Binte M. Yusof

Singapore, Singapore

Last Updated: 09/26/2026

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Found 14 publications

Convergent and Divergent Molecular Pathways in FMR1-, TSC2- and FMR1/TSC2 Knockout Neurons.

Convergent and Divergent Molecular Pathways in FMR1-, TSC2- and FMR1/TSC2 Knockout Neurons.

Journal: Molecular neurobiology
Published: May 05, 2026

Environmental Deprivation Effects on Myelin Ultrastructure in Huntington Disease and Wildtype Mice.

Environmental Deprivation Effects on Myelin Ultrastructure in Huntington Disease and Wildtype Mice.

Journal: Molecular neurobiology
Published: July 13, 2023

Dysregulated COMT Expression in Fragile X Syndrome.

Dysregulated COMT Expression in Fragile X Syndrome.

Journal: Neuromolecular medicine
Published: May 15, 2023

Widespread dysregulation of mRNA splicing implicates RNA processing in the development and progression of Huntington's disease.

Widespread dysregulation of mRNA splicing implicates RNA processing in the development and progression of Huntington's disease.

Journal: EBioMedicine
Published: February 02, 2023

Ermin deficiency leads to compromised myelin, inflammatory milieu, and susceptibility to demyelinating insult.

Ermin deficiency leads to compromised myelin, inflammatory milieu, and susceptibility to demyelinating insult.

Journal: Brain pathology (Zurich, Switzerland)
Published: September 16, 2021

Abnormal Spinal Cord Myelination due to Oligodendrocyte Dysfunction in a Model of Huntington's Disease.

Abnormal Spinal Cord Myelination due to Oligodendrocyte Dysfunction in a Model of Huntington's Disease.

Journal: Journal of Huntington's disease
Published: August 09, 2021

pS421 huntingtin modulates mitochondrial phenotypes and confers neuroprotection in an HD hiPSC model.

pS421 huntingtin modulates mitochondrial phenotypes and confers neuroprotection in an HD hiPSC model.

Journal: Cell death & disease
Published: April 23, 2020

Elevated de novo protein synthesis in FMRP-deficient human neurons and its correction by metformin treatment.

Elevated de novo protein synthesis in FMRP-deficient human neurons and its correction by metformin treatment.

Journal: Molecular autism
Published: October 31, 2019

Integrative Analysis Identifies Key Molecular Signatures Underlying Neurodevelopmental Deficits in Fragile X Syndrome.

Integrative Analysis Identifies Key Molecular Signatures Underlying Neurodevelopmental Deficits in Fragile X Syndrome.

Journal: Biological psychiatry
Published: April 10, 2019

Impaired Remyelination in a Mouse Model of Huntington Disease.

Impaired Remyelination in a Mouse Model of Huntington Disease.

Journal: Molecular neurobiology
Published: February 06, 2019

Laquinimod Treatment Improves Myelination Deficits at the Transcriptional and Ultrastructural Levels in the YAC128 Mouse Model of Huntington Disease.

Laquinimod Treatment Improves Myelination Deficits at the Transcriptional and Ultrastructural Levels in the YAC128 Mouse Model of Huntington Disease.

Journal: Molecular neurobiology
Published: September 05, 2018

Manipulation of microbiota reveals altered callosal myelination and white matter plasticity in a model of Huntington disease.

Manipulation of microbiota reveals altered callosal myelination and white matter plasticity in a model of Huntington disease.

Journal: Neurobiology of disease
Published: September 04, 2018
Showing 1-12 of 14

Last Updated: 09/26/2026