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Jamie E Craig

Showing results (111-120 of 352) with videos related to

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Familial Cancer|September 1, 2006
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial colorectal cancerCelia S Chen, Kerry D Phillips, Scott Grist, et al.
Molecular Vision|January 11, 2013
Compound heterozygote myocilin mutations in a pedigree with high prevalence of primary open-angle glaucomaThomas K Young, Emmanuelle Souzeau, Lance Liu, et al.
Acta Ophthalmologica|December 5, 2009
Systemic disease associations of familial and sporadic glaucoma: the Glaucoma Inheritance Study in TasmaniaAlex W Hewitt, Johnny Wu, Catherine M Green, 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.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|December 24, 2005
Confirmation of the adult-onset primary open angle glaucoma locus GLC1B at 2cen-q13 in an Australian familyJac C Charlesworth, James M Stankovich, David A Mackey, et al.
Acta Ophthalmologica|October 6, 2023
Genetic risk of glaucoma is associated with vascular and retinal nerve fibre wedge defectsDanit G Saks, Angela Schulz, Ayub Qassim, et al.
Diabetes Care|August 14, 2009
Diabetic retinopathy is associated with elevated serum asymmetric and symmetric dimethylargininesSotoodeh Abhary, Nicholas Kasmeridis, Kathryn P Burdon, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 13, 2006
Disease severity of familial glaucoma compared with sporadic glaucomaJohnny Wu, Alex W Hewitt, Catherine M Green, et al.
Molecular Vision|October 10, 2008
Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataractKathryn P Burdon, Kathryn Hattersley, Salil A Lachke, 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 36

Showing results (111-120 of 352) with videos related to

Sort By:
Pageof 36
Familial Cancer|September 1, 2006
Congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial colorectal cancerCelia S Chen, Kerry D Phillips, Scott Grist, et al.
Molecular Vision|January 11, 2013
Compound heterozygote myocilin mutations in a pedigree with high prevalence of primary open-angle glaucomaThomas K Young, Emmanuelle Souzeau, Lance Liu, et al.
Acta Ophthalmologica|December 5, 2009
Systemic disease associations of familial and sporadic glaucoma: the Glaucoma Inheritance Study in TasmaniaAlex W Hewitt, Johnny Wu, Catherine M Green, 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.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|December 24, 2005
Confirmation of the adult-onset primary open angle glaucoma locus GLC1B at 2cen-q13 in an Australian familyJac C Charlesworth, James M Stankovich, David A Mackey, et al.
Acta Ophthalmologica|October 6, 2023
Genetic risk of glaucoma is associated with vascular and retinal nerve fibre wedge defectsDanit G Saks, Angela Schulz, Ayub Qassim, et al.
Diabetes Care|August 14, 2009
Diabetic retinopathy is associated with elevated serum asymmetric and symmetric dimethylargininesSotoodeh Abhary, Nicholas Kasmeridis, Kathryn P Burdon, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 13, 2006
Disease severity of familial glaucoma compared with sporadic glaucomaJohnny Wu, Alex W Hewitt, Catherine M Green, et al.
Molecular Vision|October 10, 2008
Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataractKathryn P Burdon, Kathryn Hattersley, Salil A Lachke, 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 36