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Showing 1–12 of 12 results

Advanced filters: Author: Rashmi Kothary Clear advanced filters

The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1

Arthur Brown
Gilbert Bernier
Rashmi Kothary
Research01 Jul 1995
Nature Genetics

Volume: 10, P: 301-306
An induction gene trap for identifying a homeoprotein-regulated locus

Gaëll Mainguy
María Luz Montesinos
Michel Volovitch
Research01 Jul 2000
Nature Biotechnology

Volume: 18, P: 746-749
Optimization of base editors for the functional correction of SMN2 as a treatment for spinal muscular atrophy

Optimized base editors targeting the exon-7 mutation in SMN2 restore expression of the survival motor neuron (SMN) protein to normal levels, as shown in mice with spinal muscular atrophy and in fibroblasts from patients with this genetic disease.

Christiano R. R. Alves
Leillani L. Ha
Benjamin P. Kleinstiver
Research06 Dec 2023
Nature Biomedical Engineering

Volume: 8, P: 118-131
Snf2h-mediated chromatin organization and histone H1 dynamics govern cerebellar morphogenesis and neural maturation

The chromatin remodelling proteins Snf2h and Snf2l regulate nucleosome spacing. Here, the authors show that Snf2hablation impairs chromatin organization of neuronal lineages during mouse embryonic and post-natal cerebellar development.

Matías Alvarez-Saavedra
Yves De Repentigny
David J. Picketts
ResearchOpen Access20 Jun 2014
Nature Communications

Volume: 5, P: 1-18
Correction: Corrigendum: Establishment of a cone photoreceptor transplantation platform based on a novel cone-GFP reporter mouse line

Sheila Smiley
Philip E. Nickerson
Valerie A. Wallace
Amendments and CorrectionsOpen Access22 Apr 2016
Scientific Reports

Volume: 6, P: 1
Survival Motor Neuron Protein is Released from Cells in Exosomes: A Potential Biomarker for Spinal Muscular Atrophy

Leslie A. Nash
Emily R. McFall
Robin J. Parks
ResearchOpen Access24 Oct 2017
Scientific Reports

Volume: 7, P: 1-15
Differential induction of muscle atrophy pathways in two mouse models of spinal muscular atrophy

Marc-Olivier Deguise
Justin G. Boyer
Rashmi Kothary
ResearchOpen Access28 Jun 2016
Scientific Reports

Volume: 6, P: 1-13
Loss of miR-145 promotes remyelination and functional recovery in a model of chronic central demyelination

Loss of miR-145 promotes remyelination in a chronically demyelinated animal model, implicating it as a factor in remyelination failure in human Multiple Sclerosis lesions and highlighting in as a potential therapeutic target for progressive MS.

Samantha F. Kornfeld
Sarah E. Cummings
Rashmi Kothary
ResearchOpen Access04 Jul 2024
Communications Biology

Volume: 7, P: 1-19
Central and peripheral delivered AAV9-SMN are both efficient but target different pathomechanisms in a mouse model of spinal muscular atrophy

Aoife Reilly
Marc-Olivier Deguise
Rashmi Kothary
Research25 Apr 2022
Gene Therapy

Volume: 29, P: 544-554
Establishment of a cone photoreceptor transplantation platform based on a novel cone-GFP reporter mouse line

Sheila Smiley
Philip E. Nickerson
Valerie A. Wallace
ResearchOpen Access11 Mar 2016
Scientific Reports

Volume: 6, P: 1-15
The α Subunit of the Epithelial Sodium Channel in the Mouse: Developmental Regulation of Its Expression

André Dagenais
Rashmi Kothary
Yves Berthiaume
Research01 Sept 1997
Pediatric Research

Volume: 42, P: 327-334
Curing SMA: Are we there yet?

Aoife Reilly
Lucia Chehade
Rashmi Kothary
Reviews26 May 2022
Gene Therapy

Volume: 30, P: 8-17

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The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1

An induction gene trap for identifying a homeoprotein-regulated locus

Optimization of base editors for the functional correction of SMN2 as a treatment for spinal muscular atrophy

Snf2h-mediated chromatin organization and histone H1 dynamics govern cerebellar morphogenesis and neural maturation

Correction: Corrigendum: Establishment of a cone photoreceptor transplantation platform based on a novel cone-GFP reporter mouse line

Survival Motor Neuron Protein is Released from Cells in Exosomes: A Potential Biomarker for Spinal Muscular Atrophy

Differential induction of muscle atrophy pathways in two mouse models of spinal muscular atrophy

Loss of miR-145 promotes remyelination and functional recovery in a model of chronic central demyelination

Central and peripheral delivered AAV9-SMN are both efficient but target different pathomechanisms in a mouse model of spinal muscular atrophy

Establishment of a cone photoreceptor transplantation platform based on a novel cone-GFP reporter mouse line

The α Subunit of the Epithelial Sodium Channel in the Mouse: Developmental Regulation of Its Expression

Curing SMA: Are we there yet?

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