Search research articles
Contact Us
Filters
Showing results (1-10 of 30) with videos related to
Page
of 3
Sort By:
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 neurons
John F Staropoli, Asa Abeliovich
Journal of Clinical Microbiology
|
June 27, 2008
Cord formation in a clinical isolate of Mycobacterium marinum
John 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 trafficking
Susan 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-p11.4
John 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 resistance
John 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 spectrum
Susan 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 excitotoxicity
John 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 mutation
John 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 mutation
Annette Leon, John F Staropoli, Jesus M Hernandez, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 30) with videos related to
Sort By:
Page
of 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 neurons
John F Staropoli, Asa Abeliovich
Journal of Clinical Microbiology
|
June 27, 2008
Cord formation in a clinical isolate of Mycobacterium marinum
John 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 trafficking
Susan 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-p11.4
John 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 resistance
John 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 spectrum
Susan 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 excitotoxicity
John 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 mutation
John 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 mutation
Annette Leon, John F Staropoli, Jesus M Hernandez, et al.
Page
of 3