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Molecular Biology and Evolution|March 19, 2013
Evolutionary analysis of the contact system indicates that kininogen evolved adaptively in mammals and in human populationsRachele Cagliani, Diego Forni, Stefania Riva, et al.
Molecular Biology Reports|January 24, 2014
In vitro analysis of splice site mutations in the CLCN1 gene using the minigene assayGianna Ulzi, Valeria A Sansone, Francesca Magri, et al.
The Journal of Experimental Medicine|May 27, 2009
Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditionsMatteo Fumagalli, Uberto Pozzoli, Rachele Cagliani, et al.
Biochemical and Biophysical Research Communications|August 25, 2004
Over-representation of exonic splicing enhancers in human intronless genes suggests multiple functions in mRNA processingUberto Pozzoli, Laura Riva, Giorgia Menozzi, et al.
BMC Evolutionary Biology|March 29, 2008
Both selective and neutral processes drive GC content evolution in the human genomeUberto Pozzoli, Giorgia Menozzi, Matteo Fumagalli, et al.
Cellular and Molecular Life Sciences : CMLS|June 19, 2013
Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophyAlessandra Govoni, Francesca Magri, Simona Brajkovic, et al.
Molecular Biology and Evolution|March 19, 2010
Polymorphisms in the CPB2 gene are maintained by balancing selection and result in haplotype-preferential splicing of exon 7Rachele Cagliani, Matteo Fumagalli, Stefania Riva, et al.
Genome Research|November 11, 2008
Widespread balancing selection and pathogen-driven selection at blood group antigen genesMatteo Fumagalli, Rachele Cagliani, Uberto Pozzoli, et al.
Human Mutation|November 25, 2003
POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletionsAlessio Di Fonzo, Andreina Bordoni, Marco Crimi, et al.
Therapeutic Advances in Neurological Disorders|May 21, 2019
Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophiesDaniela Piga, Sabrina Salani, Francesca Magri, et al.
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