John J. Moran

发表

Schwann cell transcript biomarkers for hereditary neuropathy skin biopsies

J. Svaren, John J. Moran, Xingyao Wu, 2019, Annals of neurology.

Genome-wide analysis of EGR2/SOX10 binding in myelinating peripheral nerve

Sunduz Keles, Guannan Sun, S. Keleş, 2012, Nucleic acids research.

Transmembrane protease serine 5: a novel Schwann cell plasma marker for CMT1A

J. Svaren, K. Call, John J. Moran, 2019, Annals of clinical and translational neurology.

Myelin protein zero mutations and the unfolded protein response in Charcot Marie Tooth disease type 1B

J. Svaren, John J. Moran, Xingyao Wu, 2018, Annals of clinical and translational neurology.

Pmp22 Super-enhancer Deletion Causes Tomacula Formation and Conduction Block in Peripheral Nerves.

J. Svaren, John J. Moran, Jun Li, 2020, Human molecular genetics.

Analysis of copy number variation in dogs implicates genomic structural variation in the development of anterior cruciate ligament rupture

C. Engelman, John J. Moran, P. Muir, 2020, PloS one.

Polycomb repression regulates Schwann cell proliferation and axon regeneration after nerve injury

J. Svaren, John J. Moran, Phu Duong, 2018, Glia.

H3K27 demethylases are dispensable for activation of Polycomb-regulated injury response genes in peripheral nerve

J. Svaren, John J. Moran, Raghu Ramesh, 2021, The Journal of biological chemistry.

Genome-Edited Cell Lines for High-Throughput Screening.

James Inglese, J. Svaren, John J. Moran, 2018, Methods in molecular biology.

Variation in SIPA1L2 is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1A

F. Baas, S. Züchner, G. Beecham, 2019, Annals of neurology.

Regulation of the neuropathy-associated Pmp22 gene by a distal super-enhancer

A. Dutra, J. Svaren, John J. Moran, 2018, Human molecular genetics.

Tead1 regulates the expression of Peripheral Myelin Protein 22 during Schwann cell development.

J. Svaren, A. Antonellis, John J. Moran, 2016, Human molecular genetics.

Genome Editing-Enabled HTS Assays Expand Drug Target Pathways for Charcot–Marie–Tooth Disease

R. Guha, James Inglese, Yolanda Santiago, 2014, ACS chemical biology.

Genome-Edited Coincidence and PMP22-HiBiT Fusion Reporter Cell Lines Enable an Artifact-Suppressive Quantitative High-Throughput Screening Strategy for PMP22 Gene-Dosage Disorder Drug Discovery.

A. Dutra, James Inglese, J. Svaren, 2021, ACS pharmacology & translational science.

ACTL6a coordinates axonal caliber recognition and myelination in the peripheral nerve

G. Crabtree, J. Svaren, John J. Moran, 2022, iScience.

A mutation in the Tubb4a gene leads to microtubule accumulation with hypomyelination and demyelination

I. Duncan, J. Svaren, John J. Moran, 2017, Annals of neurology.

Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study

F. Baas, S. Züchner, G. Beecham, 2019, Journal of neuromuscular diseases.