Characterizing and predicting ccRCC-causing missense mutations in Von Hippel-Lindau disease.
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| Title: | Characterizing and predicting ccRCC-causing missense mutations in Von Hippel-Lindau disease. |
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| Authors: | Serghini A; School of Chemistry and Molecular Biosciences, Chemistry Building 68, Cooper Road, The University of Queensland, St Lucia, QLD 4072, Queensland, Australia., Portelli S; School of Chemistry and Molecular Biosciences, Chemistry Building 68, Cooper Road, The University of Queensland, St Lucia, QLD 4072, Queensland, Australia., Troadec G; School of Computing and Information Systems, University of Melbourne, Melbourne, VIC 3010, Australia., Song C; School of Computing and Information Systems, University of Melbourne, Melbourne, VIC 3010, Australia., Pan Q; School of Chemistry and Molecular Biosciences, Chemistry Building 68, Cooper Road, The University of Queensland, St Lucia, QLD 4072, Queensland, Australia.; Computational Biology and Clinical Informatics, Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne, VIC 3004, Australia., Pires DEV; School of Computing and Information Systems, University of Melbourne, Melbourne, VIC 3010, Australia.; Computational Biology and Clinical Informatics, Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne, VIC 3004, Australia., Ascher DB; School of Chemistry and Molecular Biosciences, Chemistry Building 68, Cooper Road, The University of Queensland, St Lucia, QLD 4072, Queensland, Australia.; Computational Biology and Clinical Informatics, Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne, VIC 3004, Australia. |
| Source: | Human molecular genetics [Hum Mol Genet] 2024 Jan 20; Vol. 33 (3), pp. 224-232. |
| 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: 37883464 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Characterizing and predicting ccRCC-causing missense mutations in Von Hippel-Lindau disease. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Serghini+A%22">Serghini A</searchLink>; School of Chemistry and Molecular Biosciences, Chemistry Building 68, Cooper Road, The University of Queensland, St Lucia, QLD 4072, Queensland, Australia.<br /><searchLink fieldCode="AU" term="%22Portelli+S%22">Portelli S</searchLink>; School of Chemistry and Molecular Biosciences, Chemistry Building 68, Cooper Road, The University of Queensland, St Lucia, QLD 4072, Queensland, Australia.<br /><searchLink fieldCode="AU" term="%22Troadec+G%22">Troadec G</searchLink>; School of Computing and Information Systems, University of Melbourne, Melbourne, VIC 3010, Australia.<br /><searchLink fieldCode="AU" term="%22Song+C%22">Song C</searchLink>; School of Computing and Information Systems, University of Melbourne, Melbourne, VIC 3010, Australia.<br /><searchLink fieldCode="AU" term="%22Pan+Q%22">Pan Q</searchLink>; School of Chemistry and Molecular Biosciences, Chemistry Building 68, Cooper Road, The University of Queensland, St Lucia, QLD 4072, Queensland, Australia.; Computational Biology and Clinical Informatics, Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne, VIC 3004, Australia.<br /><searchLink fieldCode="AU" term="%22Pires+DEV%22">Pires DEV</searchLink>; School of Computing and Information Systems, University of Melbourne, Melbourne, VIC 3010, Australia.; Computational Biology and Clinical Informatics, Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne, VIC 3004, Australia.<br /><searchLink fieldCode="AU" term="%22Ascher+DB%22">Ascher DB</searchLink>; School of Chemistry and Molecular Biosciences, Chemistry Building 68, Cooper Road, The University of Queensland, St Lucia, QLD 4072, Queensland, Australia.; Computational Biology and Clinical Informatics, Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne, VIC 3004, Australia. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2024 Jan 20; Vol. 33 (3), pp. 224-232. – 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=37883464 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1093/hmg/ddad181 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 224 Titles: – TitleFull: Characterizing and predicting ccRCC-causing missense mutations in Von Hippel-Lindau disease. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Serghini A – PersonEntity: Name: NameFull: Portelli S – PersonEntity: Name: NameFull: Troadec G – PersonEntity: Name: NameFull: Song C – PersonEntity: Name: NameFull: Pan Q – PersonEntity: Name: NameFull: Pires DEV – PersonEntity: Name: NameFull: Ascher DB IsPartOfRelationships: – BibEntity: Dates: – D: 20 M: 01 Text: 2024 Jan 20 Type: published Y: 2024 Identifiers: – Type: issn-electronic Value: 1460-2083 Numbering: – Type: volume Value: 33 – Type: issue Value: 3 Titles: – TitleFull: Human molecular genetics Type: main |
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