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Biological Reviews of the Cambridge Philosophical Society|December 20, 2018
Animal movements in fire-prone landscapesDale G Nimmo, Sarah Avitabile, Sam C Banks, et al.
The Journal of Infectious Diseases|June 5, 2024
Pharmacokinetics and Safety of Remdesivir in Pregnant and Nonpregnant Women With COVID-19: Results From IMPAACT 2032Kristina M Brooks, Kristin Baltrusaitis, Diana F Clarke, et al.
Pediatric Neurology|March 19, 2026
Corpus Callosotomy or Focal Surgery in Children Presenting With Generalized Tonic Seizures: Findings From the Pediatric Epilepsy Research ConsortiumCemal Karakas, Aaron E L Warren, Juliet K Knowles, et al.
Genome Biology|December 1, 2007
Application of phage display to high throughput antibody generation and characterizationDarren J Schofield, Anthony R Pope, Veronica Clementel, et al.
American Journal of Human Genetics|November 26, 2013
Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline MyopathyVandana A Gupta, Gianina Ravenscroft, Ranad Shaheen, et al.
Neurology. Genetics|May 12, 2021
WGS and RNA Studies Diagnose Noncoding <i>DMD</i> Variants in Males With High Creatine KinaseLeigh B Waddell, Samantha J Bryen, Beryl B Cummings, et al.
Nature|May 16, 2014
The metabolite α-ketoglutarate extends lifespan by inhibiting ATP synthase and TORRandall M Chin, Xudong Fu, Melody Y Pai, et al.
Human Mutation|April 3, 2014
Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathiesMinttu Marttila, Vilma-Lotta Lehtokari, Steven Marston, et al.
Science Translational Medicine|April 21, 2017
Improving genetic diagnosis in Mendelian disease with transcriptome sequencingBeryl B Cummings, Jamie L Marshall, Taru Tukiainen, et al.
The Journal of Clinical Investigation|November 26, 2013
ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruptionShazia Ashraf, Heon Yung Gee, Stephanie Woerner, et al.
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