Ceccherini I - Search Results

1

The OSMR Gene Is Involved in Hirschsprung Associated Enterocolitis Susceptibility through an Altered Downstream Signaling.

Bachetti T, Rosamilia F, Bartolucci M, Santamaria G, Mosconi M, Sartori S, De Filippo MR, Di Duca M, Obino V, Avanzini S, Mavilio D, Candiani S, Petretto A, Pini Prato A, Ceccherini I, Lantieri F. Bachetti T, et al. Among authors: ceccherini i. Int J Mol Sci. 2021 Apr 7;22(8):3831. doi: 10.3390/ijms22083831. Int J Mol Sci. 2021. PMID: 33917126 Free PMC article.

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

3

Pathogenesis of Hirschsprung's disease.

Martucciello G, Ceccherini I, Lerone M, Jasonni V. Martucciello G, et al. Among authors: ceccherini i. J Pediatr Surg. 2000 Jul;35(7):1017-25. doi: 10.1053/jpsu.2000.7763. J Pediatr Surg. 2000. PMID: 10917288 Review.

4

Hirschsprung associated GDNF mutations do not prevent RET activation.

Borghini S, Bocciardi R, Bonardi G, Matera I, Santamaria G, Ravazzolo R, Ceccherini I. Borghini S, et al. Among authors: ceccherini i. Eur J Hum Genet. 2002 Mar;10(3):183-7. doi: 10.1038/sj.ejhg.5200785. Eur J Hum Genet. 2002. PMID: 11973622

5

Mutational analysis of the RNX gene in congenital central hypoventilation syndrome.

Matera I, Bachetti T, Cinti R, Lerone M, Gagliardi L, Morandi F, Motta M, Mosca F, Ottonello G, Piumelli R, Schober JG, Ravazzolo R, Ceccherini I. Matera I, et al. Among authors: ceccherini i. Am J Med Genet. 2002 Nov 22;113(2):178-82. doi: 10.1002/ajmg.10746. Am J Med Genet. 2002. PMID: 12407709

6

A common haplotype at the 5' end of the RET proto-oncogene, overrepresented in Hirschsprung patients, is associated with reduced gene expression.

Griseri P, Bachetti T, Puppo F, Lantieri F, Ravazzolo R, Devoto M, Ceccherini I. Griseri P, et al. Among authors: ceccherini i. Hum Mutat. 2005 Feb;25(2):189-95. doi: 10.1002/humu.20135. Hum Mutat. 2005. PMID: 15643606

7

PHOX2B mutations and genetic predisposition to neuroblastoma.

Perri P, Bachetti T, Longo L, Matera I, Seri M, Tonini GP, Ceccherini I. Perri P, et al. Among authors: ceccherini i. Oncogene. 2005 Apr 21;24(18):3050-3. doi: 10.1038/sj.onc.1208532. Oncogene. 2005. PMID: 15735672

8

Distinct pathogenetic mechanisms for PHOX2B associated polyalanine expansions and frameshift mutations in congenital central hypoventilation syndrome.

Bachetti T, Matera I, Borghini S, Di Duca M, Ravazzolo R, Ceccherini I. Bachetti T, et al. Among authors: ceccherini i. Hum Mol Genet. 2005 Jul 1;14(13):1815-24. doi: 10.1093/hmg/ddi188. Epub 2005 May 11. Hum Mol Genet. 2005. PMID: 15888479

9

An in vitro approach to test the possible role of candidate factors in the transcriptional regulation of the RET proto-oncogene.

Bachetti T, Borghini S, Ravazzolo R, Ceccherini I. Bachetti T, et al. Among authors: ceccherini i. Gene Expr. 2005;12(3):137-49. doi: 10.3727/000000005783992106. Gene Expr. 2005. PMID: 16127999 Free PMC article.

10

Comparative genomic sequence analysis coupled to chromatin immunoprecipitation: a screening procedure applied to search for regulatory elements at the RET locus.

Puppo F, Musso M, Pirulli D, Griseri P, Bachetti T, Crovella S, Patrone G, Ceccherini I, Ravazzolo R. Puppo F, et al. Among authors: ceccherini i. Physiol Genomics. 2005 Nov 17;23(3):269-74. doi: 10.1152/physiolgenomics.00036.2005. Epub 2005 Sep 6. Physiol Genomics. 2005. PMID: 16144862

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