Barone V - Search Results

1

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease.

Romeo G, Ronchetto P, Luo Y, Barone V, Seri M, Ceccherini I, Pasini B, Bocciardi R, Lerone M, Kääriäinen H, et al. Romeo G, et al. Among authors: barone v. Nature. 1994 Jan 27;367(6461):377-8. doi: 10.1038/367377a0. Nature. 1994. PMID: 8114938

2

Identification of the Cys634-->Tyr mutation of the RET proto-oncogene in a pedigree with multiple endocrine neoplasia type 2A and localized cutaneous lichen amyloidosis.

Ceccherini I, Romei C, Barone V, Pacini F, Martino E, Loviselli A, Pinchera A, Romeo G. Ceccherini I, et al. Among authors: barone v. J Endocrinol Invest. 1994 Mar;17(3):201-4. doi: 10.1007/BF03347719. J Endocrinol Invest. 1994. PMID: 7914213

3

DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the ret proto-oncogene.

Ceccherini I, Hofstra RM, Luo Y, Stulp RP, Barone V, Stelwagen T, Bocciardi R, Nijveen H, Bolino A, Seri M, et al. Ceccherini I, et al. Among authors: barone v. Oncogene. 1994 Oct;9(10):3025-9. Oncogene. 1994. PMID: 8084609

4

Exclusion of linkage between RET and neuronal intestinal dysplasia type B.

Barone V, Weber D, Luo Y, Brancolini V, Devoto M, Romeo G. Barone V, et al. Am J Med Genet. 1996 Mar 15;62(2):195-8. doi: 10.1002/(SICI)1096-8628(19960315)62:2<195::AID-AJMG15>3.0.CO;2-J. Am J Med Genet. 1996. PMID: 8882403

5

Prevalence and parental origin of de novo RET mutations in Hirschsprung's disease.

Yin L, Seri M, Barone V, Tocco T, Scaranari M, Romeo G. Yin L, et al. Among authors: barone v. Eur J Hum Genet. 1996;4(6):356-8. doi: 10.1159/000472232. Eur J Hum Genet. 1996. PMID: 9043870

6

Frequency of RET mutations in long- and short-segment Hirschsprung disease.

Seri M, Yin L, Barone V, Bolino A, Celli I, Bocciardi R, Pasini B, Ceccherini I, Lerone M, Kristoffersson U, Larsson LT, Casasa JM, Cass DT, Abramowicz MJ, Vanderwinden JM, Kravcenkiene I, Baric I, Silengo M, Martucciello G, Romeo G. Seri M, et al. Among authors: barone v. Hum Mutat. 1997;9(3):243-9. doi: 10.1002/(SICI)1098-1004(1997)9:3<243::AID-HUMU5>3.0.CO;2-8. Hum Mutat. 1997. PMID: 9090527

7

Heterogeneity and low detection rate of RET mutations in Hirschsprung disease.

Yin L, Barone V, Seri M, Bolino A, Bocciardi R, Ceccherini I, Pasini B, Tocco T, Lerone M, Cywes S, et al. Yin L, et al. Among authors: barone v. Eur J Hum Genet. 1994;2(4):272-80. doi: 10.1159/000472371. Eur J Hum Genet. 1994. PMID: 7704557

8

Close linkage with the RET protooncogene and boundaries of deletion mutations in autosomal dominant Hirschsprung disease.

Luo Y, Ceccherini I, Pasini B, Matera I, Bicocchi MP, Barone V, Bocciardi R, Kääriäinen H, Weber D, Devoto M, et al. Luo Y, et al. Among authors: barone v. Hum Mol Genet. 1993 Nov;2(11):1803-8. doi: 10.1093/hmg/2.11.1803. Hum Mol Genet. 1993. PMID: 7904208

9

DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the ret proto-oncogene.

Ceccherini I, Hofstra RM, Luo Y, Stulp RP, Barone V, Stelwagen T, Bocciardi R, Nijveen H, Bolino A, Seri M, et al. Ceccherini I, et al. Among authors: barone v. Oncogene. 1995 Mar 16;10(6):1257. Oncogene. 1995. PMID: 7700653 No abstract available.

10

A chloride conductance evoked by hypotonic shock in epithelial cells.

Galietta LJ, Barone V, Gruenert DC, Romeo G. Galietta LJ, et al. Among authors: barone v. Adv Exp Med Biol. 1991;290:307-16; discussion 316-7. doi: 10.1007/978-1-4684-5934-0_29. Adv Exp Med Biol. 1991. PMID: 1659143 No abstract available.

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