Genetic alterations in SUPT6H are associated with neurodevelopmental disorders.
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| Title: | Genetic alterations in SUPT6H are associated with neurodevelopmental disorders. |
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| Authors: | Carabelli B; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, 08854, United States., Kim HG; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, 08854, United States., Ku B; Orphan Disease Therapeutic Target Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea., Berdasco C; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, 08854, United States., Jeong YY; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, 08854, United States., Lai T; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, 08854, United States., Jang MH; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, 08854, United States; Brain Health Institute, Rutgers University, Piscataway, NJ, 08854, United States; Rutgers Cancer Institute, New Brunswick, NJ, 08904, United States., Boison D; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, 08854, United States; Brain Health Institute, Rutgers University, Piscataway, NJ, 08854, United States; Rutgers Cancer Institute, New Brunswick, NJ, 08904, United States., Kim Y; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, 08854, United States; Brain Health Institute, Rutgers University, Piscataway, NJ, 08854, United States. Electronic address: yk539@rwjms.rutgers.edu. |
| Source: | Biochimica et biophysica acta. Molecular basis of disease [Biochim Biophys Acta Mol Basis Dis] 2026 Jun; Vol. 1872 (5), pp. 168226. Date of Electronic Publication: 2026 Mar 19. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101731730 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-260X (Electronic) Linking ISSN: 09254439 NLM ISO Abbreviation: Biochim Biophys Acta Mol Basis Dis Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 41864309 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Genetic alterations in SUPT6H are associated with neurodevelopmental disorders. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Carabelli+B%22">Carabelli B</searchLink>; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, 08854, United States.<br /><searchLink fieldCode="AU" term="%22Kim+HG%22">Kim HG</searchLink>; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, 08854, United States.<br /><searchLink fieldCode="AU" term="%22Ku+B%22">Ku B</searchLink>; Orphan Disease Therapeutic Target Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea.<br /><searchLink fieldCode="AU" term="%22Berdasco+C%22">Berdasco C</searchLink>; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, 08854, United States.<br /><searchLink fieldCode="AU" term="%22Jeong+YY%22">Jeong YY</searchLink>; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, 08854, United States.<br /><searchLink fieldCode="AU" term="%22Lai+T%22">Lai T</searchLink>; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, 08854, United States.<br /><searchLink fieldCode="AU" term="%22Jang+MH%22">Jang MH</searchLink>; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, 08854, United States; Brain Health Institute, Rutgers University, Piscataway, NJ, 08854, United States; Rutgers Cancer Institute, New Brunswick, NJ, 08904, United States.<br /><searchLink fieldCode="AU" term="%22Boison+D%22">Boison D</searchLink>; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, 08854, United States; Brain Health Institute, Rutgers University, Piscataway, NJ, 08854, United States; Rutgers Cancer Institute, New Brunswick, NJ, 08904, United States.<br /><searchLink fieldCode="AU" term="%22Kim+Y%22">Kim Y</searchLink>; Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, 08854, United States; Brain Health Institute, Rutgers University, Piscataway, NJ, 08854, United States. Electronic address: yk539@rwjms.rutgers.edu. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101731730%22">Biochimica et biophysica acta. Molecular basis of disease</searchLink> [Biochim Biophys Acta Mol Basis Dis] 2026 Jun; Vol. 1872 (5), pp. 168226. <i>Date of Electronic Publication: </i>2026 Mar 19. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier%22">Elsevier </searchLink><i>Country of Publication: </i>Netherlands <i>NLM ID: </i>101731730 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1879-260X (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209254439%22">09254439 </searchLink><i>NLM ISO Abbreviation: </i>Biochim Biophys Acta Mol Basis Dis <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=41864309 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.bbadis.2026.168226 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 168226 Titles: – TitleFull: Genetic alterations in SUPT6H are associated with neurodevelopmental disorders. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Carabelli B – PersonEntity: Name: NameFull: Kim HG – PersonEntity: Name: NameFull: Ku B – PersonEntity: Name: NameFull: Berdasco C – PersonEntity: Name: NameFull: Jeong YY – PersonEntity: Name: NameFull: Lai T – PersonEntity: Name: NameFull: Jang MH – PersonEntity: Name: NameFull: Boison D – PersonEntity: Name: NameFull: Kim Y IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: 2026 Jun Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 1879-260X Numbering: – Type: volume Value: 1872 – Type: issue Value: 5 Titles: – TitleFull: Biochimica et biophysica acta. Molecular basis of disease Type: main |
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