review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0074-7696(08)62385-2 |
P698 | PubMed publication ID | 8575894 |
P2093 | author name string | Maison C | |
Georgatos SD | |||
P2860 | cites work | A leucine----proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosis | Q24293187 |
Plakoglobin, or an 83-kD homologue distinct from beta-catenin, interacts with E-cadherin and N-cadherin | Q24300513 | ||
Identification of the ubiquitous human desmoglein, Dsg2, and the expression catalogue of the desmoglein subfamily of desmosomal cadherins | Q24309399 | ||
A serine kinase regulates intracellular localization of splicing factors in the cell cycle | Q24317050 | ||
Functional expression of cloned human splicing factor SF2: homology to rna-binding proteins, U1 70K, and drosophila splicing regulators | Q24317722 | ||
Contributions of cytoplasmic domains of desmosomal cadherins to desmosome assembly and intermediate filament anchorage | Q24337693 | ||
Immunological characterization of the subunit of the 100 A filaments from muscle cells | Q24561559 | ||
Filensin: a new vimentin-binding, polymerization-competent, and membrane-associated protein of the lens fiber cell | Q24644180 | ||
A lamin B receptor in the nuclear envelope | Q24645398 | ||
Making a connection: direct binding between keratin intermediate filaments and desmosomal proteins | Q24651318 | ||
The 47-kD lens-specific protein phakinin is a tailless intermediate filament protein and an assembly partner of filensin | Q24657689 | ||
Epithelial integrin alpha 6 beta 4: complete primary structure of alpha 6 and variant forms of beta 4 | Q24678880 | ||
A new high molecular mass protein showing unique localization in desmosomal plaque | Q24679384 | ||
Integral membrane proteins specific to the inner nuclear membrane and associated with the nuclear lamina | Q24679481 | ||
The expression of mutant epidermal keratin cDNAs transfected in simple epithelial and squamous cell carcinoma lines | Q24680145 | ||
Organization of actin, myosin, and intermediate filaments in the brush border of intestinal epithelial cells | Q24681056 | ||
A large particle associated with the perimeter of the nuclear pore complex | Q24681457 | ||
Increased expression of neurofilament subunit NF-L produces morphological alterations that resemble the pathology of human motor neuron disease | Q70633175 | ||
Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: a mouse model of amyotrophic lateral sclerosis | Q70633178 | ||
The synthesis and distribution of desmin and vimentin during myogenesis in vitro | Q70645926 | ||
Identification of spectrin and protein 4.1-like proteins in mammalian lens | Q71319790 | ||
Dynamic aspects of the supramolecular organization of intermediate filament networks in cultured epidermal cells | Q71461438 | ||
Association between intermediate-sized filaments and mitochondria in rat Leydig cells | Q71511330 | ||
The lamin B receptor-associated protein p34 shares sequence homology and antigenic determinants with the splicing factor 2-associated protein p32 | Q71629755 | ||
The interaction in vitro of the intermediate filament protein vimentin with synthetic polyribo- and polydeoxyribonucleotides | Q71794281 | ||
Mid-gestational lethality in mice lacking keratin 8 | Q72085734 | ||
Concomitant changes in mitochondria and intermediate filaments during heat shock and recovery of chicken embryo fibroblasts | Q72231182 | ||
Conformational changes in myocardial nuclei of rats | Q72337521 | ||
The interaction between microtubules and intermediate filaments in cultured cells treated with taxol and nocodazole | Q72548044 | ||
Vimentin filaments and centrosomes. Are they associated? | Q72571020 | ||
Localization of the centriole and keratin intermediate filaments in PtK1 cells by double immunofluorescence | Q72745300 | ||
Tenacious binding of lipids to vimentin during its isolation and purification from Ehrlich ascites tumor cells | Q93647109 | ||
Potassium chloride-insoluble myofilaments in vertebrate smooth muscle cells | Q93703583 | ||
Fractionation of the avian erythrocyte: an ultrastructural study | Q93708040 | ||
A protein antigenically related to nuclear lamin B mediates the association of intermediate filaments with desmosomes | Q36223413 | ||
Regulated expression of vimentin cDNA in cells in the presence and absence of a preexisting vimentin filament network | Q36223423 | ||
Lamins A and C bind and assemble at the surface of mitotic chromosomes | Q36223712 | ||
Stepwise reassembly of the nuclear envelope at the end of mitosis | Q36232741 | ||
Inhibition of desmin expression blocks myoblast fusion and interferes with the myogenic regulators MyoD and myogenin | Q36233766 | ||
Intermediate filaments and disease: mutations that cripple cell strength | Q36233886 | ||
IFAP 300 is common to desmosomes and hemidesmosomes and is a possible linker of intermediate filaments to these junctions | Q36234080 | ||
Intermediate filaments in monkey kidney TC7 cells: focal centers and interrelationship with other cytoskeletal systems | Q36249401 | ||
Lenticular intermediate-sized filaments: biosynthesis and interaction with plasma membrane | Q36296241 | ||
Differential organization of desmin and vimentin in muscle is due to differences in their head domains. | Q36382852 | ||
Association of microtubules and intermediate filaments in chicken gizzard cells as detected by double immunofluorescence | Q36402634 | ||
Specific disruption of vimentin filament organization in monkey kidney CV-1 cells by diphtheria toxin, exotoxin A, and cycloheximide | Q36419020 | ||
New views of smooth muscle structure using freezing, deep-etching and rotary shadowing | Q69949954 | ||
Band 3 and ankyrin homologues are present in eye lens: evidence for all major erythrocyte membrane components in same non-erythroid cell | Q70042342 | ||
Chromatin motion in neuronal interphase nuclei: changes induced by disruption of intermediate filaments | Q70118325 | ||
Reorganization of HeLa cell cytoskeleton induced by an uncoupler of oxidative phosphorylation | Q70215330 | ||
The intracellular localization of the microvillus 110K protein, a component considered to be involved in side-on membrane attachment of F-actin | Q70225077 | ||
Structural features in the heptad substructure and longer range repeats of two-stranded alpha-fibrous proteins | Q70264848 | ||
Structure and composition of the cytoskeleton of nucleated erythrocytes: III. Organization of the cytoskeleton of Bufo marinus erythrocytes as revealed by freeze-dried platinum-carbon replicas and immunofluorescence microscopy | Q70305256 | ||
The nuclear matrix: three-dimensional architecture and protein composition | Q70538958 | ||
Isolation of an immunoreactive analogue of brain fodrin that is associated with the cell cortex of Dictyostelium amoebae | Q36440320 | ||
The CaaX motif is required for isoprenylation, carboxyl methylation, and nuclear membrane association of lamin B2. | Q36529485 | ||
Viscoelastic properties of vimentin compared with other filamentous biopolymer networks | Q36529508 | ||
Integrin alpha 6/beta 4 complex is located in hemidesmosomes, suggesting a major role in epidermal cell-basement membrane adhesion | Q36529725 | ||
Cloning and sequencing of rat plectin indicates a 466-kD polypeptide chain with a three-domain structure based on a central alpha-helical coiled coil. | Q36529960 | ||
Characterization of A 54-kD protein of the inner nuclear membrane: evidence for cell cycle-dependent interaction with the nuclear lamina | Q36530128 | ||
The desmoplakin carboxyl terminus coaligns with and specifically disrupts intermediate filament networks when expressed in cultured cells | Q36531032 | ||
The vertebrate adhesive junction proteins beta-catenin and plakoglobin and the Drosophila segment polarity gene armadillo form a multigene family with similar properties | Q36531649 | ||
Identification of an epithelial protein related to the desmosome and intermediate filament network | Q36531882 | ||
Host cell factors controlling vimentin organization in the Xenopus oocyte | Q36532211 | ||
Cytoplasmic fibrils in living cultured cells. A light and electron microscope study | Q36533593 | ||
The role of CaaX-dependent modifications in membrane association of Xenopus nuclear lamin B3 during meiosis and the fate of B3 in transfected mitotic cells | Q36534715 | ||
Regulated docking of nuclear membrane vesicles to vimentin filaments during mitosis. | Q36534819 | ||
Putative association of mitochondria with a subpopulation of intermediate-sized filaments in cultured human skin fibroblasts | Q36591123 | ||
Complexity and expression patterns of the desmosomal cadherins. | Q36773470 | ||
Transient, localized accumulation of alpha-spectrin during sea urchin morphogenesis | Q36774664 | ||
Recent insights into the assembly, dynamics, and function of intermediate filament networks | Q37267883 | ||
Desmocollins form a distinct subset of the cadherin family of cell adhesion molecules | Q37516317 | ||
Fluorescent localization of membrane sites in glycerinated chicken skeletal muscle fibers and the relationship of these sites to the protein composition of the Z disc | Q37592000 | ||
Association of mitochondria with microtubules in cultured cells | Q37592671 | ||
Interactions of intermediate filaments with cell structures | Q37804797 | ||
Desmosomes and hemidesmosomes: constitutive molecular components. | Q38023534 | ||
Interaction of intermediate filaments with nuclear lamina and cell periphery | Q38218937 | ||
Binding of matrix attachment regions to lamin B1 | Q38508299 | ||
Toward a more complete 3-D structure of the nuclear pore complex | Q39244460 | ||
Interactions between IFs, microtubules, and myofibrils in fibrogenic and myogenic cells | Q39414563 | ||
Molecular and cellular biology of intermediate filaments | Q39532153 | ||
Intermediate filaments: possible functions as cytoskeletal connecting links between the nucleus and the cell surface | Q39838476 | ||
Intermediate filaments in skeletal and cardiac muscle tissue in embryonic and adult chicken | Q39838492 | ||
Different distribution of pattern of 100-Å filaments in resting and locomotive leukaemia cells | Q39997599 | ||
The beta 4 subunit cytoplasmic domain mediates the interaction of alpha 6 beta 4 integrin with the cytoskeleton of hemidesmosomes | Q40241664 | ||
Intermediate filaments: new proteins, some answers, more questions | Q40400823 | ||
Lamins and lamin-associated proteins. | Q40626423 | ||
A function for the integrin alpha 6 beta 4 in the hemidesmosome | Q40642598 | ||
The beaded intermediate filaments and their potential functions in eye lens | Q40699517 | ||
Nuclear shape in muscle cells. | Q41106267 | ||
Ultrastructure of desmosomes in mammalian intercalated disc; appearances after lanthanum treatment | Q41106313 | ||
Cytoplasmic domain of the 180-kD bullous pemphigoid antigen, a hemidesmosomal component: molecular and cell biologic characterization | Q41109698 | ||
Desmin and vimentin coexist at the periphery of the myofibril Z disc | Q41142942 | ||
Immunoelectron microscopic studies of desmin (skeletin) localization and intermediate filament organization in chicken skeletal muscle | Q41413282 | ||
Mitosis and intermediate-sized filaments in developing skeletal muscle | Q24682562 | ||
Tpr, a large coiled coil protein whose amino terminus is involved in activation of oncogenic kinases, is localized to the cytoplasmic surface of the nuclear pore complex | Q28118819 | ||
Integral membrane proteins of the nuclear envelope interact with lamins and chromosomes, and binding is modulated by mitotic phosphorylation | Q28260206 | ||
Network antibodies identify nuclear lamin B as a physiological attachment site for peripherin intermediate filaments | Q28262899 | ||
Attachment of vimentin filaments to desmosomal plaques in human meningiomal cells and arachnoidal tissue | Q28266932 | ||
Association of spectrin with desmin intermediate filaments | Q28285104 | ||
Functional analysis of desmoplakin domains: specification of the interaction with keratin versus vimentin intermediate filament networks | Q28298571 | ||
Plakoglobin: a protein common to different kinds of intercellular adhering junctions | Q28299999 | ||
Assembly properties of dominant and recessive mutations in the small mouse neurofilament (NF-L) subunit | Q28512783 | ||
cDNA sequence analysis of CP94: rat lens fiber cell beaded-filament structural protein shows homology to cytokeratins | Q28565737 | ||
cDNA cloning and characterization of lamina-associated polypeptide 1C (LAP1C), an integral protein of the inner nuclear membrane | Q28582051 | ||
Gene targeting of BPAG1: abnormalities in mechanical strength and cell migration in stratified epithelia and neurologic degeneration | Q28593672 | ||
Mitochondrial Membrane Potential in Living Cells | Q29037927 | ||
Intermediate filaments: structure, dynamics, function, and disease | Q29615442 | ||
Junctional complexes in various epithelia | Q29620435 | ||
Peripherin expression in hippocampal neurons induced by muscle soluble factor(s). | Q30442260 | ||
Transgenic mice expressing a mutant keratin 10 gene reveal the likely genetic basis for epidermolytic hyperkeratosis | Q30990411 | ||
Isolation of cDNAs encoding desmosomal plaque proteins: evidence that bovine desmoplakins I and II are derived from two mRNAs and a single gene | Q33567256 | ||
The complete sequence of Drosophila beta-spectrin reveals supra-motifs comprising eight 106-residue segments | Q33613345 | ||
Alpha 6 beta 4 integrin heterodimer is a component of hemidesmosomes | Q33899956 | ||
The lamin B receptor of the nuclear envelope inner membrane: a polytopic protein with eight potential transmembrane domains | Q33942800 | ||
In vitro assembly of intermediate filaments from baby hamster kidney (BHK-21) cells | Q33986578 | ||
Mice lacking vimentin develop and reproduce without an obvious phenotype | Q34059745 | ||
Characterization of keratocalmin, a calmodulin-binding protein from human epidermis | Q34225971 | ||
Identification of two collagen domains within the bullous pemphigoid autoantigen, BP180 | Q34238421 | ||
cDNA analysis of the 49 kDa lens fiber cell cytoskeletal protein: a new, lens-specific member of the intermediate filament family? | Q34305777 | ||
Binding of two desmin derivatives to the plasma membrane and the nuclear envelope of avian erythrocytes: evidence for a conserved site-specificity in intermediate filament-membrane interactions | Q34349736 | ||
Identification of a new hemidesmosomal protein, HD1: a major, high molecular mass component of isolated hemidesmosomes | Q34551234 | ||
The importance of intramolecular ion pairing in intermediate filaments | Q34805039 | ||
Suppression by antisense mRNA demonstrates a requirement for the glial fibrillary acidic protein in the formation of stable astrocytic processes in response to neurons | Q35016705 | ||
Desmocalmin: a calmodulin-binding high molecular weight protein isolated from desmosomes | Q35024950 | ||
Cytokeratin filaments are present in golden hamster oocytes and early embryos. | Q35168588 | ||
Assembly-disassembly of the nuclear lamina | Q35978070 | ||
Fine structure of desmosomes. , hemidesmosomes, and an adepidermal globular layer in developing newt epidermis | Q36187694 | ||
The role of three cytoplasmic fibers in BHK-21 cell motility. I. Microtubules and the effects of colchicine | Q36191940 | ||
Cytoplasmic filaments in developing and adult vertebrate smooth muscle | Q36192794 | ||
Observation of filaments in the adrenal of androgen-treated rats | Q36193209 | ||
A filamentous cytoskeleton in vertebrate smooth muscle fibers | Q36197810 | ||
Structure and biochemical composition of desmosomes and tonofilaments isolated from calf muzzle epidermis | Q36200082 | ||
Redistribution of intermediate filament subunits during skeletal myogenesis and maturation in vitro | Q36200884 | ||
Organelle relationships in cultured 3T3-L1 preadipocytes | Q36201851 | ||
Isolation of epidermal desmosomes | Q36202379 | ||
Nucleus-associated intermediate filaments from chicken erythrocytes | Q36203541 | ||
The terminal web. A reevaluation of its structure and function | Q36203784 | ||
Fodrin: axonally transported polypeptides associated with the internal periphery of many cells | Q36205287 | ||
Synemin and vimentin are components of intermediate filaments in avian erythrocytes | Q36205902 | ||
A network of transverse and longitudinal intermediate filaments is associated with sarcomeres of adult vertebrate skeletal muscle | Q36206680 | ||
Distribution of alpha-actinin in single isolated smooth muscle cells | Q36207175 | ||
Visualization of longitudinally-oriented intermediate filaments in frozen sections of chicken cardiac muscle by a new staining method | Q36207636 | ||
Morphological characterization of the cholesteryl ester cycle in cultured mouse macrophage foam cells | Q36207926 | ||
Distributions of vimentin and desmin in developing chick myotubes in vivo. I. Immunofluorescence study | Q36209818 | ||
Epithelial cytoskeletal framework and nuclear matrix-intermediate filament scaffold: three-dimensional organization and protein composition | Q36209887 | ||
10-nm filaments are induced to collapse in living cells microinjected with monoclonal and polyclonal antibodies against tubulin | Q36210136 | ||
Immunoprecipitation of nonerythrocyte spectrin within live cells following microinjection of specific antibodies: relation to cytoskeletal structures | Q36210572 | ||
Distributions of vimentin and desmin in developing chick myotubes in vivo. II. Immunoelectron microscopic study | Q36212924 | ||
The 4.1-like proteins of the bovine lens: spectrin-binding proteins closely related in structure to red blood cell protein 4.1. | Q36213021 | ||
Lamin B constitutes an intermediate filament attachment site at the nuclear envelope | Q36218105 | ||
Identification of a basic protein of Mr 75,000 as an accessory desmosomal plaque protein in stratified and complex epithelia. | Q36218624 | ||
The fates of chicken nuclear lamin proteins during mitosis: evidence for a reversible redistribution of lamin B2 between inner nuclear membrane and elements of the endoplasmic reticulum. | Q36219284 | ||
Concurrent collapse of keratin filaments, aggregation of organelles, and inhibition of protein synthesis during the heat shock response in mammary epithelial cells | Q36219958 | ||
Expression of mutant keratin cDNAs in epithelial cells reveals possible mechanisms for initiation and assembly of intermediate filaments | Q36220461 | ||
Assembly and exchange of intermediate filament proteins of neurons: neurofilaments are dynamic structures | Q36220502 | ||
An epithelium-type cytoskeleton in a glial cell: astrocytes of amphibian optic nerves contain cytokeratin filaments and are connected by desmosomes. | Q36221264 | ||
Presence of a protein immunologically related to lamin B in the postsynaptic membrane of Torpedo marmorata electrocyte | Q36221624 | ||
Overexpression of the vimentin gene in transgenic mice inhibits normal lens cell differentiation | Q36221672 | ||
The complete sequence of Drosophila alpha-spectrin: conservation of structural domains between alpha-spectrins and alpha-actinin | Q36221839 | ||
The conserved carboxy-terminal cysteine of nuclear lamins is essential for lamin association with the nuclear envelope | Q36221975 | ||
Immunochemical characterization of three components of the hemidesmosome and their expression in cultured epithelial cells | Q36222087 | ||
Dense bodies and actin polarity in vertebrate smooth muscle | Q41446325 | ||
Site specificity in vimentin-membrane interactions: intermediate filament subunits associate with the plasma membrane via their head domains | Q41474882 | ||
The binding of vimentin to human erythrocyte membranes: a model system for the study of intermediate filament-membrane interactions | Q41475472 | ||
The complement of desmosomal plaque proteins in different cell types | Q41491027 | ||
The first membrane spanning region of the lamin B receptor is sufficient for sorting to the inner nuclear membrane | Q41576875 | ||
Transient storage of a nuclear matrix protein along intermediate-type filaments during mitosis: a novel function of cytoplasmic intermediate filaments | Q41637573 | ||
Coalignment of vimentin intermediate filaments with microtubules depends on kinesin | Q41661593 | ||
Desmin/vimentin intermediate filaments are dispensable for many aspects of myogenesis | Q41666693 | ||
The CaaX motif of lamin A functions in conjunction with the nuclear localization signal to target assembly to the nuclear envelope | Q41757861 | ||
Band 4.1-like proteins of the bovine lens. Effects of differentiation, distribution and extraction characteristics | Q41909461 | ||
On the cell-free association of lamins A and C with metaphase chromosomes | Q41950432 | ||
Bovine filensin possesses primary and secondary structure similarity to intermediate filament proteins | Q42280000 | ||
Is the hemidesmosome a half desmosome? An immunological comparison of mammalian desmosomes and hemidesmosomes | Q42522002 | ||
On the primary site of nuclear RNA synthesis. A retraction | Q42746787 | ||
Rearrangement of the vimentin cytoskeleton during adipose conversion: formation of an intermediate filament cage around lipid globules | Q42808320 | ||
Intermediate filaments formed de novo from tail-less cytokeratins in the cytoplasm and in the nucleus | Q42825574 | ||
Intermediate filaments in 3T3 cells collapse after intracellular injection of a monoclonal anti-intermediate filament antibody | Q42826905 | ||
Cell type-specific association between two types of spectrin and two types of intermediate filaments | Q43405618 | ||
The cytoskeleton of chick lens cells | Q43498478 | ||
Probing mitochondria in living cells with rhodamine 123. | Q43563228 | ||
A novel hemidesmosomal plaque component: tissue distribution and incorporation into assembling hemidesmosomes in an in vitro model | Q43702686 | ||
Effect of anabolic steroids on rat heart muscle cells. I. Intermediate filaments | Q43920972 | ||
Nucleic acid-binding activities of the intermediate filament subunit proteins desmin and glial fibrillary acidic protein. | Q44192358 | ||
Binding of nucleic acids to intermediate filaments of the vimentin type and their effects on filament formation and stability | Q44949252 | ||
Immunocytochemical identification of cytoskeletal linkages to smooth muscle cell nuclei and mitochondria | Q45252452 | ||
Biochemical and immunological characterization of desmoplakins I and II, the major polypeptides of the desmosomal plaque | Q46167586 | ||
Location of a protein of the fodrin-spectrin-TW260/240 family in the mouse intestinal brush border | Q46545422 | ||
Localization of newly synthesized vimentin subunits reveals a novel mechanism of intermediate filament assembly | Q46891122 | ||
Intermyofibrillar and nuclear-myofibrillar connections in human and canine myocardium an ultrastructural study | Q47983818 | ||
Reorganization of brain spectrin (fodrin) during differentiation of PC12 cells. | Q48356790 | ||
Assembly of contractile and cytoskeletal elements in developing smooth muscle cells | Q52233121 | ||
Association of mitochondria with intermediate filaments and of polyribosomes with cytoplasmic actin. | Q52504265 | ||
Antibodies to epithelial desmosomes show wide tissue and species cross-reactivity | Q53924957 | ||
Connections of intermediate filaments with the nuclear lamina and the cell periphery. | Q54418009 | ||
Association of glycosphingolipids with intermediate filaments of human umbilical vein endothelial cells. | Q54678730 | ||
De novo synthesis and specific assembly of keratin filaments in nonepithelial cells after microinjection of mRNA for epidermal keratin | Q58439357 | ||
Desmoplakins of Epithelial and Myocardial Desmosomes are Immunologically and Biochemically Related | Q58439470 | ||
Structures Indicative of Keratinization in Lactating Cells of Bovine Mammary Gland | Q58439738 | ||
Relationship of nuclear membranes with filaments and microtubules | Q58439983 | ||
Intermediate filaments as mechanical integrators of cellular space | Q59070780 | ||
Intermediate filaments anchor the nuclei in nuclear monolayers of cultured human fibroblasts | Q59075173 | ||
Association of mitochondria with desmosomes in the rat thyroid gland | Q67326940 | ||
The existence of an insoluble Z disc scaffold in chicken skeletal muscle | Q67427728 | ||
Attachment of mitochondria to intermediate filaments in adrenal cells: Relevance to the regulation of steroid synthesis | Q67487955 | ||
Structure of alpha-keratin: structural implication of the amino acid sequences of the type I and type II chain segments | Q67601009 | ||
Lipids noncovalently associated with keratins and other cytoskeletal proteins of mouse mammary epithelial cells in primary culture | Q67663224 | ||
Arrangement of desmin intermediate filaments in smooth muscle cells as shown by high-resolution immunocytochemistry | Q67969115 | ||
Plakoglobin and beta-catenin: distinct but closely related | Q68024015 | ||
Association of glycosphingolipids with intermediate filaments of mesenchymal, epithelial, glial, and muscle cells | Q68202502 | ||
Interaction in vitro of the neurofilament triplet proteins from porcine spinal cord with natural RNA and DNA | Q68941340 | ||
Cross-linking of cytokeratins to DNA in vivo by chromium salt and cis-diamminedichloroplatinum(II) | Q68957187 | ||
Alteration of the distribution of intermediate filaments in PtK1 cells by acrylamide. II: Effect on the organization of cytoplasmic organelles | Q69485535 | ||
P304 | page(s) | 91-138 | |
P577 | publication date | 1996-01-01 | |
P1433 | published in | International Review of Cytology | Q2687019 |
P1476 | title | Integration of intermediate filaments into cellular organelles | |
P478 | volume | 164 |
Q95720983 | A novel interaction of the Golgi complex with the vimentin intermediate filament cytoskeleton |
Q36916944 | Chemotactic peptide-induced changes of intermediate filament organization in neutrophils during granule secretion: role of cyclic guanosine monophosphate |
Q36288151 | Desmin cytoskeleton in healthy and failing heart |
Q36293799 | Desmin cytoskeleton linked to muscle mitochondrial distribution and respiratory function. |
Q34395897 | Disruption of muscle architecture and myocardial degeneration in mice lacking desmin |
Q74521770 | Distribution and organization of desmin in cultured adult cardiac muscle cells: reflection on function |
Q54781478 | Downregulation of E-cadherin and its undercoat proteins in pituitary growth hormone cell adenomas with prominent fibrous bodies. |
Q77889890 | Expression of cytokeratins (CKs) 8, 13 and 18 and their mRNA in epithelial linings of radicular cysts: implication for the same CK profiles as nasal columnar epithelium in squamous epithelial lining |
Q36382332 | Filensin and phakinin form a novel type of beaded intermediate filaments and coassemble de novo in cultured cells |
Q34263903 | Intermediate filament-related myopathies |
Q36825339 | Muscle intermediate filaments and their links to membranes and membranous organelles |
Q42832228 | Phosphorylation of vimentin head domain inhibits interaction with the carboxyl-terminal end of alpha-helical rod domain studied by surface plasmon resonance measurements |
Q24681924 | Plectin sidearms mediate interaction of intermediate filaments with microtubules and other components of the cytoskeleton |
Q24537779 | Structural and functional roles of desmin in mouse skeletal muscle during passive deformation |
Q47578996 | The N-Terminal Domain of Vimentin Alters Bladder Permeability |
Q38248194 | The role of tubulin in the mitochondrial metabolism and arrangement in muscle cells. |
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