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Showing results (1641-1650 of 2,138) with videos related to

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Investigative Ophthalmology & Visual Science|July 7, 1999
Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerationsY Q Gao, M Danciger, R Longmuir, et al.
Sexually Transmitted Diseases|October 27, 2004
Factors predicting the acceptance of herpes simplex virus type 2 antibody testing among adolescents and young adultsGregory D Zimet, Susan L Rosenthal, J Dennis Fortenberry, et al.
Human Molecular Genetics|July 2, 2004
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degenerationSamuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
JAMA Ophthalmology|February 16, 2013
Visual acuity changes in patients with leber congenital amaurosis and mutations in CEP290J Jason McAnany, Mohamed A Genead, Saloni Walia, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|June 13, 2022
Inequities in Alliance Acute Leukemia Clinical Trial and Biobank Participation: Defining Targets for InterventionAndrew Hantel, Jessica Kohlschmidt, Ann-Kathrin Eisfeld, et al.
Vision Research|November 13, 2004
Results from screening over 9000 mutation-bearing mice for defects in the electroretinogram and appearance of the fundusLawrence H Pinto, Martha Hotz Vitaterna, Sanda M Siepka, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degenerationAnn H Milam, Linda Rose, Artur V Cideciyan, et al.
American Journal of Human Genetics|December 29, 2005
Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome geneDarryl Y Nishimura, Ruth E Swiderski, Charles C Searby, et al.
Journal of the National Cancer Institute|March 22, 2024
Racial and ethnic associations with comprehensive cancer center access and clinical trial enrollment for acute leukemiaAndrew Hantel, Andrew M Brunner, Jesse J Plascak, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
GENE EXPRESSION WITHIN A HUMAN CHOROIDAL NEOVASCULAR MEMBRANE USING SPATIAL TRANSCRIPTOMICSAndrew P Voigt, Nathaniel K Mullin, Emma M Navratil, et al.
Pageof 214

Showing results (1641-1650 of 2,138) with videos related to

Sort By:
Pageof 214
Investigative Ophthalmology & Visual Science|July 7, 1999
Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerationsY Q Gao, M Danciger, R Longmuir, et al.
Sexually Transmitted Diseases|October 27, 2004
Factors predicting the acceptance of herpes simplex virus type 2 antibody testing among adolescents and young adultsGregory D Zimet, Susan L Rosenthal, J Dennis Fortenberry, et al.
Human Molecular Genetics|July 2, 2004
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degenerationSamuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
JAMA Ophthalmology|February 16, 2013
Visual acuity changes in patients with leber congenital amaurosis and mutations in CEP290J Jason McAnany, Mohamed A Genead, Saloni Walia, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|June 13, 2022
Inequities in Alliance Acute Leukemia Clinical Trial and Biobank Participation: Defining Targets for InterventionAndrew Hantel, Jessica Kohlschmidt, Ann-Kathrin Eisfeld, et al.
Vision Research|November 13, 2004
Results from screening over 9000 mutation-bearing mice for defects in the electroretinogram and appearance of the fundusLawrence H Pinto, Martha Hotz Vitaterna, Sanda M Siepka, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degenerationAnn H Milam, Linda Rose, Artur V Cideciyan, et al.
American Journal of Human Genetics|December 29, 2005
Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome geneDarryl Y Nishimura, Ruth E Swiderski, Charles C Searby, et al.
Journal of the National Cancer Institute|March 22, 2024
Racial and ethnic associations with comprehensive cancer center access and clinical trial enrollment for acute leukemiaAndrew Hantel, Andrew M Brunner, Jesse J Plascak, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
GENE EXPRESSION WITHIN A HUMAN CHOROIDAL NEOVASCULAR MEMBRANE USING SPATIAL TRANSCRIPTOMICSAndrew P Voigt, Nathaniel K Mullin, Emma M Navratil, et al.
Pageof 214