Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia.
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| Title: | Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia. |
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| Authors: | Lokki AI; Translational Immunology Research Program, Research Programs Unit and Bacteriology and Immunology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. inkeri.lokki@helsinki.fi.; Heart and Lung Center, Helsinki University Central Hospital and University of Helsinki, Helsinki, Finland. inkeri.lokki@helsinki.fi., Triebwasser M; Department of Pediatrics, Division of Pediatric Hematology and Oncology, University of Michigan, Ann Arbor, MI, USA., Daly E; Hospital and Harvard Medical School, Boston, MA, USA., Kurki MI; Institute for Molecular Medicine Finland, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA., Perola M; Department of Public Health and Welfare, National Institute for Health and Welfare, Helsinki, Finland., Auro K; Department of Public Health and Welfare, National Institute for Health and Welfare, Helsinki, Finland., Salmon JE; Hospital for Special Surgery; Weill Medical College of Cornell University, New York, NY, USA., Anuja J; Division of Nephrology, Department of Medicine, Washington University School of Medicine in St. Louis, St. Louis, MO, USA., Daly M; Institute for Molecular Medicine Finland, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA., Atkinson JP; Division of Rheumatology, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA., Laivuori H; Institute for Molecular Medicine Finland, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.; Medical and Clinical Genetics, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Department of Obstetrics and Gynecology, Tampere University Hospital and the Wellbeing Services County of Pirkanmaa, Tampere, Finland.; Center for Child, Adolescent, and Maternal Health Research, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland., Meri S; Translational Immunology Research Program, Research Programs Unit and Bacteriology and Immunology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. seppo.meri@helsinki.fi.; HUSLAB Diagnostic Center, Helsinki University Central Hospital, Helsinki, Finland. seppo.meri@helsinki.fi. |
| Corporate Authors: | FINNPEC Core Investigator Group |
| Source: | Genes and immunity [Genes Immun] 2025 Feb; Vol. 26 (1), pp. 22-26. Date of Electronic Publication: 2024 Dec 17. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural |
| Journal Info: | Publisher: Nature Pub. Group Country of Publication: England NLM ID: 100953417 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5470 (Electronic) Linking ISSN: 14664879 NLM ISO Abbreviation: Genes Immun Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 39690307 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Lokki+AI%22">Lokki AI</searchLink>; Translational Immunology Research Program, Research Programs Unit and Bacteriology and Immunology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. inkeri.lokki@helsinki.fi.; Heart and Lung Center, Helsinki University Central Hospital and University of Helsinki, Helsinki, Finland. inkeri.lokki@helsinki.fi.<br /><searchLink fieldCode="AU" term="%22Triebwasser+M%22">Triebwasser M</searchLink>; Department of Pediatrics, Division of Pediatric Hematology and Oncology, University of Michigan, Ann Arbor, MI, USA.<br /><searchLink fieldCode="AU" term="%22Daly+E%22">Daly E</searchLink>; Hospital and Harvard Medical School, Boston, MA, USA.<br /><searchLink fieldCode="AU" term="%22Kurki+MI%22">Kurki MI</searchLink>; Institute for Molecular Medicine Finland, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.<br /><searchLink fieldCode="AU" term="%22Perola+M%22">Perola M</searchLink>; Department of Public Health and Welfare, National Institute for Health and Welfare, Helsinki, Finland.<br /><searchLink fieldCode="AU" term="%22Auro+K%22">Auro K</searchLink>; Department of Public Health and Welfare, National Institute for Health and Welfare, Helsinki, Finland.<br /><searchLink fieldCode="AU" term="%22Salmon+JE%22">Salmon JE</searchLink>; Hospital for Special Surgery; Weill Medical College of Cornell University, New York, NY, USA.<br /><searchLink fieldCode="AU" term="%22Anuja+J%22">Anuja J</searchLink>; Division of Nephrology, Department of Medicine, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.<br /><searchLink fieldCode="AU" term="%22Daly+M%22">Daly M</searchLink>; Institute for Molecular Medicine Finland, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.<br /><searchLink fieldCode="AU" term="%22Atkinson+JP%22">Atkinson JP</searchLink>; Division of Rheumatology, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.<br /><searchLink fieldCode="AU" term="%22Laivuori+H%22">Laivuori H</searchLink>; Institute for Molecular Medicine Finland, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.; Medical and Clinical Genetics, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Department of Obstetrics and Gynecology, Tampere University Hospital and the Wellbeing Services County of Pirkanmaa, Tampere, Finland.; Center for Child, Adolescent, and Maternal Health Research, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.<br /><searchLink fieldCode="AU" term="%22Meri+S%22">Meri S</searchLink>; Translational Immunology Research Program, Research Programs Unit and Bacteriology and Immunology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. seppo.meri@helsinki.fi.; HUSLAB Diagnostic Center, Helsinki University Central Hospital, Helsinki, Finland. seppo.meri@helsinki.fi. – Name: AuthorCorporate Label: Corporate Authors Group: Au Data: <searchLink fieldCode="CA" term="%22FINNPEC+Core+Investigator+Group%22">FINNPEC Core Investigator Group</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22100953417%22">Genes and immunity</searchLink> [Genes Immun] 2025 Feb; Vol. 26 (1), pp. 22-26. <i>Date of Electronic Publication: </i>2024 Dec 17. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Nature+Pub%2E+Group%22">Nature Pub. Group </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>100953417 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1476-5470 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2214664879%22">14664879 </searchLink><i>NLM ISO Abbreviation: </i>Genes Immun <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=39690307 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/s41435-024-00310-6 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 22 Titles: – TitleFull: Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Lokki AI – PersonEntity: Name: NameFull: Triebwasser M – PersonEntity: Name: NameFull: Daly E – PersonEntity: Name: NameFull: Kurki MI – PersonEntity: Name: NameFull: Perola M – PersonEntity: Name: NameFull: Auro K – PersonEntity: Name: NameFull: Salmon JE – PersonEntity: Name: NameFull: Anuja J – PersonEntity: Name: NameFull: Daly M – PersonEntity: Name: NameFull: Atkinson JP – PersonEntity: Name: NameFull: Laivuori H – PersonEntity: Name: NameFull: Meri S IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 02 Text: 2025 Feb Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 1476-5470 Numbering: – Type: volume Value: 26 – Type: issue Value: 1 Titles: – TitleFull: Genes and immunity Type: main |
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