V C Wheeler - JoVE Visualize

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Gene|November 25, 1997

Modification of the mouse mitochondrial genome by insertion of an exogenous geneV C Wheeler, M Aitken, C Coutelle

Molecular & General Genetics : MGG|February 1, 1994

Use of an operon fusion to induce expression and crystallisation of a Bacillus thuringiensis delta-endotoxin encoded by a cryptic geneN Crickmore, V C Wheeler, D J Ellar

The Journal of Biological Chemistry|February 21, 1997

Introduction of plasmid DNA into isolated mitochondria by electroporation. A novel approach toward gene correction for mitochondrial disordersJ M Collombet, V C Wheeler, F Vogel, et al.

Gene|March 9, 1996

Synthesis of a modified gene encoding human ornithine transcarbamylase for expression in mammalian mitochondrial and universal translation systems: a novel approach towards correction of a genetic defectV C Wheeler, C Prodromou, L H Pearl, et al.

Human Molecular Genetics|November 25, 2000

Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cellsF Trettel, D Rigamonti, P Hilditch-Maguire, et al.

Neuroscience|August 5, 2003

Neocortical neurons cultured from mice with expanded CAG repeats in the huntingtin gene: unaltered vulnerability to excitotoxins and other insultsB J Snider, J L Moss, F J Revilla, et al.

Journal of Medical Genetics|July 31, 2007

Factors associated with HD CAG repeat instability in Huntington diseaseV C Wheeler, F Persichetti, S M McNeil, et al.

Human Molecular Genetics|November 16, 2001

The HD mutation causes progressive lethal neurological disease in mice expressing reduced levels of huntingtinW Auerbach, M S Hurlbert, P Hilditch-Maguire, et al.

Human Molecular Genetics|January 15, 1999

Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouseV C Wheeler, W Auerbach, J K White, et al.

Human Molecular Genetics|March 4, 2000

Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in HdhQ92 and HdhQ111 knock-in miceV C Wheeler, J K White, C A Gutekunst, et al.

Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:

Pageof 1

Gene|November 25, 1997

Modification of the mouse mitochondrial genome by insertion of an exogenous geneV C Wheeler, M Aitken, C Coutelle

Molecular & General Genetics : MGG|February 1, 1994

Use of an operon fusion to induce expression and crystallisation of a Bacillus thuringiensis delta-endotoxin encoded by a cryptic geneN Crickmore, V C Wheeler, D J Ellar

The Journal of Biological Chemistry|February 21, 1997

Introduction of plasmid DNA into isolated mitochondria by electroporation. A novel approach toward gene correction for mitochondrial disordersJ M Collombet, V C Wheeler, F Vogel, et al.

Gene|March 9, 1996

Synthesis of a modified gene encoding human ornithine transcarbamylase for expression in mammalian mitochondrial and universal translation systems: a novel approach towards correction of a genetic defectV C Wheeler, C Prodromou, L H Pearl, et al.

Human Molecular Genetics|November 25, 2000

Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cellsF Trettel, D Rigamonti, P Hilditch-Maguire, et al.

Neuroscience|August 5, 2003

Neocortical neurons cultured from mice with expanded CAG repeats in the huntingtin gene: unaltered vulnerability to excitotoxins and other insultsB J Snider, J L Moss, F J Revilla, et al.

Journal of Medical Genetics|July 31, 2007

Factors associated with HD CAG repeat instability in Huntington diseaseV C Wheeler, F Persichetti, S M McNeil, et al.

Human Molecular Genetics|November 16, 2001

The HD mutation causes progressive lethal neurological disease in mice expressing reduced levels of huntingtinW Auerbach, M S Hurlbert, P Hilditch-Maguire, et al.

Human Molecular Genetics|January 15, 1999

Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouseV C Wheeler, W Auerbach, J K White, et al.

Human Molecular Genetics|March 4, 2000

Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in HdhQ92 and HdhQ111 knock-in miceV C Wheeler, J K White, C A Gutekunst, et al.

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