Talin variant P229S compromises integrin activation and associates with multifaceted clinical symptoms.
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| Title: | Talin variant P229S compromises integrin activation and associates with multifaceted clinical symptoms. |
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| Authors: | Azizi L; Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland., Varela L; School of Biosciences, University of Kent, Canterbury CT2 7NJ, UK., Turkki P; Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.; Fimlab Laboratories, Tampere, Finland., Mykuliak VV; Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland., Korpela S; Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland., Ihalainen TO; Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland., Church J; Clinical Immunology and Allergy, Children's Hospital Los Angeles, Los Angeles, CA, USA., Hytönen VP; Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.; Fimlab Laboratories, Tampere, Finland., Goult BT; School of Biosciences, University of Kent, Canterbury CT2 7NJ, UK. |
| Source: | Human molecular genetics [Hum Mol Genet] 2022 Dec 16; Vol. 31 (24), pp. 4159-4172. |
| 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 Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 35861643 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Talin variant P229S compromises integrin activation and associates with multifaceted clinical symptoms. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Azizi+L%22">Azizi L</searchLink>; Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.<br /><searchLink fieldCode="AU" term="%22Varela+L%22">Varela L</searchLink>; School of Biosciences, University of Kent, Canterbury CT2 7NJ, UK.<br /><searchLink fieldCode="AU" term="%22Turkki+P%22">Turkki P</searchLink>; Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.; Fimlab Laboratories, Tampere, Finland.<br /><searchLink fieldCode="AU" term="%22Mykuliak+VV%22">Mykuliak VV</searchLink>; Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.<br /><searchLink fieldCode="AU" term="%22Korpela+S%22">Korpela S</searchLink>; Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.<br /><searchLink fieldCode="AU" term="%22Ihalainen+TO%22">Ihalainen TO</searchLink>; Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.<br /><searchLink fieldCode="AU" term="%22Church+J%22">Church J</searchLink>; Clinical Immunology and Allergy, Children's Hospital Los Angeles, Los Angeles, CA, USA.<br /><searchLink fieldCode="AU" term="%22Hytönen+VP%22">Hytönen VP</searchLink>; Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.; Fimlab Laboratories, Tampere, Finland.<br /><searchLink fieldCode="AU" term="%22Goult+BT%22">Goult BT</searchLink>; School of Biosciences, University of Kent, Canterbury CT2 7NJ, UK. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2022 Dec 16; Vol. 31 (24), pp. 4159-4172. – 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 <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=35861643 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1093/hmg/ddac163 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 4159 Titles: – TitleFull: Talin variant P229S compromises integrin activation and associates with multifaceted clinical symptoms. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Azizi L – PersonEntity: Name: NameFull: Varela L – PersonEntity: Name: NameFull: Turkki P – PersonEntity: Name: NameFull: Mykuliak VV – PersonEntity: Name: NameFull: Korpela S – PersonEntity: Name: NameFull: Ihalainen TO – PersonEntity: Name: NameFull: Church J – PersonEntity: Name: NameFull: Hytönen VP – PersonEntity: Name: NameFull: Goult BT IsPartOfRelationships: – BibEntity: Dates: – D: 16 M: 12 Text: 2022 Dec 16 Type: published Y: 2022 Identifiers: – Type: issn-electronic Value: 1460-2083 Numbering: – Type: volume Value: 31 – Type: issue Value: 24 Titles: – TitleFull: Human molecular genetics Type: main |
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