Cargando…

The prevalence and molecular characterization of (δβ)(0)‐thalassemia and hereditary persistence of fetal hemoglobin in the Chinese Zhuang population

OBJECTIVE: To reveal the prevalence and molecular characterization of (δβ)(0)‐thalassemia [(δβ)(0)‐thal] and hereditary persistence of fetal hemoglobin (HPFH) in the Chinese Zhuang population. METHODS: A total of 105 subjects with fetal hemoglobin (Hb F) level ≥5% from 14 204 unrelated ones were sel...

Descripción completa

Detalles Bibliográficos
Autores principales:	He, Sheng, Wei, Yuan, Lin, Li, Chen, Qiuli, Yi, Shang, Zuo, Yangjin, Wei, Hongwei, Zheng, Chenguang, Chen, Biyan, Qiu, XiaoXia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2017
Materias:	Research Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5888142/ https://www.ncbi.nlm.nih.gov/pubmed/28763119 http://dx.doi.org/10.1002/jcla.22304

Ejemplares similares

Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern China
por: Zhang, Jie, et al.
Publicado: (2019)

Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China
por: Jiang, Fan, et al.
Publicado: (2020)

HbS-Sicilian (δβ)(0)-Thalassemia: A Rare Variant of Sickle Cell
por: Onimoe, Grace, et al.
Publicado: (2017)

Hereditary persistence of fetal hemoglobin
por: Sharma, Dharmesh Chandra, et al.
Publicado: (2020)

Induction of Fetal Hemoglobin by Introducing Natural Hereditary Persistence of Fetal Hemoglobin Mutations in the γ-Globin Gene Promoters for Genome Editing Therapies for β-Thalassemia
por: Lu, Dian, et al.
Publicado: (2022)

Blessing in disguise; a case of Hereditary Persistence of Fetal Hemoglobin
por: Shaukat, Irfan, et al.
Publicado: (2018)

Construction and Analysis of a Long Non-Coding RNA (lncRNA)-Associated ceRNA Network in β-Thalassemia and Hereditary Persistence of Fetal Hemoglobin
por: Jia, Wenguang, et al.
Publicado: (2019)

Haploinsufficiency for the erythroid transcription factor KLF1 causes Hereditary Persistence of Fetal Hemoglobin
por: Borg, Joseph, et al.
Publicado: (2010)

Genome-wide analysis of aberrantly expressed lncRNAs and miRNAs with associated co-expression and ceRNA networks in β-thalassemia and hereditary persistence of fetal hemoglobin
por: Lai, Ketong, et al.
Publicado: (2017)

Activation of γ-globin gene expression by GATA1 and NF-Y in hereditary persistence of fetal hemoglobin
por: Doerfler, Phillip A., et al.
Publicado: (2021)

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
por: He, Sheng, et al.
Publicado: (2021)

DNA methylation patterns of β-globin cluster in β-thalassemia patients
por: Bao, Xiuqin, et al.
Publicado: (2020)

A Conversation with Xiaowei Zhuang
por: Bourzac, Katherine
Publicado: (2015)

Homozygous Deletion Alpha-Thalassemia and Hereditary Persistence of Fetal Hemoglobin, Two Genetic Factors Predictive the Reduction of Morbidity and Mortality During Pregnancy in Sickle Cell Patients. A Report from the Democratic Republic of Congo
por: Mikobi, Tite Minga, et al.
Publicado: (2019)

Pharmacological Induction of Fetal Hemoglobin in β-Thalassemia and Sickle Cell Disease: An Updated Perspective
por: Bou-Fakhredin, Rayan, et al.
Publicado: (2022)

Lysine-specific histone demethylase 1 inhibition enhances robust fetal hemoglobin induction in human β(0)-thalassemia/hemoglobin E erythroid cells
por: Kaewsakulthong, Woratree, et al.
Publicado: (2021)

Extramedullary hematopoiesis presented as cytopenia and massive paraspinal masses leading to cord compression in a patient with hereditary persistence of fetal hemoglobin
por: Katchi, Tasleem, et al.
Publicado: (2016)

Genetic polymorphisms in very important pharmacogenomic variants in the Zhuang ethnic group of Southwestern China: A cohort study in the Zhuang population
por: Li, Jing, et al.
Publicado: (2018)

Homozygous delta-beta Thalassemia in a Child: a Rare Cause of Elevated Fetal Hemoglobin
por: Verma, S, et al.
Publicado: (2013)

A Rational Approach to Drug Repositioning in β-thalassemia: Induction of Fetal Hemoglobin by Established Drugs
por: Prosdocimi, Marco, et al.
Publicado: (2022)

Light People: Academician Songlin Zhuang
por: Wang, Hui, et al.
Publicado: (2022)

Reticulocyte hemoglobin equivalent to detect thalassemia and thalassemic hemoglobin variants
por: Sudmann, Å A, et al.
Publicado: (2012)

Down-regulation of the transcriptional repressor ZNF802 (JAZF1) reactivates fetal hemoglobin in β(0)-thalassemia/HbE
por: Wongborisuth, Chokdee, et al.
Publicado: (2022)

XmnI polymorphism frequency in heterozygote beta thalassemia subjects and its relation to Fetal hemoglobin levels
por: Chinelato, Isabela Sandrin, et al.
Publicado: (2011)

MicroRNA Expression in β-Thalassemia and Sickle Cell Disease: A Role in The Induction of Fetal Hemoglobin
por: Saki, Najmaldin, et al.
Publicado: (2016)

Diagnostic value of fetal hemoglobin Bart’s for evaluation of fetal α-thalassemia syndromes: application to prenatal characterization of fetal anemia caused by undiagnosed α-hemoglobinopathy
por: Singha, Kritsada, et al.
Publicado: (2022)

Prevention of Transcriptional γ-globin Gene Silencing by Inducing The Hereditary Persistence of Fetal Hemoglobin Point Mutation Using Chimeraplast-Mediated Gene Targeting
por: Ranjbaran, Reza, et al.
Publicado: (2018)

Los capítulos interiores de Zhuang Zi
por: Zi, Zhuang
Publicado: (1998)

Induction of fetal hemoglobin: Lentiviral shRNA knockdown of HBS1L in β(0)-thalassemia/HbE erythroid cells
por: Chumchuen, Sukanya, et al.
Publicado: (2023)

Natural Remedies for the Treatment of Beta-Thalassemia and Sickle Cell Anemia—Current Status and Perspectives in Fetal Hemoglobin Reactivation
por: Ng, Noel Yat Hey, et al.
Publicado: (2014)

Treatment of Erythroid Precursor Cells from β-Thalassemia Patients with Cinchona Alkaloids: Induction of Fetal Hemoglobin Production
por: Zuccato, Cristina, et al.
Publicado: (2021)

A combined approach for β-thalassemia based on gene therapy-mediated adult hemoglobin (HbA) production and fetal hemoglobin (HbF) induction
por: Zuccato, Cristina, et al.
Publicado: (2012)

The Hellenic type of nondeletional hereditary persistence of fetal hemoglobin results from a novel mutation (g.-109G>T) in the HBG2 gene promoter
por: Chassanidis, Christos, et al.
Publicado: (2008)

An Aγ-globin G->A gene polymorphism associated with β(0)39 thalassemia globin gene and high fetal hemoglobin production
por: Breveglieri, Giulia, et al.
Publicado: (2017)

Author Correction: Down-regulation of the transcriptional repressor ZNF802 (JAZF1) reactivates fetal hemoglobin in β(0)-thalassemia/HbE
por: Wongborisuth, Chokdee, et al.
Publicado: (2022)

Gap-PCR Screening for Common Large Deletional Mutations of β-Globin Gene Cluster Revealed a Higher Prevalence of the Turkish Inversion/Deletion (δβ)0 Mutation in Antalya
por: Bilgen, Türker, et al.
Publicado: (2016)

Role of XmnI(G) Polymorphism in Hydroxyurea Treatment and Fetal Hemoglobin Level at Isfahanian Intermediate β-Thalassemia Patients
por: Motovali-Bashi, Majid, et al.
Publicado: (2015)

Disruption of the BCL11A Erythroid Enhancer Reactivates Fetal Hemoglobin in Erythroid Cells of Patients with β-Thalassemia Major
por: Psatha, Nikoletta, et al.
Publicado: (2018)

HBG2 -158 (C>T) polymorphism and its contribution to fetal hemoglobin variability in Iraqi Kurds with beta-thalassemia minor
por: Albarawi, Dilan J., et al.
Publicado: (2018)

Thalassemia Major and Intermedia Patients in East Java do not Show Fetal Hemoglobin Level Difference in Relation to XMNI Polymorphism
por: Wulandari, Retno Dwi, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_147h1qnolcs6iass2lc0onb0pk