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V Walsh

Showing results (191-200 of 235) with videos related to

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Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|September 1, 1995
Enteropathy-associated T-cell lymphoma in the West of Ireland: low-frequency of Epstein-Barr virus in these tumorsS V Walsh, L J Egan, C E Connolly, et al.
The American Journal of Surgical Pathology|April 13, 1999
Allergic esophagitis in children: a clinicopathological entityS V Walsh, D A Antonioli, H Goldman, et al.
Journal of Gastroenterology and Hepatology|April 23, 2014
Serum proteome of nonalcoholic fatty liver disease: a multimodal approach to discovery of biomarkers of nonalcoholic steatohepatitisMichael H Miller, Shaun V Walsh, Abdel Atrih, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|April 27, 2012
Phase-I/II study of bortezomib in combination with carboplatin and bevacizumab as first-line therapy in patients with advanced non-small-cell lung cancerBilal Piperdi, William V Walsh, Kendra Bradley, et al.
Journal of Rehabilitation Research and Development|August 4, 2015
Effects of repetitive low-level blast exposure on visual system and ocular structuresJosé E Capó-Aponte, Gina M Jurek, David V Walsh, et al.
Nucleic Acids Research|February 25, 1990
A HindIII polymorphism identified by a DNA clone which maps to chromosome 17 (D17S245)J D Brook, M Upadhyaya, W Broadhead, et al.
Biochemical and Biophysical Research Communications|September 24, 1999
Inhibition of mitochondrial function in HL60 cells is associated with an increased apoptosis and expression of CD14K I Mills, L J Woodgate, A F Gilkes, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 29, 2011
Type 1 ryanodine receptor knock-in mutation causing central core disease of skeletal muscle also displays a neuronal phenotypeValerie De Crescenzo, Kevin E Fogarty, Jason J Lefkowitz, et al.
Human Genetics|August 1, 1990
Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophyK V Walsh, H G Harley, J D Brook, et al.
Military Medicine|February 3, 2015
Visual field dysfunctions in warfighters during different stages following blast and nonblast mTBIDavid V Walsh, José E Capó-Aponte, Kendra Jorgensen-Wagers, et al.
Pageof 24

Showing results (191-200 of 235) with videos related to

Sort By:
Pageof 24
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|September 1, 1995
Enteropathy-associated T-cell lymphoma in the West of Ireland: low-frequency of Epstein-Barr virus in these tumorsS V Walsh, L J Egan, C E Connolly, et al.
The American Journal of Surgical Pathology|April 13, 1999
Allergic esophagitis in children: a clinicopathological entityS V Walsh, D A Antonioli, H Goldman, et al.
Journal of Gastroenterology and Hepatology|April 23, 2014
Serum proteome of nonalcoholic fatty liver disease: a multimodal approach to discovery of biomarkers of nonalcoholic steatohepatitisMichael H Miller, Shaun V Walsh, Abdel Atrih, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|April 27, 2012
Phase-I/II study of bortezomib in combination with carboplatin and bevacizumab as first-line therapy in patients with advanced non-small-cell lung cancerBilal Piperdi, William V Walsh, Kendra Bradley, et al.
Journal of Rehabilitation Research and Development|August 4, 2015
Effects of repetitive low-level blast exposure on visual system and ocular structuresJosé E Capó-Aponte, Gina M Jurek, David V Walsh, et al.
Nucleic Acids Research|February 25, 1990
A HindIII polymorphism identified by a DNA clone which maps to chromosome 17 (D17S245)J D Brook, M Upadhyaya, W Broadhead, et al.
Biochemical and Biophysical Research Communications|September 24, 1999
Inhibition of mitochondrial function in HL60 cells is associated with an increased apoptosis and expression of CD14K I Mills, L J Woodgate, A F Gilkes, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 29, 2011
Type 1 ryanodine receptor knock-in mutation causing central core disease of skeletal muscle also displays a neuronal phenotypeValerie De Crescenzo, Kevin E Fogarty, Jason J Lefkowitz, et al.
Human Genetics|August 1, 1990
Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophyK V Walsh, H G Harley, J D Brook, et al.
Military Medicine|February 3, 2015
Visual field dysfunctions in warfighters during different stages following blast and nonblast mTBIDavid V Walsh, José E Capó-Aponte, Kendra Jorgensen-Wagers, et al.
Pageof 24