Novel haemoglobin mutation (α127Lys→Glu) increases oxygen affinity and has a minor effect on haptoglobin binding (original) (raw)

High-Oxygen-Affinity Hemoglobins—Case Series and Review of the Literature

Pagona Flevari

Journal of Clinical Medicine, 2024

View PDFchevron_right

Hb Mazandaran (α1) α51 Gly > Cys(CE9), c.154 GGC > TGC: A Novel Haemoglobin Variant of α1-Globin Gene

mahan mahdavi

Thalassemia Reports, 2022

View PDFchevron_right

Structure and function of hemoglobin variants at an internal hydrophobic site: consequences of mutations at the .beta. 27 (B9) position

Faouzi Baklouti

Biochemistry, 1990

View PDFchevron_right

Hemoglobin as oxygen-dependent glutathione buffer

Anna Bogdanova

Zenodo (CERN European Organization for Nuclear Research), 2022

View PDFchevron_right

Biochemical Fates of α Hemoglobin Bound to α Hemoglobin-stabilizing Protein AHSP

Andrew Gow

Journal of Biological Chemistry, 2006

View PDFchevron_right

Oxygen binding properties of non-mammalian nerve globins

Luc Moens

FEBS Journal, 2006

View PDFchevron_right

The Frequencies of Haptoglobin Types in Five Populations

Peter Kunstadter

Annals of Human Genetics, 1958

View PDFchevron_right

The effect of altered hemoglobin-oxygen affinity on oxygen transport by hemoglobin solution

Charles Rice

Journal of Surgical Research, 1980

View PDFchevron_right

Heme-ligand tunneling in group I truncated hemoglobins

michel guertin

2004

View PDFchevron_right

Haptoglobin polymorphism and peripheral arterial occlusive disease

Daniel A Duprez

Atherosclerosis, 1999

View PDFchevron_right

Neuroglobin and Other Hexacoordinated Hemoglobins Show a Weak Temperature Dependence of Oxygen Binding

Luc Moens

Biophysical Journal, 2004

View PDFchevron_right

Development of gene editing strategies for human β-globin (HBB) gene mutations

Medine KARADAĞ ALPASLAN

Gene, 2020

View PDFchevron_right

A novel β-thalassaemia mutation in the 5’untranslated region of the β-globin gene

Adamantia Papachatzopoulou

British Journal of Haematology, 1994

View PDFchevron_right

-Hemoglobin Stabilizing Protein (AHSP) Markedly Decreases the Redox Potential and Reactivity of -Subunits of Human HbA with Hydrogen Peroxide

sambuddha banerjee

Journal of Biological Chemistry, 2013

View PDFchevron_right

Comparison of the characteristics of two hemoglobin variants, Hb D-Iran and Hb E, eluting in the Hb A2 window

aastha gupta

Blood Research, 2017

View PDFchevron_right

Hemoglobin F level in different hemoglobin variants

Mewoyeka Olusoji

The Korean Journal of Hematology, 2011

View PDFchevron_right

Fast determination of haptoglobin phenotype and calculation of hemoglobin binding capacity using high pressure gel permeation chromatography

Joris Delanghe

Clinica Chimica Acta, 2000

View PDFchevron_right

Methods to quantitate human haptoglobin by complexation with hemoglobin

Sandra Cerda

Journal of Immunological Methods, 1990

View PDFchevron_right

Mutation near the binding interfaces at α-hemoglobin stabilizing protein is highly pathogenic

Sayed Abdulazeez

2016

View PDFchevron_right

Haemoglobin F auckland Gγ7 Asp → Asn: Further evidence for multiple genes for the gamma chain

R. Carrell

Biochimica et Biophysica Acta (BBA) - Protein Structure, 1974

View PDFchevron_right

Scanning the β-globin gene for mutations in large populations by denaturing capillary and gel electrophoresis

William Thilly

Electrophoresis, 2005

View PDFchevron_right

Expression and Developmental Control of the Human α‐Globin Gene Cluster

Stephen Liebhaber

Annals of the New York Academy of Sciences, 1998

View PDFchevron_right

Haptoglobin polymorphism as a risk factor for coronary heart disease mortality

Joris Delanghe

Atherosclerosis, 2001

View PDFchevron_right

Detection of −α 3.7 and _ _SEA deletions in α-globin gene in the Bangladeshi population

Hossain Shekhar

Research Square (Research Square), 2024

View PDFchevron_right

Oxidized hemoglobin is an endogenous proinflammatory agonist that targets vascular endothelial cells

Gabriela Silva

2009

View PDFchevron_right

Emerging Roles for Myoglobin in the Heart

Pradeep P.A. Mammen

Trends in Cardiovascular Medicine, 2003

View PDFchevron_right

Coinheritance of the different copy numbers of α-globin gene modifies severity of β-thalassemia/Hb E disease

Orapan Sripichai

Ann Hematol, 2008

View PDFchevron_right

Prevalence of haemoglobin variants among the Ika ethnic nationality of Delta state

Clement Isibor

International Journal of Medicine and Biomedical Research, 2014

View PDFchevron_right

Hemoglobin variants detected by hemoglobin A1c (HbA1c) analysis and the effects on HbA1c measurements

Nadzimah Mohd Nasir

International Journal of Diabetes in Developing Countries, 2010

View PDFchevron_right

Haptoglobin gene subtypes in three Brazilian population groups of different ethnicities

Silviene Oliveira

Genetics and Molecular Biology, 2009

View PDFchevron_right

Hemoglobin solution: Is a normal [Hb] or P50 more important?

Charles Rice

Journal of Surgical Research, 1982

View PDFchevron_right

Oxidized low-density lipoprotein, iron stores, and haptoglobin polymorphism

Joris Delanghe

Atherosclerosis, 2004

View PDFchevron_right

Site-directed mutations of human hemoglobin at residue 35β: A residue at the intersection of the α1β1, α1β2, and α1α2 interfaces

Stefano Bruno

Protein Science, 2001

View PDFchevron_right

Semisynthetic hemoglobin A: reconstitution of functional tetramer from semisynthetic .alpha.-globin

Md. Shabbir Khan

Biochemistry, 1989

View PDFchevron_right

Modification of globin gene expression by RNA targeting strategies

Heather Rogers

Experimental Hematology, 2007

View PDFchevron_right