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Clinical Case Reports
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March 27, 2023
Supraventricular tachycardia and deep vein thrombosis following Moderna vaccination: A case series
Niroj Bhandari, Aashutosh Chaudhary, Suyash Acharya, et al.
Plos One
|
September 27, 2013
Ocular expression and distribution of products of the POAG-associated chromosome 9p21 gene region
Glyn Chidlow, John P M Wood, Shiwani Sharma, et al.
Experimental Eye Research
|
May 16, 2009
Identification of LOXL1 protein and Apolipoprotein E as components of surgically isolated pseudoexfoliation material by direct mass spectrometry
Shiwani Sharma, Tim Chataway, Kathryn P Burdon, et al.
European Journal of Human Genetics : EJHG
|
January 12, 2012
Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process
Abraham Kuot, Alex W Hewitt, Kim Griggs, et al.
BMC Research Notes
|
February 13, 2016
Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataract
Shari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Experimental Eye Research
|
July 6, 2021
Differential gene expression analysis of corneal endothelium indicates involvement of phagocytic activity in Fuchs' endothelial corneal dystrophy
Abraham Kuot, Mark A Corbett, Richard A Mills, et al.
Molecular Vision
|
September 23, 2008
Genetic analysis of the clusterin gene in pseudoexfoliation syndrome
Kathryn P Burdon, Shiwani Sharma, Alex W Hewitt, et al.
Experimental Eye Research
|
March 22, 2016
Biological effect of LOXL1 coding variants associated with pseudoexfoliation syndrome
Shiwani Sharma, Sarah Martin, Matthew J Sykes, et al.
Investigative Ophthalmology & Visual Science
|
September 8, 2021
Genotype, Age, Genetic Background, and Sex Influence Epha2-Related Cataract Development in Mice
Alpana Dave, Jamie E Craig, Mohammad Alamein, et al.
Molecular Vision
|
October 25, 2008
Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoform
Shiwani Sharma, Kathryn P Burdon, Alpana Dave, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 71) with videos related to
Sort By:
Page
of 8
Clinical Case Reports
|
March 27, 2023
Supraventricular tachycardia and deep vein thrombosis following Moderna vaccination: A case series
Niroj Bhandari, Aashutosh Chaudhary, Suyash Acharya, et al.
Plos One
|
September 27, 2013
Ocular expression and distribution of products of the POAG-associated chromosome 9p21 gene region
Glyn Chidlow, John P M Wood, Shiwani Sharma, et al.
Experimental Eye Research
|
May 16, 2009
Identification of LOXL1 protein and Apolipoprotein E as components of surgically isolated pseudoexfoliation material by direct mass spectrometry
Shiwani Sharma, Tim Chataway, Kathryn P Burdon, et al.
European Journal of Human Genetics : EJHG
|
January 12, 2012
Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process
Abraham Kuot, Alex W Hewitt, Kim Griggs, et al.
BMC Research Notes
|
February 13, 2016
Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataract
Shari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Experimental Eye Research
|
July 6, 2021
Differential gene expression analysis of corneal endothelium indicates involvement of phagocytic activity in Fuchs' endothelial corneal dystrophy
Abraham Kuot, Mark A Corbett, Richard A Mills, et al.
Molecular Vision
|
September 23, 2008
Genetic analysis of the clusterin gene in pseudoexfoliation syndrome
Kathryn P Burdon, Shiwani Sharma, Alex W Hewitt, et al.
Experimental Eye Research
|
March 22, 2016
Biological effect of LOXL1 coding variants associated with pseudoexfoliation syndrome
Shiwani Sharma, Sarah Martin, Matthew J Sykes, et al.
Investigative Ophthalmology & Visual Science
|
September 8, 2021
Genotype, Age, Genetic Background, and Sex Influence Epha2-Related Cataract Development in Mice
Alpana Dave, Jamie E Craig, Mohammad Alamein, et al.
Molecular Vision
|
October 25, 2008
Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoform
Shiwani Sharma, Kathryn P Burdon, Alpana Dave, et al.
Page
of 8