Monoallelic loss-of-function THPO variants cause heritable thrombocytopenia.
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| Title: | Monoallelic loss-of-function THPO variants cause heritable thrombocytopenia. |
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| Authors: | Cornish N; Bristol Medical School., Aungraheeta MR; School of Cellular and Molecular Medicine, and., FitzGibbon L; School of Cellular and Molecular Medicine, and., Burley K; School of Cellular and Molecular Medicine, and., Alibhai D; Wolfson Bioimaging Facility, Faculty of Life Sciences, University of Bristol, Bristol, United Kingdom., Collins J; Department of Haematology, University of Cambridge, Cambridge, United Kingdom., Greene D; Department of Haematology, University of Cambridge, Cambridge, United Kingdom.; Medical Research Council Biostatistics Unit, Cambridge Institute of Public Health, Cambridge, United Kingdom.; NIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge, United Kingdom; and., Downes K; Department of Haematology, University of Cambridge, Cambridge, United Kingdom.; NIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge, United Kingdom; and., Westbury SK; School of Cellular and Molecular Medicine, and., Turro E; Department of Haematology, University of Cambridge, Cambridge, United Kingdom.; Medical Research Council Biostatistics Unit, Cambridge Institute of Public Health, Cambridge, United Kingdom.; NIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge, United Kingdom; and.; NHS Blood and Transplant, Cambridge Biomedical Campus, Cambridge, United Kingdom., Mumford AD; School of Cellular and Molecular Medicine, and. |
| Corporate Authors: | NIHR BioResource |
| Source: | Blood advances [Blood Adv] 2020 Mar 10; Vol. 4 (5), pp. 920-924. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: American Society of Hematology Country of Publication: United States NLM ID: 101698425 Publication Model: Print Cited Medium: Internet ISSN: 2473-9537 (Electronic) Linking ISSN: 24739529 NLM ISO Abbreviation: Blood Adv Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 32150607 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Monoallelic loss-of-function THPO variants cause heritable thrombocytopenia. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Cornish+N%22">Cornish N</searchLink>; Bristol Medical School.<br /><searchLink fieldCode="AU" term="%22Aungraheeta+MR%22">Aungraheeta MR</searchLink>; School of Cellular and Molecular Medicine, and.<br /><searchLink fieldCode="AU" term="%22FitzGibbon+L%22">FitzGibbon L</searchLink>; School of Cellular and Molecular Medicine, and.<br /><searchLink fieldCode="AU" term="%22Burley+K%22">Burley K</searchLink>; School of Cellular and Molecular Medicine, and.<br /><searchLink fieldCode="AU" term="%22Alibhai+D%22">Alibhai D</searchLink>; Wolfson Bioimaging Facility, Faculty of Life Sciences, University of Bristol, Bristol, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Collins+J%22">Collins J</searchLink>; Department of Haematology, University of Cambridge, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Greene+D%22">Greene D</searchLink>; Department of Haematology, University of Cambridge, Cambridge, United Kingdom.; Medical Research Council Biostatistics Unit, Cambridge Institute of Public Health, Cambridge, United Kingdom.; NIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge, United Kingdom; and.<br /><searchLink fieldCode="AU" term="%22Downes+K%22">Downes K</searchLink>; Department of Haematology, University of Cambridge, Cambridge, United Kingdom.; NIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge, United Kingdom; and.<br /><searchLink fieldCode="AU" term="%22Westbury+SK%22">Westbury SK</searchLink>; School of Cellular and Molecular Medicine, and.<br /><searchLink fieldCode="AU" term="%22Turro+E%22">Turro E</searchLink>; Department of Haematology, University of Cambridge, Cambridge, United Kingdom.; Medical Research Council Biostatistics Unit, Cambridge Institute of Public Health, Cambridge, United Kingdom.; NIHR BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge, United Kingdom; and.; NHS Blood and Transplant, Cambridge Biomedical Campus, Cambridge, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Mumford+AD%22">Mumford AD</searchLink>; School of Cellular and Molecular Medicine, and. – Name: AuthorCorporate Label: Corporate Authors Group: Au Data: <searchLink fieldCode="CA" term="%22NIHR+BioResource%22">NIHR BioResource</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101698425%22">Blood advances</searchLink> [Blood Adv] 2020 Mar 10; Vol. 4 (5), pp. 920-924. – 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="%22American+Society+of+Hematology%22">American Society of Hematology </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101698425 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>2473-9537 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2224739529%22">24739529 </searchLink><i>NLM ISO Abbreviation: </i>Blood Adv <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=32150607 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1182/bloodadvances.2019001293 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 920 Titles: – TitleFull: Monoallelic loss-of-function THPO variants cause heritable thrombocytopenia. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Cornish N – PersonEntity: Name: NameFull: Aungraheeta MR – PersonEntity: Name: NameFull: FitzGibbon L – PersonEntity: Name: NameFull: Burley K – PersonEntity: Name: NameFull: Alibhai D – PersonEntity: Name: NameFull: Collins J – PersonEntity: Name: NameFull: Greene D – PersonEntity: Name: NameFull: Downes K – PersonEntity: Name: NameFull: Westbury SK – PersonEntity: Name: NameFull: Turro E – PersonEntity: Name: NameFull: Mumford AD IsPartOfRelationships: – BibEntity: Dates: – D: 10 M: 03 Text: 2020 Mar 10 Type: published Y: 2020 Identifiers: – Type: issn-electronic Value: 2473-9537 Numbering: – Type: volume Value: 4 – Type: issue Value: 5 Titles: – TitleFull: Blood advances Type: main |
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