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Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
April 1, 1997
Are mitochondrial DNA deletions causative in chronic progressive external ophthalmoplegia patients?
M J Jean-Francois, S Collins, N Kotsimbos, et al.
Immunology and Cell Biology
|
April 1, 1991
The nature of immunoglobulin idiotypes and idiotype-anti-idiotype interactions in immunological networks
D C Poskitt, M J Jean-Francois, S Turnbull, et al.
Vaccine
|
November 1, 1991
Internal image (Ab2 beta) anti-idiotype vaccines. Theoretical and practical aspects
D C Poskitt, M J Jean-Francois, S Turnbull, et al.
Microbiology and Immunology
|
January 1, 1993
Production of monoclonal anti-idiotype antibodies which mimic an M-like protein of Streptococcus equi
M J Jean-Francois, D C Poskitt, L M MacDonald, et al.
Nucleic Acids Research
|
September 22, 1998
mtDNA replicative potential remains constant during ageing: polymerase gamma activity does not correlate with age related cytochrome oxidase activity decline in platelets
R M Kapsa, A F Quigley, T F Han, et al.
Australian and New Zealand Journal of Medicine
|
April 1, 1994
Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathies
M J Jean-Francois, P Lertrit, S F Berkovic, et al.
Human Molecular Genetics
|
November 1, 1994
Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunction
P Lertrit, R M Kapsa, M J Jean-Francois, et al.
Muscle & Nerve
|
December 18, 2001
Presymptomatic motor neuron loss and reactive astrocytosis in the SOD1 mouse model of amyotrophic lateral sclerosis
S J Feeney, P A McKelvie, L Austin, et al.
Journal of the Neurological Sciences
|
December 1, 1996
Mitochondrial DNA polymorphism in substantia nigra
R M Kapsa, M J Jean-Francois, P Lertrit, et al.
American Journal of Human Genetics
|
September 1, 1992
A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I
P Lertrit, A S Noer, M J Jean-Francois, et al.
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of 2
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Showing results (1-10 of 12) with videos related to
Sort By:
Page
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Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
April 1, 1997
Are mitochondrial DNA deletions causative in chronic progressive external ophthalmoplegia patients?
M J Jean-Francois, S Collins, N Kotsimbos, et al.
Immunology and Cell Biology
|
April 1, 1991
The nature of immunoglobulin idiotypes and idiotype-anti-idiotype interactions in immunological networks
D C Poskitt, M J Jean-Francois, S Turnbull, et al.
Vaccine
|
November 1, 1991
Internal image (Ab2 beta) anti-idiotype vaccines. Theoretical and practical aspects
D C Poskitt, M J Jean-Francois, S Turnbull, et al.
Microbiology and Immunology
|
January 1, 1993
Production of monoclonal anti-idiotype antibodies which mimic an M-like protein of Streptococcus equi
M J Jean-Francois, D C Poskitt, L M MacDonald, et al.
Nucleic Acids Research
|
September 22, 1998
mtDNA replicative potential remains constant during ageing: polymerase gamma activity does not correlate with age related cytochrome oxidase activity decline in platelets
R M Kapsa, A F Quigley, T F Han, et al.
Australian and New Zealand Journal of Medicine
|
April 1, 1994
Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathies
M J Jean-Francois, P Lertrit, S F Berkovic, et al.
Human Molecular Genetics
|
November 1, 1994
Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunction
P Lertrit, R M Kapsa, M J Jean-Francois, et al.
Muscle & Nerve
|
December 18, 2001
Presymptomatic motor neuron loss and reactive astrocytosis in the SOD1 mouse model of amyotrophic lateral sclerosis
S J Feeney, P A McKelvie, L Austin, et al.
Journal of the Neurological Sciences
|
December 1, 1996
Mitochondrial DNA polymorphism in substantia nigra
R M Kapsa, M J Jean-Francois, P Lertrit, et al.
American Journal of Human Genetics
|
September 1, 1992
A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I
P Lertrit, A S Noer, M J Jean-Francois, et al.
Page
of 2