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M Downes

Showing results (201-210 of 295) with videos related to

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Ophthalmic Genetics|June 17, 2020
Next generation sequencing using phenotype-based panels for genetic testing in inherited retinal diseasesMital Shah, Morag Shanks, Emily Packham, et al.
Journal of the American Chemical Society|March 26, 2011
Quorum sensing between Pseudomonas aeruginosa biofilms accelerates cell growthShane T Flickinger, Matthew F Copeland, Eric M Downes, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 21, 2026
Geographic atrophy in age-related macular degeneration: phenotypic characterisation for clinical trial considerationGrace A Borchert, Peter Charbel Issa, Kanmin Xue, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|March 27, 2003
A pilot study of adjuvant intraperitoneal 5-fluorouracil using 4% icodextrin as a novel carrier solutionK B Hosie, D J Kerr, J A Gilbert, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 26, 1999
Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 familiesS M Downes, F W Fitzke, G E Holder, et al.
BMC Ophthalmology|April 10, 2021
Targeted next generation sequencing and family survey enable correct genetic diagnosis in CRX associated macular dystrophy - a case reportSaoud Al-Khuzaei, Karl A Z Hudspith, Suzanne Broadgate, et al.
JAMA Network Open|June 15, 2019
Clinical and Molecular Characterization of PROM1-Related Retinal DegenerationJasmina Cehajic-Kapetanovic, Johannes Birtel, Michelle E McClements, et al.
Human Molecular Genetics|March 21, 1998
A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1A M Payne, S M Downes, D A Bessant, et al.
Genes|December 16, 2020
Genetic and Clinical Findings in an Ethnically Diverse Cohort with Retinitis Pigmentosa Associated with Pathogenic Variants in CERKLSusan M Downes, Tham Nguyen, Vicky Tai, et al.
Rheumatology Advances in Practice|August 22, 2019
An audit of the use of hydroxychloroquine in rheumatology clinicsClaudia Worth, Imran H Yusuf, Bethany Turner, et al.
Pageof 30

Showing results (201-210 of 295) with videos related to

Sort By:
Pageof 30
Ophthalmic Genetics|June 17, 2020
Next generation sequencing using phenotype-based panels for genetic testing in inherited retinal diseasesMital Shah, Morag Shanks, Emily Packham, et al.
Journal of the American Chemical Society|March 26, 2011
Quorum sensing between Pseudomonas aeruginosa biofilms accelerates cell growthShane T Flickinger, Matthew F Copeland, Eric M Downes, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 21, 2026
Geographic atrophy in age-related macular degeneration: phenotypic characterisation for clinical trial considerationGrace A Borchert, Peter Charbel Issa, Kanmin Xue, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|March 27, 2003
A pilot study of adjuvant intraperitoneal 5-fluorouracil using 4% icodextrin as a novel carrier solutionK B Hosie, D J Kerr, J A Gilbert, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 26, 1999
Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 familiesS M Downes, F W Fitzke, G E Holder, et al.
BMC Ophthalmology|April 10, 2021
Targeted next generation sequencing and family survey enable correct genetic diagnosis in CRX associated macular dystrophy - a case reportSaoud Al-Khuzaei, Karl A Z Hudspith, Suzanne Broadgate, et al.
JAMA Network Open|June 15, 2019
Clinical and Molecular Characterization of PROM1-Related Retinal DegenerationJasmina Cehajic-Kapetanovic, Johannes Birtel, Michelle E McClements, et al.
Human Molecular Genetics|March 21, 1998
A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1A M Payne, S M Downes, D A Bessant, et al.
Genes|December 16, 2020
Genetic and Clinical Findings in an Ethnically Diverse Cohort with Retinitis Pigmentosa Associated with Pathogenic Variants in CERKLSusan M Downes, Tham Nguyen, Vicky Tai, et al.
Rheumatology Advances in Practice|August 22, 2019
An audit of the use of hydroxychloroquine in rheumatology clinicsClaudia Worth, Imran H Yusuf, Bethany Turner, et al.
Pageof 30