Standout Papers
Citation Impact
Citing Papers
Recognition of Cognate Transfer RNA by the 30 S Ribosomal Subunit
2001 StandoutScienceNobel
Hepcidin Regulates Cellular Iron Efflux by Binding to Ferroportin and Inducing Its Internalization
2004 StandoutScience
A primer on ankyrin repeat function in TRP channels and beyond
2008
Regulation of growth differentiation factor 15 expression by intracellular iron
2008 StandoutNobel
Epidermal Merkel cells are mechanosensory cells that tune mammalian touch receptors
2014 StandoutNatureNobel
Targeted deletion of the gene encoding iron regulatory protein-2 causes misregulation of iron metabolism and neurodegenerative disease in mice
2001
Structure of the TRPA1 ion channel suggests regulatory mechanisms
2015 StandoutNatureNobel
TAN-1, the human homolog of the Drosophila Notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms
1991
Regulation of progression through the Gl phase of the cell cycle by the rum1+ gene
1994 StandoutNatureNobel
Molecular domains of myelinated axons
2000
Roles of the ankyrin repeats and C-terminal region of the mouse Notch1 intracellular region
1998 StandoutNobel
Disrupted hepcidin regulation in HFE -associated haemochromatosis and the liver as a regulator of body iron homoeostasis
2003
Animal models of human disease: zebrafish swim into view
2007 Standout
CASK and Protein 4.1 Support F-actin Nucleation on Neurexins
2001 StandoutNobel
FADD, a novel death domain-containing protein, interacts with the death domain of fas and initiates apoptosis
1995 Standout
Physiological roles of axonal ankyrins in survival of premyelinated axons and localization of voltage-gated sodium channels
1999
Hepcidin regulation of ferroportin 1 expression in the liver and intestine of the rat
2004
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
Structure of the 30S ribosomal subunit
2000 StandoutNatureNobel
Structures of Two Repeats of Spectrin Suggest Models of Flexibility
1999
An Iron-responsive Element Type II in the 5′-Untranslated Region of the Alzheimer's Amyloid Precursor Protein Transcript
2002
Sct1 functions in partnership with Cdc10 in a transcription complex that activates cell cycle START and inhibits differentiation
1993
Distribution of divalent metal transporter 1 and metal transport protein 1 in the normal and Belgrade rat
2001
Mouse brains deficient in H‐ferritin have normal iron concentration but a protein profile of iron deficiency and increased evidence of oxidative stress
2002
Regulation of Reticuloendothelial Iron Transporter MTP1 (Slc11a3) by Inflammation
2002
Both ankyrin and band 4.1 are required to restrict the rotational mobility of band 3 in the human erythrocyte membrane
1992
Balancing Acts
2004 Standout
Mutant β-spectrin 4 causes auditory and motor neuropathies in quivering mice
2001
Involvement of p34cdc2 in establishing the dependency of S phase on mitosis
1991 StandoutNatureNobel
IκBγ, a 70 kd protein identical to the C-terminal half of p110 NF-κB: A new member of the IκB family
1992
Transferrin receptor is necessary for development of erythrocytes and the nervous system
1999
Novel Roles for Iron Regulatory Proteins in the Adaptive Response to Iron Deficiency
2003
Structure of a bacterial 30S ribosomal subunit at 5.5 Å resolution
1999 StandoutNatureNobel
Labile iron pool: the main determinant of cellular response to oxidative stress
2003
Hephaestin is a ferroxidase that maintains partial activity in sex-linked anemia mice
2004
βIII Spectrin Binds to the Arp1 Subunit of Dynactin
2001
Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis.
1988 StandoutNobel
Characterization of an immediate-early gene induced in adherent monocytes that encodes IκB-like activity
1991
Band 3 and glycophorin are progressively aggregated in density-fractionated sickle and normal red blood cells. Evidence from rotational and lateral mobility studies.
1993
Molecular basis for membrane rigidity of hereditary ovalocytosis. A novel mechanism involving the cytoplasmic domain of band 3.
1992
Two to Tango: Regulation of Mammalian Iron Metabolism
2010 Standout
Ferroportin1 and hephaestin are involved in the nigral iron accumulation of 6‐OHDA‐lesioned rats
2007
Autosomal-dominant hemochrom-atosis is associated with a mutation in the ferroportin (SLC11A3) gene
2001
Role of the Ferroportin Iron-Responsive Element in Iron and Nitric Oxide Dependent Gene Regulation
2002
Distribution of Ferroportin1 Protein in Different Regions of Developing Rat Brain
2002
Defining of the Minimal Domain of Protein 4.1 Involved in Spectrin-Actin Binding
1995
Differential control of band 3 lateral and rotational mobility in intact red cells.
1994 StandoutNobel
[10] Electron-density map interpretation
1997
Reductions of erythrocyte membrane viscoelastic coefficients reflect spectrin deficiencies in hereditary spherocytosis.
1988 StandoutNobel
Rel-Associated pp40: an Inhibitor of the Rel Family of Transcription Factors
1991 ScienceNobel
Structure of the TRPV1 ion channel determined by electron cryo-microscopy
2013 StandoutNatureNobel
A Novel Mammalian Iron-regulated Protein Involved in Intracellular Iron Metabolism
2000
Membrane skeleton-bilayer interaction is not the major determinant of membrane phospholipid asymmetry in human erythrocytes
1990
Red Cell Membrane Disorders
2005
Identification of the haemoglobin scavenger receptor
2001 StandoutNature
Neuroligins and neurexins link synaptic function to cognitive disease
2008 StandoutNatureNobel
Ankyrin facilitates intracellular trafficking of α1-Na+-K+-ATPase in polarized cells
2008
Molecular Defect of the Band 3 Protein in Southeast Asian Ovalocytosis
1990
Multiple intercellular signalling systems control the development of the Caenorhabditis elegans vulva
1991 StandoutNatureNobel
Hepcidin expression inversely correlates with the expression of duodenal iron transporters and iron absorption in rats
2002
An Ankyrin-like Protein with Transmembrane Domains Is Specifically Lost after Oncogenic Transformation of Human Fibroblasts
1999
Crystal structure of a 12 ANK repeat stack from human ankyrinR
2002
Hepcidin, A New Iron Regulatory Peptide
2002
Identification of the Membrane Attachment Sites for Protein 4.1 in the Human Erythrocyte
1995
HFE and Transferrin Directly Compete for Transferrin Receptor in Solution and at the Cell Surface
2004
Asparagine and Aspartate Hydroxylation of the Cytoskeletal Ankyrin Family Is Catalyzed by Factor-inhibiting Hypoxia-inducible Factor
2010 StandoutNobel
The inhibitory ankyrin and activator Rel proteins
1992 Nobel
The novel Notch homologue mouse Notch 3 lacks specific epidermal growth factor-repeats and is expressed in proliferating neuroepithelium
1994
Regulation of the transient receptor potential channel TRPA1 by its N-terminal ankyrin repeat domain
2012
Ferroportin: Lack of evidence for multimers
2007
Mustard oils and cannabinoids excite sensory nerve fibres through the TRP channel ANKTM1
2004 StandoutNatureNobel
Glycosylphosphatidylinositol-anchored Ceruloplasmin Is Required for Iron Efflux from Cells in the Central Nervous System
2003
Iron‐dependent regulation of the divalent metal ion transporter
2001
βIV Spectrins Are Essential for Membrane Stability and the Molecular Organization of Nodes of Ranvier
2004
Essential functions of synapsins I and II in synaptic vesicle regulation
1995 StandoutNatureNobel
Yeast as a model system for understanding the control of DNA replication in eukaryotes
1990 StandoutNobel
Specific Role of the Truncated βIV-Spectrin Σ6 in Sodium Channel Clustering at Axon Initial Segments and Nodes of Ranvier
2006 StandoutNobel
Cellular and subcellular localization of a newly identified member of the protein 4.1 family, brain 4.1, in the cerebellum of adult and postnatally developing rats
1999
cactus, a gene involved in dorsoventral pattern formation of Drosophila, is related to the IκB gene family of vertebrates
1992 StandoutNobel
The synaptic vesicle cycle: a cascade of protein–protein interactions
1995 StandoutNatureNobel
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis
2001
Anemia of Chronic Disease
2005 Standout
Developmental Clustering of Ion Channels at and near the Node of Ranvier
2001
Decreased rotational diffusion of band 3 in melanesian ovalocytes from Papua, New Guinea
1991
Biochemical Analysis of Potential Sites for Protein 4.1-mediated Anchoring of the Spectrin-Actin Skeleton to the Erythrocyte Membrane
1998
Beyond hemoglobin polymerization: the red blood cell membrane and sickle disease pathophysiology
1991
Spectrin mutations cause spinocerebellar ataxia type 5
2006
CERULOPLASMIN METABOLISM AND FUNCTION
2002
Coated pits, coated vesicles, and receptor-mediated endocytosis
1979 StandoutNatureNobel
A structural model of human erythrocyte spectrin. Alignment of chemical and functional domains.
1982
Modulation of red cell band 4.1 function by cAMP-dependent kinase and protein kinase C phosphorylation.
1988
In Vivo Imaging of Membrane-Associated Glycans in Developing Zebrafish
2008 StandoutScienceNobel
Ankyrin-G coordinates assembly of the spectrin-based membrane skeleton, voltage-gated sodium channels, and L1 CAMs at Purkinje neuron initial segments
2001
Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 ( USF2 ) knockout mice
2001
Expression pattern of Motch, a mouse homolog of Drosophila Notch, suggests an important role in early postimplantation mouse development
1992
Differential phosphorylation of multiple sites in protein 4.1 and protein 4.9 by phorbol ester-activated and cyclic AMP-dependent protein kinases.
1985
Spectrin-actin interaction. Phosphorylated and dephosphorylated spectrin tetramer cross-link F-actin.
1979
Altered assembly of spectrin in red cell membranes in hereditary pyropoikilocytosis
1981
Convergence of Ets- and Notch-Related Structural Motifs in a Heteromeric DNA Binding Complex
1991 Science
Spectrin tethers and mesh in the biosynthetic pathway
2000
Molecular and functional changes in spectrin from patients with hereditary pyropoikilocytosis.
1983
Disruption of ferroportin 1 regulation causes dynamic alterations in iron homeostasis and erythropoiesis in polycythaemia mice
2004
Accelerated transbilayer movement of phosphatidylcholine in sickled erythrocytes. A reversible process.
1983
Matrix control of protein diffusion in biological membranes.
1981
Identification and Location of Brain Protein 4.1
1984 Science
Mammalian reticulocytes lose adhesion to fibronectin during maturation to erythrocytes.
1985 StandoutNobel
Structural studies on serum lipoproteins
1972
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
1976 Standout
Molar absorptivity and A1cm1% values for proteins at selected wavelengths of the ultraviolet and visible regions. VIII
1973
Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosis.
1984
Adenylyl Cyclase Amino Acid Sequence: Possible Channel- or Transporter-Like Structure
1989 StandoutScienceNobel
Xotch , the Xenopus Homolog of Drosophila Notch
1990 Science
IRON REGULATORY PROTEINS AND THE MOLECULAR CONTROL OF MAMMALIAN IRON METABOLISM
2000
Developing nodes of Ranvier are defined by ankyrin-G clustering and are independent of paranodal axoglial adhesion
2002
The Molecular Basis for Membrane – Cytoskeleton Association in Human Erythrocytes
1982
The ankyrin repeat domains of the NF-kappa B precursor p105 and the protooncogene bcl-3 act as specific inhibitors of NF-kappa B DNA binding.
1992
Spectrin deficient inherited hemolytic anemias in the mouse: Characterization by spectrin synthesis and mRNA activity in reticulocytes
1984
Platelets contain proteins immunologically related to red cell spectrin and protein 4.1
1985
Familial Hypercholesterolemia: A Genetic Defect in the Low-Density Lipoprotein Receptor
1976
Regulation of Plasma Cholesterol by Lipoprotein Receptors
1981 StandoutScienceNobel
Tryptic digestion of spectrin in variants of hereditary elliptocytosis.
1981
The discovery of the new haemochromatosis gene
2003
Regulation of the association of membrane skeletal protein 4.1 with glycophorin by a polyphosphoinositide
1985 Nature
Molecular Epitopes of the Ankyrin−Spectrin Interaction
2008
A Novel Neuron-Enriched Homolog of the Erythrocyte Membrane Cytoskeletal Protein 4.1
1999
Inheritance Pattern and Clinical Response to Splenectomy as a Reflection of Erythrocyte Spectrin Deficiency in Hereditary Spherocytosis
1986 StandoutNobel
The distribution of erythrocyte phospholipids in hereditary spherocytosis demonstrates a minimal role for erythrocyte spectrin on phospholipid diffusion and asymmetry
1993 StandoutNobel
2,3-Diphosphoglycerate and ATP dissociate erythrocyte membrane skeletons.
1980
The `Spectraplakins': cytoskeletal giants with characteristics of both spectrin and plakin families
2002
Uncoupling of the Spectrin-Based Skeleton from the Lipid Bilayer in Sickled Red Cells
1991 Science
Structure and function of the cytoplasmic domain of band 3: center of erythrocyte membrane—peripheral protein interactions
1986
Novel Proteinaceous Infectious Particles Cause Scrapie
1982 StandoutScienceNobel
The structure of the ankyrin-binding site of β-spectrin reveals how tandem spectrin-repeats generate unique ligand-binding properties
2009 StandoutNobel
Restoration of normal membrane stability to unstable protein 4.1-deficient erythrocyte membranes by incorporation of purified protein 4.1.
1986
A molecular study of heterozygous protein 4.1 deficiency in hereditary elliptocytosis
1988
Desensitization of turkey erythrocyte adenylate cyclase. Beta-adrenergic receptor phosphorylation is correlated with attenuation of adenylate cyclase activity.
1984 StandoutNobel
Cytokine-mediated regulation of iron transport in human monocytic cells
2003
Regulation of cell cycle-dependent gene expression in yeast.
1990
Iron Homeostasis
2006
The LDL Pathway in Human Fibroblasts: A Receptor-Mediated Mechanism for the Regulation of Cholesterol Metabolism
1976 StandoutNobel
Spectrin tetramer–dimer equilibrium and the stability of erythrocyte membrane skeletons
1980 Nature
A homolog of Drosophila Notch expressed during mammalian development
1991
Interchain binding at the tail end of the Drosophila spectrin molecule.
1994
Fas Preassociation Required for Apoptosis Signaling and Dominant Inhibition by Pathogenic Mutations
2000 StandoutScienceNobel
The DNA binding subunit of NF-κB is identical to factor KBF1 and homologous to the rel oncogene product
1990
Analysis of membrane and surface protein sequences with the hydrophobic moment plot
1984 Standout
Restriction of the lateral motion of band 3 in the erythrocyte membrane by the cytoskeletal network: dependence on spectrin association state
1986
Mechanisms of cytoskeletal regulation: Modulation of aortic endothelial cell protein band 4.1 by the extracellular matrix
1986
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
The complete cDNA and polypeptide sequences of human erythroid alpha-spectrin.
1990
Molecular cloning of protein 4.1, a major structural element of the human erythrocyte membrane skeleton.
1986
A structural model of human erythrocyte protein 4.1.
1984
A mutation that impairs the ability of lipoprotein receptors to localise in coated pits on the cell surface of human fibroblasts
1977 StandoutNatureNobel
Cellular localization of divalent metal transporter DMT-1 in rat kidney
2001
Defects in ankyrin-based cellular pathways in metazoan physiology
2005
Hormonal control of Na+-K+ co-transport in turkey erythrocytes. Multiple site phosphorylation of goblin, a high molecular weight protein of the plasma membrane.
1980
Specific 33-residue repeat(s) of erythrocyte ankyrin associate with the anion exchanger
1991
Anchorage of a band 3 population at the erythrocyte cytoplasmic membrane surface: protein rotational diffusion measurements.
1980
Ankyrin binds to the 15th repetitive unit of erythroid and nonerythroid beta-spectrin.
1991
Interaction of cytoskeletal proteins on the human erythrocyte membrane
1981
Severe iron deficiency anemia in transgenic mice expressing liver hepcidin
2002
Sodium channel Na v 1.6 is localized at nodes of Ranvier, dendrites, and synapses
2000
Full-length sequence of the cDNA for human erythroid beta-spectrin.
1990
Analysis of a mutant strain of human fibroblasts with a defect in the internalization of receptor-bound low density lipoprotein
1976
Molecular Basis of Hereditary Elliptocytosis Due to Protein 4.1 Deficiency
1986
Notch2: a second mammalian Notch gene
1992
In vitro formation of a complex between cytoskeletal proteins of the human erythrocyte
1979 Nature
Molecular mechanisms of receptor desensitization using the β-adrenergic receptor-coupled adenylate cyclase system as a model
1985 StandoutNatureNobel
Partial deficiency of erythrocyte spectrin in hereditary spherocytosis
1985 StandoutNatureNobel
Abnormalities in membrane phospholipid organization in sickled erythrocytes.
1981
Synapsin I is a spectrin-binding protein immunologically related to erythrocyte protein 4.1
1985 Nature
An activated Notch suppresses neurogenesis and myogenesis but not gliogenesis in mammalian cells
1994 StandoutNobel
Synapsins: Mosaics of Shared and Individual Domains in a Family of Synaptic Vesicle Phosphoproteins
1989 StandoutScienceNobel
Identification of the functional site of erythrocyte protein 4.1 involved in spectrin-actin associations.
1986
A molecular defect in two families with hemolytic poikilocytic anemia: reduction of high affinity membrane binding sites for ankyrin.
1981 StandoutNobel
Autosomal-dominant hemochrom-atosis is associated with a mutation in the ferroportin (SLC11A3) gene
2001
Selective expression of an erythroid-specific isoform of protein 4.1.
1988
Expression of the DMT1 (NRAMP2/DCT1) iron transporter in mice with genetic iron overload disorders
2001
Regulation of ferritin genes and protein
2002
Metals in Neurobiology: Probing Their Chemistry and Biology with Molecular Imaging
2008 Standout
Spectrin and Ankyrin-Based Pathways: Metazoan Inventions for Integrating Cells Into Tissues
2001
βIVΣ1 spectrin stabilizes the nodes of Ranvier and axon initial segments
2004
A technique to detect reduced mechanical stability of red cell membranes: relevance to elliptocytic disorders
1982
The heterozygous form of 4.1(-) hereditary elliptocytosis [the 4.1(-) trait]
1985
βIV-spectrin regulates sodium channel clustering through ankyrin-G at axon initial segments and nodes of Ranvier
2002
SynCAM, a Synaptic Adhesion Molecule That Drives Synapse Assembly
2002 StandoutScienceNobel
In vitro functional analysis of human ferroportin (FPN) and hemochromatosis-associated FPN mutations
2005
Deficient Red-Cell Spectrin in Severe, Recessively Inherited Spherocytosis
1982 StandoutNobel
Works of Samuel E. Lux being referenced
A New Spectrin, βIV, Has a Major Truncated Isoform That Associates with Promyelocytic Leukemia Protein Nuclear Bodies and the Nuclear Matrix
2001
Characterization of the Binary Interaction Between Human Erythrocyte Protein 4.1 and Actin
1995
Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1.
1993
Analysis of cDNA for human erythrocyte ankyrin indicates a repeated structure with homology to tissue-differentiation and cell-cycle control proteins
1990 Nature
Anion Exchanger 1 (Band 3) Is Required to Prevent Erythrocyte Membrane Surface Loss but Not to Form the Membrane Skeleton
1996
Radiolabel‐transfer cross‐linking demonstrates that protein 4.1 binds to the N‐terminal region of β spectrin and to actin in binary interactions
1990
Red blood cell membrane disorders
1999
Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8
1990 Nature
Isolation and chromosomal localization of a novel nonerythroid ankyrin gene
1991
Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter
2000 StandoutNature
Hereditary spherocytosis—defects in proteins that connect the membrane skeleton to the lipid bilayer
2004
Structure and Organization of the Human Ankyrin-1 Gene
1997
Linkage of Dominant Hereditary Spherocytosis to the Gene for the Erythrocyte Membrane-Skeleton Protein Ankyrin
1990 StandoutNobel
Ankyrin–1 mutations are a major cause of dominant and recessive hereditary spherocytosis
1996
Structural characterization of the phosphorylation sites of human erythrocyte spectrin.
1980
Dependence of Nodal Sodium Channel Clustering on Paranodal Axoglial Contact in the Developing CNS
1999
Cloning and characterization of band 3, the human erythrocyte anion-exchange protein (AE1).
1989
Membrane protein phosphorylation of intact normal and hereditary spherocytic erythrocytes.
1978
Abnormal oxidant sensitivity and beta-chain structure of spectrin in hereditary spherocytosis associated with defective spectrin-protein 4.1 binding.
1987
The effect of mild diamide oxidation on the structure and function of human erythrocyte spectrin.
1986
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
Isoforms of Ankyrin-3 That Lack the NH2-terminal Repeats Associate with Mouse Macrophage Lysosomes
1997
Inherited Disorders of the Red Cell Membrane Skeleton
1980
Dissecting the red cell membrane skeleton
1979 Nature
Exercise-induced hemolysis in xerocytosis. Erythrocyte dehydration and shear sensitivity.
1981
Identification and Functional Characterization of Protein 4.1R and Actin-Binding Sites in Erythrocyte β Spectrin: Regulation of the Interactions by Phosphatidylinositol-4,5-bisphosphate
2005
A highly conserved region of human erythrocyte ankyrin contains the capacity to bind spectrin.
1993
Electron microscopic study on reassembly of plasma high density apoprotein with various lipids
1971
Energy Reserve and Cation Composition of Irreversibly Sickled Cell in Vivo
1978
Cation depletion by the sodium pump in red cells with pathologic cation leaks. Sickle cells and xerocytes.
1986
Mapping the ankyrin-binding site of the human erythrocyte anion exchanger
1989
Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice.
1991
Molecular defect in the sickle erythrocyte skeleton. Abnormal spectrin binding to sickle inside-our vesicles.
1985
Hereditary Spherocytosis and Related Disorders
1985
Characterization of the Binary Interaction Between Human Erythrocyte Protein 4.1 and Actin
1995
Hereditary disorders of the red cell membrane skeleton
1989
Homozygous Familial Hypercholesterolemia
1975
A widely expressed βIII spectrin associated with Golgi and cytoplasmic vesicles
1998
Distribution of epithelial ankyrin (Ank3) spliceoforms in renal proximal and distal tubules
1998
Human Plasma High Density Lipoprotein
1973
Lipoprotein regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in rat liver cell cultures.
1977
Diminished spectrin extraction from ATP-depleted human erythrocytes. Evidence relating spectrin to changes in erythrocyte shape and deformability.
1978
Analysis of the ternary interaction of the red cell membrane skeletal proteins, spectrin, actin, and 4.1
1984
Hemolytic anemias associated with deficient or dysfunctional spectrin.
1979
Increased cation permeability in mutant mouse red blood cells with defective membrane skeletons
1995
Ankyrin and the hemolytic anemia mutation, nb, map to mouse chromosome 8: presence of the nb allele is associated with a truncated erythrocyte ankyrin.
1990
An analogue of the erythroid membrane skeletal protein 4.1 in nonerythroid cells.
1984
Constitutively active human Notch1 binds to the transcription factor CBF1 and stimulates transcription through a promoter containing a CBF1-responsive element.
1996
Irreversible deformation of the spectrin-actin lattice in irreversibly sickled cells.
1976
Isolation and Characterization of ApoLp-Gln-II (ApoA-II), a Plasma High Density Apolipoprotein Containing Two Identical Polypeptide Chains
1972
Elliptical erythrocyte membrane skeletons and heat-sensitive spectrin in hereditary elliptocytosis.
1981
The Influence of Lipid on the Conformation of Human Plasma High Density Apolipoproteins
1972
Hemolytic anemia in the mouse
1983
A Genetic Defect in the Binding of Protein 4.1 to Spectrin in a Kindred with Hereditary Spherocytosis
1982
Ankyrins: structure and function in normal cells and hereditary spherocytes.
1993