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Robyn V Jamieson

Showing results (31-40 of 78) with videos related to

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Stem Cell Reports|January 11, 2023
Comprehensive characterization of fetal and mature retinal cell identity to assess the fidelity of retinal organoidsHani Jieun Kim, Michelle O'Hara-Wright, Daniel Kim, et al.
Clinical & Experimental Ophthalmology|February 25, 2022
Electronegative electroretinogram in the modern multimodal imaging eraDhimas H Sakti, Haipha Ali, Maria Korsakova, et al.
European Journal of Human Genetics : EJHG|November 28, 2013
Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1Ivan Prokudin, Cas Simons, John R Grigg, et al.
The Medical Journal of Australia|June 10, 2023
The health care and societal costs of inherited retinal diseases in Australia: a microsimulation modelling studyDeborah Schofield, Joshua Kraindler, Owen Tan, et al.
Molecular Vision|October 25, 2008
Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoformShiwani Sharma, Kathryn P Burdon, Alpana Dave, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|July 22, 2008
Chromosomal rearrangements and novel genes in disorders of eye development, cataract and glaucomaMarija Mihelec, Luke St Heaps, Maree Flaherty, et al.
Translational Vision Science & Technology|December 28, 2020
Assessing Residual Cone Function in Retinitis Pigmentosa PatientsTasneem A Arsiwalla, Elisa E Cornish, Phuc Vuong Nguyen, et al.
American Journal of Medical Genetics. Part A|July 13, 2006
Deletion at 14q22-23 indicates a contiguous gene syndrome comprising anophthalmia, pituitary hypoplasia, and ear anomaliesLeisha D Nolen, David Amor, Ashley Haywood, et al.
Clinical Genetics|February 28, 2024
A founder variant expands the phenotype of WNT7B-related PDAC syndromeLama AlAbdi, Zuhair Rahbeeni, Sateesh Maddirevula, et al.
Stem Cell Reports|November 21, 2025
Connecting cilium, stress response, and proteostasis abnormalities inform variant and therapy assessment in RPGRIP1 retinal organoidsTo Ha Loi, Anson Cheng, Hani Jieun Kim, et al.
Pageof 8

Showing results (31-40 of 78) with videos related to

Sort By:
Pageof 8
Stem Cell Reports|January 11, 2023
Comprehensive characterization of fetal and mature retinal cell identity to assess the fidelity of retinal organoidsHani Jieun Kim, Michelle O'Hara-Wright, Daniel Kim, et al.
Clinical & Experimental Ophthalmology|February 25, 2022
Electronegative electroretinogram in the modern multimodal imaging eraDhimas H Sakti, Haipha Ali, Maria Korsakova, et al.
European Journal of Human Genetics : EJHG|November 28, 2013
Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1Ivan Prokudin, Cas Simons, John R Grigg, et al.
The Medical Journal of Australia|June 10, 2023
The health care and societal costs of inherited retinal diseases in Australia: a microsimulation modelling studyDeborah Schofield, Joshua Kraindler, Owen Tan, et al.
Molecular Vision|October 25, 2008
Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoformShiwani Sharma, Kathryn P Burdon, Alpana Dave, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|July 22, 2008
Chromosomal rearrangements and novel genes in disorders of eye development, cataract and glaucomaMarija Mihelec, Luke St Heaps, Maree Flaherty, et al.
Translational Vision Science & Technology|December 28, 2020
Assessing Residual Cone Function in Retinitis Pigmentosa PatientsTasneem A Arsiwalla, Elisa E Cornish, Phuc Vuong Nguyen, et al.
American Journal of Medical Genetics. Part A|July 13, 2006
Deletion at 14q22-23 indicates a contiguous gene syndrome comprising anophthalmia, pituitary hypoplasia, and ear anomaliesLeisha D Nolen, David Amor, Ashley Haywood, et al.
Clinical Genetics|February 28, 2024
A founder variant expands the phenotype of WNT7B-related PDAC syndromeLama AlAbdi, Zuhair Rahbeeni, Sateesh Maddirevula, et al.
Stem Cell Reports|November 21, 2025
Connecting cilium, stress response, and proteostasis abnormalities inform variant and therapy assessment in RPGRIP1 retinal organoidsTo Ha Loi, Anson Cheng, Hani Jieun Kim, et al.
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