Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A Fryer

Showing results (201-210 of 378) with videos related to

Pageof 38
Sort By:
Clinical Chemistry|February 21, 2012
Inappropriate requesting of glycated hemoglobin (Hb A1c) is widespread: assessment of prevalence, impact of national guidance, and practice-to-practice variabilityOwen J Driskell, David Holland, Fahmy W Hanna, et al.
British Journal of Cancer|October 1, 1994
Progression of cervical intraepithelial neoplasia to cervical cancer: interactions of cytochrome P450 CYP2D6 EM and glutathione s-transferase GSTM1 null genotypes and cigarette smokingA P Warwick, C W Redman, P W Jones, et al.
Journal of the American Society of Nephrology : JASN|December 26, 2001
Vascular endothelial growth factor gene polymorphisms are associated with acute renal allograft rejectionMajid Shahbazi, Anthony A Fryer, Vera Pravica, et al.
Biochimica Et Biophysica Acta|October 15, 1987
Studies on the developmental expression of glutathione S-transferase isoenzymes in human heart and diaphragmP A Hirrell, R Hume, A A Fryer, et al.
Cornea|January 1, 1997
Histopathology and molecular cytogenetics of a corneal opacity associated with the trisomy 8 mosaic syndrome (46,XY/47,XY, +8)J A Scott, P J Howard, P A Smith, et al.
Carcinogenesis|September 5, 2001
Outcome in prostate cancer associations with skin type and polymorphism in pigmentation-related genesC J Luscombe, M E French, S Liu, et al.
Respiratory Medicine|December 20, 2003
The association of maternal but not paternal genetic variation in GSTP1 with asthma phenotypes in childrenFrances Child, Warren Lenney, Sadie Clayton, et al.
Clinical and Experimental Dermatology|May 15, 2014
Novel compound heterozygous mutations in the desmoplakin gene cause hair shaft abnormalities and culminate in lethal cardiomyopathyP D Yesudian, R M Cabral, E Ladusans, et al.
Journal of Neurology|August 10, 2000
A pilot study of the relationship between gadolinium-enhancing lesions, gender effect and polymorphisms of antioxidant enzymes in multiple sclerosisS J Weatherby, C L Mann, M B Davies, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 1, 1997
Selective O-desulfation produces nonanticoagulant heparin that retains pharmacological activity in the lungA Fryer, Y C Huang, G Rao, et al.
Pageof 38

Showing results (201-210 of 378) with videos related to

Sort By:
Pageof 38
Clinical Chemistry|February 21, 2012
Inappropriate requesting of glycated hemoglobin (Hb A1c) is widespread: assessment of prevalence, impact of national guidance, and practice-to-practice variabilityOwen J Driskell, David Holland, Fahmy W Hanna, et al.
British Journal of Cancer|October 1, 1994
Progression of cervical intraepithelial neoplasia to cervical cancer: interactions of cytochrome P450 CYP2D6 EM and glutathione s-transferase GSTM1 null genotypes and cigarette smokingA P Warwick, C W Redman, P W Jones, et al.
Journal of the American Society of Nephrology : JASN|December 26, 2001
Vascular endothelial growth factor gene polymorphisms are associated with acute renal allograft rejectionMajid Shahbazi, Anthony A Fryer, Vera Pravica, et al.
Biochimica Et Biophysica Acta|October 15, 1987
Studies on the developmental expression of glutathione S-transferase isoenzymes in human heart and diaphragmP A Hirrell, R Hume, A A Fryer, et al.
Cornea|January 1, 1997
Histopathology and molecular cytogenetics of a corneal opacity associated with the trisomy 8 mosaic syndrome (46,XY/47,XY, +8)J A Scott, P J Howard, P A Smith, et al.
Carcinogenesis|September 5, 2001
Outcome in prostate cancer associations with skin type and polymorphism in pigmentation-related genesC J Luscombe, M E French, S Liu, et al.
Respiratory Medicine|December 20, 2003
The association of maternal but not paternal genetic variation in GSTP1 with asthma phenotypes in childrenFrances Child, Warren Lenney, Sadie Clayton, et al.
Clinical and Experimental Dermatology|May 15, 2014
Novel compound heterozygous mutations in the desmoplakin gene cause hair shaft abnormalities and culminate in lethal cardiomyopathyP D Yesudian, R M Cabral, E Ladusans, et al.
Journal of Neurology|August 10, 2000
A pilot study of the relationship between gadolinium-enhancing lesions, gender effect and polymorphisms of antioxidant enzymes in multiple sclerosisS J Weatherby, C L Mann, M B Davies, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 1, 1997
Selective O-desulfation produces nonanticoagulant heparin that retains pharmacological activity in the lungA Fryer, Y C Huang, G Rao, et al.
Pageof 38