Massively parallel functional testing of MSH2 missense variants conferring Lynch syndrome risk.
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| Title: | Massively parallel functional testing of MSH2 missense variants conferring Lynch syndrome risk. |
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| Authors: | Jia X; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA., Burugula BB; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA., Chen V; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA., Lemons RM; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA., Jayakody S; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA., Maksutova M; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA., Kitzman JO; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA; Department of Computational Medicine & Bioinformatics, University of Michigan, Ann Arbor, MI 48109, USA. Electronic address: kitzmanj@umich.edu. |
| Source: | American journal of human genetics [Am J Hum Genet] 2021 Jan 07; Vol. 108 (1), pp. 163-175. Date of Electronic Publication: 2020 Dec 23. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 33357406 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Massively parallel functional testing of MSH2 missense variants conferring Lynch syndrome risk. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Jia+X%22">Jia X</searchLink>; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA.<br /><searchLink fieldCode="AU" term="%22Burugula+BB%22">Burugula BB</searchLink>; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA.<br /><searchLink fieldCode="AU" term="%22Chen+V%22">Chen V</searchLink>; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA.<br /><searchLink fieldCode="AU" term="%22Lemons+RM%22">Lemons RM</searchLink>; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA.<br /><searchLink fieldCode="AU" term="%22Jayakody+S%22">Jayakody S</searchLink>; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA.<br /><searchLink fieldCode="AU" term="%22Maksutova+M%22">Maksutova M</searchLink>; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA.<br /><searchLink fieldCode="AU" term="%22Kitzman+JO%22">Kitzman JO</searchLink>; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA; Department of Computational Medicine & Bioinformatics, University of Michigan, Ann Arbor, MI 48109, USA. Electronic address: kitzmanj@umich.edu. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220370475%22">American journal of human genetics</searchLink> [Am J Hum Genet] 2021 Jan 07; Vol. 108 (1), pp. 163-175. <i>Date of Electronic Publication: </i>2020 Dec 23. – 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="%22Cell+Press%22">Cell Press </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>0370475 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1537-6605 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200029297%22">00029297 </searchLink><i>NLM ISO Abbreviation: </i>Am J Hum Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=33357406 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.ajhg.2020.12.003 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 163 Titles: – TitleFull: Massively parallel functional testing of MSH2 missense variants conferring Lynch syndrome risk. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Jia X – PersonEntity: Name: NameFull: Burugula BB – PersonEntity: Name: NameFull: Chen V – PersonEntity: Name: NameFull: Lemons RM – PersonEntity: Name: NameFull: Jayakody S – PersonEntity: Name: NameFull: Maksutova M – PersonEntity: Name: NameFull: Kitzman JO IsPartOfRelationships: – BibEntity: Dates: – D: 07 M: 01 Text: 2021 Jan 07 Type: published Y: 2021 Identifiers: – Type: issn-electronic Value: 1537-6605 Numbering: – Type: volume Value: 108 – Type: issue Value: 1 Titles: – TitleFull: American journal of human genetics Type: main |
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