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Jonathan H Lin

Showing results (91-100 of 100) with videos related to

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RNA (New York, N.Y.)|April 24, 2015
Transcriptome sequencing uncovers novel long noncoding and small nucleolar RNAs dysregulated in head and neck squamous cell carcinomaAngela E Zou, Jonjei Ku, Thomas K Honda, et al.
Biorxiv : the Preprint Server for Biology|July 16, 2025
Common Gene Networks Orchestrate Organelle Architecture and Inter-Organelle Metabolic Flows for Mucin Production in High Endothelial and Goblet CellsYuhan Bi, Kevin Francis Brulois, Aiman Ayesha, et al.
Acta Neuropathologica Communications|September 22, 2023
TDP43 pathology in chronic traumatic encephalopathy retinasRagini Phansalkar, Vanessa S Goodwill, Jeffrey J Nirschl, et al.
Mbio|November 22, 2018
Prion Seeds Distribute throughout the Eyes of Sporadic Creutzfeldt-Jakob Disease PatientsChristina D Orrù, Katrin Soldau, Christian Cordano, et al.
European Journal of Human Genetics : EJHG|August 17, 2017
Autosomal recessive cone-rod dystrophy can be caused by mutations in the ATF6 geneAnna Skorczyk-Werner, Wei-Chieh Chiang, Anna Wawrocka, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 25, 2021
ATF6 is essential for human cone photoreceptor developmentHeike Kroeger, Julia M D Grandjean, Wei-Chieh Jerry Chiang, et al.
Physiological Genomics|January 29, 2017
Genetic analysis of 10 pedigrees with inherited retinal degeneration by exome sequencing and phenotype-genotype associationPooja Biswas, Jacque L Duncan, Bruno Maranhao, et al.
Investigative Ophthalmology & Visual Science|June 26, 2019
Characterization of Retinal Structure in ATF6-Associated AchromatopsiaRebecca R Mastey, Michalis Georgiou, Christopher S Langlo, et al.
JCI Insight|April 10, 2020
Multiexon deletion alleles of ATF6 linked to achromatopsiaEun-Jin Lee, Wei-Chieh Jerry Chiang, Heike Kroeger, et al.
Nature Genetics|June 2, 2015
Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsiaSusanne Kohl, Ditta Zobor, Wei-Chieh Chiang, et al.
Pageof 10

Showing results (91-100 of 100) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 100 results.
RNA (New York, N.Y.)|April 24, 2015
Transcriptome sequencing uncovers novel long noncoding and small nucleolar RNAs dysregulated in head and neck squamous cell carcinomaAngela E Zou, Jonjei Ku, Thomas K Honda, et al.
Biorxiv : the Preprint Server for Biology|July 16, 2025
Common Gene Networks Orchestrate Organelle Architecture and Inter-Organelle Metabolic Flows for Mucin Production in High Endothelial and Goblet CellsYuhan Bi, Kevin Francis Brulois, Aiman Ayesha, et al.
Acta Neuropathologica Communications|September 22, 2023
TDP43 pathology in chronic traumatic encephalopathy retinasRagini Phansalkar, Vanessa S Goodwill, Jeffrey J Nirschl, et al.
Mbio|November 22, 2018
Prion Seeds Distribute throughout the Eyes of Sporadic Creutzfeldt-Jakob Disease PatientsChristina D Orrù, Katrin Soldau, Christian Cordano, et al.
European Journal of Human Genetics : EJHG|August 17, 2017
Autosomal recessive cone-rod dystrophy can be caused by mutations in the ATF6 geneAnna Skorczyk-Werner, Wei-Chieh Chiang, Anna Wawrocka, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 25, 2021
ATF6 is essential for human cone photoreceptor developmentHeike Kroeger, Julia M D Grandjean, Wei-Chieh Jerry Chiang, et al.
Physiological Genomics|January 29, 2017
Genetic analysis of 10 pedigrees with inherited retinal degeneration by exome sequencing and phenotype-genotype associationPooja Biswas, Jacque L Duncan, Bruno Maranhao, et al.
Investigative Ophthalmology & Visual Science|June 26, 2019
Characterization of Retinal Structure in ATF6-Associated AchromatopsiaRebecca R Mastey, Michalis Georgiou, Christopher S Langlo, et al.
JCI Insight|April 10, 2020
Multiexon deletion alleles of ATF6 linked to achromatopsiaEun-Jin Lee, Wei-Chieh Jerry Chiang, Heike Kroeger, et al.
Nature Genetics|June 2, 2015
Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsiaSusanne Kohl, Ditta Zobor, Wei-Chieh Chiang, et al.
Pageof 10