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Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy.
Nat Genet. 1999 Mar;21(3):285-8. doi: 10.1038/6799.
Nat Genet. 1999.
PMID: 10080180
Clinical Trial.
Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.
De Sandre-Giovannoli A, Chaouch M, Kozlov S, Vallat JM, Tazir M, Kassouri N, Szepetowski P, Hammadouche T, Vandenberghe A, Stewart CL, Grid D, Lévy N.
De Sandre-Giovannoli A, et al.
Am J Hum Genet. 2002 Mar;70(3):726-36. doi: 10.1086/339274. Epub 2002 Jan 17.
Am J Hum Genet. 2002.
PMID: 11799477
Free PMC article.
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Wolbachia utilizes host microtubules and Dynein for anterior localization in the Drosophila oocyte.
Ferree PM, Frydman HM, Li JM, Cao J, Wieschaus E, Sullivan W.
Ferree PM, et al.
PLoS Pathog. 2005 Oct;1(2):e14. doi: 10.1371/journal.ppat.0010014. Epub 2005 Oct 14.
PLoS Pathog. 2005.
PMID: 16228015
Free PMC article.
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