Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Rachayata Dharmat

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
Methods in Molecular Biology (Clifton, N.J.)|December 2, 2019
Single-Cell Capture, RNA-seq, and Transcriptome Analysis from the Neural RetinaRachayata Dharmat, Sangbae Kim, Yumei Li, et al.
Investigative Ophthalmology & Visual Science|May 2, 2017
IFT81 as a Candidate Gene for Nonsyndromic Retinal DegenerationRachayata Dharmat, Wei Liu, Zhongqi Ge, et al.
Science Signaling|May 31, 2018
Phagocytosed photoreceptor outer segments activate mTORC1 in the retinal pigment epitheliumBo Yu, Anuoluwapo Egbejimi, Rachayata Dharmat, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 29, 2016
Hypomorphic mutations identified in the candidate Leber congenital amaurosis gene CLUAP1Zachry T Soens, Yuanyuan Li, Li Zhao, et al.
Nature Communications|December 19, 2019
Single-nuclei RNA-seq on human retinal tissue provides improved transcriptome profilingQingnan Liang, Rachayata Dharmat, Leah Owen, et al.
The Journal of Cell Biology|June 15, 2018
SPATA7 maintains a novel photoreceptor-specific zone in the distal connecting ciliumRachayata Dharmat, Aiden Eblimit, Michael A Robichaux, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2019
Generation, transcriptome profiling, and functional validation of cone-rich human retinal organoidsSangbae Kim, Albert Lowe, Rachayata Dharmat, et al.
Science Advances|October 8, 2025
ASPL couples the assembly of stress granules with their VCP-mediated disassemblyGautam Pareek, Dongfang Li, Bo Wang, et al.
American Journal of Human Genetics|March 14, 2017
Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental AnomaliesMingchu Xu, Yajing Angela Xie, Hana Abouzeid, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Methods in Molecular Biology (Clifton, N.J.)|December 2, 2019
Single-Cell Capture, RNA-seq, and Transcriptome Analysis from the Neural RetinaRachayata Dharmat, Sangbae Kim, Yumei Li, et al.
Investigative Ophthalmology & Visual Science|May 2, 2017
IFT81 as a Candidate Gene for Nonsyndromic Retinal DegenerationRachayata Dharmat, Wei Liu, Zhongqi Ge, et al.
Science Signaling|May 31, 2018
Phagocytosed photoreceptor outer segments activate mTORC1 in the retinal pigment epitheliumBo Yu, Anuoluwapo Egbejimi, Rachayata Dharmat, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 29, 2016
Hypomorphic mutations identified in the candidate Leber congenital amaurosis gene CLUAP1Zachry T Soens, Yuanyuan Li, Li Zhao, et al.
Nature Communications|December 19, 2019
Single-nuclei RNA-seq on human retinal tissue provides improved transcriptome profilingQingnan Liang, Rachayata Dharmat, Leah Owen, et al.
The Journal of Cell Biology|June 15, 2018
SPATA7 maintains a novel photoreceptor-specific zone in the distal connecting ciliumRachayata Dharmat, Aiden Eblimit, Michael A Robichaux, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2019
Generation, transcriptome profiling, and functional validation of cone-rich human retinal organoidsSangbae Kim, Albert Lowe, Rachayata Dharmat, et al.
Science Advances|October 8, 2025
ASPL couples the assembly of stress granules with their VCP-mediated disassemblyGautam Pareek, Dongfang Li, Bo Wang, et al.
American Journal of Human Genetics|March 14, 2017
Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental AnomaliesMingchu Xu, Yajing Angela Xie, Hana Abouzeid, et al.
Pageof 1