Biunno I - Search Results

1

A collection of 33 novel human mtDNA homoplasmic variants.

Crimi M, Sciacco M, Galbiati S, Bordoni A, Malferrari G, Del Bo R, Biunno I, Bresolin N, Comi GP. Crimi M, et al. Among authors: biunno i. Hum Mutat. 2002 Nov;20(5):409. doi: 10.1002/humu.9079. Hum Mutat. 2002. PMID: 12402350

2

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

Del Bo R, Crimi M, Sciacco M, Malferrari G, Bordoni A, Napoli L, Prelle A, Biunno I, Moggio M, Bresolin N, Scarlato G, Pietro Comi G. Del Bo R, et al. Among authors: biunno i. Neurobiol Aging. 2003 Oct;24(6):829-38. doi: 10.1016/s0197-4580(02)00233-6. Neurobiol Aging. 2003. PMID: 12927765

3

A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome.

Crimi M, Galbiati S, Moroni I, Bordoni A, Perini MP, Lamantea E, Sciacco M, Zeviani M, Biunno I, Moggio M, Scarlato G, Comi GP. Crimi M, et al. Among authors: biunno i. Neurology. 2003 Jun 10;60(11):1857-61. doi: 10.1212/01.wnl.0000066048.72780.69. Neurology. 2003. PMID: 12796552

4

SEL1L expression in non-small cell lung cancer.

Ferrero S, Falleni M, Cattaneo M, Malferrari G, Canton C, Biagiotti L, Maggioni M, Nosotti M, Coggi G, Bosari S, Biunno I. Ferrero S, et al. Among authors: biunno i. Hum Pathol. 2006 May;37(5):505-12. doi: 10.1016/j.humpath.2005.12.012. Epub 2006 Mar 20. Hum Pathol. 2006. PMID: 16647946

5

Allelic polymorphisms in the transcriptional regulatory region of human SEL1L.

Cattaneo M, Zollo M, Malferrari G, Orlandi R, D'Angelo A, Menard S, Biunno I. Cattaneo M, et al. Among authors: biunno i. Mutat Res. 2001 Dec;458(3-4):71-6. doi: 10.1016/s0027-5107(01)00241-x. Mutat Res. 2001. PMID: 11691638

6

SEL1L, the human homolog of C. elegans sel-1: refined physical mapping, gene structure and identification of polymorphic markers.

Biunno I, Bernard L, Dear P, Cattaneo M, Volorio S, Zannini L, Bankier A, Zollo M. Biunno I, et al. Hum Genet. 2000 Feb;106(2):227-35. doi: 10.1007/s004390051032. Hum Genet. 2000. PMID: 10746565

7

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.

Saltini G, Proverbio MC, Malferrari G, Biagiotti L, Boettcher P, Dominici R, Monferini E, Lorenzini E, Cattaneo M, Antonello D, Moore PS, Zamproni I, Viscardi M, Chiumello G, Biunno I. Saltini G, et al. Among authors: biunno i. Mutat Res. 2004 Oct 4;554(1-2):159-63. doi: 10.1016/j.mrfmmm.2004.04.007. Mutat Res. 2004. PMID: 15450414

8

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

Malferrari G, Monferini E, DeBlasio P, Diaferia G, Saltini G, Del Vecchio E, Rossi-Bernardi L, Biunno I. Malferrari G, et al. Among authors: biunno i. Biotechniques. 2002 Dec;33(6):1228-30. doi: 10.2144/02336bm09. Biotechniques. 2002. PMID: 12503304 No abstract available.

9

A mitochondrial tRNA(His) gene mutation causing pigmentary retinopathy and neurosensorial deafness.

Crimi M, Galbiati S, Perini MP, Bordoni A, Malferrari G, Sciacco M, Biunno I, Strazzer S, Moggio M, Bresolin N, Comi GP. Crimi M, et al. Among authors: biunno i. Neurology. 2003 Apr 8;60(7):1200-3. doi: 10.1212/01.wnl.0000055865.30580.39. Neurology. 2003. PMID: 12682337

10

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

Liguori M, Sawcer S, Setakis E, Compston A, Giordano M, D'Alfonso S, Mellai M, Malferrari G, Trojano M, Livrea P, De Robertis F, Massacesi L, Repice A, Ballerini C, Biagioli T, Bomprezzi R, Cannoni S, Ristori G, Salvetti M, Grimaldi LM, Biunno I, Comi G, Leone M, Ferro I, Naldi P, Milanese C, Gellera C, Loredana LM, Savettieri G, Salemi G, Aridon P, Caputo D, Rosa Guerini F, Ferrante P, Momigliano-Richiardi P. Liguori M, et al. Among authors: biunno i. J Neuroimmunol. 2003 Oct;143(1-2):97-100. doi: 10.1016/j.jneuroim.2003.08.020. J Neuroimmunol. 2003. PMID: 14575923

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