Loss of PHF6 causes spontaneous seizures, enlarged brain ventricles and altered transcription in the cortex of a mouse model of the Börjeson–Forssman–Lehmann intellectual disability syndrome.
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| Title: | Loss of PHF6 causes spontaneous seizures, enlarged brain ventricles and altered transcription in the cortex of a mouse model of the Börjeson–Forssman–Lehmann intellectual disability syndrome. |
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| Authors: | McRae, Helen M.1,2 (AUTHOR), Leong, Melody P. Y.1,2 (AUTHOR), Bergamasco, Maria I.1,2 (AUTHOR), Garnham, Alexandra L.1,2 (AUTHOR), Hu, Yifang1 (AUTHOR), Corbett, Mark A.3 (AUTHOR), Whitehead, Lachlan1,2 (AUTHOR), El-Saafin, Farrah1,2 (AUTHOR), Sheikh, Bilal N.1,2 (AUTHOR), Wilcox, Stephen1,2 (AUTHOR), Hannan, Anthony J.4,5 (AUTHOR), Gécz, Jozef3,6 (AUTHOR), Smyth, Gordon K.1,7 (AUTHOR), Thomas, Tim1,2 (AUTHOR) tthomas@wehi.edu.au, Voss, Anne K.1,2 (AUTHOR) tthomas@wehi.edu.au |
| Source: | PLoS Genetics. 10/15/2024, Vol. 20 Issue 10, p1-35. 35p. |
| Database: | Academic Search Ultimate |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 180281061 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Loss of PHF6 causes spontaneous seizures, enlarged brain ventricles and altered transcription in the cortex of a mouse model of the Börjeson–Forssman–Lehmann intellectual disability syndrome. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22McRae%2C+Helen+M%2E%22">McRae, Helen M.</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Leong%2C+Melody+P%2E+Y%2E%22">Leong, Melody P. Y.</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Bergamasco%2C+Maria+I%2E%22">Bergamasco, Maria I.</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Garnham%2C+Alexandra+L%2E%22">Garnham, Alexandra L.</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hu%2C+Yifang%22">Hu, Yifang</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Corbett%2C+Mark+A%2E%22">Corbett, Mark A.</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Whitehead%2C+Lachlan%22">Whitehead, Lachlan</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22El-Saafin%2C+Farrah%22">El-Saafin, Farrah</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Sheikh%2C+Bilal+N%2E%22">Sheikh, Bilal N.</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wilcox%2C+Stephen%22">Wilcox, Stephen</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hannan%2C+Anthony+J%2E%22">Hannan, Anthony J.</searchLink><relatesTo>4,5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Gécz%2C+Jozef%22">Gécz, Jozef</searchLink><relatesTo>3,6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Smyth%2C+Gordon+K%2E%22">Smyth, Gordon K.</searchLink><relatesTo>1,7</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Thomas%2C+Tim%22">Thomas, Tim</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> tthomas@wehi.edu.au</i><br /><searchLink fieldCode="AR" term="%22Voss%2C+Anne+K%2E%22">Voss, Anne K.</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> tthomas@wehi.edu.au</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22PLoS+Genetics%22">PLoS Genetics</searchLink>. 10/15/2024, Vol. 20 Issue 10, p1-35. 35p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=180281061 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1371/journal.pgen.1011428 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 35 StartPage: 1 Titles: – TitleFull: Loss of PHF6 causes spontaneous seizures, enlarged brain ventricles and altered transcription in the cortex of a mouse model of the Börjeson–Forssman–Lehmann intellectual disability syndrome. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: McRae, Helen M. – PersonEntity: Name: NameFull: Leong, Melody P. Y. – PersonEntity: Name: NameFull: Bergamasco, Maria I. – PersonEntity: Name: NameFull: Garnham, Alexandra L. – PersonEntity: Name: NameFull: Hu, Yifang – PersonEntity: Name: NameFull: Corbett, Mark A. – PersonEntity: Name: NameFull: Whitehead, Lachlan – PersonEntity: Name: NameFull: El-Saafin, Farrah – PersonEntity: Name: NameFull: Sheikh, Bilal N. – PersonEntity: Name: NameFull: Wilcox, Stephen – PersonEntity: Name: NameFull: Hannan, Anthony J. – PersonEntity: Name: NameFull: Gécz, Jozef – PersonEntity: Name: NameFull: Smyth, Gordon K. – PersonEntity: Name: NameFull: Thomas, Tim – PersonEntity: Name: NameFull: Voss, Anne K. IsPartOfRelationships: – BibEntity: Dates: – D: 15 M: 10 Text: 10/15/2024 Type: published Y: 2024 Identifiers: – Type: issn-print Value: 15537390 Numbering: – Type: volume Value: 20 – Type: issue Value: 10 Titles: – TitleFull: PLoS Genetics Type: main |
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