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Human Genetics|April 10, 2002
Contribution of arylsulfatase A mutations located on the same allele to enzyme activity reduction and metachromatic leukodystrophy severityStefano Regis, Fabio Corsolini, Marina Stroppiano, et al.
Gene Expression|July 3, 2003
The first intron of the human osteopontin gene contains a C/EBP-beta-responsive enhancerFrancesca Giacopelli, Nadia Rosatto, Maria Teresa Divizia, et al.
Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|May 29, 2014
Complete genome sequence of chloroplast DNA (cpDNA) of Chlorella sorokinianaMassimiliano Orsini, Roberto Cusano, Cristina Costelli, et al.
Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|February 19, 2015
Complete sequence and characterization of mitochondrial and chloroplast genome of Chlorella variabilis NC64AMassimiliano Orsini, Cristina Costelli, Veronica Malavasi, et al.
Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|September 5, 2014
Complete genome sequence of mitochondrial DNA (mtDNA) of Chlorella sorokinianaMassimiliano Orsini, Cristina Costelli, Veronica Malavasi, et al.
International Journal of Molecular Sciences|October 28, 2023
Association of HLA-A*11:01, -A*24:02, and -B*18:01 with Prostate Cancer Risk: A Case-Control StudyMaria Antonietta Manca, Elena Rita Simula, Davide Cossu, et al.
International Journal of Molecular Medicine|August 4, 2005
Dissecting clinical findings: platelet defects segregate independently of deafness and cataract in a family affected by an apparent syndromic form of macrothrombocytopeniaSimone Gangarossa, Marco Seri, Alessandro Pecci, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
Genetic heterogeneity in inherited spastic paraplegia associated with epilepsyCristiana Lo Nigro, Roberto Cusano, Gian Luigi Gigli, et al.
Epigenetics Insights|April 7, 2023
Next Generation Sequencing for miRNA Detection on the Exhaled Breath Condensate: A Pilot StudyRoberto Cherchi, Roberto Cusano, Sandro Orrù, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
Previously undescribed nonsense mutation in SHH caused autosomal dominant holoprosencephaly with wide intrafamilial variabilityMonica Marini, Roberto Cusano, Pierangela De Biasio, et al.
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