Published in J Hered on June 10, 1983
The alpha-spectrin gene is on chromosome 1 in mouse and man. Proc Natl Acad Sci U S A (1985) 2.53
A mutation affecting the lactate dehydrogenase locus Ldh-1 in the mouse. II. Mechanism of the LDH-A deficiency associated with hemolytic anemia. Genetics (1993) 0.78
Clinicopathologic features of young and old sphha/sphha mice. Mutants with congenital hemolytic anemia. Am J Pathol (1988) 0.76
Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter. Nature (2000) 7.46
Cloning of mammalian heparanase, an important enzyme in tumor invasion and metastasis. Nat Med (1999) 3.06
Dependence of nodal sodium channel clustering on paranodal axoglial contact in the developing CNS. J Neurosci (1999) 3.05
Spectrin-actin membrane skeleton of normal and abnormal red blood cells. Semin Hematol (1979) 2.89
Dissecting the red cell membrane skeleton. Nature (1979) 2.30
A specific apoprotein activator for lipoprotein lipase. Biochem Biophys Res Commun (1970) 2.24
Conditioned place preference using opiate and stimulant drugs: a meta-analysis. Neurosci Biobehav Rev (1995) 2.17
The cellular basis of the genetically determined hemopoietic defect in anemic mice of genotype Sl-Sld. Blood (1965) 2.14
Is it possible to be schizophrenic yet neuropsychologically normal? Neuropsychology (1997) 2.01
Red blood cell membrane disorders. Br J Haematol (1999) 1.97
Irreversible deformation of the spectrin-actin lattice in irreversibly sickled cells. J Clin Invest (1976) 1.89
Neuroleptic withdrawal in schizophrenic patients. A review of the literature. Arch Gen Psychiatry (1995) 1.88
Anion exchanger 1 (band 3) is required to prevent erythrocyte membrane surface loss but not to form the membrane skeleton. Cell (1996) 1.85
Depressive symptoms in schizophrenia. Am J Psychiatry (1999) 1.83
Calcium measurement in isolated arterioles during myogenic and agonist stimulation. Am J Physiol (1991) 1.75
Mouse models for neural tube closure defects. Hum Mol Genet (2000) 1.73
Amino acid sequence of human apoLp-Gln-II (apoA-II), an apolipoprotein isolated from the high-density lipoprotein complex. Proc Natl Acad Sci U S A (1972) 1.68
Nondementia nonpraecox dementia praecox? Late-onset schizophrenia. Am J Geriatr Psychiatry (1997) 1.57
Notch1 inhibits neurite outgrowth in postmitotic primary neurons. Neuroscience (1999) 1.54
A widely expressed betaIII spectrin associated with Golgi and cytoplasmic vesicles. Proc Natl Acad Sci U S A (1998) 1.53
Gender-related clinical differences in older patients with schizophrenia. J Clin Psychiatry (1999) 1.49
A technique to detect reduced mechanical stability of red cell membranes: relevance to elliptocytic disorders. Blood (1982) 1.49
Controlled comparisons of clomipramine and fluoxetine in the treatment of obsessive-compulsive disorder. Behavioral and biological results. Arch Gen Psychiatry (1990) 1.46
Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrin. N Engl J Med (1990) 1.45
Growing up and growing apart: a developmental meta-analysis of twin studies. Psychol Bull (1990) 1.43
Red cell membrane skeletal defects in hereditary and acquired hemolytic anemias. Semin Hematol (1983) 1.41
Gentian violet. Med J Aust (1991) 1.40
Heme biosynthesis and drug metabolism in mice with hereditary hemolytic anemia. Heme oxygenase induction as an adaptive response for maintaining cytochrome P-450 in chronic hemolysis. J Biol Chem (1979) 1.39
Maternal postnatal depression and infant gastro-oesophageal reflux. J Paediatr Child Health (1994) 1.39
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. J Cell Biol (1995) 1.37
Typing of the common phosphoglucomutase variants using isoelectric focusing--a new interpretation of the phosphoglucomutase system. J Forensic Sci Soc (1976) 1.37
Analysis of the ternary interaction of the red cell membrane skeletal proteins spectrin, actin, and 4.1. Biochemistry (1984) 1.36
Isolation and characterization of apoLp-Gln-II (apoA-II), a plasma high density apolipoprotein containing two identical polypeptide chains. J Biol Chem (1972) 1.36
An analogue of the erythroid membrane skeletal protein 4.1 in nonerythroid cells. J Cell Biol (1984) 1.32
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis. Nat Genet (1996) 1.32
Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice. J Cell Biol (1991) 1.32
Marked reduction of spectrinin hereditary spherocytosis in the common house mouse. Blood (1978) 1.31
Constitutively active human Notch1 binds to the transcription factor CBF1 and stimulates transcription through a promoter containing a CBF1-responsive element. Proc Natl Acad Sci U S A (1996) 1.27
Chronic neutropenia and abnormal cellular immunity in cartilage-hair hypoplasia. N Engl J Med (1970) 1.27
Ankyrin and the hemolytic anemia mutation, nb, map to mouse chromosome 8: presence of the nb allele is associated with a truncated erythrocyte ankyrin. Proc Natl Acad Sci U S A (1990) 1.26
Lower incidence of tardive dyskinesia with risperidone compared with haloperidol in older patients. J Am Geriatr Soc (1999) 1.25
A genetic defect in the binding of protein 4.1 to spectrin in a kindred with hereditary spherocytosis. N Engl J Med (1982) 1.25
Mouse microcytic anaemia caused by a defect in the gene encoding the globin enhancer-binding protein NF-E2. Nature (1993) 1.23
Mild spherocytosis and altered red cell ion transport in protein 4. 2-null mice. J Clin Invest (1999) 1.19
Conventional vs. newer antipsychotics in elderly patients. Am J Geriatr Psychiatry (1999) 1.18
Isoforms of ankyrin-3 that lack the NH2-terminal repeats associate with mouse macrophage lysosomes. J Cell Biol (1997) 1.18
Platelet membrane glycoprotein IIIa contains target antigens that bind anti-platelet antibodies in immune thrombocytopenias. J Clin Invest (1984) 1.17
Tin-protoporphyrin suppression of hyperbilirubinemia in mutant mice with severe hemolytic anemia. Blood (1983) 1.15
Characterization and genetic studies of microcytic anemia in house mouse. Blood (1970) 1.15
Cow's milk allergy as a cause of infantile colic: immunofluorescent studies on jejunal mucosa. Aust Paediatr J (1977) 1.14
Tissue transplantation as an analytic and therapeutic tool in hereditary anemias. Am J Surg (1970) 1.14
Mapping the ankyrin-binding site of the human erythrocyte anion exchanger. J Biol Chem (1989) 1.13
Regional bioelectric properties of porcine airway epithelium. J Appl Physiol (1985) (1992) 1.12
The apolipoproteins. Adv Exp Med Biol (1972) 1.12
Studies on the protein defect in Tangier disease. Isolation and characterization of an abnormal high density lipoprotein. J Clin Invest (1972) 1.12
Evidence for protein kinase C involvement in arteriolar myogenic reactivity. Am J Physiol (1990) 1.11
The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter. Blood (2000) 1.11
Inherited hemolytic disease in mice: a review and update. Lab Anim Sci (1980) 1.10
Incidence of tardive dyskinesia in early stages of low-dose treatment with typical neuroleptics in older patients. Am J Psychiatry (1999) 1.10
The influence of lipid on the conformation of human plasma high density apolipoproteins. J Biol Chem (1972) 1.08
Cavernous adrenal hemangioma. Urology (1993) 1.08
Clinical and neuropsychological characteristics of patients with late-onset schizophrenia. Am J Psychiatry (1995) 1.07
Ankyrins: structure and function in normal cells and hereditary spherocytes. Semin Hematol (1993) 1.07
Complex patterns of sequence variation and multiple 5' and 3' ends are found among transcripts of the erythroid ankyrin gene. J Biol Chem (1993) 1.07
Degradation of membrane phospholipids and thiols in peroxide hemolysis: studies in vitamin E deficiency. Blood (1968) 1.06
A new spectrin, beta IV, has a major truncated isoform that associates with promyelocytic leukemia protein nuclear bodies and the nuclear matrix. J Biol Chem (2001) 1.06
Tuberculosis in socio-economically deprived neighborhoods: missed opportunities for prevention. Int J Tuberc Lung Dis (2008) 1.05
The effect of mild diamide oxidation on the structure and function of human erythrocyte spectrin. J Biol Chem (1986) 1.05
Proof of whole-cell implant in therapy of W-series anemia. Arch Biochem Biophys (1968) 1.05
Diminished spectrin extraction from ATP-depleted human erythrocytes. Evidence relating spectrin to changes in erythrocyte shape and deformability. J Clin Invest (1978) 1.04
Normal mouse strains differ in the site of initiation of closure of the cranial neural tube. Teratology (1991) 1.04
Isolation and characterization of the tryptic and cyanogen bromide peptides of apoLp-Gln-II (apoA-II), plasma high density apolipoprotein. J Biol Chem (1972) 1.04
Structure and organization of the human ankyrin-1 gene. Basis for complexity of pre-mRNA processing. J Biol Chem (1997) 1.03
Hereditary spherocytosis and related disorders. Clin Haematol (1985) 1.03
Laparoscopic management of incidentally noted omphalomesenteric duct remnant. J Endourol (1994) 1.03
Hereditary disorders of the red cell membrane skeleton. Trends Genet (1989) 1.01
Membrane protein phosphorylation of intact normal and hereditary spherocytic erythrocytes. J Biol Chem (1978) 1.01
Differential expression of Na(+)-K(+)-ATPase, ankyrin, fodrin, and E-cadherin along the kidney nephron. Am J Physiol (1995) 1.00
Structural characterization of the phosphorylation sites of human erythrocyte spectrin. J Biol Chem (1980) 1.00
Expression, purification, and characterization of the functional dimeric cytoplasmic domain of human erythrocyte band 3 in Escherichia coli. Protein Sci (1992) 0.99
Distribution of epithelial ankyrin (Ank3) spliceoforms in renal proximal and distal tubules. Am J Physiol (1998) 0.99
Radiolabel-transfer cross-linking demonstrates that protein 4.1 binds to the N-terminal region of beta spectrin and to actin in binary interactions. Eur J Biochem (1990) 0.99
Treatment of combined traction-rhegmatogenous retinal detachment in the morning glory syndrome. Retina (1985) 0.98
Immunofluorescence studies of apolipoprotein B in intestinal mucosa. Absence in abetalipoproteinemia. Gastroenterology (1979) 0.98
Cross-sectional study of older outpatients with schizophrenia and healthy comparison subjects: no differences in age-related cognitive decline. Am J Psychiatry (2000) 0.98
Hemolytic anemias associated with deficient or dysfunctional spectrin. Prog Clin Biol Res (1979) 0.98
Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis. Blood (1993) 0.97
Nitric oxide release during alpha1-adrenoceptor-mediated constriction of arterioles. Am J Physiol Heart Circ Physiol (2001) 0.97
An examination of the soluble oligomeric complexes extracted from the red cell membrane and their relation to the membrane cytoskeleton. Eur J Cell Biol (1985) 0.97
Molecular defect in the membrane skeleton of blood bank-stored red cells. Abnormal spectrin-protein 4.1-actin complex formation. J Clin Invest (1986) 0.97
Gender, estrogen, and schizophrenia. Psychopharmacol Bull (1997) 0.97
Energy reserve and cation composition of irreversibly sickled cells in vivo. Br J Haematol (1978) 0.97
Mesenteric vascular remodeling in hyperhomocysteinemia. Mol Cell Biochem (2010) 0.96
Isolation and partial characterization of a high molecular weight red cell membrane protein complex normally removed by the spleen. Blood (1977) 0.96
Abnormal oxidant sensitivity and beta-chain structure of spectrin in hereditary spherocytosis associated with defective spectrin-protein 4.1 binding. J Clin Invest (1987) 0.96
Studies on the pathogenesis of pigment gallstones in hemolytic anemia: description and characteristics of a mouse model. J Clin Invest (1980) 0.96
Relationship between ambulation and obesity in older persons with and without low back pain. Int J Obes Relat Metab Disord (2004) 0.96
The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene. Nat Genet (1992) 0.95