Red blood cells free α-haemoglobin pool: a biomarker to monitor the β-thalassemia intermedia variability. The ALPHAPOOL study-Reference-Cited by-同舟云学术

Red blood cells free α-haemoglobin pool: a biomarker to monitor the β-thalassemia intermedia variability. The ALPHAPOOL study

Published:2017-06-23 Issue:1 Volume:179 Page:142-153
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Vasseur Corinne¹²,Domingues-Hamdi Elisa¹²,Ledudal Katia³,Le Corvoisier Philippe³,Barau Caroline⁴,Ghaleh Bijan⁴,Rialland Amandine⁵,Pissard Serge¹²⁶,Galactéros Frédéric¹²⁷,Baudin-Creuza Véronique¹²^ORCID

Affiliation:

1. Institut National de la Santé et de la Recherche Médicale (Inserm)-U955; équipe 2 : Transfusion et Maladies du Globule Rouge; Institut Mondor de Recherche Biomédicale (IMRB); Université de Paris Est Créteil (UPEC); Créteil France

2. Laboratory of Excellence GR-Ex; Paris France

3. Inserm; Centre d'Investigation Clinique 1430; Hôpital Universitaire Henri Mondor Assistance Publique Hôpitaux de Paris (AP-HP); Créteil France

4. Plateforme de Ressources Biologiques; Hôpital Universitaire Henri Mondor (AP-HP); Créteil France

5. Unité de Recherche Clinique; Hôpital Universitaire Henri Mondor (AP-HP); Créteil France

6. Laboratoire de Génétique; Hôpital Universitaire Henri Mondor (AP-HP); Créteil France

7. Unité des Maladies Génétiques du Globule Rouge; Hôpital Universitaire Henri Mondor (AP-HP); Créteil France

Funder

Institut National de la Santé et de la Recherche Médicale

Assistance Publique - Hôpitaux de Paris

University of Paris Est Créteil (UPEC)

DGOS

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.14800/fullpdf

Reference36 articles.

1. Importance of RDW value in differential diagnosis of hypochrome anemias;Aslan;American Journal of Hematology,2002

2. Variable severity of beta-thalassaemia patients of eastern India: effect of alpha-thalassaemia and xmnI polymorphism;Bandyopadhyay;Clinical and Experimental Medicine,2001

3. Transfer of human alpha to beta haemoglobin via its chaperon protein: evidence for a new state;Baudin-Creuza;Journal of Biological Chemistry,2004

4. Functional properties of recombinant α-Hb Questembert (H14 Pro) and α-Hb Caen (H15gly), obtained by coexpression with the alpha hemoglobin stabilizing protein (AHSP);Baudin-Creuza;Clinical Biochemistry,2009

5. Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal haemoglobin;Borg;Nature Genetics,2010

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Peripheral blood circular RNA circ-0008102 may serve as a novel clinical biomarker in beta-thalassemia patients;European Journal of Pediatrics;2024-01-02

2. A survey of intracranial blood flow velocity in thalassemia intermedia in Khuzestan Province, Iran;Iranian Journal of Pediatric Hematology & Oncology;2023-01-03

3. Detection and follow-up of a soluble alpha-haemoglobin pool in the red cells of stored blood units;BLOOD TRANSFUS-ITALY;2022

4. Alpha haemoglobin‐stabilising protein concentration in the red blood cells of patients with sickle cell anaemia with and without hydroxycarbamide treatment;British Journal of Haematology;2021-08-10

5. Compound heterozygotes of Hb Constant Spring and Hb Stanleyville II in HbE/β0-thalassemia;Clinical Chemistry and Laboratory Medicine (CCLM);2021-04-07