Solvent accessibility of E1α and E1β residues with known missense mutations causing pyruvate dehydrogenase complex (PDC) deficiency: Impact on PDC-E1 structure and function.
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| Title: | Solvent accessibility of E1α and E1β residues with known missense mutations causing pyruvate dehydrogenase complex (PDC) deficiency: Impact on PDC-E1 structure and function. |
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| Authors: | Ducich NH; Case Western Reserve University (CWRU) School of Medicine, Cleveland, Ohio, USA., Mears JA; Department of Pharmacology, CWRU, Cleveland, Ohio, USA.; Center for Mitochondrial Diseases, CWRU, Cleveland, Ohio, USA., Bedoyan JK; Division of Genetic and Genomic Medicine, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.; Department of Pediatrics, University of Pittsburgh, Pittsburgh, Pennsylvania, USA. |
| Source: | Journal of inherited metabolic disease [J Inherit Metab Dis] 2022 May; Vol. 45 (3), pp. 557-570. Date of Electronic Publication: 2022 Feb 01. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Wiley Country of Publication: United States NLM ID: 7910918 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-2665 (Electronic) Linking ISSN: 01418955 NLM ISO Abbreviation: J Inherit Metab Dis Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 35038180 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Solvent accessibility of E1α and E1β residues with known missense mutations causing pyruvate dehydrogenase complex (PDC) deficiency: Impact on PDC-E1 structure and function. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Ducich+NH%22">Ducich NH</searchLink>; Case Western Reserve University (CWRU) School of Medicine, Cleveland, Ohio, USA.<br /><searchLink fieldCode="AU" term="%22Mears+JA%22">Mears JA</searchLink>; Department of Pharmacology, CWRU, Cleveland, Ohio, USA.; Center for Mitochondrial Diseases, CWRU, Cleveland, Ohio, USA.<br /><searchLink fieldCode="AU" term="%22Bedoyan+JK%22">Bedoyan JK</searchLink>; Division of Genetic and Genomic Medicine, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.; Department of Pediatrics, University of Pittsburgh, Pittsburgh, Pennsylvania, USA. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%227910918%22">Journal of inherited metabolic disease</searchLink> [J Inherit Metab Dis] 2022 May; Vol. 45 (3), pp. 557-570. <i>Date of Electronic Publication: </i>2022 Feb 01. – 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="%22Wiley%22">Wiley </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>7910918 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1573-2665 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2201418955%22">01418955 </searchLink><i>NLM ISO Abbreviation: </i>J Inherit Metab Dis <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=35038180 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/jimd.12477 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 557 Titles: – TitleFull: Solvent accessibility of E1α and E1β residues with known missense mutations causing pyruvate dehydrogenase complex (PDC) deficiency: Impact on PDC-E1 structure and function. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ducich NH – PersonEntity: Name: NameFull: Mears JA – PersonEntity: Name: NameFull: Bedoyan JK IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 05 Text: 2022 May Type: published Y: 2022 Identifiers: – Type: issn-electronic Value: 1573-2665 Numbering: – Type: volume Value: 45 – Type: issue Value: 3 Titles: – TitleFull: Journal of inherited metabolic disease Type: main |
| ResultId | 1 |
