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M A Simpson

Showing results (111-120 of 153) with videos related to

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Clinical Genetics|August 28, 2007
Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian familiesM Hashemzadeh Chaleshtori, M A Simpson, E Farrokhi, et al.
Archives of Surgery (Chicago, Ill. : 1960)|March 1, 1995
Kidney transplantation in diabetic patients using cyclosporine. Five-year follow-upD Shaffer, M A Simpson, P N Madras, et al.
Neurology|October 25, 2002
Diagnostic strategies in CADASILH S Markus, R J Martin, M A Simpson, et al.
The Journal of Biological Chemistry|March 30, 2001
Hyaluronan synthase elevation in metastatic prostate carcinoma cells correlates with hyaluronan surface retention, a prerequisite for rapid adhesion to bone marrow endothelial cellsM A Simpson, J Reiland, S R Burger, et al.
Transplantation|February 1, 1989
Sequential determinations of urinary cytology and plasma and urinary lymphokines in the management of renal allograft recipientsM A Simpson, P N Madras, A J Cornaby, et al.
Free Radical Biology & Medicine|July 27, 2019
Serum electrolytes can promote hydroxyl radical-initiated biomolecular damage from inflammationYukako Komaki, Adam M-A Simpson, Jong Kwon Choe, et al.
Cardiology|October 30, 2008
Homozygous mutation of desmocollin-2 in arrhythmogenic right ventricular cardiomyopathy with mild palmoplantar keratoderma and woolly hairM A Simpson, S Mansour, D Ahnood, et al.
Australian Veterinary Journal|May 1, 1988
Prevalence of bovine venereal disease in the Victoria River District of the Northern Territory: likely economic effects and practicable control measuresC J McCool, M P Townsend, S G Wolfe, et al.
Transplantation Proceedings|February 1, 1991
Sequential IL-2 and IL-2R levels predict rejection in liver allograft recipientsM A Simpson, T Young-Fadok, P N Madras, et al.
Neurology|May 9, 2008
A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23K J Dick, R Al-Mjeni, W Baskir, et al.
Pageof 16

Showing results (111-120 of 153) with videos related to

Sort By:
Pageof 16
Clinical Genetics|August 28, 2007
Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian familiesM Hashemzadeh Chaleshtori, M A Simpson, E Farrokhi, et al.
Archives of Surgery (Chicago, Ill. : 1960)|March 1, 1995
Kidney transplantation in diabetic patients using cyclosporine. Five-year follow-upD Shaffer, M A Simpson, P N Madras, et al.
Neurology|October 25, 2002
Diagnostic strategies in CADASILH S Markus, R J Martin, M A Simpson, et al.
The Journal of Biological Chemistry|March 30, 2001
Hyaluronan synthase elevation in metastatic prostate carcinoma cells correlates with hyaluronan surface retention, a prerequisite for rapid adhesion to bone marrow endothelial cellsM A Simpson, J Reiland, S R Burger, et al.
Transplantation|February 1, 1989
Sequential determinations of urinary cytology and plasma and urinary lymphokines in the management of renal allograft recipientsM A Simpson, P N Madras, A J Cornaby, et al.
Free Radical Biology & Medicine|July 27, 2019
Serum electrolytes can promote hydroxyl radical-initiated biomolecular damage from inflammationYukako Komaki, Adam M-A Simpson, Jong Kwon Choe, et al.
Cardiology|October 30, 2008
Homozygous mutation of desmocollin-2 in arrhythmogenic right ventricular cardiomyopathy with mild palmoplantar keratoderma and woolly hairM A Simpson, S Mansour, D Ahnood, et al.
Australian Veterinary Journal|May 1, 1988
Prevalence of bovine venereal disease in the Victoria River District of the Northern Territory: likely economic effects and practicable control measuresC J McCool, M P Townsend, S G Wolfe, et al.
Transplantation Proceedings|February 1, 1991
Sequential IL-2 and IL-2R levels predict rejection in liver allograft recipientsM A Simpson, T Young-Fadok, P N Madras, et al.
Neurology|May 9, 2008
A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23K J Dick, R Al-Mjeni, W Baskir, et al.
Pageof 16