Published in Exp Cell Res on March 01, 1971
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Fluorescent antibody localization of myosin in the cytoplasm, cleavage furrow, and mitotic spindle of human cells. J Cell Biol (1976) 6.94
Actin in dividing cells: contractile ring filaments bind heavy meromyosin. Proc Natl Acad Sci U S A (1973) 4.61
A highly ordered ring of membrane-associated filaments in budding yeast. J Cell Biol (1976) 4.24
Actin in the brush-border of epithelial cells of the chicken intestine. Proc Natl Acad Sci U S A (1971) 4.00
The effect of myosin antibody on the division of starfish blastomeres. J Cell Biol (1977) 3.92
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Brush border motility. Microvillar contraction in triton-treated brush borders isolated from intestinal epithelium. J Cell Biol (1976) 3.12
Changing patterns of actin localization during cell division. Proc Natl Acad Sci U S A (1975) 3.07
Preparation and purification of polymerized actin from sea urchin egg extracts. J Cell Biol (1975) 2.92
Characterization and localization of myosin in the brush border of intestinal epithelial cells. J Cell Biol (1978) 2.47
The distribution, ultrastructure, and chemistry of microfilaments in cultured chick embryo fibroblasts. J Cell Biol (1973) 2.12
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Filament ring formation in the dimorphic yeast Candida albicans. J Cell Biol (1983) 1.95
Orientation and three-dimensional organization of actin filaments in dividing cultured cells. J Cell Biol (1993) 1.94
Actin associated with membranes from 3T3 mouse fibroblast and HeLa cells. J Cell Biol (1975) 1.93
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Concentration of an integral membrane protein, CD43 (leukosialin, sialophorin), in the cleavage furrow through the interaction of its cytoplasmic domain with actin-based cytoskeletons. J Cell Biol (1993) 1.88
Alpha-actinin localization in the cleavage furrow during cytokinesis. J Cell Biol (1978) 1.84
Cytoskeletal distribution and function during the maturation and enucleation of mammalian erythroblasts. J Cell Biol (1989) 1.84
Microfilaments in Chaos carolinensis. Membrane association, distribution, and heavy meromyosin binding in the glycerinated cell. J Cell Biol (1973) 1.84
Cytochalasin B inhibits actin-related gelation of HeLa cell extracts. J Cell Biol (1976) 1.80
Mechanism of the formation of contractile ring in dividing cultured animal cells. I. Recruitment of preexisting actin filaments into the cleavage furrow. J Cell Biol (1990) 1.80
Extraction of an actin-like protein from the prokaryote Mycoplasma pneumoniae. Proc Natl Acad Sci U S A (1977) 1.38
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Effect of microinjected N-ethylmaleimide-modified heavy meromyosin on cell division in amphibian eggs. J Cell Biol (1980) 1.09
Actin in Xenopus oocytes. II. Intracellular distribution and polymerizability. J Cell Biol (1978) 1.02
A myosin-like protein in the cortical layer of the sea urchin egg. J Cell Biol (1973) 0.94
Microfilaments in the polar lobe constriction of fertilized eggs of Ilyanassa obsoleta. J Cell Biol (1973) 0.84
Ultrastructure of blebbing and phagocytosis of blebs by hyperplastic thyroid epithelial cells in vivo. J Cell Biol (1977) 0.79
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Microfilaments in spermatocytes of Nephrotoma suturalis. J Cell Biol (1974) 0.75
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Molecular cloning and characterization of the human double-stranded RNA-activated protein kinase induced by interferon. Cell (1990) 7.12
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Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome. J Med Genet (1983) 2.16
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The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes. J Med Genet (2005) 1.94
A pseudoautosomal gene in man. Science (1986) 1.94
Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences. Hum Genet (1984) 1.74
Development of antibodies to unprotected glycosylation sites on recombinant human GM-CSF. Lancet (1990) 1.71
Ultrastructural changes in the surface layers of the newt's egg in relation to the mechanism of its cleavage. J Cell Sci (1970) 1.66
Detection of myosin heavy chain mRNA during myogenesis in tissue culture by in vitro and in situ hybridization. Cell (1977) 1.66
Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines. Am J Hum Genet (1990) 1.60
The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders. Am J Med Genet (2001) 1.54
Becker muscular dystrophy: correlation of deletion type with clinical severity. J Med Genet (1990) 1.50
Cyclin D3 compensates for loss of cyclin D2 in mouse B-lymphocytes activated via the antigen receptor and CD40. J Biol Chem (2000) 1.39
Investigation of association between alpha-1 proteinase inhibitor haplotype and endometritis in the thoroughbred mare. Equine Vet J (1994) 1.39
Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy. Hum Genet (1985) 1.33
Yolk transport in the ovarian follicle of the hen (Gallus domesticus): lipoprotein-like particles at the periphery of the oocyte in the rapid growth phase. J Cell Sci (1979) 1.33
X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localization. Hum Genet (1987) 1.31
Mapping genetic markers on human chromosome 19 using subchromosomal fragments in somatic cell hybrids. Cytogenet Cell Genet (1986) 1.29
Clinical findings in 33 subjects with large supernumerary marker(15) chromosomes and 3 subjects with triplication of 15q11-q13. Am J Med Genet A (2006) 1.28
Electron microscope observations on some structural proteins of the chick lens. Exp Eye Res (1972) 1.28
Further studies on the development of the eye of Drosophila melanogaster. I. The ommatidia. J Morphol (1968) 1.28
The glutamine 27 beta2-adrenoceptor polymorphism is associated with elevated IgE levels in asthmatic families. J Allergy Clin Immunol (1997) 1.25
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Distribution of reversing factor in reticulocyte lysates during active protein synthesis and on inhibition by heme deprivation or double-stranded RNA. Proc Natl Acad Sci U S A (1984) 1.23
Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes. J Med Genet (2004) 1.22
X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis. Am J Hum Genet (1988) 1.21
BCR-ABL and interleukin 3 promote haematopoietic cell proliferation and survival through modulation of cyclin D2 and p27Kip1 expression. J Biol Chem (2001) 1.10
The A-Myb transcription factor is a marker of centroblasts in vivo. J Immunol (1998) 1.10
The 60 S ribosomal subunit as a carrier of eukaryotic initiation factor 2 and the site of reversing factor activity during protein synthesis. J Biol Chem (1985) 1.08
Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexity. Am J Hum Genet (2003) 1.08
A study of females with deletions of the short arm of the X chromosome. Hum Genet (1998) 1.07
Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafness. Am J Med Genet (1992) 1.07
Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNA. Clin Genet (1990) 1.06
Lck is a key target of imatinib and dasatinib in T-cell activation. Leukemia (2010) 1.04
Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studies. J Med Genet (1986) 1.04
Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome. J Med Genet (1986) 1.03
BCR signals target p27(Kip1) and cyclin D2 via the PI3-K signalling pathway to mediate cell cycle arrest and apoptosis of WEHI 231 B cells. Oncogene (2001) 1.03
Electron microscope observations on the ovarian follicle of the domestic fowl during the rapid growth phase. J Anat (1978) 1.02
Duchenne muscular dystrophy in Wales: impact of DNA linkage analysis and cDNA deletion screening. J Med Genet (1989) 1.02
The B-cell and neuronal forms of the octamer-binding protein Oct-2 differ in DNA-binding specificity and functional activity. Mol Cell Biol (1991) 1.02
Molecular deletion analysis in Duchenne muscular dystrophy. J Med Genet (1986) 1.02
Characterization of cell cycle status and E2F complexes in mobilized CD34+ cells before and after cytokine stimulation. Blood (1997) 1.01
The influence of INK4 proteins on growth and self-renewal kinetics of hematopoietic progenitor cells. Blood (2001) 1.01
A method for separating the granulosa cells, the basal lamina and the theca of the preovulatory ovarian follicle of the domestic fowl (Gallus domesticus). J Reprod Fertil (1977) 0.99
Epimutation of the TNDM locus and the Beckwith-Wiedemann syndrome centromeric locus in individuals with transient neonatal diabetes mellitus. Hum Genet (2006) 0.99
The fine structure of the eye of a visual mutant, A-type of Drosophila melanogaster. J Insect Physiol (1972) 0.97
Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysis. J Pediatr (1989) 0.97
Fragile X mental retardation and the iduronate sulphatase locus: testing Laird's model of fra(X) inheritance. Am J Med Genet (1992) 0.96
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Antituberculosis drugs and new drug development. Curr Opin Pulm Med (2001) 0.95
Identification of glycogen in thin sections of amphibian embryos. J Cell Sci (1967) 0.95
Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1). Hum Genet (1992) 0.95
Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment. Am J Hum Genet (1993) 0.95
Ultrastructure of the blastopore cells in the newt. J Embryol Exp Morphol (1966) 0.94
A note on the mechanisms of cell deformation in the neural folds of the Amphibia. Exp Cell Res (1966) 0.94
CBP associates with the p42/p44 MAPK enzymes and is phosphorylated following NGF treatment. Neuroreport (1999) 0.94
Fanconi anaemia complementation group B presenting as X linked VACTERL with hydrocephalus syndrome. J Med Genet (2006) 0.93
Characterization of 34 novel and six known MTM1 gene mutations in 47 unrelated X-linked myotubular myopathy patients. Neuromuscul Disord (1999) 0.93
DNA and enzyme studies on chorionic villi for use in antenatal diagnosis. Clin Chim Acta (1984) 0.92
Cell cycle arrest of proliferating neuronal cells by serum deprivation can result in either apoptosis or differentiation. J Neurochem (1993) 0.92
Preferential induction of apoptosis of leukaemic cells by farnesol. FEBS Lett (2000) 0.92
A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions. Hum Genet (2005) 0.92
Role of different sponge cell types in species specific cell aggregation. Nat New Biol (1971) 0.91
Modulation of E2F complexes during G0 to S phase transition in human primary B-lymphocytes. J Biol Chem (1999) 0.91
The myosin of developing and dystrophic skeletal muscle. FEBS Lett (1974) 0.91
Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysis. Am J Med Genet (1990) 0.91
Oct-1 [corrected] and Oct-2 DNA-binding site specificity is regulated in vitro by different kinases. Biochem J (1996) 0.91
X chromosome linkage studies in familial Rett syndrome. Hum Genet (1993) 0.90
Microfilaments in the external surface layer of the early amphibian embryo. J Embryol Exp Morphol (1975) 0.90
Maternal folate polymorphisms and the etiology of human nondisjunction. Am J Hum Genet (2001) 0.90
Further studies on the development of the of Drosophila melanogaster. II. The interommatidial bristles. J Morphol (1968) 0.89
Transdermal delivery of naloxone: effect of water, propylene glycol, ethanol and their binary combinations on permeation through rat skin. Int J Pharm (2001) 0.89
Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implications. J Med Genet (1998) 0.89
Detection of de novo mutations and analysis of their origin in families with X linked hypohidrotic ectodermal dysplasia. J Med Genet (1994) 0.89
Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred. J Med Genet (1991) 0.87
Linkage of asthma to markers on chromosome 12 in a sample of 240 families using quantitative phenotype scores. Genomics (1998) 0.87
Polyribosome binding of rabbit globin messenger RNA and messenger ribonucleoprotein labelled with bacteriophage-T4 RNA ligase and 5'-[32P] phosphocytidine 3'-phosphate. Nucleic Acids Res (1983) 0.87
Report on the 20th ENMC sponsored international workshop: myotubular/centronuclear myopathy. Neuromuscul Disord (1994) 0.87
X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684). J Med Genet (1994) 0.86
Linkage analysis of the 5q31-33 candidate region for asthma in 240 UK families. Genes Immun (2001) 0.86
The structure of the germinal disc region of the hen's ovarian follicle during the rapid growth phase. J Anat (1978) 0.86
The blebbing response of 2-4 cell stage mouse embryos to cytochalasin B. Dev Biol (1975) 0.86
Role of atresia in establishing the follicular hierarchy in the ovary of the domestic hen (Gallus domesticus). J Reprod Fertil (1983) 0.85
The binding of very low density and low density lipoproteins to the plasma membrane of the hen's oocyte. A morphological study. Exp Cell Res (1984) 0.85
Genetic heterogeneity in X-linked amelogenesis imperfecta. Genomics (1992) 0.84
Pure populations of transduced primary human cells can be produced using GFP expressing herpes virus vectors and flow cytometry. Gene Ther (1998) 0.84
Recognition and reanalysis of a cell line from a manifesting female with X linked hypohidrotic ectodermal dysplasia and an X; autosome balanced translocation. J Med Genet (1988) 0.84
A comparison of human lens epithelial cells in situ and in vitro in relation to aging: an ultrastructural study. Exp Eye Res (1979) 0.84
Assignment of Emery-Dreifuss muscular dystrophy to the distal region of Xq28: the results of a collaborative study. Am J Hum Genet (1991) 0.82
Oestriol and oestradiol increase cell to cell communication and connexin43 protein expression in human myometrium. Mol Hum Reprod (2001) 0.82
A complex medical phenotype in a patient with triplication of 2q12.3 to 2q13 characterized with oligonucleotide array CGH. Cytogenet Genome Res (2009) 0.82
Localisation of the gene for Hunter syndrome on the long arm of X chromosome. Hum Genet (1986) 0.82
Comparative studies of the Spi1 proteins of three equine alpha-1-proteinase inhibitor haplotypes following isolation by affinity chromatography. Int J Biochem (1993) 0.81
The genes and mRNA coding for the heavy chains of chick embryonic skeletal myosin. Cell (1977) 0.81
A method to demonstrate the fine structural components of lens fibre cells. Exp Eye Res (1976) 0.81