Huiru Cheng

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.

Mutation spectrum of the fibrillin‐1 (FBN1) gene in Taiwanese patients with Marfan syndrome

Chih-ping Chen, Chien-Nan Lee, Shuan-Pei Lin, 2009, Annals of human genetics.

Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis.

Chien-Nan Lee, Shuan-Pei Lin, Huiru Cheng, 2009, Analytical biochemistry.

Genetic detection of Chinese hereditary nonpolyposis colorectal cancer.

Huiru Cheng, R. Meng, Hei-ying Jin, 2004, World journal of gastroenterology.

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.

Bi‐allelic mutations in MCIDAS and CCNO cause human infertility associated with abnormal gamete transport

F. Tao, Yiyuan Liu, Yunxia Cao, 2021, Clinical genetics.

Homozygous mutations in DZIP1 can induce asthenoteratospermia with severe MMAF

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

Maternal cadmium exposure impairs placental angiogenesis in preeclampsia through disturbing thyroid hormone receptor signaling.

Yuehua Wu, Huiru Cheng, Zhaolian Wei, 2022, Ecotoxicology and environmental safety.

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.

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.

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 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 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.

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.

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.

Clinicopathologic characteristics of Chinese hereditary non-polyposis colorectal cancer

Huiru Cheng, R. Meng, Hei-ying Jin, 2003 .

Triphenyltin chloride exposure inhibits meiotic maturation of mouse oocytes by disrupting cytoskeleton assembly and cell cycle progression.

Huiru Cheng, Zuying Xu, Dan Liang, 2024, Toxicology in vitro : an international journal published in association with BIBRA.

Homozygous deleterious variants in the C-terminal of TDRD5 impair spermiogenesis, causing severe oligoasthenoteratozoospermia in humans.

Mingxi Liu, Xiaojin He, Huiru Cheng, 2024, Andrology.

Carbendazim exposure inhibits mouse oocytes meiotic maturation in vitro by destroying spindle assembly.

Yu Cao, Siyuan Wang, Huiru Cheng, 2023, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.