Search research articles
Contact Us
Filters
Showing results (891-900 of 1,250) with videos related to
Page
of 125
Sort By:
Bioorganic & Medicinal Chemistry Letters
|
June 26, 2003
1H-Pyrazolo[3,4-b]pyridine inhibitors of cyclin-dependent kinases: highly potent 2,6-Difluorophenacyl analogues
Raj 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 correlations
Kaoru 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 maculopathy
M 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 calving
K 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 History
Thales 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 oculopathy
Rajarshi 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 History
Malena Daich Varela, Michalis Georgiou, Yahya Alswaiti, et al.
Ophthalmology
|
June 18, 2013
The clinical effect of homozygous ABCA4 alleles in 18 patients
Kaoru 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 mutations
Donna 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 transformation
Sujata Jana, Rucha Deo, Rowan P Hough, et al.
Page
of 125
Search research articles
Search
Showing results (891-900 of 1,250) with videos related to
Sort By:
Page
of 125
Bioorganic & Medicinal Chemistry Letters
|
June 26, 2003
1H-Pyrazolo[3,4-b]pyridine inhibitors of cyclin-dependent kinases: highly potent 2,6-Difluorophenacyl analogues
Raj 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 correlations
Kaoru 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 maculopathy
M 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 calving
K 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 History
Thales 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 oculopathy
Rajarshi 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 History
Malena Daich Varela, Michalis Georgiou, Yahya Alswaiti, et al.
Ophthalmology
|
June 18, 2013
The clinical effect of homozygous ABCA4 alleles in 18 patients
Kaoru 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 mutations
Donna 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 transformation
Sujata Jana, Rucha Deo, Rowan P Hough, et al.
Page
of 125