نتائج البحث

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.

• Authors : McRae HM; Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.; Department of Medical Biology, The University of Melbourne, Parkville, Victoria, Australia.

Subjects: Mental Retardation, X-Linked*/Mental Retardation, X-Linked*/Mental Retardation, X-Linked*/genetics ; Mental Retardation, X-Linked*/Mental Retardation, X-Linked*/Mental Retardation, X-Linked*/pathology ; Repressor Proteins*/Repressor Proteins*/Repressor Proteins*/genetics Borjeson-Forssman-Lehmann syndrome

• Source: PLoS genetics [PLoS Genet] 2024 Oct 15; Vol. 20 (10), pp. e1011428. Date of Electronic Publication: 2024 Oct 15 (Print Publication: 2024).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet

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Tracking the Fragile X Mental Retardation Protein in a Highly Ordered Neuronal RiboNucleoParticles Population: A Link between Stalled Polyribosomes and RNA Granules.

• Authors : El Fatimy R; Institut universitaire en santé mentale de Québec, Quebec, Canada.; Département de Psychiatrie et de Neurosciences, Faculté de Médecine, Université Laval, Québec, Quebec, Canada.

Subjects: Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/*genetics ; Fragile X Syndrome/Fragile X Syndrome/Fragile X Syndrome/*genetics ; RNA-Binding Proteins/RNA-Binding Proteins/RNA-Binding Proteins/*genetics

• Source: PLoS genetics [PLoS Genet] 2016 Jul 27; Vol. 12 (7), pp. e1006192. Date of Electronic Publication: 2016 Jul 27 (Print Publication: 2016).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet

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Nuclear Fragile X Mental Retardation Protein is localized to Cajal bodies.

• Authors : Dury AY; Centre de recherche, Institut en santé mentale de Québec, Québec, Québec, Canada ; Département de psychiatrie et des neurosciences, Faculté de médecine, Université Laval, Québec, Québec, Canada.

Subjects: Coiled Bodies/Coiled Bodies/Coiled Bodies/*genetics ; Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/*genetics ; Fragile X Syndrome/Fragile X Syndrome/Fragile X Syndrome/*genetics

• Source: PLoS genetics [PLoS Genet] 2013 Oct; Vol. 9 (10), pp. e1003890. Date of Electronic Publication: 2013 Oct 31.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: Print-Electronic Cited Medium: Internet

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The bantam microRNA is associated with drosophila fragile X mental retardation protein and regulates the fate of germline stem cells.

• Authors : Yang Y; State Key Laboratory of Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, People's Republic of China.; Xu S

Subjects: Cell Differentiation*; Drosophila/Drosophila/Drosophila/*metabolism ; Drosophila Proteins/Drosophila Proteins/Drosophila Proteins/*metabolism

• Source: PLoS genetics [PLoS Genet] 2009 Apr; Vol. 5 (4), pp. e1000444. Date of Electronic Publication: 2009 Apr 03.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: Print-Electronic Cited Medium: Internet

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Tracking the Fragile X Mental Retardation Protein in a Highly Ordered Neuronal RiboNucleoParticles Population: A Link between Stalled Polyribosomes and RNA Granules.

• Authors : Rachid El Fatimy; Laetitia Davidovic; Sandra Tremblay

Subjects: Genetics; QH426-470

• Source: PLoS Genetics, Vol 12, Iss 7, p e1006192 (2016)

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Fragile X Mental Retardation Protein Regulates Proliferation and Differentiation of Adult Neural Stem/Progenitor Cells.

• Authors : Yuping Luo¹; Ge Shan^2,3; Weixiang Guo¹

• Source: PLoS Genetics. Apr2010, Vol. 6 Issue 4, p1-15. 15p. 7 Graphs.

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The Bantam microRNA Is Associated with Drosophila Fragile X Mental Retardation Protein and Regulates the Fate of Germline Stem Cells.

• Authors : Yingyue Yang¹; Shunliang Xu^2,3,4; Laixin Xia¹

• Source: PLoS Genetics. Apr2009, Vol. 5 Issue 4, p1-10. 10p. 1 Color Photograph, 1 Diagram, 1 Chart, 4 Graphs.

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Forging Links between Human Mental Retardation-Associated CNVs and Mouse Gene Knockout Models.

• Authors : Webber, Caleb¹; Hehir-Kwa, Jayne Y.²; Duc-Quang Nguyen¹

• Source: PLoS Genetics. Jun2009, Vol. 5 Issue 6, p1-12. 12p. 2 Charts, 4 Graphs.

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CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait.

• Authors : Türkmen, Seval¹; Gao Guo¹; Garshasbi, Masoud^2,3

• Source: PLoS Genetics. May2009, Vol. 5 Issue 5, p1-8. 8p. 1 Diagram, 1 Chart, 4 Graphs.

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SIRT1 Inhibition Alleviates Gene Silencing in Fragile X Mental Retardation Syndrome.

• Authors : Biacsi, Rea^1,2 (AUTHOR); Kumari, Daman¹ (AUTHOR); Usdin, Karen¹ (AUTHOR)

• Source: PLoS Genetics. Mar2008, Vol. 4 Issue 3, p1-9. 9p. 1 Diagram, 7 Graphs.

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