang, Guihu Zhao, 2023, EBioMedicine.