Citation Impact
Citing Papers
The emerging landscape of novel 4-1BB (CD137) agonistic drugs for cancer immunotherapy
2023
Target-conditioned diffusion generates potent TNFR superfamily antagonists and agonists
2024 StandoutScienceNobel
Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis.
1989 StandoutNobel
Amino-acid substitution in α-spectrin commonly coinherited with nondominant hereditary spherocytosis
1997 StandoutNobel
30 Years of NF-κB: A Blossoming of Relevance to Human Pathobiology
2017 Nobel
Calcium's Role in Mechanotransduction during Muscle Development
2014 Standout
GPI Mount Scopus — a variant of glucosephosphate isomerase deficiency
1993
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. I. Biochemical identification of rearrangements in the spectrin/actin binding domain and functional characterizations.
1990 StandoutNobel
Spectrin Oligomerization is Cooperatively Coupled to Membrane Assembly: A Linkage Targeted by Many Hereditary Hemolytic Anemias?
2001
Active site-directed antibodies identify calpain II as an early-appearing and pervasive component of neurofibrillary pathology in Alzheimer's disease
1997
Calcium oxalate nephrolithiasis: Defective oxalate transport
1991
A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.
1996
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins of rearrangements.
1990 StandoutNobel
Nitric Oxide and Peroxynitrite in Health and Disease
2007 Standout
Very fast empirical prediction and rationalization of protein pKa values
2005 Standout
Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis.
1988 StandoutNobel
Role of Oxidative Modifications in Atherosclerosis
2004 Standout
Crystal Structure of Bovine Heart Phosphotyrosyl Phosphatase at 2.2-.ANG. Resolution
1994
Glutaminolysis and Transferrin Regulate Ferroptosis
2015 Standout
Differential control of band 3 lateral and rotational mobility in intact red cells.
1994 StandoutNobel
Reductions of erythrocyte membrane viscoelastic coefficients reflect spectrin deficiencies in hereditary spherocytosis.
1988 StandoutNobel
Development of a chitosan-based wound dressing with improved hemostatic and antimicrobial properties
2008 Standout
A Prospective Study of Dietary Calcium and Other Nutrients and the Risk of Symptomatic Kidney Stones
1993 Standout
Sp alpha V/41: a common spectrin polymorphism at the alpha IV-alpha V domain junction. Relevance to the expression level of hereditary elliptocytosis due to alpha-spectrin variants located in trans.
1991
Combination of two mutant alpha spectrin alleles underlies a severe spherocytic hemolytic anemia.
1996
Mapping the Human Erythrocyte β-Spectrin Dimer Initiation Site Using Recombinant Peptides and Correlation of Its Phasing with the α-Actinin Dimer Site
1996
Calpain Mediates Integrin-induced Signaling at a Point Upstream of Rho Family Members
1999
Asparagine and Aspartate Hydroxylation of the Cytoskeletal Ankyrin Family Is Catalyzed by Factor-inhibiting Hypoxia-inducible Factor
2010 StandoutNobel
Non-classical processes in surface hemostasis: mechanisms for the poly- N -acetyl glucosamine-induced alteration of red blood cell morphology and surface prothrombogenicity
2008
Cutting to the chase: calpain proteases in cell motility
2002
Food allergy: A review and update on epidemiology, pathogenesis, diagnosis, prevention, and management
2017 Standout
Defining trained immunity and its role in health and disease
2020 Standout
Linkage of Dominant Hereditary Spherocytosis to the Gene for the Erythrocyte Membrane-Skeleton Protein Ankyrin
1990 StandoutNobel
Specific Role of the Truncated βIV-Spectrin Σ6 in Sodium Channel Clustering at Axon Initial Segments and Nodes of Ranvier
2006 StandoutNobel
NF-κB, inflammation, immunity and cancer: coming of age
2018 Standout
Uridine monophosphate kinase: A new genetic polymorphism with possible clinical implications.
1974
Multiple protein 4.1 isoforms produced by alternative splicing in human erythroid cells.
1988
Construction of a genetic linkage map in man using restriction fragment length polymorphisms.
1980 Standout
Abnormal spectrin in hereditary elliptocytosis
1986
Cell Migration: Integrating Signals from Front to Back
2003 StandoutScience
Hereditary elliptocytosis, spherocytosis and related disorders: Consequences of a deficiency or a mutation of membrane skeletal proteins
1987
Proposals for the classification of the myelodysplastic syndromes
1982 Standout
Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis
1993
Red cell membrane sialoglycoptein β in homozygous and heterozygous 4.1(−) hereditary elliptocytosis
1985
Molecular determinants of clinical expression of hereditary elliptocytosis and pyropoikilocytosis
1987
The tra-3 sex determination gene of Caenorhabditis elegans encodes a member of the calpain regulatory protease family.
1996
Molecular heterogeneity of hereditary pyropoikilocytosis: identification of a second variant of the spectrin alpha-subunit
1983
Location of the human red cell spectrin tetramer binding site and detection of a related “closed” hairpin loop dimer using proteolytic footprinting.
1993
Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosis.
1984
Classification of Acute Leukemia
1977
Hereditary Elliptocytosis and Related Disorders
1985
Alteration of the erythrocyte membrane skeletal ultrastructure in hereditary spherocytosis, hereditary elliptocytosis, and pyropoikilocytosis
1990 StandoutNobel
The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1
1985
Glutathione peroxidase: A selenoenzyme
1973 Standout
Selenium: Biochemical Role as a Component of Glutathione Peroxidase
1973 StandoutScience
Inheritance Pattern and Clinical Response to Splenectomy as a Reflection of Erythrocyte Spectrin Deficiency in Hereditary Spherocytosis
1986 StandoutNobel
The Calpain System
2003 Standout
Mutant forms of spectrin alpha-subunits in hereditary elliptocytosis.
1987 StandoutNobel
The distribution of erythrocyte phospholipids in hereditary spherocytosis demonstrates a minimal role for erythrocyte spectrin on phospholipid diffusion and asymmetry
1993 StandoutNobel
Hereditary Spherocytosis and Related Disorders
1985
Purification of the major protein-tyrosine-phosphatases of human placenta.
1988 StandoutNobel
Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis
1986
The structure of the ankyrin-binding site of β-spectrin reveals how tandem spectrin-repeats generate unique ligand-binding properties
2009 StandoutNobel
Binding of G protein beta gamma-subunits to pleckstrin homology domains.
1994 StandoutNobel
Die Glutathionperoxidase: Enzymologie und biologische Aspekte
1971
Characterization of the major protein-tyrosine-phosphatases of human placenta.
1988 StandoutNobel
Stem cells repurpose proliferation to contain a breach in their niche barrier
2018
Nitric oxide causes inactivation of the low molecular weight phosphotyrosine protein phosphatase.
1994
Reconstitution of spectrin-deficient, spherocytic mouse erythrocyte membranes.
1979
Three cases of hereditary nonspherocytic hemolytic anemia associated with red blood cell glutathione deficiency
1996
Identification of the hereditary pyropoikilocytosis carrier state
1984
Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.
1987
Erythrocyte Enzymopathies in the Newborn
1981
Structure analysis and molecular model of the selenoenzyme glutathione peroxidase at 2.8 Å resolution
1979 StandoutNobel
Molecular biology of the Rh antigens
1991 StandoutNobel
Distinct variants of erythrocyte protein 4.1 inherited in linkage with elliptocytosis and Rh type in three white families
1988 StandoutNobel
Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis
1990
Protein band 3 phosphotyrosyl phosphatase. purification and characterization
1987
A new abnormal variant of spectrin in black patients with hereditary elliptocytosis
1985
Sertoli-Sertoli and Sertoli-Germ Cell Interactions and Their Significance in Germ Cell Movement in the Seminiferous Epithelium during Spermatogenesis
2004 Standout
PLATELET DYSFUNCTION IN PRELEUKEMIC STATES AND IN VARIOUS TYPES OF LEUKEMIA
1972
Glucose-6-phosphate dehydrogenase deficiency
2008 Standout
Full-length sequence of the cDNA for human erythroid beta-spectrin.
1990
Molecular Basis of Hereditary Elliptocytosis Due to Protein 4.1 Deficiency
1986
Partial deficiency of erythrocyte spectrin in hereditary spherocytosis
1985 StandoutNatureNobel
Kinetics of activation and inactivation of swelling-stimulated K+/Cl- transport. The volume-sensitive parameter is the rate constant for inactivation.
1990
Functional Significance of Cell Volume Regulatory Mechanisms
1998 Standout
Identification of a functional role for human erythrocyte sialoglycoproteins beta and gamma
1987
The return of metabolism: biochemistry and physiology of the pentose phosphate pathway
2014 Standout
A molecular defect of spectrin in a subset of patients with hereditary elliptocytosis. Alterations in the alpha-subunit domain involved in spectrin self-association.
1984
A molecular defect in two families with hemolytic poikilocytic anemia: reduction of high affinity membrane binding sites for ankyrin.
1981 StandoutNobel
Spα1/65 hereditary elliptocytosis in North Africa
1986
Partial purification and characterization of phosphotyrosyl-protein phosphatase(S) from human erythrocyte cytosol
1986
Frequency of enzyme deficiency variants in erythrocytes of newborn infants.
1981
Spectrin and Ankyrin-Based Pathways: Metazoan Inventions for Integrating Cells Into Tissues
2001
Beta spectrin in human skeletal muscle. Tissue-specific differential processing of 3' beta spectrin pre-mRNA generates a beta spectrin isoform with a unique carboxyl terminus
1990
Platelet Physiology and Abnormalities of Platelet Function
1975 Standout
The heterozygous form of 4.1(-) hereditary elliptocytosis [the 4.1(-) trait]
1985
Deficient Red-Cell Spectrin in Severe, Recessively Inherited Spherocytosis
1982 StandoutNobel
Works of C Galand being referenced
Déficit en glutathion-synthétase avec 5-oxoprolinurie. Deux nouveaux cas et revue de la littérature.
1978
Spectrin ?IIa variant in dominant and non-dominant spherocytosis
1993
IL-33 promotes food anaphylaxis in epicutaneously sensitized mice by targeting mast cells
2016
Severe recessive poikilocytic anaemia with a new spectrin α chain variant
1990
In vitro digestion of spectrin, protein 4.1 and ankyrin by erythrocyte calcium dependent neutral protease (Calpain I)
1990
377 AGEN2373 is a CD137 agonist antibody designed to leverage optimal CD137 and FcγR co-targeting to promote antitumor immunologic effects
2020
[Glutathione synthesis during congenital hemolytic anemia with reduced glutathione deficiency. Congenital erythrocytic glutathione-synthetase deficiency?].
1966
Spectrin beta-chain variant associated with hereditary elliptocytosis.
1982
Hereditary elliptocytosis: clinical, morphological and biochemical studies of 38 cases.
1986
Defective lymphoid organogenesis underlies the immune deficiency caused by a heterozygous S32I mutation in IκBα
2015
Hereditary Elliptocytosis with a Spectrin Molecular Defect in a White Patient
1984
Anomalies of Blood Group Antigens and Erythrocyte Enzymes in Two Types of Chronic Refractory Anaemia
1969
Spectrin ?IIa variant in dominant and non-dominant spherocytosis
1994
IL-23 induced in keratinocytes by endogenous TLR4 ligands polarizes dendritic cells to drive IL-22 responses to skin immunization
2016
Erythrocyte membrane phosphorylation in hereditary spherocytosis.
1977
Molecular Defect of Spectrin in the Family of a Child with Congenital Hemolytic Poikilocytic Anemia
1984
[Hereditary elliptocytosis in West Africa: frequency and repartition of spectrin variants].
1988
Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypes
1989
A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosis
1984
Causal mechanisms of multiple acquired red cell enzyme defects in a patient with acquired dyserythropoiesis
1976
A New Variant of Glucosephosphate Isomerase Deficiency with Mild Haemolytic Anaemia (GPI‐MYTHO)
1978
[Hemolytic anemia with glutathione peroxidase deficiency in an adult].
1969
[Erythrocyte and leucocyte 3-phosphoglycerate kinase deficiency. Studies of properties of the enzyme, phagocytic activity of the polymorphonuclear leucoytes and a review of the literature].
1975
The human red cell acid phosphatase is a phosphotyrosine protein phosphatase which dephosphorylates the membrane protein band 3
1986
Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact site
1994
Interactions of the human red cell membrane tyrosine kinase with heparin
1985
Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypes
1989
[A new erythroenzymopathy: congenital non-spherocytic hemolytic anemia and hereditary erythrocytic adenylate kinase deficiency].
1971
A shortened variant of red cell membrane protein 4.1
1982
Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain
1990