Standout Papers
Citation Impact
Citing Papers
Hereditary Anemias of the Mouse: A Review for Geneticists
1979
Lipoprotein abnormalities in primary biliary cirrhosis. Association with hepatic lipase inhibition as well as altered cholesterol esterification.
1985
Effects of an Rb mutation in the mouse
1992 StandoutNature
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
The ANK Repeats of Erythrocyte Ankyrin Form Two Distinct but Cooperative Binding Sites for the Erythrocyte Anion Exchanger
1995
Ion Transport Pathology in the Mechanism of Sickle Cell Dehydration
2004
Regression of Coronary Artery Disease as a Result of Intensive Lipid-Lowering Therapy in Men with High Levels of Apolipoprotein B
1990 Standout
Physiological roles of axonal ankyrins in survival of premyelinated axons and localization of voltage-gated sodium channels
1999
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
The act cluster contains regulatory and antibiotic export genes, direct targets for translational control by the bldA tRNA gene of streptomyces
1991
A New Human Hereditary Amyloidosis: The Result of a Stop-Codon Mutation in the Apolipoprotein AII Gene
2001
Sorting of GPI-anchored proteins to glycolipid-enriched membrane subdomains during transport to the apical cell surface
1992 Standout
The bone marrow niche for haematopoietic stem cells
2014 StandoutNature
Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels
2013 StandoutNobel
Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis.
1988 StandoutNobel
Band 3 and glycophorin are progressively aggregated in density-fractionated sickle and normal red blood cells. Evidence from rotational and lateral mobility studies.
1993
Severe hypercholesterolemia and atherosclerosis in apolipoprotein E-deficient mice created by homologous recombination in ES cells
1992 Standout
High affinity VEGF binding and developmental expression suggest Flk-1 as a major regulator of vasculogenesis and angiogenesis
1993 Standout
Molecular basis for membrane rigidity of hereditary ovalocytosis. A novel mechanism involving the cytoplasmic domain of band 3.
1992
Differential control of band 3 lateral and rotational mobility in intact red cells.
1994 StandoutNobel
Bcl-2-deficient mice demonstrate fulminant lymphoid apoptosis, polycystic kidneys, and hypopigmented hair
1993 Standout
Plant pathogens and integrated defence responses to infection
2001 StandoutNature
Expression and purification of recombinant cytoplasmic domain of human erythrocyte band 3 with hexahistidine tag or chitin-binding tag in Escherichia coli
2004
Reductions of erythrocyte membrane viscoelastic coefficients reflect spectrin deficiencies in hereditary spherocytosis.
1988 StandoutNobel
Conformation and elasticity of the isolated red blood cell membrane skeleton
1992
The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene
1988 Standout
The Ankyrin-B C-terminal Domain Determines Activity of Ankyrin-B/G Chimeras in Rescue of Abnormal Inositol 1,4,5-Trisphosphate and Ryanodine Receptor Distribution in Ankyrin-B (−/−) Neonatal Cardiomyocytes
2002
Molecular Defect of the Band 3 Protein in Southeast Asian Ovalocytosis
1990
Isochorismate synthase is required to synthesize salicylic acid for plant defence
2001 StandoutNature
Asparagine and Aspartate Hydroxylation of the Cytoskeletal Ankyrin Family Is Catalyzed by Factor-inhibiting Hypoxia-inducible Factor
2010 StandoutNobel
Protein composition determines the anti-atherogenic properties of HDL in transgenic mice
1993 Nature
Structure of the Calmodulin αII-Spectrin Complex Provides Insight into the Regulation of Cell Plasticity
2006 StandoutNobel
Degradation of CFTR by the ubiquitin-proteasome pathway
1995 Standout
TGFα deficiency results in hair follicle and eye abnormalities in targeted and waved-1 mice
1993 StandoutNobel
Specific Role of the Truncated βIV-Spectrin Σ6 in Sodium Channel Clustering at Axon Initial Segments and Nodes of Ranvier
2006 StandoutNobel
Molecular Mechanisms of Amyloidosis
2003 Standout
Effect of Band 3 Subunit Equilibrium on the Kinetics and Affinity of Ankyrin Binding to Erythrocyte Membrane Vesicles
1998
Decreased rotational diffusion of band 3 in melanesian ovalocytes from Papua, New Guinea
1991
Spectrin rearrangement early in erythrocyte ghost endocytosis.
1979
Membrane protein phosphorylation of intact normal and hereditary spherocytic erythrocytes.
1978
Abnormal spectrin in hereditary elliptocytosis
1986
Spontaneous Hypercholesterolemia and Arterial Lesions in Mice Lacking Apolipoprotein E
1992 StandoutScience
Genetic Models of Human Vascular Disease
1995 StandoutNobel
Identification, purification, and partial characterization of a novel Mr 28,000 integral membrane protein from erythrocytes and renal tubules.
1988 StandoutNobel
Reconstitution and functional comparison of purified GlpF and AqpZ, the glycerol and water channels from Escherichia coli
2001 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
Cetiedil inhibition of calmodulin-stimulated enzyme activity
1984
Primary Biliary Cirrhosis
1987 Standout
Mammalian reticulocytes lose adhesion to fibronectin during maturation to erythrocytes.
1985 StandoutNobel
The alpha-spectrin gene is on chromosome 1 in mouse and man.
1985
The role of spectrin in erythrocyte ghost endocytosis
1978
The DNA sequences encoding plsB and dgk loci of Escherichia coli.
1983 StandoutNobel
Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosis.
1984
Spectrin beta-chain variant associated with hereditary elliptocytosis.
1982
The Molecular Basis for Membrane – Cytoskeleton Association in Human Erythrocytes
1982
Rigid membranes of Malayan ovalocytes: a likely genetic barrier against malaria
1984
Spectrin deficient inherited hemolytic anemias in the mouse: Characterization by spectrin synthesis and mRNA activity in reticulocytes
1984
Regulation of Plasma Cholesterol by Lipoprotein Receptors
1981 StandoutScienceNobel
β-Arrestin2-mediated inotropic effects of the angiotensin II type 1A receptor in isolated cardiac myocytes
2006 StandoutNobel
Inheritance Pattern and Clinical Response to Splenectomy as a Reflection of Erythrocyte Spectrin Deficiency in Hereditary Spherocytosis
1986 StandoutNobel
Gain-of-Function Mutations of c- kit in Human Gastrointestinal Stromal Tumors
1998 StandoutScience
Mutant forms of spectrin alpha-subunits in hereditary elliptocytosis.
1987 StandoutNobel
Hereditary Spherocytosis and Related Disorders
1985
Fate of the transferrin receptor during maturation of sheep reticulocytes in vitro: Selective externalization of the receptor
1983 Standout
Desensitization of turkey erythrocyte adenylate cyclase. Beta-adrenergic receptor phosphorylation is correlated with attenuation of adenylate cyclase activity.
1984 StandoutNobel
The Arabidopsis NPR1 Gene That Controls Systemic Acquired Resistance Encodes a Novel Protein Containing Ankyrin Repeats
1997
Avermectin Biosynthesis
1997 StandoutNobel
Apolipoprotein E: Cholesterol Transport Protein with Expanding Role in Cell Biology
1988 StandoutScience
The gene encoding the T-cell surface protein T4 is located on human chromosome 12.
1986 StandoutNobel
Genetic control of lipid transport in mice. I. Structural properties and polymorphisms of plasma lipoproteins.
1983
The Intrinsic Electrophysiological Properties of Mammalian Neurons: Insights into Central Nervous System Function
1988 StandoutScience
βiv Spectrin, a New Spectrin Localized at Axon Initial Segments and Nodes of Ranvier in the Central and Peripheral Nervous System
2000
Reconstitution of spectrin-deficient, spherocytic mouse erythrocyte membranes.
1979
Optical trapping and manipulation of neutral particles using lasers
1997 StandoutNobel
On the Subunit Structure of the Protein of Human Serum High Density Lipoprotein
1972
Identification of the hereditary pyropoikilocytosis carrier state
1984
Bepridil and cetiedil. Vasodilators which inhibit Ca2+-dependent calmodulin interactions with erythrocyte membranes.
1984 StandoutNobel
Functional differences among nonerythroid anion exchangers expressed in a transfected human cell line
1991
Mammalian red cell membrane Rh polypeptides are selectively palmitoylated subunits of a macromolecular complex.
1992 StandoutNobel
The Measurement of Apolipoprotein A-I and A-II Levels in Men and Women by Immunoassay
1977
Type III Hyperlipoproteinemia: Diagnosis, Molecular Defects, Pathology, and Treatment
1983
A mouse model for beta 0-thalassemia.
1995 StandoutNobel
Dynamics of membrane-skeleton (fodrin) organization during development of polarity in Madin-Darby canine kidney epithelial cells.
1986
Interaction of cytoskeletal proteins on the human erythrocyte membrane
1981
A new abnormal variant of spectrin in black patients with hereditary elliptocytosis
1985
Amphipathic helixes and plasma lipoproteins: A computer study
1977
An analogue of the erythroid membrane skeletal protein 4.1 in nonerythroid cells.
1984
Separate mechanisms for the uptake of high and low density lipoproteins by mouse adrenal gland in vivo.
1979 StandoutNobel
Partial deficiency of erythrocyte spectrin in hereditary spherocytosis
1985 StandoutNatureNobel
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
Enzymic basis for the Ca2+ion-induced crosslinking of membrane proteins in intact human erythrocytes
1978
Apoprotein (E–A-II) complex of human plasma lipoproteins. I. Characterization of this mixed disulfide and its identification in a high density lipoprotein subfraction.
1978
A molecular theory of lipid—protein interactions in the plasma lipoproteins
1974
Palmitoylation of cysteine 69 from the COOH-terminal of band 3 protein in the human erythrocyte membrane. Acylation occurs in the middle of the consensus sequence of F–I-IICLAVL found in band 3 protein and G2 protein of Rift Valley fever virus.
1991
Spectrin and Ankyrin-Based Pathways: Metazoan Inventions for Integrating Cells Into Tissues
2001
Isolation and characterization of a human serum cholesteryl ester transfer protein.
1978
A Genetic Defect in the Binding of Protein 4.1 to Spectrin in a Kindred with Hereditary Spherocytosis
1982
Deficient Red-Cell Spectrin in Severe, Recessively Inherited Spherocytosis
1982 StandoutNobel
Works of K M John being referenced
Linkage of Dominant Hereditary Spherocytosis to the Gene for the Erythrocyte Membrane-Skeleton Protein Ankyrin
1990 StandoutNobel
Cloning and characterization of band 3, the human erythrocyte anion-exchange protein (AE1).
1989
Ank3 (epithelial ankyrin), a widely distributed new member of the ankyrin gene family and the major ankyrin in kidney, is expressed in alternatively spliced forms, including forms that lack the repeat domain.
1995
Diminished spectrin extraction from ATP-depleted human erythrocytes. Evidence relating spectrin to changes in erythrocyte shape and deformability.
1978
Hemolytic anemias associated with deficient or dysfunctional spectrin.
1979
Irreversible deformation of the spectrin-actin lattice in irreversibly sickled cells.
1976
Elliptical erythrocyte membrane skeletons and heat-sensitive spectrin in hereditary elliptocytosis.
1981
Amino Acid Sequence of Human apoLp-Gln-II (apoA-II), an Apolipoprotein Isolated from the High-Density Lipoprotein Complex
1972