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From Cytoskeleton to Gene Expression: Actin in the Nucleus
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cm.20437openalex-snapshot
WASH and the Arp2/3 complex regulate endosome shape and trafficking
inferredcites →https://doi.org/10.1002/cm.21116openalex-snapshot
Steady‐state nuclear actin levels are determined by export competent actin pool
inferredcites →https://doi.org/10.1002/j.1460-2075.1984.tb02141.xopenalex-snapshot
Is actin a transcription initiation factor for RNA polymerase B?
inferredcites →https://doi.org/10.1007/s00018-007-7316-3openalex-snapshot
CAP2, cyclase-associated protein 2, is a dual compartment protein
inferredcites →https://doi.org/10.1016/0006-291x(79)90395-4openalex-snapshot
Actin co-purifies with RNA polymerase II
inferredcites →https://doi.org/10.1016/0014-4827(74)90787-3openalex-snapshot
Slime mould actin: Homology to vertebrate actin and presence in the nucleus
inferredcites →https://doi.org/10.1016/0014-4827(79)90412-9openalex-snapshot
Nuclear actin bundles in Amoeba, dictyostelium and human HeLa cells induced by dimethyl sulfoxide
inferredcites →https://doi.org/10.1016/0092-8674(77)90152-0openalex-snapshot
Diffusible and bound actin in nuclei of xenopus laevis oocytes
inferredcites →https://doi.org/10.1016/0092-8674(79)90223-xopenalex-snapshot
An actin filament matrix in hand-isolated nuclei of X. laevis oocytes
inferredcites →https://doi.org/10.1016/j.bbagrm.2012.01.010openalex-snapshot
The transcription cycle in eukaryotes: From productive initiation to RNA polymerase II recycling
inferredcites →https://doi.org/10.1016/j.bbamcr.2013.06.002openalex-snapshot
Stimulation of in vivo nuclear transport dynamics of actin and its co-factors IQGAP1 and Rac1 in response to DNA replication stress
inferredcites →https://doi.org/10.1016/j.cell.2006.08.045openalex-snapshot
Gradients of the Drosophila Chinmo BTB-Zinc Finger Protein Govern Neuronal Temporal Identity
inferredcites →https://doi.org/10.1016/j.cell.2013.12.035openalex-snapshot
Redox Modification of Nuclear Actin by MICAL-2 Regulates SRF Signaling
inferredcites →https://doi.org/10.1016/j.chom.2013.05.006openalex-snapshot
Proximity to PML Nuclear Bodies Regulates HIV-1 Latency in CD4+ T Cells
inferredcites →https://doi.org/10.1016/j.cub.2006.03.059openalex-snapshot
Long-Range Directional Movement of an Interphase Chromosome Site
inferredcites →https://doi.org/10.1016/j.cub.2014.03.053openalex-snapshot
HSP70 Transgene Directed Motion to Nuclear Speckles Facilitates Heat Shock Activation
inferredcites →https://doi.org/10.1016/j.cub.2015.01.052openalex-snapshot
Wash Interacts with Lamin and Affects Global Nuclear Organization
inferredcites →https://doi.org/10.1016/j.yexcr.2003.10.028openalex-snapshot
An actin–myosin complex on actively transcribing genes
inferredcites →https://doi.org/10.1016/j.yexcr.2004.06.034openalex-snapshot
Nuclear actin is partially associated with Cajal bodies in human cells in culture and relocates to the nuclear periphery after infection of cells by adenovirus 5
inferredcites →https://doi.org/10.1016/s0002-9440(10)61236-9openalex-snapshot
Cytoplasmic YY1 Is Associated with Increased Smooth Muscle-Specific Gene Expression
inferredcites →https://doi.org/10.1016/s0014-4827(03)00102-2openalex-snapshot
Profilin I colocalizes with speckles and Cajal bodies:
inferredcites →https://doi.org/10.1016/s0092-8674(00)00051-9openalex-snapshot
Involvement of the TIP60 Histone Acetylase Complex in DNA Repair and Apoptosis
inferredcites →https://doi.org/10.1016/s0092-8674(00)81633-5openalex-snapshot
Rapid and Phosphoinositol-Dependent Binding of the SWI/SNF-like BAF Complex to Chromatin after T Lymphocyte Receptor Signaling
inferredcites →https://doi.org/10.1016/s0092-8674(01)00450-0openalex-snapshot
The p400 Complex Is an Essential E1A Transformation Target
inferredcites →https://doi.org/10.1016/s0092-8674(03)00278-2openalex-snapshot
Actin Dynamics Control SRF Activity by Regulation of Its Coactivator MAL
inferredcites →https://doi.org/10.1016/s1097-2765(00)80258-0openalex-snapshot
Multiple Links between the NuA4 Histone Acetyltransferase Complex and Epigenetic Control of Transcription
inferredcites →https://doi.org/10.1038/35020123openalex-snapshot
A chromatin remodelling complex involved in transcription and DNA processing
inferredcites →https://doi.org/10.1038/emboj.2010.216openalex-snapshot
An actin‐regulated importin α/β‐dependent extended bipartite NLS directs nuclear import of MRTF‐A
inferredcites →https://doi.org/10.1038/emboj.2011.118openalex-snapshot
Structural biochemistry of nuclear actin‐related proteins 4 and 8 reveals their interaction with actin
inferredcites →https://doi.org/10.1038/nature09703openalex-snapshot
Coronin 2A mediates actin-dependent de-repression of inflammatory response genes
inferredcites →https://doi.org/10.1038/nature12105openalex-snapshot
Lamin A/C and emerin regulate MKL1–SRF activity by modulating actin dynamics
inferredcites →https://doi.org/10.1038/ncb1182openalex-snapshot
Actin is part of pre-initiation complexes and is necessary for transcription by RNA polymerase II
inferredcites →https://doi.org/10.1038/ncb1190openalex-snapshot
Nuclear actin and myosin I are required for RNA polymerase I transcription
inferredcites →https://doi.org/10.1038/ncb1357openalex-snapshot
A selective block of nuclear actin export stabilizes the giant nuclei of Xenopus oocytes
inferredcites →https://doi.org/10.1038/ncb1433openalex-snapshot
Regulation of RNA-polymerase-II-dependent transcription by N-WASP and its nuclear-binding partners
inferredcites →https://doi.org/10.1038/ncb1852openalex-snapshot
p53-cofactor JMY is a multifunctional actin nucleation factor
inferredcites →https://doi.org/10.1038/ncb2364openalex-snapshot
Nuclear actin and myosins: Life without filaments
inferredcites →https://doi.org/10.1038/ncb2830openalex-snapshot
A nuclear F-actin scaffold stabilizes ribonucleoprotein droplets against gravity in large cells
inferredcites →https://doi.org/10.1038/ncb740openalex-snapshot
Metabolic-energy-dependent movement of PML bodies within the mammalian cell nucleus
inferredcites →https://doi.org/10.1038/nmeth.1220openalex-snapshot
Lifeact: a versatile marker to visualize F-actin
inferredcites →https://doi.org/10.1038/nrm2145openalex-snapshot
Histone acetyltransferase complexes: one size doesn't fit all
inferredcites →https://doi.org/10.1038/nsmb.1403openalex-snapshot
The HSA domain binds nuclear actin-related proteins to regulate chromatin-remodeling ATPases
inferredcites →https://doi.org/10.1038/nsmb.2529openalex-snapshot
Evidence for monomeric actin function in INO80 chromatin remodeling
inferredcites →https://doi.org/10.1038/nsmb904openalex-snapshot
Actin and hnRNP U cooperate for productive transcription by RNA polymerase II
inferredcites →https://doi.org/10.1038/sj.embor.7400657openalex-snapshot
The chromatin remodelling complex WSTF–SNF2h interacts with nuclear myosin 1 and has a role in RNA polymerase I transcription
inferredcites →https://doi.org/10.1038/sj.embor.7400855openalex-snapshot
Mdm2 targets the p53 transcription cofactor JMY for degradation
inferredcites →https://doi.org/10.1042/bj20100396openalex-snapshot
Functional diversity of the hnRNPs: past, present and perspectives
inferredcites →https://doi.org/10.1073/pnas.1118880109openalex-snapshot
Active maintenance of nuclear actin by importin 9 supports transcription
inferredcites →https://doi.org/10.1073/pnas.1131933100openalex-snapshot
An actin–ribonucleoprotein interaction is involved in transcription by RNA polymerase II
inferredcites →https://doi.org/10.1074/jbc.m110.184374openalex-snapshot
G-actin Participates in RNA Polymerase II-dependent Transcription Elongation by Recruiting Positive Transcription Elongation Factor b (P-TEFb)
inferredcites →https://doi.org/10.1074/jbc.m114.627166openalex-snapshot
Nuclear F-actin Formation and Reorganization upon Cell Spreading
inferredcites →https://doi.org/10.1074/jbc.m206393200openalex-snapshot
Latrunculin B or ATP Depletion Induces Cofilin-dependent Translocation of Actin into Nuclei of Mast Cells
inferredcites →https://doi.org/10.1074/jbc.m302845200openalex-snapshot
Cytoplasmic Nuclear Transfer of the Actin-capping Protein Tropomodulin
inferredcites →https://doi.org/10.1074/jbc.m406046200openalex-snapshot
Subcellular Localization of Multiple PREP2 Isoforms Is Regulated by Actin, Tubulin, and Nuclear Export
inferredcites →https://doi.org/10.1074/jbc.m500001200openalex-snapshot
The Mammalian YL1 Protein Is a Shared Subunit of the TRRAP/TIP60 Histone Acetyltransferase and SRCAP Complexes
inferredcites →https://doi.org/10.1074/jbc.m600233200openalex-snapshot
The WSTF-SNF2h Chromatin Remodeling Complex Interacts with Several Nuclear Proteins in Transcription
inferredcites →https://doi.org/10.1074/jbc.m607596200openalex-snapshot
A Novel Role of the Actin-nucleating Arp2/3 Complex in the Regulation of RNA Polymerase II-dependent Transcription
inferredcites →https://doi.org/10.1083/jcb.101.4.1198openalex-snapshot
Morphological study of the mammalian stress response: characterization of changes in cytoplasmic organelles, cytoskeleton, and nucleoli, and appearance of intranuclear actin filaments in rat fibroblasts after heat-shock treatment.
inferredcites →https://doi.org/10.1083/jcb.153.1.229openalex-snapshot
Actin Bound to the Heterogeneous Nuclear Ribonucleoprotein Hrp36 Is Associated with Balbiani Ring mRNA from the Gene to Polysomes
inferredcites →https://doi.org/10.1083/jcb.200507101openalex-snapshot
Nucleoplasmic β-actin exists in a dynamic equilibrium between low-mobility polymeric species and rapidly diffusing populations
inferredcites →https://doi.org/10.1083/jcb.200710058openalex-snapshot
Actin-dependent intranuclear repositioning of an active gene locus in vivo
inferredcites →https://doi.org/10.1083/jcb.201103168openalex-snapshot
Comparative RNAi screening identifies a conserved core metazoan actinome by phenotype
inferredcites →https://doi.org/10.1083/jcb.201409047openalex-snapshot
Accessorizing and anchoring the LINC complex for multifunctionality
inferredcites →https://doi.org/10.1083/jcb.40.1.286openalex-snapshot
INTRANUCLEAR FIBRILLAR BODIES IN ACTINOMYCIN D-TREATED OOCYTES
inferredcites →https://doi.org/10.1084/jem.20140169openalex-snapshot
WASH is required for the differentiation commitment of hematopoietic stem cells in a c-Myc–dependent manner
inferredcites →https://doi.org/10.1091/mbc.e09-02-0114openalex-snapshot
Induction of HoxB Transcription by Retinoic Acid Requires Actin Polymerization
inferredcites →https://doi.org/10.1091/mbc.e09-06-0534openalex-snapshot
Nuclear Translocation of β-Actin Is Involved in Transcriptional Regulation during Macrophage Differentiation of HL-60 Cells
inferredcites →https://doi.org/10.1091/mbc.e12-09-0685openalex-snapshot
Visualization of actin filaments and monomers in somatic cell nuclei
inferredcites →https://doi.org/10.1093/brain/awm247openalex-snapshot
Mechanisms underlying intranuclear rod formation
inferredcites →https://doi.org/10.1093/emboj/cdg565openalex-snapshot
Exportin 6: a novel nuclear export receptor that is specific for profilin·actin complexes
inferredcites →https://doi.org/10.1093/nar/30.8.1725openalex-snapshot
Nuclear actin is associated with a specific subset of hnRNP A/B-type proteins
inferredcites →https://doi.org/10.1101/cshperspect.a000562openalex-snapshot
The Nuclear Pore Complex and Nuclear Transport
inferredcites →https://doi.org/10.1101/gad.1250804openalex-snapshot
A role for β-actin in RNA polymerase III transcription
inferredcites →https://doi.org/10.1101/gad.455908openalex-snapshot
Nuclear myosin I acts in concert with polymeric actin to drive RNA polymerase I transcription
inferredcites →https://doi.org/10.1101/gad.615211openalex-snapshot
Nuclear actin polymerization is required for transcriptional reprogramming of Oct4 by oocytes
inferredcites →https://doi.org/10.1126/science.1090701openalex-snapshot
ATP-Driven Exchange of Histone H2AZ Variant Catalyzed by SWR1 Chromatin Remodeling Complex
inferredcites →https://doi.org/10.1126/science.1141084openalex-snapshot
Nuclear Actin Regulates Dynamic Subcellular Localization and Activity of the SRF Cofactor MAL
inferredcites →https://doi.org/10.1126/science.1175862openalex-snapshot
Actin, a Central Player in Cell Shape and Movement
inferredcites →https://doi.org/10.1126/science.1235038openalex-snapshot
Nuclear Actin Network Assembly by Formins Regulates the SRF Coactivator MAL
inferredcites →https://doi.org/10.1126/science.1240376openalex-snapshot
Nuclear Wave1 Is Required for Reprogramming Transcription in Oocytes and for Normal Development
inferredcites →https://doi.org/10.1126/scisignal.2001750openalex-snapshot
Structure of a Pentavalent G-Actin•MRTF-A Complex Reveals How G-Actin Controls Nucleocytoplasmic Shuttling of a Transcriptional Coactivator
inferredcites →https://doi.org/10.1128/jb.108.2.705-714.1971openalex-snapshot
Synthesis and Some Properties of an Actin-Like Nuclear Protein in the Slime Mold Physarum polycephalum
inferredcites →https://doi.org/10.1128/mcb.00766-08openalex-snapshot
The Histone Acetyltransferase PCAF Associates with Actin and hnRNP U for RNA Polymerase II Transcription
inferredcites →https://doi.org/10.1128/mcb.01623-07openalex-snapshot
RPEL Motifs Link the Serum Response Factor Cofactor MAL but Not Myocardin to Rho Signaling via Actin Binding
inferredcites →https://doi.org/10.1152/physrev.00005.2014openalex-snapshot
The Biology of YAP/TAZ: Hippo Signaling and Beyond
inferredcites →https://doi.org/10.1158/0008-5472.can-03-1856openalex-snapshot
Nuclear Accumulation of Globular Actin as a Cellular Senescence Marker
inferredcites →https://doi.org/10.1186/gb-2010-11-1-r5openalex-snapshot
Rapid chromosome territory relocation by nuclear motor activity in response to serum removal in primary human fibroblasts
inferredcites →https://doi.org/10.1186/s12915-015-0147-zopenalex-snapshot
Nuclear myosin 1 contributes to a chromatin landscape compatible with RNA polymerase II transcription activation
inferredcites →https://doi.org/10.1242/jcs.01404openalex-snapshot
Nuclear localisation of the G-actin sequestering peptide thymosin β4
inferredcites →https://doi.org/10.1242/jcs.01410openalex-snapshot
Increased importin-β-dependent nuclear import of the actin modulating protein CapG promotes cell invasion
inferredcites →https://doi.org/10.1242/jcs.073197openalex-snapshot
Depletion of nuclear actin is a key mediator of quiescence in epithelial cells
inferredcites →https://doi.org/10.1242/jcs.104349openalex-snapshot
Heterocomplex Formation by Arp4 and β-Actin Involved in Integrity of the Brg1 Chromatin Remodeling Complex
inferredcites →https://doi.org/10.1242/jcs.169441openalex-snapshot
Genome-wide RNAi screen for nuclear actin reveals a network of cofilin regulators
inferredcites →https://doi.org/10.1371/journal.pbio.0020231openalex-snapshot
Emerin Caps the Pointed End of Actin Filaments: Evidence for an Actin Cortical Network at the Nuclear Inner Membrane
inferredcites →https://doi.org/10.1371/journal.pgen.1003397openalex-snapshot
Nuclear Myosin 1c Facilitates the Chromatin Modifications Required to Activate rRNA Gene Transcription and Cell Cycle Progression
inferredcites →https://doi.org/10.1371/journal.pgen.1004390openalex-snapshot
Glycogen Synthase Kinase (GSK) 3β Phosphorylates and Protects Nuclear Myosin 1c from Proteasome-Mediated Degradation to Activate rDNA Transcription in Early G1 Cells
inferredcites →https://doi.org/10.4161/nucl.1.3.11799openalex-snapshot
Direct actin binding to A- and B-type lamin tails and actin filament bundling by the lamin A tail
inferredcites →https://doi.org/10.4161/nucl.14508openalex-snapshot
The F-actin severing protein cofilin-1 is required for RNA polymerase II transcription elongation
inferredcites →https://doi.org/10.4161/nucl.2.1.14510openalex-snapshot
Actin-related proteins localized in the nucleus: from discovery to novel roles in nuclear organization
inferredcites →https://doi.org/10.4161/nucl.25751openalex-snapshot
The nuclear envelope LEM-domain protein emerin
inferredcites →https://doi.org/10.4161/sgtp.27539openalex-snapshot
Rho, nuclear actin, and actin-binding proteins in the regulation of transcription and gene expression
inferredcites →https://doi.org/10.7554/elife.07735openalex-snapshot
DNA damage induces nuclear actin filament assembly by Formin-2 and Spire-1/2 that promotes efficient DNA repair
inferredcites →https://doi.org/10.7554/elife.11935openalex-snapshot
Correction: DNA damage induces nuclear actin filament assembly by Formin-2 and Spire-1/2 that promotes efficient DNA repair
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/1873-3468.13173openalex-snapshot
Actin dynamics in host–pathogen interaction
inferred← citeshttps://doi.org/10.1002/ar.23958openalex-snapshot
Posttranscriptional and Posttranslational Regulation of Actin
inferred← citeshttps://doi.org/10.1002/ar.23959openalex-snapshot
Nuclear Actin: From Discovery to Function
inferred← citeshttps://doi.org/10.1002/glia.23735openalex-snapshot
The oligodendrocyte growth cone and its actin cytoskeleton: A fundamental element for progenitor cell migration and CNS myelination
inferred← citeshttps://doi.org/10.1007/164_2016_43openalex-snapshot
Mammalian Actins: Isoform-Specific Functions and Diseases
inferred← citeshttps://doi.org/10.1007/s00418-018-1693-6openalex-snapshot
Nuclear actin: ancient clue to evolution in eukaryotes?
inferred← citeshttps://doi.org/10.1007/s10974-019-09515-zopenalex-snapshot
The discovery of actin: “to see what everyone else has seen, and to think what nobody has thought”*
inferred← citeshttps://doi.org/10.1007/s13402-018-00419-7openalex-snapshot
Nuclear localization of PD-L1: artifact or reality?
inferred← citeshttps://doi.org/10.1016/j.acthis.2017.10.008openalex-snapshot
Stemness distinctions between the ectomesenchymal stem cells from neonatal and adult mice
inferred← citeshttps://doi.org/10.1016/j.bbamem.2020.183278openalex-snapshot
Relationship between apical junction proteins, gene expression and cancer
inferred← citeshttps://doi.org/10.1016/j.bbapap.2026.141139openalex-snapshot
Structural and biophysical features of α- and β-actin isoforms in native and inactivated states
inferred← citeshttps://doi.org/10.1016/j.ceb.2020.01.012openalex-snapshot
Regulation of nuclear actin dynamics in development and disease
inferred← citeshttps://doi.org/10.1016/j.cophys.2019.10.018openalex-snapshot
Molecular studies on pregnancy with mouse models
inferred← citeshttps://doi.org/10.1016/j.gene.2021.146129openalex-snapshot
Molecular mechanism responsible for the hyperexpression of baculovirus polyhedrin
inferred← citeshttps://doi.org/10.1016/j.isci.2023.107707openalex-snapshot
Seizure enhances SUMOylation and zinc-finger transcriptional repression in neuronal nuclei
inferred← citeshttps://doi.org/10.1016/j.jbc.2025.111123openalex-snapshot
A revised model of nuclear actin import: Importin 9 competes with cofilin, profilin, and RanGTP for actin binding
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.133819openalex-snapshot
Exposure to virgin and marine incubated microparticles of biodegradable and conventional polymers modulates the hepatopancreas transcriptome of Mytilus galloprovincialis
inferred← citeshttps://doi.org/10.1016/j.jplph.2018.11.002openalex-snapshot
A roadmap towards a functional paradigm for learning & memory in plants
inferred← citeshttps://doi.org/10.1016/j.plrev.2024.03.011openalex-snapshot
Perception and response of skeleton to mechanical stress
inferred← citeshttps://doi.org/10.1016/j.semcdb.2019.12.003openalex-snapshot
Regulation of actin isoforms in cellular and developmental processes
inferred← citeshttps://doi.org/10.1016/j.tcb.2019.02.010openalex-snapshot
Nuclear Actin and Actin-Binding Proteins in DNA Repair
inferred← citeshttps://doi.org/10.1038/s41419-023-05985-9openalex-snapshot
JUN-induced super-enhancer RNA forms R-loop to promote nasopharyngeal carcinoma metastasis
inferred← citeshttps://doi.org/10.1038/s41467-018-06713-0openalex-snapshot
Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia
inferred← citeshttps://doi.org/10.1042/bsr20181312openalex-snapshot
AKT/protein kinase B associates with β-actin in the nucleus of melanoma cells
inferred← citeshttps://doi.org/10.1080/17425255.2018.1487397openalex-snapshot
Regulation of cytochrome P450 gene expression by ketamine: a review
inferred← citeshttps://doi.org/10.1091/mbc.e15-09-0634openalex-snapshot
Fascin regulates nuclear actin duringDrosophilaoogenesis
inferred← citeshttps://doi.org/10.1101/641266openalex-snapshot
Human cytomegalovirus nuclear capsid motility is non-directed and independent of nuclear actin bundles
inferred← citeshttps://doi.org/10.1111/ijlh.14011openalex-snapshot
The identification of giant platelets with disorganized granules can suggest ACTB gene mutation
inferred← citeshttps://doi.org/10.1134/s1990519x18010029openalex-snapshot
pH Change in Culture Medium Induces Reorganization of Intranuclear Actin in Two-Cell Mouse Embryos
inferred← citeshttps://doi.org/10.1134/s1990519x19010036openalex-snapshot
Intranuclear Actin Distribution at the Four- and Eight-Cell Stages of Mouse Embryo Development
inferred← citeshttps://doi.org/10.1242/jcs.215509openalex-snapshot
The makings of the ‘actin code': regulation of actin's biological function at the amino acid and nucleotide level
inferred← citeshttps://doi.org/10.1242/jcs.226852openalex-snapshot
Nuclear actin interactome analysis links actin to KAT14 histone acetyl transferase and mRNA splicing
inferred← citeshttps://doi.org/10.1261/rna.079615.123openalex-snapshot
The importance of m 6 A topology in chicken embryo mRNA: a precise mapping of m 6 A at the conserved chicken β-actin zipcode
inferred← citeshttps://doi.org/10.1515/bmc-2016-0022openalex-snapshot
Matrix metalloproteinases: an emerging role in regulation of actin microfilament system
inferred← citeshttps://doi.org/10.1681/asn.2018111160openalex-snapshot
The Extracellular Matrix Receptor Discoidin Domain Receptor 1 Regulates Collagen Transcription by Translocating to the Nucleus
inferred← citeshttps://doi.org/10.2139/ssrn.5414175openalex-snapshot
Spectral properties of rabbit muscle α-actin and recombinant β-actin
inferred← citeshttps://doi.org/10.26508/lsa.202201484openalex-snapshot
The conserved Pelado/ZSWIM8 protein regulates actin dynamics by promoting linear actin filament polymerization
inferred← citeshttps://doi.org/10.3389/fcell.2020.588836openalex-snapshot
Loss of β-Cytoplasmic Actin in the Intestinal Epithelium Increases Gut Barrier Permeability in vivo and Exaggerates the Severity of Experimental Colitis
inferred← citeshttps://doi.org/10.3390/cancers13133197openalex-snapshot
Imaging Mass Spectrometry-Based Proteomic Analysis to Differentiate Melanocytic Nevi and Malignant Melanoma
inferred← citeshttps://doi.org/10.3390/ijtm1010002openalex-snapshot
Development of Multilayer Mesenchymal Stem Cell Cell Sheets
inferred← citeshttps://doi.org/10.7868/s0041377118090096openalex-snapshot
ВНУТРИЯДЕРНОЕ РАСПРЕДЕЛЕНИЕ АКТИНА НА ЧЕТЫРЕХКЛЕТОЧНОЙ И ВОСЬМИКЛЕТОЧНОЙ СТАДИЯХ РАЗВИТИЯ ЗАРОДЫШЕЙ МЫШИ, "Цитология"
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