P. Zhu

发表

Targeted next generation sequencing identified novel loss‐of‐function mutations in MERTK gene in Chinese patients with retinitis pigmentosa

D. Tang, Yong Dai, Song Liu, 2019, Molecular genetics & genomic medicine.

Prenatal screening and prenatal diagnosis with cordocentesis for prenatal chromosome abnormalities

Hui Guo, Yong Xu, Yan Wu, 2018 .

Identification of 11 potentially relevant gene mutations involved in growth retardation, intellectual disability, joint contracture, and hepatopathy

Wenbiao Chen, H. Diao, P. Zhu, 2018, Medicine.

Classification and Prognostic Characteristics of Hepatocellular Carcinoma Based on Glycolysis Cholesterol Synthesis Axis

Wenbiao Chen, X. Hou, P. Zhu, 2022, Journal of oncology.

The Association between Immune Subgroups and Gene Modules for the Clinical, Cellular, and Molecular Characteristic of Hepatocellular Carcinoma

Wenbiao Chen, X. Hou, P. Zhu, 2022, Journal of oncology.

Identification of Genomic Rare Variants by Whole Genome Sequencing in Primary Torsion Dystonia

D. Tang, Bo Li, P. Zhu, 2020 .

Association of the characteristics of B- and T-cell repertoires with papillary thyroid carcinoma

Ni Xie, Song Liu, C. Zou, 2018, Oncology letters.

Rapid gene identification in a Chinese osteopetrosis family by whole exome sequencing.

Jianguo Zhang, Min Ding, W. Sui, 2013, Gene.

Genotyping, generation and proteomic profiling of the first human autosomal dominant osteopetrosis type II-specific induced pluripotent stem cells

D. Tang, W. Sui, Jiansheng Xie, 2019, Stem Cell Research & Therapy.

Integrated analysis of B-cell and T-cell receptors by high-throughput sequencing reveals conserved repertoires in IgA nephropathy

D. Tang, F. Zheng, Song Liu, 2018, Molecular medicine reports.

Multiomics landscape of the autosomal dominant osteopetrosis type II disease-specific induced pluripotent stem cells

Y. Shangguan, D. Tang, W. Dai, 2021, Hereditas.

Bioinformatics Analysis of the Core Genes Related to Lupus Nephritis Through a Network and Pathway-Based Approach.

Wenbiao Chen, P. Zhu, Y. Dai, 2019, DNA and cell biology.

Integrative analysis of the characteristics of lipid metabolism-related genes as prognostic prediction markers for hepatocellular carcinoma.

J. Zeng, Desheng Tang, P. Zhu, 2021, European review for medical and pharmacological sciences.

A genetic risk factor for thrombophilia in a Han Chinese family

W. Sui, S. Cong, Yadan Luo, 2017, Molecular medicine reports.

A Chinese family with congenital Dysfibrinogenemia carries a heterozygous missense mutation in FGA: Concerning the genetic abnormality and clinical treatment

Xinyou Zhang, P. Zhu, Jihao Zhou, 2017, Pakistan journal of medical sciences.

Characterization of the T-cell receptor repertoire by deep T cell receptor sequencing in tissues from patients with prostate cancer

Song Liu, Xinzhou Zhang, Yunlong Hu, 2017, Oncology letters.

Identification of a novel COL4A5 mutation in the proband initially diagnosed as IgAN from a Chinese family with X-linked Alport syndrome

Saijun Liu, Hui Huang, Jing Wu, 2019, Science China Life Sciences.

Determination of the complexity and diversity of the TCR β-chain CDR3 repertoire in bladder cancer using high-throughput sequencing

W. Sui, Song Liu, C. Zou, 2019, Oncology letters.

Single-cell RNA sequencing reveals the mediatory role of cancer-associated fibroblast PTN in hepatitis B virus cirrhosis-HCC progression

Yeda Chen, Chenhong Lin, P. Zhu, 2023, Gut Pathogens.

Identification of Pathogenic Mutations and Investigation of the NOTCH Pathway Activation in Kartagener Syndrome

Xuemei Han, L. Cheng, Yingyun Fu, 2019, Front. Genet..

Identification of a novel COL4A5 mutation in the proband initially diagnosed as IgAN from a Chinese family with X-linked Alport syndrome

Saijun Liu, Hui Huang, Jing Wu, 2019, Science China Life Sciences.