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Shiwani Sharma

Showing results (21-30 of 71) with videos related to

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Clinical & Experimental Ophthalmology|October 2, 2015
Role of the nucleolus in neurodegenerative diseases with particular reference to the retina: a reviewPaul I Sia, John Pm Wood, Glyn Chidlow, et al.
Biophysical Journal|September 7, 2010
Detecting protein aggregates on untreated human tissue samples by atomic force microscopy recognition imagingRhiannon Creasey, Shiwani Sharma, Jamie E Craig, et al.
Human Mutation|June 21, 2007
A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start siteKathryn P Burdon, Shiwani Sharma, Celia S Chen, et al.
Journal of Proteome Research|June 14, 2011
MALDI-MS-imaging of whole human lens capsuleMaurizio Ronci, Shiwani Sharma, Tim Chataway, et al.
Annals of Medicine and Surgery (2012)|June 23, 2022
Traumatic gastric laceration with injury of splenic and celiac vessel following intentional self-harm by crashing of motor vehicle: A case reportShiwani Sharma Acharya, Robin Man Karmacharya, Satish Vaidya, et al.
Human Molecular Genetics|May 6, 2006
Nance-Horan syndrome protein, NHS, associates with epithelial cell junctionsShiwani Sharma, Sharyn L Ang, Marie Shaw, et al.
JAMA Ophthalmology|May 24, 2014
Mutation in TMEM98 in a large white kindred with autosomal dominant nanophthalmos linked to 17p12-q12Mona S Awadalla, Kathryn P Burdon, Emmanuelle Souzeau, et al.
BMC Medical Genetics|May 10, 2017
Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)Shari Javadiyan, Jamie E Craig, Shiwani Sharma, et al.
Ultramicroscopy|July 12, 2011
Atomic force microscopy-based antibody recognition imaging of proteins in the pathological deposits in pseudoexfoliation syndromeRhiannon Creasey, Shiwani Sharma, Christopher T Gibson, et al.
Plos One|August 24, 2017
TGC repeat expansion in the TCF4 gene increases the risk of Fuchs' endothelial corneal dystrophy in Australian casesAbraham Kuot, Alex W Hewitt, Grant R Snibson, et al.
Pageof 8

Showing results (21-30 of 71) with videos related to

Sort By:
Pageof 8
Clinical & Experimental Ophthalmology|October 2, 2015
Role of the nucleolus in neurodegenerative diseases with particular reference to the retina: a reviewPaul I Sia, John Pm Wood, Glyn Chidlow, et al.
Biophysical Journal|September 7, 2010
Detecting protein aggregates on untreated human tissue samples by atomic force microscopy recognition imagingRhiannon Creasey, Shiwani Sharma, Jamie E Craig, et al.
Human Mutation|June 21, 2007
A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start siteKathryn P Burdon, Shiwani Sharma, Celia S Chen, et al.
Journal of Proteome Research|June 14, 2011
MALDI-MS-imaging of whole human lens capsuleMaurizio Ronci, Shiwani Sharma, Tim Chataway, et al.
Annals of Medicine and Surgery (2012)|June 23, 2022
Traumatic gastric laceration with injury of splenic and celiac vessel following intentional self-harm by crashing of motor vehicle: A case reportShiwani Sharma Acharya, Robin Man Karmacharya, Satish Vaidya, et al.
Human Molecular Genetics|May 6, 2006
Nance-Horan syndrome protein, NHS, associates with epithelial cell junctionsShiwani Sharma, Sharyn L Ang, Marie Shaw, et al.
JAMA Ophthalmology|May 24, 2014
Mutation in TMEM98 in a large white kindred with autosomal dominant nanophthalmos linked to 17p12-q12Mona S Awadalla, Kathryn P Burdon, Emmanuelle Souzeau, et al.
BMC Medical Genetics|May 10, 2017
Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)Shari Javadiyan, Jamie E Craig, Shiwani Sharma, et al.
Ultramicroscopy|July 12, 2011
Atomic force microscopy-based antibody recognition imaging of proteins in the pathological deposits in pseudoexfoliation syndromeRhiannon Creasey, Shiwani Sharma, Christopher T Gibson, et al.
Plos One|August 24, 2017
TGC repeat expansion in the TCF4 gene increases the risk of Fuchs' endothelial corneal dystrophy in Australian casesAbraham Kuot, Alex W Hewitt, Grant R Snibson, et al.
Pageof 8