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American Journal of Human Genetics|October 18, 2016
Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar DisorganizationGina L O'Grady, Heather A Best, Tamar E Sztal, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 28, 2012
The CD47-signal regulatory protein alpha (SIRPa) interaction is a therapeutic target for human solid tumorsStephen B Willingham, Jens-Peter Volkmer, Andrew J Gentles, et al.
The Journal of Clinical Investigation|May 5, 2011
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafnessSaskia F Heeringa, Gil Chernin, Moumita Chaki, et al.
American Journal of Human Genetics|June 11, 2013
Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathyGianina Ravenscroft, Satoko Miyatake, Vilma-Lotta Lehtokari, et al.
The Journal of Clinical Investigation|September 25, 2014
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathyMichaela Yuen, Sarah A Sandaradura, James J Dowling, et al.
BMC Biology|August 1, 2017
Genomic innovations, transcriptional plasticity and gene loss underlying the evolution and divergence of two highly polyphagous and invasive Helicoverpa pest speciesS L Pearce, D F Clarke, P D East, et al.
Annals of Neurology|April 26, 2018
Congenital Titinopathy: Comprehensive characterization and pathogenic insightsEmily C Oates, Kristi J Jones, Sandra Donkervoort, et al.
Insect Biochemistry and Molecular Biology|August 16, 2016
Multifaceted biological insights from a draft genome sequence of the tobacco hornworm moth, Manduca sextaMichael R Kanost, Estela L Arrese, Xiaolong Cao, et al.
Genome Biology|April 25, 2015
The genomes of two key bumblebee species with primitive eusocial organizationBen M Sadd, Seth M Barribeau, Guy Bloch, et al.
Science (New York, N.Y.)|May 13, 2022
The Tabula Sapiens: A multiple-organ, single-cell transcriptomic atlas of humans, Robert C Jones, Jim Karkanias, et al.
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