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C Bruno

Showing results (211-220 of 355) with videos related to

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Neuromuscular Disorders : NMD|November 2, 1999
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathyC Bruno, M DiRocco, L D Lamba, et al.
La Clinica Terapeutica|July 7, 2007
[HAV infection in patients with chronic hepatitis C]G Bertino, A M Ardiri, M C Bruno, et al.
Molecular Cancer Research : MCR|August 26, 2018
A Role for Tryptophan-2,3-dioxygenase in CD8 T-cell Suppression and Evidence of Tryptophan Catabolism in Breast Cancer Patient PlasmaLisa I Greene, Tullia C Bruno, Jessica L Christenson, et al.
Archives of Neurology|February 19, 2000
A novel missense mutation (W797R) in the myophosphorylase gene in Spanish patients with McArdle diseaseR Fernández, C Navarro, A L Andreu, et al.
Plos One|April 6, 2012
Phenotypic and functional properties of Helios+ regulatory T cellsDaniel J Zabransky, Christopher J Nirschl, Nicholas M Durham, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 24, 2010
McArdle disease: a clinical reviewR Quinlivan, J Buckley, M James, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 4, 2008
Phenotypic analysis of prostate-infiltrating lymphocytes reveals TH17 and Treg skewingKaren Sandell Sfanos, Tullia C Bruno, Charles H Maris, et al.
La Clinica Terapeutica|May 1, 1997
[Comparative study of the modification of arterial pressure in adult and aged subjects treated with hemofiltration. Preliminary results]G E Russo, S Giusti, E Vitaliano, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 19, 2006
Granulocyte colony-stimulating factor preferentially stimulates proliferation of monosomy 7 cells bearing the isoform IV receptorElaine M Sloand, Agnes S M Yong, Shakti Ramkissoon, et al.
American Journal of Human Genetics|August 12, 1999
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IVC Bruno, A Martinuzzi, Y Tang, et al.
Pageof 36

Showing results (211-220 of 355) with videos related to

Sort By:
Pageof 36
Neuromuscular Disorders : NMD|November 2, 1999
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathyC Bruno, M DiRocco, L D Lamba, et al.
La Clinica Terapeutica|July 7, 2007
[HAV infection in patients with chronic hepatitis C]G Bertino, A M Ardiri, M C Bruno, et al.
Molecular Cancer Research : MCR|August 26, 2018
A Role for Tryptophan-2,3-dioxygenase in CD8 T-cell Suppression and Evidence of Tryptophan Catabolism in Breast Cancer Patient PlasmaLisa I Greene, Tullia C Bruno, Jessica L Christenson, et al.
Archives of Neurology|February 19, 2000
A novel missense mutation (W797R) in the myophosphorylase gene in Spanish patients with McArdle diseaseR Fernández, C Navarro, A L Andreu, et al.
Plos One|April 6, 2012
Phenotypic and functional properties of Helios+ regulatory T cellsDaniel J Zabransky, Christopher J Nirschl, Nicholas M Durham, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 24, 2010
McArdle disease: a clinical reviewR Quinlivan, J Buckley, M James, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 4, 2008
Phenotypic analysis of prostate-infiltrating lymphocytes reveals TH17 and Treg skewingKaren Sandell Sfanos, Tullia C Bruno, Charles H Maris, et al.
La Clinica Terapeutica|May 1, 1997
[Comparative study of the modification of arterial pressure in adult and aged subjects treated with hemofiltration. Preliminary results]G E Russo, S Giusti, E Vitaliano, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 19, 2006
Granulocyte colony-stimulating factor preferentially stimulates proliferation of monosomy 7 cells bearing the isoform IV receptorElaine M Sloand, Agnes S M Yong, Shakti Ramkissoon, et al.
American Journal of Human Genetics|August 12, 1999
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IVC Bruno, A Martinuzzi, Y Tang, et al.
Pageof 36