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A Patton

Showing results (321-330 of 412) with videos related to

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Nature Genetics|July 23, 2002
SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegiaHeema Patel, Harold Cross, Christos Proukakis, et al.
Journal of Science and Medicine in Sport|April 20, 2019
An assessment of the utility and functionality of wearable head impact sensors in Australian FootballAndrew S McIntosh, Catherine Willmott, Declan A Patton, et al.
Heart (British Cardiac Society)|May 10, 2008
Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the AmishK Zahka, K Kalidas, M A Simpson, et al.
The Biochemical Journal|October 15, 1995
Identification of a heparin-binding protein using monoclonal antibodies that block heparin binding to porcine aortic endothelial cellsW A Patton, C A Granzow, L A Getts, et al.
Journal of Dairy Science|March 2, 2015
Effects of slow-release urea and rumen-protected methionine and histidine on performance of dairy cowsF Giallongo, A N Hristov, J Oh, et al.
Human Molecular Genetics|January 15, 2005
Common arterial trunk associated with a homeodomain mutation of NKX2.6Kirsten Heathcote, Claire Braybrook, Lulu Abushaban, et al.
American Journal of Medical Genetics|December 1, 1994
Small terminal deletions of the long arm of chromosome 2: two new casesA M Fisher, K H Ellis, C E Browne, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 9, 2002
Growth hormone therapy in Noonan's syndrome: non-cardiomyopathic congenital heart disease does not adversely affect growth improvementD C Brown, C E Macfarlane, W J McKenna, et al.
Advanced Materials (Deerfield Beach, Fla.)|October 14, 2017
Engineering Cell Surface Function with DNA OrigamiEhsan Akbari, Molly Y Mollica, Christopher R Lucas, et al.
Nature Genetics|September 18, 2001
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossiaC Braybrook, K Doudney, A C Marçano, et al.
Pageof 42

Showing results (321-330 of 412) with videos related to

Sort By:
Pageof 42
Nature Genetics|July 23, 2002
SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegiaHeema Patel, Harold Cross, Christos Proukakis, et al.
Journal of Science and Medicine in Sport|April 20, 2019
An assessment of the utility and functionality of wearable head impact sensors in Australian FootballAndrew S McIntosh, Catherine Willmott, Declan A Patton, et al.
Heart (British Cardiac Society)|May 10, 2008
Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the AmishK Zahka, K Kalidas, M A Simpson, et al.
The Biochemical Journal|October 15, 1995
Identification of a heparin-binding protein using monoclonal antibodies that block heparin binding to porcine aortic endothelial cellsW A Patton, C A Granzow, L A Getts, et al.
Journal of Dairy Science|March 2, 2015
Effects of slow-release urea and rumen-protected methionine and histidine on performance of dairy cowsF Giallongo, A N Hristov, J Oh, et al.
Human Molecular Genetics|January 15, 2005
Common arterial trunk associated with a homeodomain mutation of NKX2.6Kirsten Heathcote, Claire Braybrook, Lulu Abushaban, et al.
American Journal of Medical Genetics|December 1, 1994
Small terminal deletions of the long arm of chromosome 2: two new casesA M Fisher, K H Ellis, C E Browne, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 9, 2002
Growth hormone therapy in Noonan's syndrome: non-cardiomyopathic congenital heart disease does not adversely affect growth improvementD C Brown, C E Macfarlane, W J McKenna, et al.
Advanced Materials (Deerfield Beach, Fla.)|October 14, 2017
Engineering Cell Surface Function with DNA OrigamiEhsan Akbari, Molly Y Mollica, Christopher R Lucas, et al.
Nature Genetics|September 18, 2001
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossiaC Braybrook, K Doudney, A C Marçano, et al.
Pageof 42