Saturation genome editing of 11 codons and exon 13 of BRCA2 coupled with chemotherapeutic drug response accurately determines pathogenicity of variants.
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| Title: | Saturation genome editing of 11 codons and exon 13 of BRCA2 coupled with chemotherapeutic drug response accurately determines pathogenicity of variants. |
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| Authors: | Sahu S; Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America., Sullivan TL; Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America., Mitrophanov AY; Statistical Consulting and Scientific Programming, Frederick National Laboratory for Cancer Research, National Institutes of Health, Frederick, Maryland, United States of America., Galloux M; Independent bioinformatician, Marseille, France., Nousome D; CCR Bioinformatics Resource, Leidos Biomedical Sciences, Inc. Frederick National Laboratory for Cancer Research, Frederick, Maryland, United States of America., Southon E; Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America., Caylor D; Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America., Mishra AP; Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America., Evans CN; Genome Modification Core, Laboratory Animal Sciences Program, Frederick National Laboratory for Cancer Research, Frederick, Maryland, United States of America., Clapp ME; Genome Modification Core, Laboratory Animal Sciences Program, Frederick National Laboratory for Cancer Research, Frederick, Maryland, United States of America., Burkett S; Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America., Malys T; Statistical Consulting and Scientific Programming, Frederick National Laboratory for Cancer Research, National Institutes of Health, Frederick, Maryland, United States of America., Chari R; Genome Modification Core, Laboratory Animal Sciences Program, Frederick National Laboratory for Cancer Research, Frederick, Maryland, United States of America., Biswas K; Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America., Sharan SK; Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America. |
| Source: | PLoS genetics [PLoS Genet] 2023 Sep 15; Vol. 19 (9), pp. e1010940. Date of Electronic Publication: 2023 Sep 15 (Print Publication: 2023). |
| Publication Type: | Journal Article; Research Support, N.I.H., Intramural; Research Support, N.I.H., Extramural |
| Journal Info: | Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7404 (Electronic) Linking ISSN: 15537390 NLM ISO Abbreviation: PLoS Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 37713444 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Saturation genome editing of 11 codons and exon 13 of BRCA2 coupled with chemotherapeutic drug response accurately determines pathogenicity of variants. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Sahu+S%22">Sahu S</searchLink>; Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Sullivan+TL%22">Sullivan TL</searchLink>; Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Mitrophanov+AY%22">Mitrophanov AY</searchLink>; Statistical Consulting and Scientific Programming, Frederick National Laboratory for Cancer Research, National Institutes of Health, Frederick, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Galloux+M%22">Galloux M</searchLink>; Independent bioinformatician, Marseille, France.<br /><searchLink fieldCode="AU" term="%22Nousome+D%22">Nousome D</searchLink>; CCR Bioinformatics Resource, Leidos Biomedical Sciences, Inc. Frederick National Laboratory for Cancer Research, Frederick, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Southon+E%22">Southon E</searchLink>; Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Caylor+D%22">Caylor D</searchLink>; Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Mishra+AP%22">Mishra AP</searchLink>; Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Evans+CN%22">Evans CN</searchLink>; Genome Modification Core, Laboratory Animal Sciences Program, Frederick National Laboratory for Cancer Research, Frederick, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Clapp+ME%22">Clapp ME</searchLink>; Genome Modification Core, Laboratory Animal Sciences Program, Frederick National Laboratory for Cancer Research, Frederick, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Burkett+S%22">Burkett S</searchLink>; Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Malys+T%22">Malys T</searchLink>; Statistical Consulting and Scientific Programming, Frederick National Laboratory for Cancer Research, National Institutes of Health, Frederick, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Chari+R%22">Chari R</searchLink>; Genome Modification Core, Laboratory Animal Sciences Program, Frederick National Laboratory for Cancer Research, Frederick, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Biswas+K%22">Biswas K</searchLink>; Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America.<br /><searchLink fieldCode="AU" term="%22Sharan+SK%22">Sharan SK</searchLink>; Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101239074%22">PLoS genetics</searchLink> [PLoS Genet] 2023 Sep 15; Vol. 19 (9), pp. e1010940. <i>Date of Electronic Publication: </i>2023 Sep 15 (<i>Print Publication: </i>2023). – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, N.I.H., Intramural; Research Support, N.I.H., Extramural – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Public+Library+of+Science%22">Public Library of Science </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101239074 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Internet <i>ISSN: </i>1553-7404 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2215537390%22">15537390 </searchLink><i>NLM ISO Abbreviation: </i>PLoS Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=37713444 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1371/journal.pgen.1010940 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: e1010940 Titles: – TitleFull: Saturation genome editing of 11 codons and exon 13 of BRCA2 coupled with chemotherapeutic drug response accurately determines pathogenicity of variants. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Sahu S – PersonEntity: Name: NameFull: Sullivan TL – PersonEntity: Name: NameFull: Mitrophanov AY – PersonEntity: Name: NameFull: Galloux M – PersonEntity: Name: NameFull: Nousome D – PersonEntity: Name: NameFull: Southon E – PersonEntity: Name: NameFull: Caylor D – PersonEntity: Name: NameFull: Mishra AP – PersonEntity: Name: NameFull: Evans CN – PersonEntity: Name: NameFull: Clapp ME – PersonEntity: Name: NameFull: Burkett S – PersonEntity: Name: NameFull: Malys T – PersonEntity: Name: NameFull: Chari R – PersonEntity: Name: NameFull: Biswas K – PersonEntity: Name: NameFull: Sharan SK IsPartOfRelationships: – BibEntity: Dates: – D: 15 M: 09 Text: 2023 Sep 15 Type: published Y: 2023 Identifiers: – Type: issn-electronic Value: 1553-7404 Numbering: – Type: volume Value: 19 – Type: issue Value: 9 Titles: – TitleFull: PLoS genetics Type: main |
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