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Journal of Molecular Biology
|
April 15, 1981
Partial duplication of the large ribosomal RNA sequence in an inverted repeat in circular mitochondrial DNA from Kloeckera africana. Implications for mechanisms of the petite mutation
G D Clark-Walker, C R McArthur, K S Sriprakash
Current Genetics
|
November 5, 2013
Does mitochondrial DNA length influence the frequency of spontaneous petite mutants in yeasts?
G D Clark-Walker, C R McArthur, D J Daley
Nucleic Acids Research
|
July 25, 1993
MGM101, a nuclear gene involved in maintenance of the mitochondrial genome in Saccharomyces cerevisiae
X J Chen, M X Guan, G D Clark-Walker
Molecular & General Genetics : MGG
|
October 28, 1998
Suppression of rho0 lethality by mitochondrial ATP synthase F1 mutations in Kluyveromyces lactis occurs in the absence of F0
X J Chen, P M Hansbro, G D Clark-Walker
Journal of Bacteriology
|
July 1, 1971
Fatty acid and sterol composition of Mucor genevensis in relation to dimorphism and anaerobic growth
P A Gordon, P R Stewart, G D Clark-Walker
Current Genetics
|
July 1, 1991
A mobile group II intron of a naturally occurring rearranged mitochondrial genome in Kluyveromyces lactis
P J Skelly, C M Hardy, G D Clark-Walker
Journal of Neuropathology and Experimental Neurology
|
September 18, 1997
Predominant localization of the LIS family of gene products to Cajal-Retzius cells and ventricular neuroepithelium in the developing human cortex
G D Clark, M Mizuguchi, B Antalffy, et al.
Nature
|
February 23, 1978
Naturally occurring respiratory deficient Candida slooffii strains resemble petite mutants
H Arthur, K Watson, C R McArthur, et al.
Nature
|
January 13, 1994
Platelet-activating factor as a potential retrograde messenger in CA1 hippocampal long-term potentiation
K Kato, G D Clark, N G Bazan, et al.
Pediatrics
|
December 1, 1984
Munchausen's syndrome by proxy (child abuse) presenting as apparent autoerythrocyte sensitization syndrome: an unusual presentation of Polle syndrome
G D Clark, J D Key, P Rutherford, et al.
Page
of 12
Search research articles
Search
Showing results (71-80 of 112) with videos related to
Sort By:
Page
of 12
Journal of Molecular Biology
|
April 15, 1981
Partial duplication of the large ribosomal RNA sequence in an inverted repeat in circular mitochondrial DNA from Kloeckera africana. Implications for mechanisms of the petite mutation
G D Clark-Walker, C R McArthur, K S Sriprakash
Current Genetics
|
November 5, 2013
Does mitochondrial DNA length influence the frequency of spontaneous petite mutants in yeasts?
G D Clark-Walker, C R McArthur, D J Daley
Nucleic Acids Research
|
July 25, 1993
MGM101, a nuclear gene involved in maintenance of the mitochondrial genome in Saccharomyces cerevisiae
X J Chen, M X Guan, G D Clark-Walker
Molecular & General Genetics : MGG
|
October 28, 1998
Suppression of rho0 lethality by mitochondrial ATP synthase F1 mutations in Kluyveromyces lactis occurs in the absence of F0
X J Chen, P M Hansbro, G D Clark-Walker
Journal of Bacteriology
|
July 1, 1971
Fatty acid and sterol composition of Mucor genevensis in relation to dimorphism and anaerobic growth
P A Gordon, P R Stewart, G D Clark-Walker
Current Genetics
|
July 1, 1991
A mobile group II intron of a naturally occurring rearranged mitochondrial genome in Kluyveromyces lactis
P J Skelly, C M Hardy, G D Clark-Walker
Journal of Neuropathology and Experimental Neurology
|
September 18, 1997
Predominant localization of the LIS family of gene products to Cajal-Retzius cells and ventricular neuroepithelium in the developing human cortex
G D Clark, M Mizuguchi, B Antalffy, et al.
Nature
|
February 23, 1978
Naturally occurring respiratory deficient Candida slooffii strains resemble petite mutants
H Arthur, K Watson, C R McArthur, et al.
Nature
|
January 13, 1994
Platelet-activating factor as a potential retrograde messenger in CA1 hippocampal long-term potentiation
K Kato, G D Clark, N G Bazan, et al.
Pediatrics
|
December 1, 1984
Munchausen's syndrome by proxy (child abuse) presenting as apparent autoerythrocyte sensitization syndrome: an unusual presentation of Polle syndrome
G D Clark, J D Key, P Rutherford, et al.
Page
of 12