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John F Staropoli

Showing results (1-10 of 30) with videos related to

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Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|July 16, 2008
Tumorigenesis and neurodegeneration: two sides of the same coin?John F Staropoli
Journal of Molecular Neuroscience : MN|September 28, 2005
The ubiquitin-proteasome pathway is necessary for maintenance of the postmitotic status of neuronsJohn F Staropoli, Asa Abeliovich
Journal of Clinical Microbiology|June 27, 2008
Cord formation in a clinical isolate of Mycobacterium marinumJohn F Staropoli, John A Branda
Clinical Lipidology|May 1, 2012
The juvenile Batten disease protein, CLN3, and its role in regulating anterograde and retrograde post-Golgi traffickingSusan L Cotman, John F Staropoli
Journal of Medical Genetics|August 4, 2010
Co-segregation of Norrie disease and idiopathic pulmonary hypertension in a family with a microdeletion of the NDP region at Xp11.3-p11.4John F Staropoli, Winnie Xin, Katherine B Sims
Transfusion|August 5, 2008
Membrane autoantibodies in systemic lupus erythematosus: a case of autoimmune hemolytic anemia, antiphospholipid antibodies, and transient acquired activated protein C resistanceJohn F Staropoli, Elizabeth M Van Cott, Robert S Makar
Current Neurology and Neuroscience Reports|June 19, 2013
Neuronal ceroid lipofuscinosis: impact of recent genetic advances and expansion of the clinicopathologic spectrumSusan L Cotman, Amel Karaa, John F Staropoli, et al.
Neuron|March 12, 2003
Parkin is a component of an SCF-like ubiquitin ligase complex and protects postmitotic neurons from kainate excitotoxicityJohn F Staropoli, Caroline McDermott, Cécile Martinat, et al.
BMC Medical Genetics|June 26, 2012
An atypical case of neuronal ceroid lipofuscinosis with co-inheritance of a variably penetrant POLG1 mutationJohn F Staropoli, Winnie Xin, Rosemary Barone, et al.
Leukemia Research|March 8, 2011
Translocation t(1;9) is a recurrent cytogenetic abnormality associated with progression of essential thrombocythemia patients displaying the JAK2 V617F mutationAnnette Leon, John F Staropoli, Jesus M Hernandez, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|July 16, 2008
Tumorigenesis and neurodegeneration: two sides of the same coin?John F Staropoli
Journal of Molecular Neuroscience : MN|September 28, 2005
The ubiquitin-proteasome pathway is necessary for maintenance of the postmitotic status of neuronsJohn F Staropoli, Asa Abeliovich
Journal of Clinical Microbiology|June 27, 2008
Cord formation in a clinical isolate of Mycobacterium marinumJohn F Staropoli, John A Branda
Clinical Lipidology|May 1, 2012
The juvenile Batten disease protein, CLN3, and its role in regulating anterograde and retrograde post-Golgi traffickingSusan L Cotman, John F Staropoli
Journal of Medical Genetics|August 4, 2010
Co-segregation of Norrie disease and idiopathic pulmonary hypertension in a family with a microdeletion of the NDP region at Xp11.3-p11.4John F Staropoli, Winnie Xin, Katherine B Sims
Transfusion|August 5, 2008
Membrane autoantibodies in systemic lupus erythematosus: a case of autoimmune hemolytic anemia, antiphospholipid antibodies, and transient acquired activated protein C resistanceJohn F Staropoli, Elizabeth M Van Cott, Robert S Makar
Current Neurology and Neuroscience Reports|June 19, 2013
Neuronal ceroid lipofuscinosis: impact of recent genetic advances and expansion of the clinicopathologic spectrumSusan L Cotman, Amel Karaa, John F Staropoli, et al.
Neuron|March 12, 2003
Parkin is a component of an SCF-like ubiquitin ligase complex and protects postmitotic neurons from kainate excitotoxicityJohn F Staropoli, Caroline McDermott, Cécile Martinat, et al.
BMC Medical Genetics|June 26, 2012
An atypical case of neuronal ceroid lipofuscinosis with co-inheritance of a variably penetrant POLG1 mutationJohn F Staropoli, Winnie Xin, Rosemary Barone, et al.
Leukemia Research|March 8, 2011
Translocation t(1;9) is a recurrent cytogenetic abnormality associated with progression of essential thrombocythemia patients displaying the JAK2 V617F mutationAnnette Leon, John F Staropoli, Jesus M Hernandez, et al.
Pageof 3