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M A Reddy

Showing results (21-30 of 32) with videos related to

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Diabetologia|December 13, 2005
Increased expression of cyclooxygenase-2 in human pancreatic islets treated with high glucose or ligands of the advanced glycation endproduct-specific receptor (AGER), and in islets from diabetic miceN Shanmugam, I T Todorov, I Nair, et al.
The Cochrane Database of Systematic Reviews|June 8, 2017
Focal laser treatment in addition to chemotherapy for retinoblastomaIdo D Fabian, Kenneth P Johnson, Andrew W Stacey, et al.
Infection and Immunity|October 18, 2000
Involvement of focal adhesion kinase in Escherichia coli invasion of human brain microvascular endothelial cellsM A Reddy, C A Wass, K S Kim, et al.
Comparative Medicine|November 14, 2008
Platelets from diabetic pigs exhibit hypersensitivity to thrombinShivendra D Shukla, Sanjay V Kansra, M A Reddy, et al.
Kidney International|March 4, 2006
Relationship between 12/15-lipoxygenase and COX-2 in mesangial cells: potential role in diabetic nephropathyZ-G Xu, S-L Li, L Lanting, et al.
The Journal of Infectious Diseases|August 23, 2001
Differential role of cytosolic phospholipase A2 in the invasion of brain microvascular endothelial cells by Escherichia coli and Listeria monocytogenesA Das, L Asatryan, M A Reddy, et al.
The Journal of Experimental Medicine|December 1, 1994
Opposing actions of c-ets/PU.1 and c-myb protooncogene products in regulating the macrophage-specific promoters of the human and mouse colony-stimulating factor-1 receptor (c-fms) genesM A Reddy, B S Yang, X Yue, et al.
The British Journal of Ophthalmology|January 25, 2003
A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphylomaM A Reddy, P J Francis, V Berry, et al.
American Journal of Human Genetics|September 29, 2001
Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humansV Berry, P Francis, M A Reddy, et al.
Human Molecular Genetics|March 16, 2004
Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataractM A Reddy, O A Bateman, C Chakarova, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Diabetologia|December 13, 2005
Increased expression of cyclooxygenase-2 in human pancreatic islets treated with high glucose or ligands of the advanced glycation endproduct-specific receptor (AGER), and in islets from diabetic miceN Shanmugam, I T Todorov, I Nair, et al.
The Cochrane Database of Systematic Reviews|June 8, 2017
Focal laser treatment in addition to chemotherapy for retinoblastomaIdo D Fabian, Kenneth P Johnson, Andrew W Stacey, et al.
Infection and Immunity|October 18, 2000
Involvement of focal adhesion kinase in Escherichia coli invasion of human brain microvascular endothelial cellsM A Reddy, C A Wass, K S Kim, et al.
Comparative Medicine|November 14, 2008
Platelets from diabetic pigs exhibit hypersensitivity to thrombinShivendra D Shukla, Sanjay V Kansra, M A Reddy, et al.
Kidney International|March 4, 2006
Relationship between 12/15-lipoxygenase and COX-2 in mesangial cells: potential role in diabetic nephropathyZ-G Xu, S-L Li, L Lanting, et al.
The Journal of Infectious Diseases|August 23, 2001
Differential role of cytosolic phospholipase A2 in the invasion of brain microvascular endothelial cells by Escherichia coli and Listeria monocytogenesA Das, L Asatryan, M A Reddy, et al.
The Journal of Experimental Medicine|December 1, 1994
Opposing actions of c-ets/PU.1 and c-myb protooncogene products in regulating the macrophage-specific promoters of the human and mouse colony-stimulating factor-1 receptor (c-fms) genesM A Reddy, B S Yang, X Yue, et al.
The British Journal of Ophthalmology|January 25, 2003
A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphylomaM A Reddy, P J Francis, V Berry, et al.
American Journal of Human Genetics|September 29, 2001
Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humansV Berry, P Francis, M A Reddy, et al.
Human Molecular Genetics|March 16, 2004
Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataractM A Reddy, O A Bateman, C Chakarova, et al.
Pageof 4