Qian Li

发表

A novel T→G splice site mutation of CRYBA1/A3 associated with autosomal dominant nuclear cataracts in a Chinese family

Xu Ma, Siquan Zhu, Fan Yang, 2012, Molecular vision.

A G→T splice site mutation of CRYBA1/A3 associated with autosomal dominant suture cataracts in a Chinese family

Yuanyuan Guo, Xu Ma, Siquan Zhu, 2011, Molecular vision.

Elevated MST1 leads to apoptosis via depletion of YAP1 in cardiomyocytes exposed to high glucose

Xu Ma, C. Shi, D. Su, 2021, Molecular medicine.

A novel mutation in CRYAA is associated with autosomal dominant suture cataracts in a Chinese family

Yuanyuan Guo, Xu Ma, Siquan Zhu, 2012, Molecular vision.

Mutation Analysis in Chinese Families with Autosomal Dominant Hereditary Cataracts

Xu Ma, Zhenfei Yang, Qian Li, 2015, Current eye research.

Role of Nodal-PITX2C signaling pathway in glucose-induced cardiomyocyte hypertrophy.

Xu Ma, D. Su, Qian Li, 2014, Biochemistry and cell biology = Biochimie et biologie cellulaire.

Thyroid antibodies and gestational diabetes mellitus: a meta-analysis.

Qian Li, Qianqian Wang, Ying Yang, 2015, Fertility and sterility.

Preconception diabetes mellitus and adverse pregnancy outcomes in over 6.4 million women: A population-based cohort study in China

Huixia Yang, Yumei Wei, Long Wang, 2019, PLoS medicine.

MDM2 phosphorylation mediates H2O2-induced lens epithelial cells apoptosis and age-related cataract.

Lei Sun, Xu Ma, Shanshan Hu, 2020, Biochemical and biophysical research communications.

Abnormal Expression of MST1 and YAP1 in Fetal Heart Tissue in a Hyperglycemic Environment and Their Roles in Mediating Apoptosis

Yanhua Li, Xu Ma, C. Shi, 2020 .

Role of GAB1/PI3K/AKT signaling high glucose-induced cardiomyocyte apoptosis.

Yingyu Chen, Xu Ma, Shanshan Hu, 2017, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

ROCK1/p53/NOXA signaling mediates cardiomyocyte apoptosis in response to high glucose in vitro and vivo.

J. Zhao, Lei Sun, Xu Ma, 2017, Biochimica et biophysica acta. Molecular basis of disease.

Cited2 participates in cardiomyocyte apoptosis and maternal diabetes-induced congenital heart abnormality.

Xu Ma, C. Shi, D. Su, 2016, Biochemical and biophysical research communications.

Down-regulation of EBAF in the heart with ventricular septal defects and its regulation by histone acetyltransferase p300 and transcription factors smad2 and cited2.

Xu Ma, D. Su, Qian Li, 2013, Biochimica et biophysica acta.

Role of EBAF/Nodal/p27 signaling pathway in development of placenta in normal and diabetic rats.

Xu Ma, Yining Jin, C. Shi, 2021, Developmental Biology.

A R54L Mutation of CRYAA Associated with Autosomal Dominant Nuclear Cataracts in a Chinese Family

Xu Ma, Siquan Zhu, Fan Yang, 2013, Current eye research.

GSK3β and MCL-1 mediate cardiomyocyte apoptosis in response to high glucose

J. Zhao, Xu Ma, Shanshan Hu, 2019, Histochemistry and Cell Biology.

The DNA methylation profile of PLA2G4C gene promoter in schizophrenia

Xu Ma, Qiong Yu, C. Kou, 2012, Psychiatry Research.

A G57W Mutation of CRYGS Associated with Autosomal Dominant Pulverulent Cataracts in a Chinese Family

Xu Ma, Siquan Zhu, Zhenfei Yang, 2015, Ophthalmic genetics.

lncRNA TUG1 modulates proliferation, apoptosis, invasion, and angiogenesis via targeting miR-29b in trophoblast cells

Xu Ma, D. Su, Qian Li, 2019, Human Genomics.

Downregulation of SOX11 in fetal heart tissue, under hyperglycemic environment, mediates cardiomyocytes apoptosis

Xu Ma, C. Shi, D. Su, 2020, Journal of biochemical and molecular toxicology.

Clinical heterogeneity and intrafamilial variability of Joubert syndrome in two siblings with CPLANE1 variants

Zongfu Cao, Ruikun Cai, Yufei Yu, 2021, Molecular genetics & genomic medicine.

A nonsense mutation of CRYGC associated with autosomal dominant congenital nuclear cataracts and microcornea in a Chinese pedigree

Xu Ma, Siquan Zhu, Zhenfei Yang, 2012, Molecular vision.

Identification of two novel pathogenic variants of PIBF1 by whole exome sequencing in a 2-year-old boy with Joubert syndrome

Yun Peng, Zongfu Cao, Ruikun Cai, 2020, BMC medical genetics.

Prevention and Control of Pathogens Based on Big-Data Mining and Visualization Analysis

Hao Lin, Zongfu Cao, Ruikun Cai, 2021, Frontiers in Molecular Biosciences.

Preconception blood pressure and risk of preterm birth: a large historical cohort study in a Chinese rural population.

Yuan He, Qian Li, Ying Yang, 2015, Fertility and sterility.

CITED2 mutation links congenital heart defects to dysregulation of the cardiac gene VEGF and PITX2C expression.

Xu Ma, D. Su, Qian Li, 2012, Biochemical and biophysical research communications.

Association of Husband Smoking With Wife's Hypertension Status in Over 5 Million Chinese Females Aged 20 to 49 Years

Fangchao Liu, Xingyu Wang, Long Wang, 2017, Journal of the American Heart Association.

Preconception Hb concentration and risk of preterm birth in over 2·7 million Chinese women aged 20–49 years: a population-based cohort study

Fangchao Liu, Long Wang, Yuan He, 2018, British Journal of Nutrition.

Identification and Functional Analysis of GJA8 Mutation in a Chinese Family with Autosomal Dominant Perinuclear Cataracts

Lei Zhang, Xu Ma, Zhenfei Yang, 2013, PloS one.

Tanshinone l exhibits anticancer effects in human endometrial carcinoma HEC-1-A cells via mitochondrial mediated apoptosis, cell cycle arrest and inhibition of JAK/STAT signalling pathway.

Xu Ma, Qian Li, Ying Liang, 2018, Journal of B.U.ON. : official journal of the Balkan Union of Oncology.

Sequencing Analysis of mRNA Profile in Endothelial Cells in Response to ox-LDL

Xu Ma, C. Shi, D. Su, 2021, Biochemical Genetics.

Genome-wide analysis of methylation in rat fetal heart under hyperglycemia by methylation-dependent restriction site–associated DNA sequencing

Rui Meng, C. Shi, D. Su, 2022, PloS one.