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M A Farrar

Showing results (21-30 of 30) with videos related to

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The Journal of Experimental Medicine|October 9, 1998
Regulation of L-selectin-mediated rolling through receptor dimerizationX Li, D A Steeber, M L Tang, et al.
Journal of Endovascular Therapy : an Official Journal of the International Society of Endovascular Specialists|February 28, 2001
Combined endovascular and open surgery for four-vessel cerebrovascular occlusive diseaseM S Barakate, C M Fisher, M Appleberg, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1989
Cloning and expression of the cDNA for the murine interferon gamma receptorP W Gray, S Leong, E H Fennie, et al.
Circulation|April 1, 1995
Histomorphometric and biochemical correlates of arterial procollagen gene expression during vascular repair after experimental angioplastyM A Karim, D D Miller, M A Farrar, et al.
Human Immunology|September 1, 1989
Evidence for heterogeneity of the DPA and DPB alleles derived from a DRw11,DQw7,DPw4 cell lineS L Woulfe, K Rice, D K Didier, et al.
Oncogene|October 27, 2015
Sleeping Beauty transposon screen identifies signaling modules that cooperate with STAT5 activation to induce B-cell acute lymphoblastic leukemiaL M Heltemes-Harris, J D Larson, T K Starr, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 18, 2020
Changes in long term peripheral nerve biophysical properties in childhood cancer survivors following neurotoxic chemotherapyT Kandula, M A Farrar, R J Cohn, et al.
Coronary Artery Disease|December 1, 1995
Immunohistochemical characterization of immune cell composition and cytokine receptor expression in human coronary atherectomy tissueD D Miller, F E Craig, F A Dressler, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 7, 2026
Evidence-based multidisciplinary model of care for newborn screening in spinal muscular atrophyDidu S Kariyawasam, C E Meagher, A Kay, et al.
Acta Neuropathologica|August 30, 2019
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvementS Donkervoort, R Sabouny, P Yun, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
The Journal of Experimental Medicine|October 9, 1998
Regulation of L-selectin-mediated rolling through receptor dimerizationX Li, D A Steeber, M L Tang, et al.
Journal of Endovascular Therapy : an Official Journal of the International Society of Endovascular Specialists|February 28, 2001
Combined endovascular and open surgery for four-vessel cerebrovascular occlusive diseaseM S Barakate, C M Fisher, M Appleberg, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1989
Cloning and expression of the cDNA for the murine interferon gamma receptorP W Gray, S Leong, E H Fennie, et al.
Circulation|April 1, 1995
Histomorphometric and biochemical correlates of arterial procollagen gene expression during vascular repair after experimental angioplastyM A Karim, D D Miller, M A Farrar, et al.
Human Immunology|September 1, 1989
Evidence for heterogeneity of the DPA and DPB alleles derived from a DRw11,DQw7,DPw4 cell lineS L Woulfe, K Rice, D K Didier, et al.
Oncogene|October 27, 2015
Sleeping Beauty transposon screen identifies signaling modules that cooperate with STAT5 activation to induce B-cell acute lymphoblastic leukemiaL M Heltemes-Harris, J D Larson, T K Starr, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 18, 2020
Changes in long term peripheral nerve biophysical properties in childhood cancer survivors following neurotoxic chemotherapyT Kandula, M A Farrar, R J Cohn, et al.
Coronary Artery Disease|December 1, 1995
Immunohistochemical characterization of immune cell composition and cytokine receptor expression in human coronary atherectomy tissueD D Miller, F E Craig, F A Dressler, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 7, 2026
Evidence-based multidisciplinary model of care for newborn screening in spinal muscular atrophyDidu S Kariyawasam, C E Meagher, A Kay, et al.
Acta Neuropathologica|August 30, 2019
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvementS Donkervoort, R Sabouny, P Yun, et al.
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