Yao-Bin Zhu

发表

Genetic analysis of a congenital split-hand/split-foot malformation 4 pedigree

X. Yang, Jie-wei Luo, Xin-fu Lin, 2018, Molecular medicine reports.

Effect of superselective prostatic artery embolization on benign prostatic hyperplasia

Jian-Hui Zhang, Jie-wei Luo, Yao-Bin Zhu, 2020, Abdominal Radiology.

Genetic diagnosis history and osteoarticular phenotype of a non-transfusion secondary hemochromatosis

Dan-dan Ruan, Jie-wei Luo, Fa-qiang Tang, 2020, World journal of clinical cases.

Genetic diagnosis history and osteoarticular phenotype of a non-transfusion secondary hemochromatosis

Dan-dan Ruan, Jie-wei Luo, Fa-qiang Tang, 2020, World journal of clinical cases.

Association of Tongue Bacterial Flora and Subtypes of Liver-Fire Hyperactivity Syndrome in Hypertensive Patients

X. Yang, Jie-wei Luo, Yao-Bin Zhu, 2018, Evidence-based complementary and alternative medicine : eCAM.

A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency

Dan-dan Ruan, Jie-wei Luo, Fa-qiang Tang, 2021, The journal of gene medicine.

Genetic analysis of three families with X-linked dominant hypophosphatemic rickets

Jie-wei Luo, Xin-fu Lin, Yao-Bin Zhu, 2018, Journal of pediatric endocrinology & metabolism : JPEM.

Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A

W. Chen, Dan-dan Ruan, Jian-Hui Zhang, 2022, Cardiology research and practice.

Function of PHEX mutations p.Glu145* and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription

Dan-dan Ruan, Jie-wei Luo, Fa-qiang Tang, 2022, Cell Death & Disease.

Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations

X. Yang, Dan-dan Ruan, Jian-Hui Zhang, 2021, BioMed research international.

Astragaloside-IV protects H9C2(2-1) cardiomyocytes from high glucose-induced injury via miR-34a-mediated autophagy pathway

Jie-wei Luo, X. Qian, Jingjing Li, 2019, Artificial cells, nanomedicine, and biotechnology.

Han family with essential tremor caused by the P421L variant of the TENM4 gene in China

Jie-wei Luo, Han-Lu Wang, Xing-Lin Ruan, 2023, Neurological Sciences.

Screening and function discussion of a hereditary renal tubular acidosis family pathogenic gene

Li Chen, Jie-wei Luo, Han-Lu Wang, 2020, Cell Death & Disease.

Genetic mutation of familial dilated cardiomyopathy based on next-generation semiconductor sequencing

Jie-wei Luo, Xin-fu Lin, Yao-Bin Zhu, 2018, Molecular medicine reports.

Genetic analysis of sick sinus syndrome in a family harboring compound CACNA1C and TTN mutations

Jie-wei Luo, Yao-Bin Zhu, Fen Jiang, 2018, Molecular medicine reports.

Analysis of mutations in six Chinese families with autosomal dominant polycystic kidney disease.

Jian-Hui Zhang, Yi Li, Jie-wei Luo, 2020, American journal of translational research.

Clinical phenotype and genetic function analysis of a rare family with hereditary leiomyomatosis and renal cell carcinoma complicated with Birt–Hogg–Dubé syndrome

Dan-dan Ruan, Jie-wei Luo, Guokai Yang, 2023, Journal of medical genetics.