Citation Impact
Citing Papers
De novo design of allosterically switchable protein assemblies
2024 StandoutNatureNobel
THE SENSITIVITY OF GEL ELECTROPHORESIS AS A DETECTOR OF GENETIC VARIATION
1979
Duration of Red-Cell Storage and Complications after Cardiac Surgery
2008 Standout
Peptide-binding specificity of the molecular chaperone BiP
1991 StandoutNatureNobel
The Systemic Amyloidoses
1997 Standout
Pathogenesis and Treatment of Sickle Cell Disease
1997
TIGAR, a p53-Inducible Regulator of Glycolysis and Apoptosis
2006 Standout
Hoxb8 Is Required for Normal Grooming Behavior in Mice
2002 StandoutNobel
Hemoglobin: Structure, Function and Allostery
2020
Nonenzymatic Deamidation of Asparaginyl and Glutaminyl Residues in Protein
1991
Effects of storage on efficacy of red cell transfusion: When is it not safe?
2003
The β-Thalassemias
1999 Standout
Hemoglobin Jamaica Plain — A Sickling Hemoglobin with Reduced Oxygen Affinity
2004
1 The population genetics of the haemoglobinopathies
1998
Balancing Acts
2004 Standout
The molecular basis of blood coagulation
1988 Standout
The Utility of DNA Typing in Forensic Work
1991 StandoutScience
Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels
2013 StandoutNobel
Position effects in mice carrying a lacZ transgene in cis with the -globin LCR can be explained by a graded model
1997
Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia
2002 StandoutNobel
Synthesis and evaluation of a new inhibitor of phosphoglucose isomerases: the enediolate analogue 5-phospho-D-arabinohydroxamate
1998
Mechanistic implications for Escherichia coli cofactor-dependent phosphoglycerate mutase based on the high-resolution crystal structure of a vanadate complex
2002
Unusually large von willebrand factor multimers preferentially promote young sickle and nonsickle erythrocyte adhesion to endothelial cells
1993
8 The population genetics of the haemoglobinopathies
1993
Rates of Hyperkalemia after Publication of the Randomized Aldactone Evaluation Study
2004 Standout
Sickle Cell Hemoglobin Polymerization
1990
Prevention of a First Stroke by Transfusions in Children with Sickle Cell Anemia and Abnormal Results on Transcranial Doppler Ultrasonography
1998 Standout
Sickle-cell disease
2010 Standout
Sickle Cell Disease in a Patient with Sickle Cell Trait and Compound Heterozygosity for Hemoglobin S and Hemoglobin Quebec–Chori
1991
GlcNAc 2-Epimerase Can Serve a Catabolic Role in Sialic Acid Metabolism
2003 StandoutNobel
Identification of the haemoglobin scavenger receptor
2001 StandoutNature
Significant haemoglobinopathies: guidelines for screening and diagnosis
2010
A Liquid-to-Solid Phase Transition of the ALS Protein FUS Accelerated by Disease Mutation
2015 Standout
Selection of Mutant CHO Cells with Constitutive Activation of the HIF System and Inactivation of the von Hippel-Lindau Tumor Suppressor
2001 StandoutNobel
Molecular characterisation of the enolase gene from the human malaria parasite Plasmodium falciparum Evidence for ancestry within a photosynthetic lineage
1994
Molecular basis for polycythemia
1999
Regulation of the Erythropoietin Gene
1989
Effect of Population-Based Interventions on Laboratory Utilization
1998
Prion (PrPSc)-specific epitope defined by a monoclonal antibody
1997 StandoutNatureNobel
Position-independent, high-level expression of the human β-globin gene in transgenic mice
1987 Standout
Seeding “one-dimensional crystallization” of amyloid: A pathogenic mechanism in Alzheimer's disease and scrapie?
1993 Standout
The inheritance of hemoglobin types and other biochemical traits in mammals
1960
Fetal Hemoglobin Variants in Mice
1968 StandoutScienceNobel
Tritium labeling of proteins to high specific radioactivity by reduction methylation.
1980
A role for clathrin light chains in the recognition of clathrin cages by ‘uncoating ATPase’
1984 StandoutNatureNobel
The ATPase core of a clathrin uncoating protein.
1987 StandoutNobel
A monoclonal antibody specific for mouse dendritic cells.
1982 StandoutNobel
Stem cell factor is encoded at the SI locus of the mouse and is the ligand for the c-kit tyrosine kinase receptor
1990 Standout
THE GREEN FLUORESCENT PROTEIN
1998 StandoutNobel
Mössbauer studies of cytochrome P-450cam
1973
Crystallization by particle attachment in synthetic, biogenic, and geologic environments
2015 StandoutScience
MOLECULAR GENETICS OF HUMAN HEMOGLOBIN
1976
Human and murine phosphorycholine-binding immunoglobulins: conserved subgroup and first hypervariable region of heavy chains.
1976
An enzyme that removes clathrin coats: purification of an uncoating ATPase.
1984 StandoutNobel
Regulation of hypoxia-inducible factor is preserved in the absence of a functioning mitochondrial respiratory chain
2001 StandoutNobel
Relation between Complications of Type I Diabetes Mellitus and Collagen-Linked Fluorescence
1986 Standout
A Plastid of Probable Green Algal Origin in Apicomplexan Parasites
1997 StandoutScience
Inherited Electrophoretic Hemoglobin Patterns among 20 Inbred Strains of Mice
1958 Science
Separation by hybrid isoelectric focusing of normal human plasma transthyretin (prealbumin) and a variant with a methionine for valine substitution associated with familial amyloidotic polyneuropathy
1986
Abnormal processing of beta Knossos RNA
1984
Protein synthesis elongation factor EF-1 alpha is essential for ubiquitin-dependent degradation of certain N alpha-acetylated proteins and may be substituted for by the bacterial elongation factor EF-Tu.
1994 StandoutNobel
Molecular basis of hemophilia B: a defective enzyme due to an unprocessed propeptide is caused by a point mutation in the factor IX precursor.
1986
The clinical utility of glycosylated hemoglobin
1981
Identification of the Cystic Fibrosis Gene: Genetic Analysis
1989 StandoutScience
A mouse model of familial porphyria cutanea tarda
2000
Strategy linking several analytical methods of neonatal screening for sickle cell disease
2001
The Chemistry and Biochemistry of Vanadium and the Biological Activities Exerted by Vanadium Compounds
2004 Standout
Evolution of a bifunctional enzyme: 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase.
1989
In Vivo Half-Life of a Protein Is a Function of Its Amino-Terminal Residue
1986 StandoutScience
A Common Human β Globin Splicing Mutation Modeled in Mice
1998 StandoutNobel
Peptide Binding and Release by Proteins Implicated as Catalysts of Protein Assembly
1989 StandoutScienceNobel
The Gárdos channel: a review of the Ca2+-activated K+ channel in human erythrocytes
2003
HEL Cells: A New Human Erythroleukemia Cell Line with Spontaneous and Induced Globin Expression
1982 Science
Regulation of the Erythropoietin Gene
1999
Amino-terminal processing of proteins: hemoglobin South Florida, a variant with retention of initiator methionine and N alpha-acetylation.
1985
Developmental genetics of the human haemoglobins
1983
Liquid–liquid separation in solutions of normal and sickle cell hemoglobin
2002
Idiotypic analysis of antibodies to poly(Glu60Ala30Tyr10): interstrain and interspecies idiotypic crossreactions.
1978 StandoutNobel
Molecular analysis of spontaneous somatic mutants
1977 StandoutNatureNobel
Degradation of the tumor suppressor protein p53 by the ubiquitin-mediated proteolytic system requires a novel species of ubiquitin-carrier protein, E2
1994 StandoutNobel
Basal and human papillomavirus E6 oncoprotein-induced degradation of Myc proteins by the ubiquitin pathway
1998 StandoutNobel
The silent carrier allele: β thalassemia without a mutation in the β-globin gene or its immediate flanking regions
1984 StandoutNobel
Molecular basis and prenatal diagnosis of beta-thalassemia
1988
Affinity purification of ubiquitin-protein ligase on immobilized protein substrates. Evidence for the existence of separate NH2-terminal binding sites on a single enzyme.
1990 StandoutNobel
Ubiquitin-mediated protein degradation.
1988 StandoutNobel
Refined crystal structure of deoxyhemoglobin S. II. Molecular interactions in the crystal.
1985
Self-catalyzed growth of S layers via an amorphous-to-crystalline transition limited by folding kinetics
2010 StandoutNobel
Silent β-Thalassemia Associated with Hb Knossos β27 (B9) Ala→Ser in Algeria
1983
Hemoglobin casper: β 106 (G8) Leu→Pro
1973
An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the X-linked factor, beta-globin haplotypes, alpha-globin gene number, gender, and age
1995
HbS-Oman Heterozygote: A New Dominant Sickle Syndrome
1998
Enzymatic dissociation of clathrin cages in a two-stage process.
1985 StandoutNobel
Liquid phase condensation in cell physiology and disease
2017 StandoutScience
Cotranslational amino-terminal processing of cytosolic proteins. Cell-free expression of site-directed mutants of human hemoglobin.
1988
Structure and Chemistry of Cytochrome P450
2005 Standout
Quantification of the close association between DNA haplotypes and specific β-thalassaemia mutations in Mediterraneans
1984 Nature
Works of J. Rosa being referenced
Reducing unnecessary laboratory use with new test request form: example of tumour markers
1993
Molecular cloning and nucleotide sequence of murine 2,3-bisphosphoglycerate mutase cDNA
1988
The peculiar spectrum of ?-thalassemia genes in Tunisia
1988
Clinical manifestations and erythrocyte adhesion to endothelium in sickle cell syndrome
1985
Isoelectric focusing of human hemoglobin: its application to screening, to the characterization of 70 variants, and to the study of modified fractions of normal hemoglobins
1978
Polymorphism of human fetal haemoglobin studied by isoelectric focusing
1980
Acquired unbalanced hemoglobin chain synthesis during HIV infection.
1993
Cord blood screening for hemoglobin abnormalities by thin layer isoelectric focusing
1980
The enzymes of the glycolytic pathway in erythrocytes infected with Plasmodium falciparum malaria parasites
1988
Genetic regulation of ? gene expression: Study of the interaction of ?-thalassemia with heterocellular HPFH
1981
Haemoglobin I Toulouse: β66 (E 10) Lys → Glu: a New Abnormal Haemoglobin with a Mutation localized on the E 10 Porphyrin Surrounding Zone
1969 Nature
Description d'une ultramicrométrode d'analyse séquentielle des peptides
1970
Structural study of hemoglobin Knossos, β27 (B9) Ala→Ser
1982
Elevated Hb F Associated with β‐Thalassaemia Trait: Haemoglobin Synthesis in Reticulocytes and in Blood BFU‐E
1981
A new Case of Hemoglobin Providence (α2β282 (Ef6) Lys → Asn or Asp) Discovered in a French Caucasian Family. Structural and Functional Studies
1985
β-Chain contact sites in the haemoglobin S polymer
1980 Nature
Hemoglobin toulouse α2β266 (E 10) Lys→Glu
1971
Modification of the Electronic Structure of Ferrous Iron in Hemoglobin by Ligandation and by Alterations of the Protein Structure Inferred from Mössbauer Measurements
1970
Hemoglobin C Ziguinchor αA2β62 (A3)Glu → Val β58(E2)→ Arg: The second sickling variant with amino acid substitutions in 2 residues of the β polypeptide chain
1975
Isolation and identification of a cDNA clone coding for rat uroporphyrinogen decarboxylase.
1984
Sequence of the human erythrocyte phosphoglycerate mutase by microsequencer and mass spectrometry.
1988
The first case of a complete deficiency of diphosphoglycerate mutase in human erythrocytes.
1978
Isolation, characterization, and structure of a mutant 89 Arg → Cys bisphosphoglycerate mutase
1989
Hb Marseille [α2β2 N methionyl ‐ 2 (NA2) His → Pro]: a new β chain variant having an extended N‐terminus
1984
Hemoglobin S Antilles: a variant with lower solubility than hemoglobin S and producing sickle cell disease in heterozygotes.
1986
Different Heterogeneities of Mouse Hæmoglobin according to Strains
1958 Nature