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M Downes

Showing results (171-180 of 295) with videos related to

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Mutation Research|August 1, 1989
Base-pair substitutions alter the site-specific mutagenicity of UV and MNNG in the SUP4-o gene of yeastB A Kunz, B G Ayre, A M Downes, et al.
Exploratory Research in Clinical and Social Pharmacy|April 28, 2022
An exploratory survey on the awareness and usage of clinical practice guidelines among clinical pharmacistsJessica M Downes, Lisa A Appeddu, Jeremy L Johnson, et al.
Eye (London, England)|February 26, 2025
Sleep and mood in central serous chorioretinopathyYunfei Yang, Victoria S Foster, Sophie Marlowe, et al.
BMC Ophthalmology|July 14, 2023
Combined central serous chorioretinopathy, hypermetropia, short axial length, chorioretinal folds, enlarged/thickened ocular coats, with varying association of scleral changes (CHAFES)Susan M Downes, Sonia P Mall, Saoud Al-Khuzaei, et al.
American Journal of Health-System Pharmacy : AJHP : Official Journal of the American Society of Health-System Pharmacists|August 15, 2015
Identifying opportunities to improve medication management in transitions of careJessica M Downes, Katherine S O'Neal, Michael J Miller, et al.
Molecular Pharmaceutics|November 12, 2025
Engineered Nonhormonal, Cationic Proinsulin Variants Prolong Lymphatic DrainageGrant M Downes, Amber S Griffith, Kyle D Apley, et al.
Translational Vision Science & Technology|December 10, 2016
A Novel Method for Quantitative Serial Autofluorescence Analysis in Retinitis Pigmentosa Using Image CharacteristicsJasleen K Jolly, Siegfried K Wagner, Jonathan Moules, et al.
Bioconjugate Chemistry|October 26, 2023
CD22L Conjugation to Insulin Attenuates Insulin-Specific B Cell ActivationKyle D Apley, Amber S Griffith, Grant M Downes, et al.
JAMA Ophthalmology|September 6, 2019
Clinical Characterization of Retinitis Pigmentosa Associated With Variants in SNRNP200Imran H Yusuf, Johannes Birtel, Morag E Shanks, et al.
Journal of Medical Genetics|October 3, 1999
Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophiesA M Payne, S M Downes, D A Bessant, et al.
Pageof 30

Showing results (171-180 of 295) with videos related to

Sort By:
Pageof 30
Mutation Research|August 1, 1989
Base-pair substitutions alter the site-specific mutagenicity of UV and MNNG in the SUP4-o gene of yeastB A Kunz, B G Ayre, A M Downes, et al.
Exploratory Research in Clinical and Social Pharmacy|April 28, 2022
An exploratory survey on the awareness and usage of clinical practice guidelines among clinical pharmacistsJessica M Downes, Lisa A Appeddu, Jeremy L Johnson, et al.
Eye (London, England)|February 26, 2025
Sleep and mood in central serous chorioretinopathyYunfei Yang, Victoria S Foster, Sophie Marlowe, et al.
BMC Ophthalmology|July 14, 2023
Combined central serous chorioretinopathy, hypermetropia, short axial length, chorioretinal folds, enlarged/thickened ocular coats, with varying association of scleral changes (CHAFES)Susan M Downes, Sonia P Mall, Saoud Al-Khuzaei, et al.
American Journal of Health-System Pharmacy : AJHP : Official Journal of the American Society of Health-System Pharmacists|August 15, 2015
Identifying opportunities to improve medication management in transitions of careJessica M Downes, Katherine S O'Neal, Michael J Miller, et al.
Molecular Pharmaceutics|November 12, 2025
Engineered Nonhormonal, Cationic Proinsulin Variants Prolong Lymphatic DrainageGrant M Downes, Amber S Griffith, Kyle D Apley, et al.
Translational Vision Science & Technology|December 10, 2016
A Novel Method for Quantitative Serial Autofluorescence Analysis in Retinitis Pigmentosa Using Image CharacteristicsJasleen K Jolly, Siegfried K Wagner, Jonathan Moules, et al.
Bioconjugate Chemistry|October 26, 2023
CD22L Conjugation to Insulin Attenuates Insulin-Specific B Cell ActivationKyle D Apley, Amber S Griffith, Grant M Downes, et al.
JAMA Ophthalmology|September 6, 2019
Clinical Characterization of Retinitis Pigmentosa Associated With Variants in SNRNP200Imran H Yusuf, Johannes Birtel, Morag E Shanks, et al.
Journal of Medical Genetics|October 3, 1999
Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophiesA M Payne, S M Downes, D A Bessant, et al.
Pageof 30