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Showing results (971-980 of 1,001) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|September 4, 2025
Complementary biomolecular coassemblies direct energy transport for cardiac photostimulatorsZe-Fan Yao, Sujeung Lim, Yuyao Kuang, et al.
Human Molecular Genetics|November 10, 2012
iPS cell modeling of Best disease: insights into the pathophysiology of an inherited macular degenerationRuchira Singh, Wei Shen, David Kuai, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|August 3, 2016
Executive Summary: Practice Guidelines for the Diagnosis and Management of Aspergillosis: 2016 Update by the Infectious Diseases Society of AmericaThomas F Patterson, George R Thompson, David W Denning, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|July 2, 2016
Practice Guidelines for the Diagnosis and Management of Aspergillosis: 2016 Update by the Infectious Diseases Society of AmericaThomas F Patterson, George R Thompson, David W Denning, et al.
Translational Vision Science & Technology|June 10, 2021
Examining Whether AOSLO-Based Foveal Cone Metrics in Achromatopsia and Albinism Are Representative of Foveal Cone StructureKatie M Litts, Erica N Woertz, Niamh Wynne, et al.
American Journal of Human Genetics|May 7, 2002
A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosaDebra K Breuer, Beverly M Yashar, Elena Filippova, et al.
Investigative Ophthalmology & Visual Science|December 7, 2007
Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarraysAnneke I den Hollander, Irma Lopez, Suzanne Yzer, et al.
The New England Journal of Medicine|January 25, 2008
HLA-mismatched renal transplantation without maintenance immunosuppressionTatsuo Kawai, A Benedict Cosimi, Thomas R Spitzer, et al.
Human Molecular Genetics|August 2, 2014
Analysis of the ABCA4 genomic locus in Stargardt diseaseJana Zernant, Yajing Angela Xie, Carmen Ayuso, et al.
Retina (Philadelphia, Pa.)|February 2, 2017
REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIAChristopher S Langlo, Laura R Erker, Maria Parker, et al.
Pageof 101

Showing results (971-980 of 1,001) with videos related to

Sort By:
Pageof 101
Proceedings of the National Academy of Sciences of the United States of America|September 4, 2025
Complementary biomolecular coassemblies direct energy transport for cardiac photostimulatorsZe-Fan Yao, Sujeung Lim, Yuyao Kuang, et al.
Human Molecular Genetics|November 10, 2012
iPS cell modeling of Best disease: insights into the pathophysiology of an inherited macular degenerationRuchira Singh, Wei Shen, David Kuai, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|August 3, 2016
Executive Summary: Practice Guidelines for the Diagnosis and Management of Aspergillosis: 2016 Update by the Infectious Diseases Society of AmericaThomas F Patterson, George R Thompson, David W Denning, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|July 2, 2016
Practice Guidelines for the Diagnosis and Management of Aspergillosis: 2016 Update by the Infectious Diseases Society of AmericaThomas F Patterson, George R Thompson, David W Denning, et al.
Translational Vision Science & Technology|June 10, 2021
Examining Whether AOSLO-Based Foveal Cone Metrics in Achromatopsia and Albinism Are Representative of Foveal Cone StructureKatie M Litts, Erica N Woertz, Niamh Wynne, et al.
American Journal of Human Genetics|May 7, 2002
A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosaDebra K Breuer, Beverly M Yashar, Elena Filippova, et al.
Investigative Ophthalmology & Visual Science|December 7, 2007
Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarraysAnneke I den Hollander, Irma Lopez, Suzanne Yzer, et al.
The New England Journal of Medicine|January 25, 2008
HLA-mismatched renal transplantation without maintenance immunosuppressionTatsuo Kawai, A Benedict Cosimi, Thomas R Spitzer, et al.
Human Molecular Genetics|August 2, 2014
Analysis of the ABCA4 genomic locus in Stargardt diseaseJana Zernant, Yajing Angela Xie, Carmen Ayuso, et al.
Retina (Philadelphia, Pa.)|February 2, 2017
REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIAChristopher S Langlo, Laura R Erker, Maria Parker, et al.
Pageof 101