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H Watkins

Showing results (151-160 of 212) with videos related to

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Journal of Neurophysiology|July 26, 2018
Differential effects of radiant and mechanically applied thermal stimuli on human C-tactile afferent firing patternsRochelle Ackerley, Katarina Wiklund Fernström, Helena Backlund Wasling, et al.
Biophysical Journal|November 4, 2009
Synchronous in situ ATPase activity, mechanics, and Ca2+ sensitivity of human and porcine myocardiumP J Griffiths, H Isackson, R Pelc, et al.
The Journal of Emergency Medicine|July 1, 1997
Technical considerations in knot construction. Part II. Interrupted dermal suture closureP M Mazzarese, B C Faulkner, A J Gear, et al.
Journal of Long-Term Effects of Medical Implants|December 9, 1995
Evolution of hydrogel polymers as contact lenses, surface coatings, dressings, and drug delivery systemsJ C Wheeler, J A Woods, M J Cox, et al.
Neuropsychologia|June 6, 2000
Impaired planning but intact decision making in early Huntington's disease: implications for specific fronto-striatal pathologyL H Watkins, R D Rogers, A D Lawrence, et al.
Journal of Neurophysiology|January 27, 2017
Optimal delineation of single C-tactile and C-nociceptive afferents in humans by latency slowingRoger H Watkins, Johan Wessberg, Helena Backlund Wasling, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|January 20, 2004
In vivo exposure to hyperoxia induces DNA damage in a population of alveolar type II epithelial cellsJason M Roper, Dawn J Mazzatti, Richard H Watkins, et al.
American Journal of Human Genetics|December 1, 1993
Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathyH Watkins, L Thierfelder, R Anan, et al.
Human Molecular Genetics|May 24, 2001
Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesisE Blair, C Redwood, H Ashrafian, et al.
Cell|June 3, 1994
Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomereL Thierfelder, H Watkins, C MacRae, et al.
Pageof 22

Showing results (151-160 of 212) with videos related to

Sort By:
Pageof 22
Journal of Neurophysiology|July 26, 2018
Differential effects of radiant and mechanically applied thermal stimuli on human C-tactile afferent firing patternsRochelle Ackerley, Katarina Wiklund Fernström, Helena Backlund Wasling, et al.
Biophysical Journal|November 4, 2009
Synchronous in situ ATPase activity, mechanics, and Ca2+ sensitivity of human and porcine myocardiumP J Griffiths, H Isackson, R Pelc, et al.
The Journal of Emergency Medicine|July 1, 1997
Technical considerations in knot construction. Part II. Interrupted dermal suture closureP M Mazzarese, B C Faulkner, A J Gear, et al.
Journal of Long-Term Effects of Medical Implants|December 9, 1995
Evolution of hydrogel polymers as contact lenses, surface coatings, dressings, and drug delivery systemsJ C Wheeler, J A Woods, M J Cox, et al.
Neuropsychologia|June 6, 2000
Impaired planning but intact decision making in early Huntington's disease: implications for specific fronto-striatal pathologyL H Watkins, R D Rogers, A D Lawrence, et al.
Journal of Neurophysiology|January 27, 2017
Optimal delineation of single C-tactile and C-nociceptive afferents in humans by latency slowingRoger H Watkins, Johan Wessberg, Helena Backlund Wasling, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|January 20, 2004
In vivo exposure to hyperoxia induces DNA damage in a population of alveolar type II epithelial cellsJason M Roper, Dawn J Mazzatti, Richard H Watkins, et al.
American Journal of Human Genetics|December 1, 1993
Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathyH Watkins, L Thierfelder, R Anan, et al.
Human Molecular Genetics|May 24, 2001
Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesisE Blair, C Redwood, H Ashrafian, et al.
Cell|June 3, 1994
Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomereL Thierfelder, H Watkins, C MacRae, et al.
Pageof 22