View in EDS HTML Full Text PDF Full Text

TorsinA dysfunction causes persistent neuronal nuclear pore defects.

Saved in:
Bibliographic Details
Title: TorsinA dysfunction causes persistent neuronal nuclear pore defects.
Authors: Pappas SS; Department of Neurology., Liang CC; Department of Neurology., Kim S; Cellular and Molecular Biology Program., Rivera CO; Department of Neurology., Dauer WT; Department of Neurology.; Cellular and Molecular Biology Program.; Department of Cell and Developmental Biology.; VA Ann Arbor Health System, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Source: Human molecular genetics [Hum Mol Genet] 2018 Feb 01; Vol. 27 (3), pp. 407-420.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 29186574
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: TorsinA dysfunction causes persistent neuronal nuclear pore defects.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Pappas+SS%22">Pappas SS</searchLink>; Department of Neurology.<br /><searchLink fieldCode="AU" term="%22Liang+CC%22">Liang CC</searchLink>; Department of Neurology.<br /><searchLink fieldCode="AU" term="%22Kim+S%22">Kim S</searchLink>; Cellular and Molecular Biology Program.<br /><searchLink fieldCode="AU" term="%22Rivera+CO%22">Rivera CO</searchLink>; Department of Neurology.<br /><searchLink fieldCode="AU" term="%22Dauer+WT%22">Dauer WT</searchLink>; Department of Neurology.; Cellular and Molecular Biology Program.; Department of Cell and Developmental Biology.; VA Ann Arbor Health System, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2018 Feb 01; Vol. 27 (3), pp. 407-420.
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
– Name: TitleSource
  Label: Journal Info
  Group: Src
  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22IRL+Press+at+Oxford+University+Press%22">IRL Press at Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9208958 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1460-2083 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209646906%22">09646906 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mol Genet <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=29186574
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1093/hmg/ddx405
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 407
    Titles:
      – TitleFull: TorsinA dysfunction causes persistent neuronal nuclear pore defects.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Pappas SS
      – PersonEntity:
          Name:
            NameFull: Liang CC
      – PersonEntity:
          Name:
            NameFull: Kim S
      – PersonEntity:
          Name:
            NameFull: Rivera CO
      – PersonEntity:
          Name:
            NameFull: Dauer WT
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 02
              Text: 2018 Feb 01
              Type: published
              Y: 2018
          Identifiers:
            – Type: issn-electronic
              Value: 1460-2083
          Numbering:
            – Type: volume
              Value: 27
            – Type: issue
              Value: 3
          Titles:
            – TitleFull: Human molecular genetics
              Type: main
ResultId 1