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The Journal of Investigative Dermatology
|
April 14, 1999
Skin type, melanoma, and melanocortin 1 receptor variants
E Healy, C Todd, I J Jackson, et al.
Annals of the New York Academy of Sciences
|
May 19, 2000
Genetic studies of the human melanocortin-1 receptor
J L Rees, M Birch-Machin, N Flanagan, et al.
Lancet (London, England)
|
July 1, 1989
Mitochondrial function in Parkinson's disease
L A Bindoff, M Birch-Machin, N E Cartlidge, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 7, 1999
[Leigh syndrome and leukodystrophy due to partial succinate dehydrogenase deficiency: regression with riboflavin]
J M Pinard, C Marsac, E Barkaoui, et al.
Biochemical and Biophysical Research Communications
|
September 15, 1989
Multiple defects of the respiratory chain including complex II in a family with myopathy and encephalopathy
C Desnuelle, M Birch-Machin, J F Pellissier, et al.
Nature Genetics
|
October 1, 1995
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency
T Bourgeron, P Rustin, D Chretien, et al.
British Journal of Cancer
|
March 24, 2011
Mitochondrial DNA mutations in head and neck cancer are infrequent and lack prognostic utility
C Challen, H Brown, C Cai, et al.
British Journal of Cancer
|
March 14, 2007
Targeting homeostatic mechanisms of endoplasmic reticulum stress to increase susceptibility of cancer cells to fenretinide-induced apoptosis: the role of stress proteins ERdj5 and ERp57
M Corazzari, P E Lovat, J L Armstrong, et al.
The Journal of Investigative Dermatology
|
November 6, 1998
A mutational hotspot in the 2B domain of human hair basic keratin 6 (hHb6) in monilethrix patients
B P Korge, E Healy, C S Munro, et al.
The Journal of Investigative Dermatology
|
October 3, 1999
Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotype
B P Korge, H Hamm, C S Jury, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
The Journal of Investigative Dermatology
|
April 14, 1999
Skin type, melanoma, and melanocortin 1 receptor variants
E Healy, C Todd, I J Jackson, et al.
Annals of the New York Academy of Sciences
|
May 19, 2000
Genetic studies of the human melanocortin-1 receptor
J L Rees, M Birch-Machin, N Flanagan, et al.
Lancet (London, England)
|
July 1, 1989
Mitochondrial function in Parkinson's disease
L A Bindoff, M Birch-Machin, N E Cartlidge, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
May 7, 1999
[Leigh syndrome and leukodystrophy due to partial succinate dehydrogenase deficiency: regression with riboflavin]
J M Pinard, C Marsac, E Barkaoui, et al.
Biochemical and Biophysical Research Communications
|
September 15, 1989
Multiple defects of the respiratory chain including complex II in a family with myopathy and encephalopathy
C Desnuelle, M Birch-Machin, J F Pellissier, et al.
Nature Genetics
|
October 1, 1995
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency
T Bourgeron, P Rustin, D Chretien, et al.
British Journal of Cancer
|
March 24, 2011
Mitochondrial DNA mutations in head and neck cancer are infrequent and lack prognostic utility
C Challen, H Brown, C Cai, et al.
British Journal of Cancer
|
March 14, 2007
Targeting homeostatic mechanisms of endoplasmic reticulum stress to increase susceptibility of cancer cells to fenretinide-induced apoptosis: the role of stress proteins ERdj5 and ERp57
M Corazzari, P E Lovat, J L Armstrong, et al.
The Journal of Investigative Dermatology
|
November 6, 1998
A mutational hotspot in the 2B domain of human hair basic keratin 6 (hHb6) in monilethrix patients
B P Korge, E Healy, C S Munro, et al.
The Journal of Investigative Dermatology
|
October 3, 1999
Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotype
B P Korge, H Hamm, C S Jury, et al.
Page
of 2