View in EDS PDF Full Text

Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus.

Saved in:
Bibliographic Details
Title: Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus.
Authors: Roberts NA; Centre for Genomic Medicine and Centre for Paediatrics and Child Health, Institute of Human Development, Faculty of Medical and Human Sciences., Woolf AS; Centre for Paediatrics and Child Health, Institute of Human Development, Faculty of Medical and Human Sciences., Stuart HM; Centre for Genomic Medicine and., Thuret R; Developmental Biology and., McKenzie EA; Protein Expression Facility, Faculty of Life Sciences, University of Manchester, Manchester M13 9PT, UK., Newman WG; Centre for Genomic Medicine and., Hilton EN; Centre for Genomic Medicine and Centre for Paediatrics and Child Health, Institute of Human Development, Faculty of Medical and Human Sciences, emma.hilton@manchester.ac.uk.
Source: Human molecular genetics [Hum Mol Genet] 2014 Aug 15; Vol. 23 (16), pp. 4302-14. Date of Electronic Publication: 2014 Apr 01.
Publication Type: Journal Article; 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-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
FullText Links:
  – Type: pdflink
Text:
  Availability: 0
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 24691552
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Roberts+NA%22">Roberts NA</searchLink>; Centre for Genomic Medicine and Centre for Paediatrics and Child Health, Institute of Human Development, Faculty of Medical and Human Sciences.<br /><searchLink fieldCode="AU" term="%22Woolf+AS%22">Woolf AS</searchLink>; Centre for Paediatrics and Child Health, Institute of Human Development, Faculty of Medical and Human Sciences.<br /><searchLink fieldCode="AU" term="%22Stuart+HM%22">Stuart HM</searchLink>; Centre for Genomic Medicine and.<br /><searchLink fieldCode="AU" term="%22Thuret+R%22">Thuret R</searchLink>; Developmental Biology and.<br /><searchLink fieldCode="AU" term="%22McKenzie+EA%22">McKenzie EA</searchLink>; Protein Expression Facility, Faculty of Life Sciences, University of Manchester, Manchester M13 9PT, UK.<br /><searchLink fieldCode="AU" term="%22Newman+WG%22">Newman WG</searchLink>; Centre for Genomic Medicine and.<br /><searchLink fieldCode="AU" term="%22Hilton+EN%22">Hilton EN</searchLink>; Centre for Genomic Medicine and Centre for Paediatrics and Child Health, Institute of Human Development, Faculty of Medical and Human Sciences, emma.hilton@manchester.ac.uk.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2014 Aug 15; Vol. 23 (16), pp. 4302-14. <i>Date of Electronic Publication: </i>2014 Apr 01.
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Journal Article; 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-Electronic <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=24691552
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1093/hmg/ddu147
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 4302
    Titles:
      – TitleFull: Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Roberts NA
      – PersonEntity:
          Name:
            NameFull: Woolf AS
      – PersonEntity:
          Name:
            NameFull: Stuart HM
      – PersonEntity:
          Name:
            NameFull: Thuret R
      – PersonEntity:
          Name:
            NameFull: McKenzie EA
      – PersonEntity:
          Name:
            NameFull: Newman WG
      – PersonEntity:
          Name:
            NameFull: Hilton EN
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 15
              M: 08
              Text: 2014 Aug 15
              Type: published
              Y: 2014
          Identifiers:
            – Type: issn-electronic
              Value: 1460-2083
          Numbering:
            – Type: volume
              Value: 23
            – Type: issue
              Value: 16
          Titles:
            – TitleFull: Human molecular genetics
              Type: main
ResultId 1