Clement Y. Chow

发表

The dynamic effect of genetic variation on the in vivo ER stress transcriptional response in different tissues

C. Y. Chow, Nikki D. Russell, Clement Y. Chow, 2022, G3.

The dynamic effect of regulatory genetic variation on the in vivo ER stress transcriptional response

C. Y. Chow, Nikki D. Russell, Clement Y. Chow, 2021, bioRxiv.

Insulin Potentiates JAK/STAT Signaling to Broadly Inhibit Flavivirus Replication in Insect Vectors

Brandi K. Torrevillas, Chasity E Trammell, S. Luckhart, 2019, bioRxiv.

Large Neurological Component to Genetic Differences Underlying Biased Sperm Use in Drosophila

A. Clark, M. Wolfner, C. Y. Chow, 2013, Genetics.

Loss of Vac14, a regulator of the signaling lipid phosphatidylinositol 3,5-bisphosphate, results in neurodegeneration in mice

S. Morrison, M. Meisler, R. Westrick, 2007, Proceedings of the National Academy of Sciences.

Causal and Candidate Gene Variants in a Large Cohort of Women with Primary Ovarian Insufficiency

E. Mardis, M. Yandell, E. Hernandez, 2021, medRxiv.

Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J

J. Lupski, K. Szigeti, M. Meisler, 2007, Nature.

Pathogenic Mechanism of the FIG4 Mutation Responsible for Charcot-Marie-Tooth Disease CMT4J

M. Meisler, J. Dowling, L. Weisman, 2011, PLoS genetics.

Deleterious variants of FIG4, a phosphoinositide phosphatase, in patients with ALS.

Robert H. Brown, J. Landers, M. Meisler, 2009, American journal of human genetics.

Mutation of FIG4 causes a rapidly progressive, asymmetric neuronal degeneration.

M. Meisler, M. Shy, Jun Li, 2008, Brain : a journal of neurology.

Deleterious Variants of FIG 4 , a Phosphoinositide Phosphatase , in Patients with ALS Citation

Robert H. Brown, J. Landers, M. Meisler, 2008 .

VAC14 nucleates a protein complex essential for the acute interconversion of PI3P and PI(3,5)P2 in yeast and mouse

R. Bronson, M. Meisler, D. Goldowitz, 2008, The EMBO journal.

Mutations in PI(3,5)P2 Signaling and Neurodegeneration in Mouse and Human.

C. Y. Chow, Clement Y. Chow, 2008 .

Roles of Female and Male Genotype in Post-Mating Responses in Drosophila melanogaster

A. Clark, M. Wolfner, C. Y. Chow, 2017, The Journal of heredity.

Induction of Excessive Endoplasmic Reticulum Stress in the Drosophila Male Accessory Gland Results in Infertility

A. Clark, M. Wolfner, C. Y. Chow, 2015, PloS one.

Molecular social interactions: Drosophila melanogaster seminal fluid proteins as a case study.

M. Wolfner, L. Sirot, C. Rubinstein, 2009, Advances in genetics.

An in vivo drug repurposing screen and transcriptional analyses reveals the serotonin pathway and GSK3 as major therapeutic targets for NGLY1 deficiency

R. Peterson, C. Y. Chow, Kevin A. Hope, 2021, bioRxiv.

Etiology of Human Genetic Disease on the Fly.

L. Reiter, C. Y. Chow, Clement Y. Chow, 2017, Trends in genetics : TIG.

The Genetic Architecture of the Genome-Wide Transcriptional Response to ER Stress in the Mouse

A. Clark, M. Wolfner, C. Y. Chow, 2015, PLoS genetics.

The Genetic Basis for Male × Female Interactions Underlying Variation in Reproductive Phenotypes of Drosophila

A. Clark, M. Wolfner, C. Y. Chow, 2010, Genetics.

A Drosophila screen identifies a role for histone methylation in ER stress preconditioning

Katie G. Owings, C. Y. Chow, Clement Y. Chow, 2023, bioRxiv.

Genetic Modifiers of Neurodegeneration in a Drosophila Model of Parkinson’s Disease

I. Martin, C. Y. Chow, Vinita G Chittoor-Vinod, 2018, Genetics.

Genetic Modifiers of Pathogenic LRRK2 G2019S Neurodegeneration in Drosophila

I. Martin, C. Y. Chow, Vinita G Chittoor-Vinod, 2018, bioRxiv.

Natural Genetic Variation Screen in Drosophila Identifies Wnt Signaling, Mitochondrial Metabolism, and Redox Homeostasis Genes as Modifiers of Apoptosis

Alan G. Goodman, Katie G. Owings, C. Y. Chow, 2019, G3: Genes, Genomes, Genetics.

A genome-wide CRISPR screen identifies DPM1 as a modifier of DPAGT1 deficiency and ER stress

N. Perrimon, S. Mohr, C. Y. Chow, 2022, PLoS genetics.

A genome-wide CRISPR screen identifies the glycosylation enzyme DPM1 as a modifier of DPAGT1 deficiency and ER stress

N. Perrimon, S. Mohr, C. Y. Chow, 2021, bioRxiv.

Bringing genetic background into focus

C. Y. Chow, Clement Y. Chow, 2015, Nature Reviews Genetics.

Baldspot/ELOVL6 is a conserved modifier of disease and the ER stress response

C. Y. Chow, Rebecca A. S. Palu, Clement Y. Chow, 2018, bioRxiv.

Using natural variation in Drosophila to discover previously unknown endoplasmic reticulum stress genes

A. Clark, M. Wolfner, C. Y. Chow, 2013, Proceedings of the National Academy of Sciences.

A Drosophila screen identifies NKCC1 as a modifier of NGLY1 deficiency

C. Lutz, Katie G. Owings, C. Y. Chow, 2020, eLife.

A Drosophila natural variation screen identifies NKCC1 as a substrate of NGLY1 deglycosylation and a modifier of NGLY1 deficiency

C. Lutz, Katie G. Owings, C. Y. Chow, 2020, bioRxiv.

Candidate genetic modifiers of retinitis pigmentosa identified by exploiting natural variation in Drosophila.

A. Clark, M. Wolfner, C. Y. Chow, 2016, Human molecular genetics.

Transcriptome and functional analysis in a Drosophila model of NGLY1 deficiency provides insight into therapeutic approaches

Matthew Might, M. Might, Katie G. Owings, 2018, Human molecular genetics.

Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers

Joshua M. Korn, M. Daly, D. Altshuler, 2011, Human Genetics.

Exaggerated emotional behavior in mice heterozygous for the sodium channel Scn 8 a ( Na v 1 . 6 )

M. Meisler, C. Y. Chow, B. McKinney, 2010 .

Exaggerated emotional behavior in mice heterozygous null for the sodium channel Scn8a (Nav1.6)

M. Meisler, C. Y. Chow, G. Murphy, 2008, Genes, brain, and behavior.

Candidate genetic modifiers of retinitis pigmentosa identified by exploiting natural variation in Drosophila.

M. Wolfner, Clement Y. Chow, A. Clark, 2016, Human molecular genetics.

Characterizing genetic variation in the regulation of the ER stress response through computational and cis-eQTL analyses

L. Jorde, Clement Y. Chow, N. D. Russell, 2023, G3.