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Items: 23

1.

A novel oncogenic BTK isoform is overexpressed in colon cancers and required for RAS-mediated transformation.

Grassilli E, Pisano F, Cialdella A, Bonomo S, Missaglia C, Cerrito MG, Masiero L, Ianzano L, Giordano F, Cicirelli V, Narloch R, D'Amato F, Noli B, Ferri GL, Leone BE, Stanta G, Bonin S, Helin K, Giovannoni R, Lavitrano M.

Oncogene. 2016 Aug 18;35(33):4368-78. doi: 10.1038/onc.2015.504. Epub 2016 Jan 25.

2.

GSK3A is redundant with GSK3B in modulating drug resistance and chemotherapy-induced necroptosis.

Grassilli E, Ianzano L, Bonomo S, Missaglia C, Cerrito MG, Giovannoni R, Masiero L, Lavitrano M.

PLoS One. 2014 Jul 1;9(7):e100947. doi: 10.1371/journal.pone.0100947. eCollection 2014.

3.

Inhibition of GSK3B bypass drug resistance of p53-null colon carcinomas by enabling necroptosis in response to chemotherapy.

Grassilli E, Narloch R, Federzoni E, Ianzano L, Pisano F, Giovannoni R, Romano G, Masiero L, Leone BE, Bonin S, Donada M, Stanta G, Helin K, Lavitrano M.

Clin Cancer Res. 2013 Jul 15;19(14):3820-31. doi: 10.1158/1078-0432.CCR-12-3289. Epub 2013 May 31.

4.

Genetic diagnosis in Lafora disease: genotype-phenotype correlations and diagnostic pitfalls.

Lohi H, Turnbull J, Zhao XC, Pullenayegum S, Ianzano L, Yahyaoui M, Mikati MA, Quinn NP, Franceschetti S, Zara F, Minassian BA.

Neurology. 2007 Mar 27;68(13):996-1001. Erratum in: Neurology. 2007 Jun 12;68(24):2153. Quinn, NP [added].

PMID:
17389303
5.

Clinical and genetic findings in 26 Italian patients with Lafora disease.

Franceschetti S, Gambardella A, Canafoglia L, Striano P, Lohi H, Gennaro E, Ianzano L, Veggiotti P, Sofia V, Biondi R, Striano S, Gellera C, Annesi G, Madia F, Civitelli D, Rocca FE, Quattrone A, Avanzini G, Minassian B, Zara F.

Epilepsia. 2006 Mar;47(3):640-3.

6.

Lafora progressive Myoclonus Epilepsy mutation database-EPM2A and NHLRC1 (EPM2B) genes.

Ianzano L, Zhang J, Chan EM, Zhao XC, Lohi H, Scherer SW, Minassian BA.

Hum Mutat. 2005 Oct;26(4):397.

PMID:
16134145
7.

Novel glycogen synthase kinase 3 and ubiquitination pathways in progressive myoclonus epilepsy.

Lohi H, Ianzano L, Zhao XC, Chan EM, Turnbull J, Scherer SW, Ackerley CA, Minassian BA.

Hum Mol Genet. 2005 Sep 15;14(18):2727-36. Epub 2005 Aug 22.

PMID:
16115820
8.

Expanded repeat in canine epilepsy.

Lohi H, Young EJ, Fitzmaurice SN, Rusbridge C, Chan EM, Vervoort M, Turnbull J, Zhao XC, Ianzano L, Paterson AD, Sutter NB, Ostrander EA, André C, Shelton GD, Ackerley CA, Scherer SW, Minassian BA.

Science. 2005 Jan 7;307(5706):81.

9.

Laforin preferentially binds the neurotoxic starch-like polyglucosans, which form in its absence in progressive myoclonus epilepsy.

Chan EM, Ackerley CA, Lohi H, Ianzano L, Cortez MA, Shannon P, Scherer SW, Minassian BA.

Hum Mol Genet. 2004 Jun 1;13(11):1117-29. Epub 2004 Apr 21.

PMID:
15102711
10.

Loss of function of the cytoplasmic isoform of the protein laforin (EPM2A) causes Lafora progressive myoclonus epilepsy.

Ianzano L, Young EJ, Zhao XC, Chan EM, Rodriguez MT, Torrado MV, Scherer SW, Minassian BA.

Hum Mutat. 2004 Feb;23(2):170-6.

PMID:
14722920
11.

Mutations in NHLRC1 cause progressive myoclonus epilepsy.

Chan EM, Young EJ, Ianzano L, Munteanu I, Zhao X, Christopoulos CC, Avanzini G, Elia M, Ackerley CA, Jovic NJ, Bohlega S, Andermann E, Rouleau GA, Delgado-Escueta AV, Minassian BA, Scherer SW.

Nat Genet. 2003 Oct;35(2):125-7. Epub 2003 Sep 7.

PMID:
12958597
12.

Identification of a novel protein interacting with laforin, the EPM2a progressive myoclonus epilepsy gene product.

Ianzano L, Zhao XC, Minassian BA, Scherer SW.

Genomics. 2003 Jun;81(6):579-87.

PMID:
12782127
13.

Laforin is a cell membrane and endoplasmic reticulum-associated protein tyrosine phosphatase.

Minassian BA, Andrade DM, Ianzano L, Young EJ, Chan E, Ackerley CA, Scherer SW.

Ann Neurol. 2001 Feb;49(2):271-5.

PMID:
11220751
14.

Mutation spectrum and predicted function of laforin in Lafora's progressive myoclonus epilepsy.

Minassian BA, Ianzano L, Meloche M, Andermann E, Rouleau GA, Delgado-Escueta AV, Scherer SW.

Neurology. 2000 Aug 8;55(3):341-6.

PMID:
10932264
15.

Identification of new and common mutations in the EPM2A gene in Lafora disease.

Minassian BA, Ianzano L, Delgado-Escueta AV, Scherer SW.

Neurology. 2000 Jan 25;54(2):488-90.

PMID:
10668720
16.

Spontaneous functional correction of homozygous fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism.

Waisfisz Q, Morgan NV, Savino M, de Winter JP, van Berkel CG, Hoatlin ME, Ianzano L, Gibson RA, Arwert F, Savoia A, Mathew CG, Pronk JC, Joenje H.

Nat Genet. 1999 Aug;22(4):379-83.

PMID:
10431244
17.

The PISSLRE gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancer.

Crawford J, Ianzano L, Savino M, Whitmore S, Cleton-Jansen AM, Settasatian C, d'apolito M, Seshadri R, Pronk JC, Auerbach AD, Verlander PC, Mathew CG, Tipping AJ, Doggett NA, Zelante L, Callen DF, Savoia A.

Genomics. 1999 Feb 15;56(1):90-7.

PMID:
10036189
18.

Fine exon-intron structure of the Fanconi anemia group A (FAA) gene and characterization of two genomic deletions.

Centra M, Memeo E, d'Apolito M, Savino M, Ianzano L, Notarangelo A, Liu J, Doggett NA, Zelante L, Savoia A.

Genomics. 1998 Aug 1;51(3):463-7.

PMID:
9721219
19.

Mutations of the Fanconi anemia group A gene (FAA) in Italian patients.

Savino M, Ianzano L, Strippoli P, Ramenghi U, Arslanian A, Bagnara GP, Joenje H, Zelante L, Savoia A.

Am J Hum Genet. 1997 Dec;61(6):1246-53.

20.

The genomic organization of the Fanconi anemia group A (FAA) gene.

Ianzano L, D'Apolito M, Centra M, Savino M, Levran O, Auerbach AD, Cleton-Jansen AM, Doggett NA, Pronk JC, Tipping AJ, Gibson RA, Mathew CG, Whitmore SA, Apostolou S, Callen DF, Zelante L, Savoia A.

Genomics. 1997 May 1;41(3):309-14.

PMID:
9169126
21.

Molecular characterization of Fanconi anaemia group C (FAC) gene polymorphisms.

Savoia A, Centra M, Ianzano L, Pio de Cillis G, Buchwald M, Zelante L.

Mol Cell Probes. 1996 Jun;10(3):213-8.

PMID:
8799375
22.

Identification of three novel mutations in the PIG-A gene in paroxysmal nocturnal haemoglobinuria (PNH) patients.

Savoia A, Ianzano L, Lunardi C, De Sandre G, Carotenuto M, Musto P, Zelante L.

Hum Genet. 1996 Jan;97(1):45-8.

PMID:
8557259
23.

Characterization of the 5' region of the Fanconi anaemia group C (FACC) gene.

Savoia A, Centra M, Ianzano L, de Cillis GP, Zelante L, Buchwald M.

Hum Mol Genet. 1995 Aug;4(8):1321-6.

PMID:
7581369

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