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Showing results (891-900 of 1,250) with videos related to

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Bioorganic & Medicinal Chemistry Letters|June 26, 2003
1H-Pyrazolo[3,4-b]pyridine inhibitors of cyclin-dependent kinases: highly potent 2,6-Difluorophenacyl analoguesRaj N Misra, Hai yun Xiao, David B Rawlins, et al.
Investigative Ophthalmology & Visual Science|November 23, 2013
A longitudinal study of Stargardt disease: quantitative assessment of fundus autofluorescence, progression, and genotype correlationsKaoru Fujinami, Noemi Lois, Rajarshi Mukherjee, et al.
The British Journal of Ophthalmology|November 21, 2007
ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathyM Michaelides, L L Chen, M A Brantley, et al.
Journal of Dairy Science|May 21, 2013
Behavioral and physiological effects of a short-term feed restriction in lactating dairy cattle with different body condition scores at calvingK E Schütz, N R Cox, K A Macdonald, et al.
Investigative Ophthalmology & Visual Science|July 17, 2024
CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural HistoryThales A C de Guimaraes, Anthony G Robson, Isabela M C de Guimaraes, et al.
Molecular Vision|April 3, 2010
A detailed phenotypic assessment of individuals affected by MFRP-related oculopathyRajarshi Mukhopadhyay, Panagiotis I Sergouniotis, Donna S Mackay, et al.
American Journal of Ophthalmology|September 13, 2022
CRB1-Associated Retinal Dystrophies: Genetics, Clinical Characteristics, and Natural HistoryMalena Daich Varela, Michalis Georgiou, Yahya Alswaiti, et al.
Ophthalmology|June 18, 2013
The clinical effect of homozygous ABCA4 alleles in 18 patientsKaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, et al.
Investigative Ophthalmology & Visual Science|February 12, 2011
Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutationsDonna S Mackay, Louise A Ocaka, Arundhati Dev Borman, et al.
JCI Insight|May 25, 2021
mRNA translation is a therapeutic vulnerability necessary for bladder epithelial transformationSujata Jana, Rucha Deo, Rowan P Hough, et al.
Pageof 125

Showing results (891-900 of 1,250) with videos related to

Sort By:
Pageof 125
Bioorganic & Medicinal Chemistry Letters|June 26, 2003
1H-Pyrazolo[3,4-b]pyridine inhibitors of cyclin-dependent kinases: highly potent 2,6-Difluorophenacyl analoguesRaj N Misra, Hai yun Xiao, David B Rawlins, et al.
Investigative Ophthalmology & Visual Science|November 23, 2013
A longitudinal study of Stargardt disease: quantitative assessment of fundus autofluorescence, progression, and genotype correlationsKaoru Fujinami, Noemi Lois, Rajarshi Mukherjee, et al.
The British Journal of Ophthalmology|November 21, 2007
ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathyM Michaelides, L L Chen, M A Brantley, et al.
Journal of Dairy Science|May 21, 2013
Behavioral and physiological effects of a short-term feed restriction in lactating dairy cattle with different body condition scores at calvingK E Schütz, N R Cox, K A Macdonald, et al.
Investigative Ophthalmology & Visual Science|July 17, 2024
CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural HistoryThales A C de Guimaraes, Anthony G Robson, Isabela M C de Guimaraes, et al.
Molecular Vision|April 3, 2010
A detailed phenotypic assessment of individuals affected by MFRP-related oculopathyRajarshi Mukhopadhyay, Panagiotis I Sergouniotis, Donna S Mackay, et al.
American Journal of Ophthalmology|September 13, 2022
CRB1-Associated Retinal Dystrophies: Genetics, Clinical Characteristics, and Natural HistoryMalena Daich Varela, Michalis Georgiou, Yahya Alswaiti, et al.
Ophthalmology|June 18, 2013
The clinical effect of homozygous ABCA4 alleles in 18 patientsKaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, et al.
Investigative Ophthalmology & Visual Science|February 12, 2011
Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutationsDonna S Mackay, Louise A Ocaka, Arundhati Dev Borman, et al.
JCI Insight|May 25, 2021
mRNA translation is a therapeutic vulnerability necessary for bladder epithelial transformationSujata Jana, Rucha Deo, Rowan P Hough, et al.
Pageof 125