Citation Impact
Citing Papers
2016 ESC Position Paper on cancer treatments and cardiovascular toxicity developed under the auspices of the ESC Committee for Practice Guidelines
2016 Standout
Cancer incidence and mortality patterns in Europe: Estimates for 40 countries in 2012
2013 Standout
Ageing populations: the challenges ahead
2009 Standout
Recent trends of cancer in Europe: A combined approach of incidence, survival and mortality for 17 cancer sites since the 1990s
2008
The global prevalence of glucose-6-phosphate dehydrogenase deficiency: A systematic review and meta-analysis
2009 Standout
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
Cardiac effects of adjuvant doxorubicin and radiation therapy in breast cancer patients.
1998
CASK and Protein 4.1 Support F-actin Nucleation on Neurexins
2001 StandoutNobel
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
Metastatic non-small-cell lung cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up
2016 Standout
2009 Focused Update Incorporated Into the ACC/AHA 2005 Guidelines for the Diagnosis and Management of Heart Failure in Adults
2009 Standout
Unstable β-globin mRNA in mRNA-deficient β0 thalassemia
1981
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins of rearrangements.
1990 StandoutNobel
Membrane Dynamics of the Water Transport Protein Aquaporin-1 in Intact Human Red Cells
1999 StandoutNobel
Hippo Pathway in Organ Size Control, Tissue Homeostasis, and Cancer
2015 Standout
Insertions, substitutions, and the origin of microsatellites
2000
Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis.
1988 StandoutNobel
Global cancer statistics
2011 Standout
Identification of the protein 4.1 binding site to phosphatidylserine vesicles
1988
Differential control of band 3 lateral and rotational mobility in intact red cells.
1994 StandoutNobel
Bladder Cancer Incidence and Mortality: A Global Overview and Recent Trends
2016 Standout
Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle
1990 Nature
Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans
1998 Standout
Identification of the Membrane Attachment Sites for Protein 4.1 in the Human Erythrocyte
1995
Homology requirements for unequal crossing over in humans.
1991 StandoutNobel
α‐Actinin is a potent regulator of G protein‐coupled receptor kinase activity and substrate specificity in vitro
2000 StandoutNobel
Targeting DNA topoisomerase II in cancer chemotherapy
2009 Standout
Interleukin-10 levels are often elevated in serum of adults with Hodgkin's disease and are associated with inferior failure-free survival
1999
Linkage of Dominant Hereditary Spherocytosis to the Gene for the Erythrocyte Membrane-Skeleton Protein Ankyrin
1990 StandoutNobel
A Putative Src Homology 3 Domain Binding Motif but Not the C-terminal Dystrophin WW Domain Binding Motif Is Required for Dystroglycan Function in Cellular Polarity in Drosophila
2007 StandoutNobel
A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff
2012 Standout
Estimates of cancer incidence and mortality in Europe in 2008
2010 Standout
Severe hemolysis and red cell fragmentation caused by the combination of a spectrin mutation with a thrombotic microangiopathy
1989
Specific Role of the Truncated βIV-Spectrin Σ6 in Sodium Channel Clustering at Axon Initial Segments and Nodes of Ranvier
2006 StandoutNobel
Microsatellites: simple sequences with complex evolution
2004 Standout
The spectrin-actin junction of erythrocyte membrane skeletons
1989
Evidence that red blood cell protein p55 may participate in the skeleton-membrane linkage that involves protein 4.1 and glycophorin C
1993
ACC/AHA 2005 Guideline Update for the Diagnosis and Management of Chronic Heart Failure in the Adult
2005 Standout
Metal-Catalyzed Intermolecular Hydrofunctionalization of Allenes: Easy Access to Allylic Structures via the Selective Formation of C–N, C–C, and C–O Bonds
2020
Abnormal oxidant sensitivity and beta-chain structure of spectrin in hereditary spherocytosis associated with defective spectrin-protein 4.1 binding.
1987
Identification, purification, and partial characterization of a novel Mr 28,000 integral membrane protein from erythrocytes and renal tubules.
1988 StandoutNobel
alpha-Thalassaemia associated with the deletion of two nucleotides at position -2 and -3 preceding the AUG codon.
1985
Hereditary elliptocytosis, spherocytosis and related disorders: Consequences of a deficiency or a mutation of membrane skeletal proteins
1987
The Spectrin-Based Membrane Skeleton and Micron-Scale Organization of the Plasma Membrane
1993
The control of globin and other eukaryotic genes
1982 StandoutNobel
Location of the human red cell spectrin tetramer binding site and detection of a related “closed” hairpin loop dimer using proteolytic footprinting.
1993
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
Stabilization and ribosome association of unspliced pre-mRNAs in a yeast upf1- mutant.
1993 StandoutNobel
Detection of a novel DNA polymorphism in the beta-globin gene cluster.
1984 StandoutNobel
Isolation of the cDNA for erythrocyte integral membrane protein of 28 kilodaltons: member of an ancient channel family.
1991 StandoutNobel
Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes
1986 Standout
Catalytic Asymmetric Hydroalkoxylation of C–C Multiple Bonds
2021 StandoutNobel
The distribution of erythrocyte phospholipids in hereditary spherocytosis demonstrates a minimal role for erythrocyte spectrin on phospholipid diffusion and asymmetry
1993 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
A molecular study of heterozygous protein 4.1 deficiency in hereditary elliptocytosis
1988
Synthesis of an ochre suppressor tRNA gene and expression in mammalian cells.
1984 StandoutNobel
Human erythrocyte glycophorin C
1989
Aplastic Anemia
1982 StandoutNobel
Interleukin-10 and the Interleukin-10 Receptor
2001 Standout
Establishment of mammalian cell lines containing multiple nonsense mutations and functional suppressor tRNA genes
1982 StandoutNobel
beta 0 thalassemia, a nonsense mutation in man.
1979
Dexrazoxane-Associated Risk for Acute Myeloid Leukemia/Myelodysplastic Syndrome and Other Secondary Malignancies in Pediatric Hodgkin's Disease
2007
Partial deletion of beta-globin gene DNA in certain patients with beta 0-thalassemia.
1979
Localization of the protein 4.1-binding site on human erythrocyte glycophorins C and D
1994
Polymorphism of the Hinf I restriction site located 1 Kb 5? to the human ?-globin gene
1982
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
Untranslated immunoglobulin kappa light chain mRNA in a lambda light chain-producing mouse myeloma, MOPC104E.
1980 StandoutNobel
Erythrocyte Mr 28,000 transmembrane protein exists as a multisubunit oligomer similar to channel proteins.
1991 StandoutNobel
Identification of a functional role for human erythrocyte sialoglycoproteins beta and gamma
1987
The scanning model for translation: an update.
1989 Standout
111Indium‐Chloride Bone Marrow Scintigraphy in Aplastic Anaemia
1981
Characterization of β-globin mRNA in the β0 thalassemias
1978
Sodium-Potassium-Chloride Cotransport
2000 Standout
Works of P Colonna being referenced
Hemoglobin H Disease from Algeria: Genetic and Molecular Characterization
1981
Fifteen‐year secondary leukaemia risk observed in 761 patients with Hodgkin's disease prospectively treated by MOPP or ABVD chemotherapy plus high‐dose irradiation
2002
Mediastinal tumor size and response to chemotherapy are the only prognostic factors in supradiaphragmatic Hodgkin's disease treated by ABVD plus radiotherapy: ten-year results of the Paris-Ouest-France 81/12 trial, including 262 patients.
1996
Predictive and discriminating three‐risk‐group prognostic scoring system for staging Hodgkin lymphomas
2006
Molecular basis of Sp alpha I/65 hereditary elliptocytosis in North Africa: insertion of a TTG triplet between codons 147 and 149 in the alpha-spectrin gene from five unrelated families
1989
Red cell membrane sialoglycoptein β in homozygous and heterozygous 4.1(−) hereditary elliptocytosis
1985
[G-6PD deficiency in newborns in Algiers (author's transl)].
1975
Gerbich reactivity in 4.1(—) hereditary elliptocytosis and protein 4.1 level in blood group Gerbich deficiency
1987
?-Thalassemia haplotypes in the Algerian population
1987
beta-O-thalassemia from Algeria: genetic and molecular characterization
1977
Heterogeneity in ?0 thalassemia from Algeria: Genetic, clinical and molecular studies
1980
Alkene Hydroamination via Earth‐Abundant Transition Metal (Iron, Cobalt, Copper and Zinc) Catalysis: A Mechanistic Overview
2019
Molecular basis of Sp alpha I/65 hereditary elliptocytosis in North Africa: insertion of a TTG triplet between codons 147 and 149 in the alpha-spectrin gene from five unrelated families
1989
Significance of bone-marrow scintigraphy in aplastic anemia: concise communication.
1980
Spα1/65 hereditary elliptocytosis in North Africa
1986
The heterozygous form of 4.1(-) hereditary elliptocytosis [the 4.1(-) trait]
1985