Jonathan H Lin

Pathology, Neuroscience University of California, San Diego, La Jolla, CA 
"Jonathan H Lin"
Mean distance: 13.91 (cluster 6)


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Thomas M. Jessell grad student 2001 Columbia
 (ETS Genes and the Assembly of a Simple Stretch Reflex Circuit Between Motor Neuron Pools and Muscle Sensory Afferent Subtypes)
Matthew LaVail research scientist 2006-2012 UCSF


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Victory T. Joseph grad student 2009- UCSD
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Lee EJ, Chiang WJ, Kroeger H, et al. (2020) Multiexon deletion alleles of ATF6 linked to achromatopsia. Jci Insight. 5
Wingard JB, Delzell DA, Houlihan NV, et al. (2019) Incidence of Glaucoma or Ocular Hypertension After Repeated Anti-Vascular Endothelial Growth Factor Injections for Macular Degeneration. Clinical Ophthalmology (Auckland, N.Z.). 13: 2563-2572
Chiang WJ, Kroeger H, Chea L, et al. (2019) Pathomechanisms of ATF6-Associated Cone Photoreceptor Diseases. Advances in Experimental Medicine and Biology. 1185: 305-310
Hiramatsu N, Chiang K, Aivati C, et al. (2019) PERK-mediated induction of microRNA-483 disrupts cellular ATP homeostasis during the unfolded protein response. The Journal of Biological Chemistry
Yuan SH, Hiramatsu N, Liu Q, et al. (2018) Tauopathy-Associated PERK Alleles are Functional Hypomorphs that Increase Neuronal Vulnerability to ER Stress. Human Molecular Genetics
Kroeger H, Chiang WC, Felden J, et al. (2018) ER Stress and Unfolded Protein Response in Ocular Health and Disease. The Febs Journal
Kroeger H, Grimsey N, Paxman R, et al. (2018) The unfolded protein response regulator ATF6 promotes mesodermal differentiation. Science Signaling. 11
Skorczyk-Werner A, Chiang WC, Wawrocka A, et al. (2017) Autosomal recessive cone-rod dystrophy can be caused by mutations in the ATF6 gene. European Journal of Human Genetics : Ejhg
Rodvold JJ, Chiu KT, Hiramatsu N, et al. (2017) Intercellular transmission of the unfolded protein response promotes survival and drug resistance in cancer cells. Science Signaling. 10
Biswas P, Duncan JL, Maranhao B, et al. (2017) Genetic analysis of ten pedigrees with inherited retinal degeneration (IRD) by exome sequencing and phenotype-genotype association. Physiological Genomics. physiolgenomics.0009
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