Xiaohui Jiang

Andrology Department, Sichuan University

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title	2024

Other Publications

Article	Year
Modification of montmorillonite surfaces using a novel class of cationic gemini surfactants. Journal of colloid and interface science\| PubMed ID: 19150079	2009
[The influence of circadian clock gene on mouse sperm fertility in RNAi]. Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition\| PubMed ID: 19253828	2008
Interaction between water-soluble rhodium complex RhCl(CO)(TPPTS)₂ and surfactants probed by spectroscopic methods. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy\| PubMed ID: 22484254	2012
Organophilic worm-like ruthenium nanoparticles catalysts by the modification of CTAB on montmorillonite supports. Journal of colloid and interface science\| PubMed ID: 23141762	2013
The noncircadian function of the circadian Clock gene in the regulation of male fertility. Journal of biological rhythms\| PubMed ID: 23735500	2013
A qPCR method to characterize the sex type of the cell strains from rats. Bioscience, biotechnology, and biochemistry\| PubMed ID: 27316703	2016
Reply. The Annals of thoracic surgery\| PubMed ID: 29856972	2018
Clinical significance of plasma anti-TOPO48 autoantibody and blood survivin-expressing circulating cancer cells in patients with early stage endometrial carcinoma. Archives of gynecology and obstetrics\| PubMed ID: 30341503	2019
A homozygous RNF220 mutation leads to male infertility with small-headed sperm. Gene\| PubMed ID: 30500349	2019
A risk prediction model of sperm retrieval failure with fine needle aspiration in males with non-obstructive azoospermia. Human reproduction (Oxford, England)\| PubMed ID: 30576444	2019
and play vital roles in occurrence of congenital bilateral absence of vas deferens (CBAVD). Asian journal of andrology\| PubMed ID: 30632488	2019
Loss-of-function mutations in QRICH2 cause male infertility with multiple morphological abnormalities of the sperm flagella. Nature communications\| PubMed ID: 30683861	2019
Author Correction: Loss-of-function mutations in QRICH2 cause male infertility with multiple morphological abnormalities of the sperm flagella. Nature communications\| PubMed ID: 31110204	2019
A novel splice site variant in ANOS1 gene leads to Kallmann syndrome in three siblings. Gene\| PubMed ID: 31669640	2020
An autoantibody against a 48-Kd fragment of human DNA-topoiomerase I in breast cancer: Implication for diagnosis and prognosis, and antibody-dependent cellular cytotoxicity in vitro. Cellular immunology\| PubMed ID: 31732123	2020
A specific autoantibody against a novel tumour-association antigen derived from human DNA-topoiomerase I is a potential biomarker for early diagnosis and favourable prognosis in patients wit... Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals\| PubMed ID: 31922440	2020
Importance and safety of autologous sperm cryopreservation for fertility preservation in young male patients with cancer. Medicine\| PubMed ID: 32282708	2020
A development strategy to fast establish the Taqman qPCR based method to detect SNP mutations. Human cell\| PubMed ID: 32613572	2020
A dual-site controlled pH probe revealing the pH of sperm cytoplasm and screening for healthy spermatozoa. Journal of materials chemistry. B\| PubMed ID: 33870986	2021
Novel Mutations in X-Linked, -Induced Asthenoteratozoospermia and Male Infertility. Cells\| PubMed ID: 34202084	2021
CEP128 is involved in spermatogenesis in humans and mice. Nature communications\| PubMed ID: 35296684	2022
Critical Roles of the Circadian Transcription Factor in Reproductive Endocrinology and Fertility. Frontiers in endocrinology\| PubMed ID: 35311235	2022
Loss-of-function p.G970D missense mutation might cause congenital bilateral absence of the vas deferens and be associated with impaired spermatogenesis. Asian journal of andrology\| PubMed ID: 35665694	2023
Case report: Biallelic variants in POLR3B gene lead to 4H leukodystrophy from the study of brother and sister. Medicine\| PubMed ID: 36042647	2022
Population-based genetic analysis in infertile men reveals novel mutations of ADAD family members in patients with impaired spermatogenesis. Human molecular genetics\| PubMed ID: 36708028	2023
The EDA/EDAR/NF-κB pathway in non-syndromic tooth agenesis: A genetic perspective. Frontiers in genetics\| PubMed ID: 37077539	2023
A novel SNP in HUWE1 promoter confers increased risk of NOA by affecting the RA/RARα pathway in Chinese individuals. Andrology\| PubMed ID: 37290064	2024
A Prediction Model of Sperm Retrieval in Males with Idiopathic Non-obstructive Azoospermia for Microdissection Testicular Sperm Extraction. Reproductive sciences (Thousand Oaks, Calif.)\| PubMed ID: 37749447	2024
Novel axonemal protein ZMYND12 interacts with TTC29 and DNAH1, and is required for male fertility and flagellum function. eLife\| PubMed ID: 37934199	2023
Outcomes comparison of testicular versus ejaculated sperm for intracytoplasmic sperm injection in infertile men with high DNA fragmentation: updated systematic review and meta-analysis. Translational andrology and urology\| PubMed ID: 38196694	2023
Case report: remedial microdissection testicular sperm extraction after onco-microdissection testicular sperm extraction failure. Medicine\| PubMed ID: 38394502	2024
HSF5 Deficiency Causes Male Infertility Involving Spermatogenic Arrest at Meiotic Prophase I in Humans and Mice. Advanced science (Weinheim, Baden-Wurttemberg, Germany)\| PubMed ID: 38958533	2024