Citation Impact
Citing Papers
Tibetans living at sea level have a hyporesponsive hypoxia-inducible factor system and blunted physiological responses to hypoxia
2013 StandoutNobel
Comparison of Two Fluid-Management Strategies in Acute Lung Injury
2006 Standout
Molecular and Cellular Aspects of Thiol–Disulfide Exchange
1990
Human high-altitude adaptation: forward genetics meets the HIF pathway
2014
Evolutionary history of Tibetans inferred from whole-genome sequencing
2017 StandoutNobel
Erythrocytosis-associated HIF-2α Mutations Demonstrate a Critical Role for Residues C-terminal to the Hydroxylacceptor Proline
2009
Genetic origins and clinical phenotype of familial and acquired erythrocytosis and thrombocytosis
2008
Involvement of oxygen-sensing pathways in physiologic and pathologic erythropoiesis
2009 StandoutNobel
Novel exon 12 mutations in the HIF2A gene associated with erythrocytosis
2008
The EGLN-HIF O 2 -Sensing System: Multiple Inputs and Feedbacks
2017 StandoutNobel
Regulation of erythropoiesis by hypoxia-inducible factors
2013
HIF Hydroxylase Pathways in Cardiovascular Physiology and Medicine
2015 StandoutNobel
Cardiopulmonary function in two human disorders of the hypoxia‐inducible factor (HIF) pathway: von Hippel‐Lindau disease and HIF‐2α gain‐of‐function mutation
2011 StandoutNobel
Hypoxia-Inducible Factors and the Response to Hypoxic Stress
2010 Standout
Hypoxia-Inducible Factors in Physiology and Medicine
2012 StandoutNobel
Extrinsic and intrinsic control by EKLF (KLF1) within a specialized erythroid niche
2014
Potent and Selective Triazole-Based Inhibitors of the Hypoxia-Inducible Factor Prolyl-Hydroxylases with Activity in the Murine Brain
2015 StandoutNobel
Structural basis for oxygen degradation domain selectivity of the HIF prolyl hydroxylases
2016 StandoutNobel
The Clinical Sequelae of Intravascular Hemolysis and Extracellular Plasma Hemoglobin
2005 Standout
Gout-associated uric acid crystals activate the NALP3 inflammasome
2006 StandoutNature
Roles of individual prolyl‐4‐hydroxylase isoforms in the first 24 hours following transient focal cerebral ischaemia: insights from genetically modified mice
2012 StandoutNobel
Evidence review of hydroxyurea for the prevention of sickle cell complications in low-income countries
2013
Genetic causes of erythrocytosis and the oxygen-sensing pathway
2008
Prolyl hydroxylase domain-containing protein inhibitors as stabilizers of hypoxia-inducible factor: small molecule-based therapeutics for anemia
2010
Hypoxia and Inflammation
2011 Standout
Juvenile idiopathic arthritis
2007 Standout
Updated Clinical Classification of Pulmonary Hypertension
2009 Standout
Targeting oxidative stress in disease: promise and limitations of antioxidant therapy
2021 Standout
Familial autoinflammatory diseases: genetics, pathogenesis and treatment
2005
Genetic Determinants and Ethnic Disparities in Sepsis-associated Acute Lung Injury
2005
A novel heterozygous HIF2AM535I mutation reinforces the role of oxygen sensing pathway disturbances in the pathogenesis of familial erythrocytosis
2008
Structure and function of haemoglobins
2017
Clinical management of adult sickle-cell disease
2012
Mammalian display screening of diverse cystine-dense peptides for difficult to drug targets
2017 StandoutNobel
Oxygen sensing and hypoxia signalling pathways in animals: the implications of physiology for cancer
2013 StandoutNobel
Distinct deregulation of the hypoxia inducible factor by PHD2 mutants identified in germline DNA of patients with polycythemia
2011
ROS as signalling molecules: mechanisms that generate specificity in ROS homeostasis
2007 Standout
PHD2 Mutation and Congenital Erythrocytosis with Paraganglioma
2008
Fevers, Genes, and Innate Immunity
2008
Updated Clinical Classification of Pulmonary Hypertension
2013 Standout
Nitric oxide's reactions with hemoglobin: a view through the SNO-storm
2003
Mutation analysis of HIF prolyl hydroxylases (PHD/EGLN) in individuals with features of phaeochromocytoma and renal cell carcinoma susceptibility
2010 StandoutNobel
Sickle cell disease: no longer a single gene disorder
2001
Effects of Iron Supplementation and Depletion on Hypoxic Pulmonary Hypertension
2009 StandoutNobel
Sickle-cell disease
2010 Standout
Physiological functions of thioredoxin and thioredoxin reductase
2000 Standout
Significant haemoglobinopathies: guidelines for screening and diagnosis
2010
Reduced water exchange in sickle cell anemia red cells: a membrane abnormality
1989
Recognition of Hyaluronan Released in Sterile Injury Involves a Unique Receptor Complex Dependent on Toll-like Receptor 4, CD44, and MD-2
2007 StandoutNobel
Microbe sensing, positive feedback loops, and the pathogenesis of inflammatory diseases
2008 StandoutNobel
Oxygen Sensing, Homeostasis, and Disease
2011 StandoutNobel
Sickle cell disease in Africa
2002
The increase in pulmonary arterial pressure caused by hypoxia depends on iron status
2008 StandoutNobel
Targeting Hypoxia-Inducible Factors for the Treatment of Anemia in Chronic Kidney Disease Patients
2017 Standout
Carotid body hyperplasia and enhanced ventilatory responses to hypoxia in mice with heterozygous deficiency of PHD2
2013 StandoutNobel
EGLN1 Inhibition and Rerouting of α-Ketoglutarate Suffice for Remote Ischemic Protection
2016 StandoutNobel
The human side of hypoxia‐inducible factor
2008 StandoutNobel
Therapeutic Manipulation of the HIF Hydroxylases
2009
Cation transport and volume regulation in sickle red blood cells
1993
Hypoxia-inducible factor induces cysteine dioxygenase and promotes cysteine homeostasis in Caenorhabditis elegans
2023 StandoutNobel
Improving Protein Expression, Stability, and Function with ProteinMPNN
2024 StandoutNobel
Clinical iron deficiency disturbs normal human responses to hypoxia
2016 StandoutNobel
Identification and transcriptome analysis of erythroblastic island macrophages
2019 StandoutNobel
Hypoxia. Cross talk between oxygen sensing and the cell cycle machinery
2011 StandoutNobel
Two Distinct Roles for EGL-9 in the Regulation of HIF-1-Mediated Gene Expression in Caenorhabditis elegans
2009
Increased Glutathionyl Hemoglobin in Diabetes Mellitus and Hyperlipidemia Demonstrated by Liquid Chromatography/Electrospray Ionization-Mass Spectrometry
2000
Phosphocreatine-dependent protein phosphorylation in rat skeletal muscle
1992
Mitochondrial Reactive Oxygen Species (ROS) and ROS-Induced ROS Release
2014 Standout
The HIF Pathway and Erythrocytosis
2011
A Feedback Loop Involving the Phd3 Prolyl Hydroxylase Tunes the Mammalian Hypoxic Response In Vivo
2009 StandoutNobel
Hypoxia. 5. Hypoxia and hematopoiesis
2011
Endothelial Hypoxia-Inducible Factor-2α Is Required for the Maintenance of Airway Microvasculature
2019 StandoutNobel
The Aquaporin Family of Water Channel Proteins in Clinical Medicine
1997 StandoutNobel
Erythrocytosis: the HIF pathway in control
2013
Oxidized Redox State of Glutathione in the Endoplasmic Reticulum
1992 StandoutScience
Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple
2001 Standout
Pathophysiology of the Aquaporin Water Channels
1996 StandoutNobel
Functional Significance of Cell Volume Regulatory Mechanisms
1998 Standout
Treatment of erythropoietin deficiency in mice with systemically administered siRNA
2012 StandoutNobel
Creatine and Creatinine Metabolism
2000 Standout
Pheochromocytoma and Paraganglioma: An Endocrine Society Clinical Practice Guideline
2014 Standout
Works of Claude Préhu being referenced
Transfer of Human α- to β-Hemoglobin via Its Chaperone Protein
2004
Rabbit M type phosphoglycermutase: comparative effects of two thiol reagents, antibody reaction and hybridization studies
1988
Glucose-6-Phosphate Dehydrogenase Deficiency and Homozygous Sickle Cell Disease in Congo
1998
Clinical Follow-Up of Hydroxyurea-Treated Adults with Sickle Cell Disease
2010
Unexpected high frequency of P46L TNFRSF1A allele in sub-Saharan West African populations
2004
Disturbance in the HIF-1α pathway associated with erythrocytosis: Further evidences brought by frameshift and nonsense mutations in the prolyl hydroxylase domain protein 2 (PHD2) gene
2007
A study of 36 unrelated cases with pure erythrocytosis revealed three new mutations in the erythropoietin receptor gene
2008
A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an α2 globin gene variant (Hb Conakry)
1998
Acquired unbalanced hemoglobin chain synthesis during HIV infection.
1993
Covalent binding of glutathione to hemoglobin. I. Inhibition of hemoglobin S polymerization.
1986
Molecular Analysis of the Rare In(Lu) Blood Type: Toward Decoding the Phenotypic Outcome of Haploinsufficiency for the Transcription Factor KLF1
2012
Kinetics of water transport in sickle cells
1985