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Proceedings of the National Academy of Sciences of the United States of America|February 23, 2021
Regulation of neonatal IgA production by the maternal microbiotaQinghui Mu, Brianna K Swartwout, Michael Edwards, et al.
Calcified Tissue International|December 26, 2016
Bone Mass and Strength are Significantly Improved in Mice Overexpressing Human WNT16 in OsteocytesImranul Alam, Austin M Reilly, Mohammed Alkhouli, et al.
Infection Control and Hospital Epidemiology|August 8, 2008
Outbreak of invasive methicillin-resistant Staphylococcus aureus infection associated with acupuncture and joint injectionR J Murray, J C Pearson, G W Coombs, et al.
Experimental Eye Research|November 21, 2020
Differential effects of Hsp90 inhibition on corneal cells in vitro and in vivoVijayKrishna Raghunathan, Sydney Garrison Edwards, Brian C Leonard, et al.
American Journal of Human Genetics|June 19, 2012
Exome sequencing identifies a REEP1 mutation involved in distal hereditary motor neuropathy type VChristian Beetz, Thomas R Pieber, Nicole Hertel, et al.
The Lancet. Neurology|March 12, 2011
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trialDavide Pareyson, Mary M Reilly, Angelo Schenone, et al.
International Journal of Genomics|October 23, 2019
Additional Evidence for <i>DDB2</i> T338M as a Genetic Risk Factor for Ocular Squamous Cell Carcinoma in HorsesMoriel H Singer-Berk, Kelly E Knickelbein, Zachary T Lounsberry, et al.
Neurology|July 1, 2011
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutationsJ M Polke, M Laurá, D Pareyson, et al.
Neurology|January 18, 2024
Multicenter Validation of the Charcot-Marie-Tooth Functional Outcome MeasureMelissa R Mandarakas, Katy J Eichinger, Paula Bray, et al.
Frontiers in Neurology|September 15, 2023
The mutational profile in a South African cohort with inherited neuropathies and spastic paraplegiaAmokelani C Mahungu, Elizabeth Steyn, Niki Floudiotis, et al.
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