Yangjin Zuo

Nanning, China

Last Updated: 09/26/2026

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Found 15 publications

Activation of γ-globin expression by LncRNA-mediated ERF promoter hypermethylation in β-thalassemia.

Activation of γ-globin expression by LncRNA-mediated ERF promoter hypermethylation in β-thalassemia.

Journal: Clinical epigenetics

Published: October 09, 2023

Reference intervals for erythrocyte parameters and hemoglobin electrophoresis parameters for young children in Guangxi.

Reference intervals for erythrocyte parameters and hemoglobin electrophoresis parameters for young children in Guangxi.

Journal: International journal of laboratory hematology

Published: March 18, 2022

Molecular Characterization of α- and β-Thalassaemia Among Children From 1 to 10 Years of Age in Guangxi, A Multi-Ethnic Region in Southern China.

Molecular Characterization of α- and β-Thalassaemia Among Children From 1 to 10 Years of Age in Guangxi, A Multi-Ethnic Region in Southern China.

Journal: Frontiers in pediatrics

Published: June 12, 2021

Epigenetic inactivation of ERF reactivates γ-globin expression in β-thalassemia.

Epigenetic inactivation of ERF reactivates γ-globin expression in β-thalassemia.

Journal: American journal of human genetics

Published: December 27, 2020

DNA methylation patterns of β-globin cluster in β-thalassemia patients.

DNA methylation patterns of β-globin cluster in β-thalassemia patients.

Journal: Clinical epigenetics

Published: October 19, 2020

A novel splicing mutation in F8 causes various aberrant transcripts in a hemophilia A patient and identifies a new transcript from healthy individuals.

A novel splicing mutation in F8 causes various aberrant transcripts in a hemophilia A patient and identifies a new transcript from healthy individuals.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis

Published: August 28, 2020

A novel missense mutation in F9 gene causes hemophilia B in a family with clinical variability.

A novel missense mutation in F9 gene causes hemophilia B in a family with clinical variability.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis

Published: January 07, 2020

A novel 223 kb deletion in the beta-globin gene cluster was identified in a Chinese thalassemia major patient.

A novel 223 kb deletion in the beta-globin gene cluster was identified in a Chinese thalassemia major patient.

Journal: International journal of laboratory hematology

Published: January 24, 2019

First Identification of the 3.5 kb Deletion (NC_000011.10: g.5224302-5227791del3490bp) on the β-Globin Gene Cluster in a Chinese Family.

First Identification of the 3.5 kb Deletion (NC_000011.10: g.5224302-5227791del3490bp) on the β-Globin Gene Cluster in a Chinese Family.

Journal: Hemoglobin

Published: January 08, 2019

Characterization of Hb Bart's Hydrops Fetalis Caused by - -SEA and a Large Novel α0-Thalassemia Deletion.

Characterization of Hb Bart's Hydrops Fetalis Caused by - -SEA and a Large Novel α0-Thalassemia Deletion.

Journal: Hemoglobin

Published: March 02, 2018

Characterization of a Large Novel α-Globin Gene Cluster Deletion Causing α0-Thalassemia in a Chinese Family.

Characterization of a Large Novel α-Globin Gene Cluster Deletion Causing α0-Thalassemia in a Chinese Family.

Journal: Hemoglobin

Published: November 23, 2017

A novel variant of osteogenesis imperfecta type IV and low serum phosphorus level caused by a Val94Asp mutation in COL1A1.

A novel variant of osteogenesis imperfecta type IV and low serum phosphorus level caused by a Val94Asp mutation in COL1A1.

Journal: Molecular medicine reports

Published: June 21, 2017

Showing 1-12 of 15

Last Updated: 09/26/2026