The maximal size of protein to diffuse through the nuclear pore is larger than 60kDa
about
Control of Protein Activity and Cell Fate Specification via Light-Mediated Nuclear TranslocationOptogenetic control of nuclear protein export.The membrane-active tri-block copolymer pluronic F-68 profoundly rescues rat hippocampal neurons from oxygen-glucose deprivation-induced death through early inhibition of apoptosisProbing formation of cargo/importin-α transport complexes in plant cells using a pathogen effectorPermeabilization activated reduction in fluorescence: A novel method to measure kinetics of protein interactions with intracellular structures.Nuclear import and dimerization of tomato ASR1, a water stress-inducible protein exclusive to plantsEnhanced core hydrophobicity, functionalization and cell penetration of polybasic nanomatrices.DNA polymerase β contains a functional nuclear localization signal at its N-terminus.Normal telomere length maintenance in Saccharomyces cerevisiae requires nuclear import of the ever shorter telomeres 1 (Est1) protein via the importin alpha pathway.Physical interaction between VIVID and white collar complex regulates photoadaptation in Neurospora.Protein-responsive ribozyme switches in eukaryotic cells.Drosophila Naked cuticle (Nkd) engages the nuclear import adaptor Importin-alpha3 to antagonize Wnt/beta-catenin signaling.Nuclear envelope disruption involving host caspases plays a role in the parvovirus replication cycle.Differential stimulation of monocytic cells results in distinct populations of microparticlesAdaptation of the Agrobacterium tumefaciens VirG response regulator to activate transcription in plants.The HEX 110 Hexamerin Is a Cytoplasmic and Nucleolar Protein in the Ovaries of Apis mellifera.Karyopherin α 3 and karyopherin α 4 proteins mediate the nuclear import of methyl-CpG binding protein 2A Cytolethal Distending Toxin Variant from Aggregatibacter actinomycetemcomitans with an Aberrant CdtB That Lacks the Conserved Catalytic Histidine 160.The Nuclear Proteome of a Vertebrate.MD simulations and FRET reveal an environment-sensitive conformational plasticity of importin-βKaryopherin Alpha Proteins Regulate Oligodendrocyte Differentiation.TDP-43 and FUS en route from the nucleus to the cytoplasm.Understanding renal nuclear protein accumulation: an in vitro approach to explain an in vivo phenomenon.Definitive localization of intracellular proteins: Novel approach using CRISPR-Cas9 genome editing, with glucose 6-phosphate dehydrogenase as a modelRegulation of hepatitis C virus replication by nuclear translocation of nonstructural 5A protein and transcriptional activation of host genes.Neutralization of Bacterial YoeBSpn Toxicity and Enhanced Plant Growth in Arabidopsis thaliana via Co-Expression of the Toxin-Antitoxin Genes.Towards reconciling structure and function in the nuclear pore complex.Identification of the nuclear export and adjacent nuclear localization signals for ORF45 of Kaposi's sarcoma-associated herpesvirusSimple rules for passive diffusion through the nuclear pore complex.Epigenetics of amphetamine-induced sensitization: HDAC5 expression and microRNA in neural remodelingCD74 is a novel transcription regulator.Mapping of functional domains of the lipid kinase phosphatidylinositol 4-kinase type III alpha involved in enzymatic activity and hepatitis C virus replication.Influence of Structural Features on the Cellular Uptake Behavior of Non-Targeted Polyester-Based Nanocarriers.Varicella zoster virus ORF25 gene product: an essential hub protein linking encapsidation proteins and the nuclear egress complex.B30.2/SPRY domain in tripartite motif-containing 22 is essential for the formation of distinct nuclear bodies.The dynamics and mechanisms of interleukin-1alpha and beta nuclear import.Identification of PIWIL1 Isoforms and Their Expression in Bovine Testes, Oocytes, and Early Embryos.Venezuelan equine encephalitis virus capsid protein inhibits nuclear import in Mammalian but not in mosquito cellsSynergy of two low-affinity NLSs determines the high avidity of influenza A virus nucleoprotein NP for human importin α isoforms.Crystal structure of the Melampsora lini effector AvrP reveals insights into a possible nuclear function and recognition by the flax disease resistance protein P.
P2860
Q27305280-C8A795E3-7B02-411D-B045-20640C0B5D2DQ27333329-764B87BC-FAA9-4571-8C77-EF112BEF321BQ28386144-DCD62211-47F0-4853-9B75-9FE0666F5F99Q29307549-9B160187-7587-4733-B55E-BE86991139A2Q30829990-3D94425C-7F37-4B29-ABBA-0CD04873859EQ31085818-05A3BADC-4190-4005-A723-1401101C460AQ33364166-3C29D11F-54E3-4A87-904C-7D3C7EFD16FBQ33557353-00735384-4313-4D68-941D-D588B99E0B50Q34057250-1F0BBCA8-FCD7-461A-AB17-9477ABC4507EQ34151948-21CAE7C7-E83A-490B-954D-02B9FE71553FQ34510072-968C2F9E-EAC0-4FD5-B096-F1E1AC135C91Q34771575-4F27D25E-DD3C-4006-B62B-18B65B0040BCQ35076773-9774D3E0-EC35-4A00-B821-497C7E028C9FQ35622927-E3E4791D-A92A-409E-816C-F0815B592397Q35863378-7D565317-4389-4CEA-9DBD-E1D515582D1FQ35949229-A64E773A-F0A9-42A7-82FF-CD2B41A66DE4Q36049921-85D17074-A7D4-4E4B-BA33-966444FCDB12Q36077181-475785BC-7954-41C1-8C74-283F777FB64BQ36200347-83F7AC13-80FB-425E-A52D-73BF5A4DF2DDQ36209867-692D3246-74C9-4856-AA6C-3F3777AA07BCQ36255930-4788294C-AECA-4CB0-B856-48F598F71762Q36336278-1C598805-C777-46C8-A18E-FF89464579E0Q36357444-B4C24C2C-54EE-4957-AAB4-6039333EA206Q36414673-13D09397-CE84-4985-B44E-BB4971AD6FD2Q36827433-F23604D2-D244-4216-BB56-B9B0F15CEB8EQ36846816-A804B9C8-29E8-49E2-A4C5-425904418D91Q37070304-727B40C6-395E-4F2D-B8B3-D659D34112D4Q37110705-137B18D0-0D7C-4AE0-9BE7-C16E8B773B3FQ37325778-089080AA-109E-44A5-86F8-4C64D6A40AEAQ37487886-9031539D-990A-4CFF-92CF-F0A77E37CB8EQ37599054-862FD812-35F7-41C5-9DEA-113682DD4724Q38985647-D72EA0E7-0576-45AD-A637-CD2E79C01D16Q39558434-72ED4E12-3350-44FB-A09A-D021950C2876Q39603845-E3D6A0FC-56A7-495D-B97A-BDA8B73B66FEQ39845286-D6E91AE1-8926-42CE-944E-45FACD5AE939Q39927034-67B69C86-2AA5-4618-925A-E316E9C834ECQ39971766-DAC961C0-ED57-45C8-90CA-147394AF0BCFQ40015798-3D82D9F8-E25A-43E3-BA1A-4AC6816AFBECQ40044584-8D0171B7-4C1E-44AA-92AE-147919EFCD60Q40090010-07AB6289-12B4-4A84-9672-CBD293D6FBB5
P2860
The maximal size of protein to diffuse through the nuclear pore is larger than 60kDa
description
2007 nî lūn-bûn
@nan
2007 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
The maximal size of protein to diffuse through the nuclear pore is larger than 60kDa
@ast
The maximal size of protein to diffuse through the nuclear pore is larger than 60kDa
@en
type
label
The maximal size of protein to diffuse through the nuclear pore is larger than 60kDa
@ast
The maximal size of protein to diffuse through the nuclear pore is larger than 60kDa
@en
prefLabel
The maximal size of protein to diffuse through the nuclear pore is larger than 60kDa
@ast
The maximal size of protein to diffuse through the nuclear pore is larger than 60kDa
@en
P2860
P1433
P1476
The maximal size of protein to diffuse through the nuclear pore is larger than 60kDa
@en
P2093
Michael G Brattain
Ruiwen Wang
P2860
P304
P356
10.1016/J.FEBSLET.2007.05.082
P407
P577
2007-06-12T00:00:00Z