Bocciardi R - Search Results

1

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: bocciardi r. 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

2

The physical map of the human RET proto-oncogene.

Pasini B, Hofstra RM, Yin L, Bocciardi R, Santamaria G, Grootscholten PM, Ceccherini I, Patrone G, Priolo M, Buys CH, et al. Pasini B, et al. Among authors: bocciardi r. Oncogene. 1995 Nov 2;11(9):1737-43. Oncogene. 1995. PMID: 7478601

3

Loss of function effect of RET mutations causing Hirschsprung disease.

Pasini B, Borrello MG, Greco A, Bongarzone I, Luo Y, Mondellini P, Alberti L, Miranda C, Arighi E, Bocciardi R, et al. Pasini B, et al. Among authors: bocciardi r. Nat Genet. 1995 May;10(1):35-40. doi: 10.1038/ng0595-35. Nat Genet. 1995. PMID: 7647787

4

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: bocciardi r. Oncogene. 1995 Mar 16;10(6):1257. Oncogene. 1995. PMID: 7700653 No abstract available.

5

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: bocciardi r. Eur J Hum Genet. 1994;2(4):272-80. doi: 10.1159/000472371. Eur J Hum Genet. 1994. PMID: 7704557

6

Exon structure and flanking intronic sequences of the human RET proto-oncogene.

Ceccherini I, Bocciardi R, Luo Y, Pasini B, Hofstra R, Takahashi M, Romeo G. Ceccherini I, et al. Among authors: bocciardi r. Biochem Biophys Res Commun. 1993 Nov 15;196(3):1288-95. doi: 10.1006/bbrc.1993.2392. Biochem Biophys Res Commun. 1993. PMID: 7902707

7

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: bocciardi r. Hum Mol Genet. 1993 Nov;2(11):1803-8. doi: 10.1093/hmg/2.11.1803. Hum Mol Genet. 1993. PMID: 7904208

8

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: bocciardi r. Oncogene. 1994 Oct;9(10):3025-9. Oncogene. 1994. PMID: 8084609

9

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: bocciardi r. Nature. 1994 Jan 27;367(6461):377-8. doi: 10.1038/367377a0. Nature. 1994. PMID: 8114938

10

The multiple endocrine neoplasia type 2B point mutation switches the specificity of the Ret tyrosine kinase towards cellular substrates that are susceptible to interact with Crk and Nck.

Bocciardi R, Mograbi B, Pasini B, Borrello MG, Pierotti MA, Bourget I, Fischer S, Romeo G, Rossi B. Bocciardi R, et al. Oncogene. 1997 Nov 6;15(19):2257-65. doi: 10.1038/sj.onc.1201413. Oncogene. 1997. PMID: 9393871

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