Xiaohui Jiang

Modification of montmorillonite surfaces using a novel class of cationic gemini surfactants.

[The influence of circadian clock gene on mouse sperm fertility in RNAi].

Interaction between water-soluble rhodium complex RhCl(CO)(TPPTS)₂ and surfactants probed by spectroscopic methods.

Organophilic worm-like ruthenium nanoparticles catalysts by the modification of CTAB on montmorillonite supports.

The noncircadian function of the circadian Clock gene in the regulation of male fertility.

A qPCR method to characterize the sex type of the cell strains from rats.

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Clinical significance of plasma anti-TOPO48 autoantibody and blood survivin-expressing circulating cancer cells in patients with early stage endometrial carcinoma.

A homozygous RNF220 mutation leads to male infertility with small-headed sperm.

A risk prediction model of sperm retrieval failure with fine needle aspiration in males with non-obstructive azoospermia.

and play vital roles in occurrence of congenital bilateral absence of vas deferens (CBAVD).

Loss-of-function mutations in QRICH2 cause male infertility with multiple morphological abnormalities of the sperm flagella.

Author Correction: Loss-of-function mutations in QRICH2 cause male infertility with multiple morphological abnormalities of the sperm flagella.

A novel splice site variant in ANOS1 gene leads to Kallmann syndrome in three siblings.

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.

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 with colorectal carcinoma.

Importance and safety of autologous sperm cryopreservation for fertility preservation in young male patients with cancer.

A development strategy to fast establish the Taqman qPCR based method to detect SNP mutations.

A dual-site controlled pH probe revealing the pH of sperm cytoplasm and screening for healthy spermatozoa.

Novel Mutations in X-Linked, -Induced Asthenoteratozoospermia and Male Infertility.

CEP128 is involved in spermatogenesis in humans and mice.

Critical Roles of the Circadian Transcription Factor in Reproductive Endocrinology and Fertility.

Loss-of-function p.G970D missense mutation might cause congenital bilateral absence of the vas deferens and be associated with impaired spermatogenesis.

Case report: Biallelic variants in POLR3B gene lead to 4H leukodystrophy from the study of brother and sister.

Population-based genetic analysis in infertile men reveals novel mutations of ADAD family members in patients with impaired spermatogenesis.

The EDA/EDAR/NF-κB pathway in non-syndromic tooth agenesis: A genetic perspective.

A novel SNP in HUWE1 promoter confers increased risk of NOA by affecting the RA/RARα pathway in Chinese individuals.

A Prediction Model of Sperm Retrieval in Males with Idiopathic Non-obstructive Azoospermia for Microdissection Testicular Sperm Extraction.

Novel axonemal protein ZMYND12 interacts with TTC29 and DNAH1, and is required for male fertility and flagellum function.

Outcomes comparison of testicular versus ejaculated sperm for intracytoplasmic sperm injection in infertile men with high DNA fragmentation: updated systematic review and meta-analysis.

Case report: remedial microdissection testicular sperm extraction after onco-microdissection testicular sperm extraction failure.

HSF5 Deficiency Causes Male Infertility Involving Spermatogenic Arrest at Meiotic Prophase I in Humans and Mice.