Search research articles
Contact Us
Filters
Showing results (151-160 of 212) with videos related to
Page
of 22
Sort By:
Journal of Neurophysiology
|
July 26, 2018
Differential effects of radiant and mechanically applied thermal stimuli on human C-tactile afferent firing patterns
Rochelle 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 myocardium
P 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 closure
P 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 systems
J 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 pathology
L 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 slowing
Roger 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 cells
Jason 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 cardiomyopathy
H 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 pathogenesis
E 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 sarcomere
L Thierfelder, H Watkins, C MacRae, et al.
Page
of 22
Search research articles
Search
Showing results (151-160 of 212) with videos related to
Sort By:
Page
of 22
Journal of Neurophysiology
|
July 26, 2018
Differential effects of radiant and mechanically applied thermal stimuli on human C-tactile afferent firing patterns
Rochelle 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 myocardium
P 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 closure
P 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 systems
J 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 pathology
L 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 slowing
Roger 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 cells
Jason 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 cardiomyopathy
H 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 pathogenesis
E 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 sarcomere
L Thierfelder, H Watkins, C MacRae, et al.
Page
of 22