Piluso G - Search Results

1

Lack of replication of genetic associations with human longevity.

Novelli V, Viviani Anselmi C, Roncarati R, Guffanti G, Malovini A, Piluso G, Puca AA. Novelli V, et al. Among authors: piluso g. Biogerontology. 2008 Apr;9(2):85-92. doi: 10.1007/s10522-007-9116-4. Epub 2007 Nov 23. Biogerontology. 2008. PMID: 18034366 Free article.

2

Identification and characterization of a novel member of the dystrobrevin gene family.

Puca AA, Nigro V, Piluso G, Belsito A, Sampaolo S, Quaderi N, Rossi E, Di Iorio G, Ballabio A, Franco B. Puca AA, et al. Among authors: piluso g. FEBS Lett. 1998 Mar 20;425(1):7-13. doi: 10.1016/s0014-5793(98)00097-0. FEBS Lett. 1998. PMID: 9540997 Free article.

3

Gamma1- and gamma2-syntrophins, two novel dystrophin-binding proteins localized in neuronal cells.

Piluso G, Mirabella M, Ricci E, Belsito A, Abbondanza C, Servidei S, Puca AA, Tonali P, Puca GA, Nigro V. Piluso G, et al. J Biol Chem. 2000 May 26;275(21):15851-60. doi: 10.1074/jbc.M000439200. J Biol Chem. 2000. PMID: 10747910 Free article.

4

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene.

Nigro V, de Sá Moreira E, Piluso G, Vainzof M, Belsito A, Politano L, Puca AA, Passos-Bueno MR, Zatz M. Nigro V, et al. Among authors: piluso g. Nat Genet. 1996 Oct;14(2):195-8. doi: 10.1038/ng1096-195. Nat Genet. 1996. PMID: 8841194

5

Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein.

Nigro V, Piluso G, Belsito A, Politano L, Puca AA, Papparella S, Rossi E, Viglietto G, Esposito MG, Abbondanza C, Medici N, Molinari AM, Nigro G, Puca GA. Nigro V, et al. Among authors: piluso g. Hum Mol Genet. 1996 Aug;5(8):1179-86. doi: 10.1093/hmg/5.8.1179. Hum Mol Genet. 1996. PMID: 8842738

6

The retinoblastoma-interacting zinc-finger protein RIZ is a downstream effector of estrogen action.

Abbondanza C, Medici N, Nigro V, Rossi V, Gallo L, Piluso G, Belsito A, Roscigno A, Bontempo P, Puca AA, Molinari AM, Moncharmont B, Puca GA. Abbondanza C, et al. Among authors: piluso g. Proc Natl Acad Sci U S A. 2000 Mar 28;97(7):3130-5. doi: 10.1073/pnas.97.7.3130. Proc Natl Acad Sci U S A. 2000. PMID: 10706618 Free PMC article.

7

Identification of a DNA binding protein cooperating with estrogen receptor as RIZ (retinoblastoma interacting zinc finger protein).

Medici N, Abbondanza C, Nigro V, Rossi V, Piluso G, Belsito A, Gallo L, Roscigno A, Bontempo P, Puca AA, Molinari AM, Moncharmont B, Puca GA. Medici N, et al. Among authors: piluso g. Biochem Biophys Res Commun. 1999 Nov 2;264(3):983-9. doi: 10.1006/bbrc.1999.1604. Biochem Biophys Res Commun. 1999. PMID: 10544042

8

A novel RAB39B mutation and concurrent de novo NF1 mutation in a boy with neurofibromatosis type 1, intellectual disability, and autism: a case report.

Santoro C, Giugliano T, Bernardo P, Palladino F, Torella A, Del Vecchio Blanco F, Onore ME, Carotenuto M, Nigro V, Piluso G. Santoro C, et al. Among authors: piluso g. BMC Neurol. 2020 Sep 1;20(1):327. doi: 10.1186/s12883-020-01911-0. BMC Neurol. 2020. PMID: 32873259 Free PMC article.

9

Genotype-Phenotype Correlations in Neurofibromatosis Type 1: Identification of Novel and Recurrent NF1 Gene Variants and Correlations with Neurocognitive Phenotype.

Napolitano F, Dell'Aquila M, Terracciano C, Franzese G, Gentile MT, Piluso G, Santoro C, Colavito D, Patanè A, De Blasiis P, Sampaolo S, Paladino S, Melone MAB. Napolitano F, et al. Among authors: piluso g. Genes (Basel). 2022 Jun 23;13(7):1130. doi: 10.3390/genes13071130. Genes (Basel). 2022. PMID: 35885913 Free PMC article.

10

A novel diagnostic method to detect truncated neurofibromin in neurofibromatosis 1.

Esposito T, Piluso G, Saracino D, Uccello R, Schettino C, Dato C, Capaldo G, Giugliano T, Varriale B, Paolisso G, Di Iorio G, Melone MA. Esposito T, et al. Among authors: piluso g. J Neurochem. 2015 Dec;135(6):1123-8. doi: 10.1111/jnc.13396. Epub 2015 Nov 12. J Neurochem. 2015. PMID: 26478990 Free article.

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