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Showing results (721-730 of 866) with videos related to

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Plos Neglected Tropical Diseases|May 24, 2014
Late onset of the serological response against the 18 kDa small heat shock protein of Mycobacterium ulcerans in childrenKatharina Röltgen, Martin W Bratschi, Amanda Ross, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|January 30, 2026
Ocular delivery of different valosin-containing protein (VCP) inhibitory formulations prevents retinal degeneration in rho<sup>∆I255</sup> miceBowen Cao, Ana-Cristina Almansa-Garcia, Merve Sen, et al.
International Journal of Health Geographics|March 14, 2007
CAALYX: a new generation of location-based services in healthcareMaged N Kamel Boulos, Artur Rocha, Angelo Martins, et al.
International Journal of Molecular Sciences|November 25, 2020
Repositioned Drugs for Chagas Disease Unveiled via Structure-Based Drug RepositioningMelissa F Adasme, Sarah Naomi Bolz, Lauren Adelmann, et al.
Investigative Ophthalmology & Visual Science|January 1, 2016
Monoallelic ABCA4 Mutations Appear Insufficient to Cause Retinopathy: A Quantitative Autofluorescence StudyPhilipp L Müller, Martin Gliem, Elisabeth Mangold, et al.
JAMA Ophthalmology|May 26, 2018
Olfactory Dysfunction in Patients With CNGB1-Associated Retinitis PigmentosaPeter Charbel Issa, Peggy Reuter, Laura Kühlewein, et al.
Orphanet Journal of Rare Diseases|March 12, 2015
OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67)Michaela Thoenes, Ulrike Zimmermann, Inga Ebermann, et al.
Journal of Immunology Research|June 23, 2017
Validation of a Novel Immunoline Assay for Patient Stratification according to Virulence of the Infecting <i>Helicobacter pylori</i> Strain and Eradication StatusLuca Formichella, Laura Romberg, Hannelore Meyer, et al.
Molecular Vision|March 31, 2010
Sequence variants of the DFNB31 gene among Usher syndrome patients of diverse originElena Aller, Teresa Jaijo, Erwin van Wijk, et al.
Human Mutation|November 24, 2015
PEX6 is Expressed in Photoreceptor Cilia and Mutated in Deafblindness with Enamel Dysplasia and MicrocephalyMaha S Zaki, Raoul Heller, Michaela Thoenes, et al.
Pageof 87

Showing results (721-730 of 866) with videos related to

Sort By:
Pageof 87
Plos Neglected Tropical Diseases|May 24, 2014
Late onset of the serological response against the 18 kDa small heat shock protein of Mycobacterium ulcerans in childrenKatharina Röltgen, Martin W Bratschi, Amanda Ross, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|January 30, 2026
Ocular delivery of different valosin-containing protein (VCP) inhibitory formulations prevents retinal degeneration in rho<sup>∆I255</sup> miceBowen Cao, Ana-Cristina Almansa-Garcia, Merve Sen, et al.
International Journal of Health Geographics|March 14, 2007
CAALYX: a new generation of location-based services in healthcareMaged N Kamel Boulos, Artur Rocha, Angelo Martins, et al.
International Journal of Molecular Sciences|November 25, 2020
Repositioned Drugs for Chagas Disease Unveiled via Structure-Based Drug RepositioningMelissa F Adasme, Sarah Naomi Bolz, Lauren Adelmann, et al.
Investigative Ophthalmology & Visual Science|January 1, 2016
Monoallelic ABCA4 Mutations Appear Insufficient to Cause Retinopathy: A Quantitative Autofluorescence StudyPhilipp L Müller, Martin Gliem, Elisabeth Mangold, et al.
JAMA Ophthalmology|May 26, 2018
Olfactory Dysfunction in Patients With CNGB1-Associated Retinitis PigmentosaPeter Charbel Issa, Peggy Reuter, Laura Kühlewein, et al.
Orphanet Journal of Rare Diseases|March 12, 2015
OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67)Michaela Thoenes, Ulrike Zimmermann, Inga Ebermann, et al.
Journal of Immunology Research|June 23, 2017
Validation of a Novel Immunoline Assay for Patient Stratification according to Virulence of the Infecting <i>Helicobacter pylori</i> Strain and Eradication StatusLuca Formichella, Laura Romberg, Hannelore Meyer, et al.
Molecular Vision|March 31, 2010
Sequence variants of the DFNB31 gene among Usher syndrome patients of diverse originElena Aller, Teresa Jaijo, Erwin van Wijk, et al.
Human Mutation|November 24, 2015
PEX6 is Expressed in Photoreceptor Cilia and Mutated in Deafblindness with Enamel Dysplasia and MicrocephalyMaha S Zaki, Raoul Heller, Michaela Thoenes, et al.
Pageof 87