Pasini B - 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: pasini b. Nature. 1994 Jan 27;367(6461):377-8. doi: 10.1038/367377a0. Nature. 1994. PMID: 8114938

2

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: pasini b. Biochem Biophys Res Commun. 1993 Nov 15;196(3):1288-95. doi: 10.1006/bbrc.1993.2392. Biochem Biophys Res Commun. 1993. PMID: 7902707

3

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

4

A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma.

Hofstra RM, Landsvater RM, Ceccherini I, Stulp RP, Stelwagen T, Luo Y, Pasini B, Höppener JW, van Amstel HK, Romeo G, et al. Hofstra RM, et al. Among authors: pasini b. Nature. 1994 Jan 27;367(6461):375-6. doi: 10.1038/367375a0. Nature. 1994. PMID: 7906866

5

RET mutations in human disease.

Pasini B, Ceccherini I, Romeo G. Pasini B, et al. Trends Genet. 1996 Apr;12(4):138-44. doi: 10.1016/0168-9525(96)10012-3. Trends Genet. 1996. PMID: 8901418 Review.

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: pasini b. 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

Somatic in frame deletions not involving juxtamembranous cysteine residues strongly activate the RET proto-oncogene.

Ceccherini I, Pasini B, Pacini F, Gullo M, Bongarzone I, Romei C, Santamaria G, Matera I, Mondellini P, Scopsi L, Pinchera A, Pierotti MA, Romeo G. Ceccherini I, et al. Among authors: pasini b. Oncogene. 1997 May 29;14(21):2609-12. doi: 10.1038/sj.onc.1201079. Oncogene. 1997. PMID: 9191060

8

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. Among authors: pasini b. Oncogene. 1997 Nov 6;15(19):2257-65. doi: 10.1038/sj.onc.1201413. Oncogene. 1997. PMID: 9393871

9

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. Oncogene. 1995 Nov 2;11(9):1737-43. Oncogene. 1995. PMID: 7478601

10

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. Nat Genet. 1995 May;10(1):35-40. doi: 10.1038/ng0595-35. Nat Genet. 1995. PMID: 7647787

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