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T P Hutchin

Showing results (1-10 of 12) with videos related to

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Cellular and Molecular Life Sciences : CMLS|February 24, 2001
Mitochondrial defects and hearing lossT P Hutchin, G A Cortopassi
Genetics|March 1, 1997
Multiple origins of a mitochondrial mutation conferring deafnessT P Hutchin, G A Cortopassi
QJM : Monthly Journal of the Association of Physicians|September 27, 2002
Antioxidant capacity after acute ischaemic strokeS E Gariballa, T P Hutchin, A J Sinclair
Neuroscience Letters|March 8, 1996
Nicotinamide as a precursor for NAD+ prevents apoptosis in the mouse brain induced by tertiary-butylhydroperoxideL K Klaidman, S K Mukherjee, T P Hutchin, et al.
Biochemical and Biophysical Research Communications|January 13, 1998
Mitochondrial DNA mutations in Alzheimer's diseaseT P Hutchin, P R Heath, R C Pearson, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Maternally inherited hearing impairment in a family with the mitochondrial DNA A7445G mutationT P Hutchin, N J Lench, S Arbuzova, et al.
Brain Research Bulletin|January 1, 1995
Apoptosis and DNA fragmentation as induced by tertiary butylhydroperoxide in the brainS K Mukherjee, R Yasharel, L K Klaidman, et al.
Journal of Medical Genetics|April 3, 2001
Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairmentT P Hutchin, K R Thompson, M Parker, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunctionT P Hutchin, N C Navarro-Coy, G Van Camp, et al.
Clinical Genetics|April 19, 2003
The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UKD C Blaydon, R F Mueller, T P Hutchin, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Cellular and Molecular Life Sciences : CMLS|February 24, 2001
Mitochondrial defects and hearing lossT P Hutchin, G A Cortopassi
Genetics|March 1, 1997
Multiple origins of a mitochondrial mutation conferring deafnessT P Hutchin, G A Cortopassi
QJM : Monthly Journal of the Association of Physicians|September 27, 2002
Antioxidant capacity after acute ischaemic strokeS E Gariballa, T P Hutchin, A J Sinclair
Neuroscience Letters|March 8, 1996
Nicotinamide as a precursor for NAD+ prevents apoptosis in the mouse brain induced by tertiary-butylhydroperoxideL K Klaidman, S K Mukherjee, T P Hutchin, et al.
Biochemical and Biophysical Research Communications|January 13, 1998
Mitochondrial DNA mutations in Alzheimer's diseaseT P Hutchin, P R Heath, R C Pearson, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Maternally inherited hearing impairment in a family with the mitochondrial DNA A7445G mutationT P Hutchin, N J Lench, S Arbuzova, et al.
Brain Research Bulletin|January 1, 1995
Apoptosis and DNA fragmentation as induced by tertiary butylhydroperoxide in the brainS K Mukherjee, R Yasharel, L K Klaidman, et al.
Journal of Medical Genetics|April 3, 2001
Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairmentT P Hutchin, K R Thompson, M Parker, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunctionT P Hutchin, N C Navarro-Coy, G Van Camp, et al.
Clinical Genetics|April 19, 2003
The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UKD C Blaydon, R F Mueller, T P Hutchin, et al.
Pageof 2