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Neuromuscular Disorders : NMD|September 1, 1994
Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9L H Yamaoka, C A Westbrook, M C Speer, et al.Neuromuscular Disorders : NMD|December 10, 1997
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutationJ M Stajich, J M Gilchrist, F Lennon, et al.Biotechniques|March 26, 2009
Flexible low-cost system for small animal aerosol inhalation exposure to drugs, proteins, inflammatory agents, and infectious agentsWilliam G Schroeder, Laura M Mitrescu, Marcia L Hart, et al.Biorxiv : the Preprint Server for Biology|June 6, 2025
Ancient convergence with prokaryote defense and recent adaptations to lentiviruses in primates characterize the ancestral immune factors SAMD9sAlexandre Legrand, Rémi Demeure, Amandine Chantharath, et al.Experimental and Molecular Pathology|June 28, 2014
Microhemorrhage is an early event in the pulmonary fibrotic disease of PECAM-1 deficient FVB/n miceMarta Lishnevsky, Lena C Young, Steven J Woods, et al.Nature Ecology & Evolution|November 11, 2025
Evolutionary characterization of antiviral SAMD9/9L across kingdoms supports ancient convergence and lineage-specific adaptationsAlexandre Legrand, Rémi Demeure, Amandine Chantharath, et al.Investigative Ophthalmology & Visual Science|November 24, 2005
Retinal vein occlusion, homocysteine, and methylene tetrahydrofolate reductase genotypeStuart J McGimpsey, Jayne V Woodside, Louise Bamford, et al.Journal of Immunology (Baltimore, Md. : 1950)|March 22, 2000
Aerosolized Syk antisense suppresses Syk expression, mediator release from macrophages, and pulmonary inflammationG R Stenton, M K Kim, O Nohara, et al.JCI Insight|February 18, 2025
CD103+ dendritic cell-fibroblast crosstalk via TLR9, TDO2, and AHR signaling drives lung fibrogenesisHannah Carter, Rita Medina Costa, Taylor S Adams, et al.Human Heredity|August 7, 1998
Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy familiesM C Speer, J M Vance, F Lennon-Graham, et al.Pageof 19