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Diabetologia
|
October 25, 2017
Correction to: Islet-intrinsic effects of CFTR mutation
Fiona N Manderson Koivula, Neville H McClenaghan, Alan G S Harper, et al.
Journal of the Neurological Sciences
|
December 1, 1988
Evidence against location of the gene for facioscapulohumeral muscular dystrophy on the distal long arm of chromosome 14
P W Lunt, J G Noades, M Upadhyaya, et al.
Clinical Genetics
|
March 1, 1988
Population studies of Huntington's disease in Wales
O W Quarrell, A Tyler, M P Jones, et al.
Progress in Clinical and Biological Research
|
January 1, 1985
Gene mapping and myotonic dystrophy
P S Harper, D Shaw, L Meredith, et al.
Nano Research
|
January 21, 2021
Controlling human platelet activation with calcium-binding nanoparticles
David Cabrera, Karen Walker, Sandhya Moise, et al.
Journal of the American Chemical Society
|
May 13, 2004
Electrochemistry and optical absorbance and luminescence of molecule-like Au38 nanoparticles
Dongil Lee, Robert L Donkers, Gangli Wang, et al.
Muscle & Nerve. Supplement
|
January 1, 1995
Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD)
M Upadhyaya, J Maynard, M Osborn, et al.
The Journal of Comparative Neurology
|
June 15, 1994
Localization of nerve growth factor (NGF) and low-affinity NGF receptors in touch domes and quantification of NGF mRNA in keratinocytes of adult rats
K B English, S Harper, N Stayner, et al.
Cellular Signalling
|
August 8, 2007
Dual role of tubulin-cytoskeleton in store-operated calcium entry in human platelets
Pedro C Redondo, Alan G S Harper, Stewart O Sage, et al.
Journal of Molecular and Cellular Cardiology
|
November 1, 1991
Myocardial membrane cholesterol: effects of ischaemia
H Venter, S Genade, R Mouton, et al.
Page
of 123
Search research articles
Search
Showing results (431-440 of 1,225) with videos related to
Sort By:
Page
of 123
Diabetologia
|
October 25, 2017
Correction to: Islet-intrinsic effects of CFTR mutation
Fiona N Manderson Koivula, Neville H McClenaghan, Alan G S Harper, et al.
Journal of the Neurological Sciences
|
December 1, 1988
Evidence against location of the gene for facioscapulohumeral muscular dystrophy on the distal long arm of chromosome 14
P W Lunt, J G Noades, M Upadhyaya, et al.
Clinical Genetics
|
March 1, 1988
Population studies of Huntington's disease in Wales
O W Quarrell, A Tyler, M P Jones, et al.
Progress in Clinical and Biological Research
|
January 1, 1985
Gene mapping and myotonic dystrophy
P S Harper, D Shaw, L Meredith, et al.
Nano Research
|
January 21, 2021
Controlling human platelet activation with calcium-binding nanoparticles
David Cabrera, Karen Walker, Sandhya Moise, et al.
Journal of the American Chemical Society
|
May 13, 2004
Electrochemistry and optical absorbance and luminescence of molecule-like Au38 nanoparticles
Dongil Lee, Robert L Donkers, Gangli Wang, et al.
Muscle & Nerve. Supplement
|
January 1, 1995
Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD)
M Upadhyaya, J Maynard, M Osborn, et al.
The Journal of Comparative Neurology
|
June 15, 1994
Localization of nerve growth factor (NGF) and low-affinity NGF receptors in touch domes and quantification of NGF mRNA in keratinocytes of adult rats
K B English, S Harper, N Stayner, et al.
Cellular Signalling
|
August 8, 2007
Dual role of tubulin-cytoskeleton in store-operated calcium entry in human platelets
Pedro C Redondo, Alan G S Harper, Stewart O Sage, et al.
Journal of Molecular and Cellular Cardiology
|
November 1, 1991
Myocardial membrane cholesterol: effects of ischaemia
H Venter, S Genade, R Mouton, et al.
Page
of 123