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Typical NF2 and LTZR1 mutations are retained in an immortalized human schwann cell model of schwannomatosis.

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Title: Typical NF2 and LTZR1 mutations are retained in an immortalized human schwann cell model of schwannomatosis.
Authors: Melfi V; Dept. of Pharmacological and Biomolecular Science 'R. Paoletti' Università degli Studi di Milano, Italy., Mohamed T; Dept. of Pharmacological and Biomolecular Science 'R. Paoletti' Università degli Studi di Milano, Italy., Colciago A; Dept. of Pharmacological and Biomolecular Science 'R. Paoletti' Università degli Studi di Milano, Italy., Fasciani A; Human Technopole, Milan, Italy., De Francesco R; Dept. of Pharmacological and Biomolecular Science 'R. Paoletti' Università degli Studi di Milano, Italy.; INGM, Istituto Nazionale Genetica Molecolare 'Romeo ed Enrica Invernizzi', Milan, Italy., Bettio D; Clinical Genetics Unit, Dept. of Women's and Children's Health, University of Padova, Italy., Cerqua C; Clinical Genetics Unit, Dept. of Women's and Children's Health, University of Padova, Italy., Boaretto F; Clinical Genetics Unit, Dept. of Women's and Children's Health, University of Padova, Italy., Basso E; Dept. of Neurosurgery, Ospedale Santa Maria della Misericordia, Rovigo, Italy., Ferraresi S; Dept. of Neurosurgery, Ospedale Santa Maria della Misericordia, Rovigo, Italy., Montini M; Dept. of Experimental and Clinical, Medical Genetics Unit, Biomedical Sciences 'Mario Serio,' University of Florence, Florence, Italy., Eoli M; Neuro Oncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Papi L; Dept. of Experimental and Clinical, Medical Genetics Unit, Biomedical Sciences 'Mario Serio,' University of Florence, Florence, Italy., Trevisson E; Clinical Genetics Unit, Dept. of Women's and Children's Health, University of Padova, Italy., Magnaghi V; Dept. of Pharmacological and Biomolecular Science 'R. Paoletti' Università degli Studi di Milano, Italy.
Source: Heliyon [Heliyon] 2024 Oct 04; Vol. 10 (19), pp. e38957. Date of Electronic Publication: 2024 Oct 04 (Print Publication: 2024).
Publication Type: Journal Article
Journal Info: Publisher: Elsevier Ltd Country of Publication: England NLM ID: 101672560 Publication Model: eCollection Cited Medium: Print ISSN: 2405-8440 (Print) Linking ISSN: 24058440 NLM ISO Abbreviation: Heliyon Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: Typical NF2 and LTZR1 mutations are retained in an immortalized human schwann cell model of schwannomatosis.
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  Data: <searchLink fieldCode="AU" term="%22Melfi+V%22">Melfi V</searchLink>; Dept. of Pharmacological and Biomolecular Science 'R. Paoletti' Università degli Studi di Milano, Italy.<br /><searchLink fieldCode="AU" term="%22Mohamed+T%22">Mohamed T</searchLink>; Dept. of Pharmacological and Biomolecular Science 'R. Paoletti' Università degli Studi di Milano, Italy.<br /><searchLink fieldCode="AU" term="%22Colciago+A%22">Colciago A</searchLink>; Dept. of Pharmacological and Biomolecular Science 'R. Paoletti' Università degli Studi di Milano, Italy.<br /><searchLink fieldCode="AU" term="%22Fasciani+A%22">Fasciani A</searchLink>; Human Technopole, Milan, Italy.<br /><searchLink fieldCode="AU" term="%22De+Francesco+R%22">De Francesco R</searchLink>; Dept. of Pharmacological and Biomolecular Science 'R. Paoletti' Università degli Studi di Milano, Italy.; INGM, Istituto Nazionale Genetica Molecolare 'Romeo ed Enrica Invernizzi', Milan, Italy.<br /><searchLink fieldCode="AU" term="%22Bettio+D%22">Bettio D</searchLink>; Clinical Genetics Unit, Dept. of Women's and Children's Health, University of Padova, Italy.<br /><searchLink fieldCode="AU" term="%22Cerqua+C%22">Cerqua C</searchLink>; Clinical Genetics Unit, Dept. of Women's and Children's Health, University of Padova, Italy.<br /><searchLink fieldCode="AU" term="%22Boaretto+F%22">Boaretto F</searchLink>; Clinical Genetics Unit, Dept. of Women's and Children's Health, University of Padova, Italy.<br /><searchLink fieldCode="AU" term="%22Basso+E%22">Basso E</searchLink>; Dept. of Neurosurgery, Ospedale Santa Maria della Misericordia, Rovigo, Italy.<br /><searchLink fieldCode="AU" term="%22Ferraresi+S%22">Ferraresi S</searchLink>; Dept. of Neurosurgery, Ospedale Santa Maria della Misericordia, Rovigo, Italy.<br /><searchLink fieldCode="AU" term="%22Montini+M%22">Montini M</searchLink>; Dept. of Experimental and Clinical, Medical Genetics Unit, Biomedical Sciences 'Mario Serio,' University of Florence, Florence, Italy.<br /><searchLink fieldCode="AU" term="%22Eoli+M%22">Eoli M</searchLink>; Neuro Oncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.<br /><searchLink fieldCode="AU" term="%22Papi+L%22">Papi L</searchLink>; Dept. of Experimental and Clinical, Medical Genetics Unit, Biomedical Sciences 'Mario Serio,' University of Florence, Florence, Italy.<br /><searchLink fieldCode="AU" term="%22Trevisson+E%22">Trevisson E</searchLink>; Clinical Genetics Unit, Dept. of Women's and Children's Health, University of Padova, Italy.<br /><searchLink fieldCode="AU" term="%22Magnaghi+V%22">Magnaghi V</searchLink>; Dept. of Pharmacological and Biomolecular Science 'R. Paoletti' Università degli Studi di Milano, Italy.
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  Data: <searchLink fieldCode="JN" term="%22101672560%22">Heliyon</searchLink> [Heliyon] 2024 Oct 04; Vol. 10 (19), pp. e38957. <i>Date of Electronic Publication: </i>2024 Oct 04 (<i>Print Publication: </i>2024).
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier+Ltd%22">Elsevier Ltd </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101672560 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>2405-8440 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2224058440%22">24058440 </searchLink><i>NLM ISO Abbreviation: </i>Heliyon <i>Subsets: </i>PubMed not MEDLINE
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              Text: 2024 Oct 04
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