Glial dysregulation in the human brain in fragile X-associated tremor/ataxia syndrome.
Saved in:
| Title: | Glial dysregulation in the human brain in fragile X-associated tremor/ataxia syndrome. |
|---|---|
| Authors: | Dias CM; Division of Developmental Medicine, Boston Children's Hospital, Boston, MA 02115.; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Department of Pediatrics, Harvard Medical School, Boston, MA 02115.; Department of Pediatrics, Section of Developmental Pediatrics, Section of Genetics and Metabolism, and Denver Fragile X Clinic and Research Center, Children's Hospital Colorado, University of Colorado Anschutz Medical Campus, Aurora, CO 80045., Issac B; Research Computing, Department of Information Technology, Boston Children's Hospital, Boston, MA 02115., Sun L; Research Computing, Department of Information Technology, Boston Children's Hospital, Boston, MA 02115., Lukowicz A; Department of Pediatrics, Section of Developmental Pediatrics, Section of Genetics and Metabolism, and Denver Fragile X Clinic and Research Center, Children's Hospital Colorado, University of Colorado Anschutz Medical Campus, Aurora, CO 80045., Talukdar M; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Harvard-Massachusetts Institute of Technology MD/PhD Program, Program in Bioinformatics & Integrative Genomics, Harvard Medical School, Boston, MA 02115., Akula SK; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Harvard-Massachusetts Institute of Technology MD/PhD Program, Program in Neuroscience, Harvard Medical School, Boston, MA 02115., Miller MB; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Department of Pathology, Brigham and Women's Hospital, Boston, MA 02115., Walsh K; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115., Rockowitz S; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Research Computing, Department of Information Technology, Boston Children's Hospital, Boston, MA 02115., Walsh CA; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Department of Pediatrics, Harvard Medical School, Boston, MA 02115.; HHMI, Boston Children's Hospital, Boston, MA 02115.; Department of Neurology, Harvard Medical School, Boston, MA 02115. |
| Source: | Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2023 Jun 06; Vol. 120 (23), pp. e2300052120. Date of Electronic Publication: 2023 May 30. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: National Academy of Sciences Country of Publication: United States NLM ID: 7505876 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1091-6490 (Electronic) Linking ISSN: 00278424 NLM ISO Abbreviation: Proc Natl Acad Sci U S A Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
|---|---|
| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 37252957 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Glial dysregulation in the human brain in fragile X-associated tremor/ataxia syndrome. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Dias+CM%22">Dias CM</searchLink>; Division of Developmental Medicine, Boston Children's Hospital, Boston, MA 02115.; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Department of Pediatrics, Harvard Medical School, Boston, MA 02115.; Department of Pediatrics, Section of Developmental Pediatrics, Section of Genetics and Metabolism, and Denver Fragile X Clinic and Research Center, Children's Hospital Colorado, University of Colorado Anschutz Medical Campus, Aurora, CO 80045.<br /><searchLink fieldCode="AU" term="%22Issac+B%22">Issac B</searchLink>; Research Computing, Department of Information Technology, Boston Children's Hospital, Boston, MA 02115.<br /><searchLink fieldCode="AU" term="%22Sun+L%22">Sun L</searchLink>; Research Computing, Department of Information Technology, Boston Children's Hospital, Boston, MA 02115.<br /><searchLink fieldCode="AU" term="%22Lukowicz+A%22">Lukowicz A</searchLink>; Department of Pediatrics, Section of Developmental Pediatrics, Section of Genetics and Metabolism, and Denver Fragile X Clinic and Research Center, Children's Hospital Colorado, University of Colorado Anschutz Medical Campus, Aurora, CO 80045.<br /><searchLink fieldCode="AU" term="%22Talukdar+M%22">Talukdar M</searchLink>; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Harvard-Massachusetts Institute of Technology MD/PhD Program, Program in Bioinformatics & Integrative Genomics, Harvard Medical School, Boston, MA 02115.<br /><searchLink fieldCode="AU" term="%22Akula+SK%22">Akula SK</searchLink>; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Harvard-Massachusetts Institute of Technology MD/PhD Program, Program in Neuroscience, Harvard Medical School, Boston, MA 02115.<br /><searchLink fieldCode="AU" term="%22Miller+MB%22">Miller MB</searchLink>; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Department of Pathology, Brigham and Women's Hospital, Boston, MA 02115.<br /><searchLink fieldCode="AU" term="%22Walsh+K%22">Walsh K</searchLink>; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.<br /><searchLink fieldCode="AU" term="%22Rockowitz+S%22">Rockowitz S</searchLink>; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Research Computing, Department of Information Technology, Boston Children's Hospital, Boston, MA 02115.<br /><searchLink fieldCode="AU" term="%22Walsh+CA%22">Walsh CA</searchLink>; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Department of Pediatrics, Harvard Medical School, Boston, MA 02115.; HHMI, Boston Children's Hospital, Boston, MA 02115.; Department of Neurology, Harvard Medical School, Boston, MA 02115. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%227505876%22">Proceedings of the National Academy of Sciences of the United States of America</searchLink> [Proc Natl Acad Sci U S A] 2023 Jun 06; Vol. 120 (23), pp. e2300052120. <i>Date of Electronic Publication: </i>2023 May 30. – 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="%22National+Academy+of+Sciences%22">National Academy of Sciences </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>7505876 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1091-6490 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200278424%22">00278424 </searchLink><i>NLM ISO Abbreviation: </i>Proc Natl Acad Sci U S A <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=37252957 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1073/pnas.2300052120 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: e2300052120 Titles: – TitleFull: Glial dysregulation in the human brain in fragile X-associated tremor/ataxia syndrome. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Dias CM – PersonEntity: Name: NameFull: Issac B – PersonEntity: Name: NameFull: Sun L – PersonEntity: Name: NameFull: Lukowicz A – PersonEntity: Name: NameFull: Talukdar M – PersonEntity: Name: NameFull: Akula SK – PersonEntity: Name: NameFull: Miller MB – PersonEntity: Name: NameFull: Walsh K – PersonEntity: Name: NameFull: Rockowitz S – PersonEntity: Name: NameFull: Walsh CA IsPartOfRelationships: – BibEntity: Dates: – D: 06 M: 06 Text: 2023 Jun 06 Type: published Y: 2023 Identifiers: – Type: issn-electronic Value: 1091-6490 Numbering: – Type: volume Value: 120 – Type: issue Value: 23 Titles: – TitleFull: Proceedings of the National Academy of Sciences of the United States of America Type: main |
| ResultId | 1 |