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Helena Lee

Showing results (61-70 of 67) with videos related to

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Scientific Reports|September 15, 2019
A small gene sequencing panel realises a high diagnostic rate in patients with congenital nystagmus following basic phenotypingLuke O'Gorman, Chelsea S Norman, Luke Michaels, et al.
Scientific Reports|July 2, 2017
Identification of a functionally significant tri-allelic genotype in the Tyrosinase gene (TYR) causing hypomorphic oculocutaneous albinism (OCA1B)Chelsea S Norman, Luke O'Gorman, Jane Gibson, et al.
Cells|March 6, 2021
Oligomeric Aβ<sub>1-42</sub> Induces an AMD-Like Phenotype and Accumulates in Lysosomes to Impair RPE FunctionSavannah A Lynn, David A Johnston, Jenny A Scott, et al.
NPJ Genomic Medicine|January 14, 2022
Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B)Siying Lin, Aida Sanchez-Bretaño, Joseph S Leslie, et al.
Behavior Research Methods|July 28, 2023
Minimal reporting guideline for research involving eye tracking (2023 edition)Matt J Dunn, Robert G Alexander, Onyekachukwu M Amiebenomo, et al.
Behavior Research Methods|May 1, 2024
Author Correction: Minimal reporting guideline for research involving eye tracking (2023 edition)Matt J Dunn, Robert G Alexander, Onyekachukwu M Amiebenomo, et al.
Behavior Research Methods|November 16, 2023
Retraction Note: Eye tracking: empirical foundations for a minimal reporting guidelineKenneth Holmqvist, Saga Lee Örbom, Ignace T C Hooge, et al.
Pageof 7

Showing results (61-70 of 67) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 67 results.
Scientific Reports|September 15, 2019
A small gene sequencing panel realises a high diagnostic rate in patients with congenital nystagmus following basic phenotypingLuke O'Gorman, Chelsea S Norman, Luke Michaels, et al.
Scientific Reports|July 2, 2017
Identification of a functionally significant tri-allelic genotype in the Tyrosinase gene (TYR) causing hypomorphic oculocutaneous albinism (OCA1B)Chelsea S Norman, Luke O'Gorman, Jane Gibson, et al.
Cells|March 6, 2021
Oligomeric Aβ<sub>1-42</sub> Induces an AMD-Like Phenotype and Accumulates in Lysosomes to Impair RPE FunctionSavannah A Lynn, David A Johnston, Jenny A Scott, et al.
NPJ Genomic Medicine|January 14, 2022
Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B)Siying Lin, Aida Sanchez-Bretaño, Joseph S Leslie, et al.
Behavior Research Methods|July 28, 2023
Minimal reporting guideline for research involving eye tracking (2023 edition)Matt J Dunn, Robert G Alexander, Onyekachukwu M Amiebenomo, et al.
Behavior Research Methods|May 1, 2024
Author Correction: Minimal reporting guideline for research involving eye tracking (2023 edition)Matt J Dunn, Robert G Alexander, Onyekachukwu M Amiebenomo, et al.
Behavior Research Methods|November 16, 2023
Retraction Note: Eye tracking: empirical foundations for a minimal reporting guidelineKenneth Holmqvist, Saga Lee Örbom, Ignace T C Hooge, et al.
Pageof 7