Xiaoya Ren

发表

Hormonal changes throughout puberty in congenital hypogonadotropic hypogonadism and Pump indication

C. Gong, B. Cao, Jiajia Chen, 2020 .

Senescence marker protein 30 inhibits tumor growth by reducing HDAC4 expression in non-small cell lung cancer

Xiaolong Yan, A. Ganti, Liqun Xu, 2021, Translational lung cancer research.

Persistent Müllerian duct syndrome: A case report and review

Di Wu, C. Gong, Xiaoya Ren, 2017, Experimental and therapeutic medicine.

Clinical characteristics and genotype‐phenotype correlations of 130 Chinese children in a high‐homogeneity single‐center cohort with 5α‐reductase 2 deficiency

M. Polak, Di Wu, C. Gong, 2020, Molecular Genetics & Genomic Medicine.

WNT5A promotes the metastasis of esophageal squamous cell carcinoma by activating the HDAC7/SNAIL signaling pathway

Xiaolong Yan, Xiaofei Li, Liqun Xu, 2022, Cell Death & Disease.

γδTFH cells promote B cell maturation and antibody production in neuroblastoma

Xi Chen, Xiaolin Wang, H. Qin, 2017, BMC Immunology.

Characteristics, Prognosis, and Competing Risk Nomograms of Cutaneous Malignant Melanoma: Evidence for Pigmentary Disorders

Tengyu Ma, Dahai Hu, Zichao Li, 2022, Frontiers in Oncology.

Efficacy and safety of human chorionic gonadotropin combined with human menopausal gonadotropin and a gonadotropin-releasing hormone pump for male adolescents with congenital hypogonadotropic hypogonadism

C. Gong, Ying Liu, Shao-ke Chen, 2021, Chinese medical journal.

The wide clinical expression spectrum presented in two families with NR5A1 mutation

C. Gong, Xiu-Ju Zhao, Xiaoya Ren, 2018 .

Increase in Peripheral Blood Intermediate Monocytes is Associated with the Development of Recent-Onset Type 1 Diabetes Mellitus in Children

C. Gong, Di Wu, B. Cao, 2017, International journal of biological sciences.

Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients

Zhihong Wu, Hengqiang Zhao, N. Wu, 2021, Frontiers in Endocrinology.

SOX2 heterozygous mutation causes multiple extra-ocular phenotypes in boys

C. Gong, Xiaoya Ren, Yi Wang, 2020 .

Novel phenotypes and genotypes in Antley-Bixler syndrome caused by cytochrome P450 oxidoreductase deficiency: based on the first cohort of Chinese children

C. Gong, Junfen Fu, C. Su, 2019, Orphanet Journal of Rare Diseases.

A novel deletion mutation in IL2RG gene results in X-linked severe combined immunodeficiency with an atypical phenotype

Bao-Ping Xu, Xiaoya Ren, W. Mou, 2016, Immunogenetics.

Ubiquitin-specific protease 28: the decipherment of its dual roles in cancer development

Xiaoxia Zhou, Xiaolong Yan, Dong Liu, 2023, Experimental Hematology & Oncology.

Growth Curves of Chinese Children with Androgen Insensitivity Syndrome: A Multicenter Registry Study

C. Gong, Shaoke Chen, Ge-li Liu, 2022, Journal of personalized medicine.

Prevalence and association of diabetic nephropathy in newly diagnosed Chinese patients with diabetes in the Hebei province: A single-center case-control study

Xianghui Yu, Ninglin Kang, Xiaoya Ren, 2023, Medicine.

Flow cytometric analyses of the viability, surface marker expression and function of lymphocytes from children following cryopreservation.

Xiaoya Ren, W. Mou, Hong Jiao, 2016, Molecular medicine reports.