G. Malferrari

发表

Ctla4 and multiple sclerosis in the Italian population.

I. Biunno, A. Stella, E. Monferini, 2005, Experimental and molecular pathology.

Low-flow Ischemia and Hypoxia Stimulate Apoptosis in Perfused Hearts Independently of Reperfusion

S. Pozzi, I. Biunno, M. Samaja, 2002, Cellular Physiology and Biochemistry.

RNA-mediated interference indicates that SEL1L plays a role in pancreatic beta-cell growth.

I. Biunno, A. Albertini, E. Monferini, 2004, DNA and cell biology.

A novel polymorphism in SEL1L confers susceptibility to Alzheimer's disease

L. Milanesi, C. Mariani, D. Galimberti, 2006, Neuroscience Letters.

Parkinson's Progression Markers Initiative brain autopsy program.

P. Muglia, J. Jankovic, M. Mintun, 2022, Parkinsonism & related disorders.

The Parkinson's progression markers initiative (PPMI) – establishing a PD biomarker cohort

Norbert Schuff, Arthur W. Toga, John Seibyl, 2018, Annals of clinical and translational neurology.

Identification of a novel polymorphism in the fibronectin type II domain of the SEL1L gene and possible relation to the persistent hyperinsulinemic hypoglycemia of infancy.

D. Antonello, P. Moore, I. Biunno, 2004, Mutation research.

Melanoma antigen genes 1 and 2 are differentially expressed in human gastric and cardial carcinomas.

I. Biunno, A. Peracchia, F. Zennaro, 2000, Scandinavian journal of gastroenterology.

The Expression of Sel1L and Tan-1 in Normal and Neoplastic Cells

S. Ménard, I. Biunno, R. Orlandi, 2000, The International journal of biological markers.

Cloning and functional analysis of the allelic polymorphism in the transcription regulatory region of interleukin-1 alpha.

C. Mariani, L. Grimaldi, I. Biunno, 2002, Immunogenetics.

A Simple Extraction Method Useful to Purify DNA from Difficult Biologic Sources

P. Blasio, I. Biunno, M. Gramegna, 2006 .

The Interleukin 1-beta exonic (+3953) polymorphism does not alter in vitro protein secretion.

C. Mariani, L. Grimaldi, I. Biunno, 2002, Experimental and molecular pathology.

Longitudinal clinical and biomarker characteristics of non-manifesting LRRK2 G2019S carriers in the PPMI cohort

Yen F. Tai, P. Muglia, J. Jankovic, 2022, npj Parkinson's Disease.

Feasibility and safety of lumbar puncture in the Parkinson's disease research participants: Parkinson's Progression Marker Initiative (PPMI).

Yen F. Tai, P. Muglia, J. Jankovic, 2019, Parkinsonism & related disorders.

SEL1L expression in non-small cell lung cancer.

S. Bosari, M. Falleni, G. Coggi, 2006, Human pathology.

Cross-species conservation of SEL1L, a human pancreas-specific expressing gene.

I. Rogozin, I. Biunno, B. Castiglioni, 2002, Omics : a journal of integrative biology.

Allelic polymorphisms in the transcriptional regulatory region of human SEL1L.

S. Ménard, I. Biunno, M. Zollo, 2001, Mutation research.

Cloning and functional analysis of SEL1L promoter region, a pancreas-specific gene.

I. Rogozin, I. Biunno, M. Zollo, 2001, DNA and cell biology.

Molecular characterization of a novel endonuclease (Xib) and possible involvement in lysosomal glycogen storage disorders.

S. Servidei, M. Mirabella, C. Tresoldi, 1999, Experimental and molecular pathology.

High-quality genomic DNA from human whole blood and mononuclear cells.

I. Biunno, E. Monferini, E. Del Vecchio, 2002, BioTechniques.

A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population

S. Sawcer, G. Comi, M. Trojano, 2003, Journal of Neuroimmunology.

Identification of single nucleotide variations in the coding and regulatory regions of the myelin-associated glycoprotein gene and study of their association with multiple sclerosis

G. Savettieri, A. Pastore, D. Caputo, 2002, Journal of Neuroimmunology.

Technical note: Improved method for rapid DNA extraction of mastitis pathogens directly from milk.

I. Biunno, S. Morandi, P. Moroni, 2006, Journal of dairy science.

Clinical and dopamine transporter imaging characteristics of non-manifest LRRK2 and GBA mutation carriers in the Parkinson's Progression Markers Initiative (PPMI): a cross-sectional study

Yen F. Tai, A. Singleton, P. Muglia, 2020, The Lancet Neurology.

Cloning and functional analysis of the allelic polymorphism in the transcription regulatory region of interleukin-1α

C. Mariani, L. Grimaldi, I. Biunno, 2002, Immunogenetics.

A collection of 33 novel human mtDNA homoplasmic variants

N. Bresolin, G. Comi, I. Biunno, 2002, Human mutation.

A mitochondrial tRNAHis gene mutation causing pigmentary retinopathy and neurosensorial deafness

N. Bresolin, I. Biunno, M. Crimi, 2003, Neurology.

Deletion polymorphism of DNASE1L1, an X-linked DNase I-like gene, in acid maltase deficiency disorders.

S. Servidei, M. Mirabella, I. Biunno, 2001, Experimental and molecular pathology.

High mutational burden in the mtDNA control region from aged muscles: a single-fiber study

N. Bresolin, G. Comi, G. Scarlato, 2003, Neurobiology of Aging.

Protozoan and Hepatitis B Virus DNA Detection in Human Samples

P. Blasio, I. Biunno, E. Monferini, 2004 .