Ceccherini I - Search Results

1

Recent advances in the developmental origin of neuroblastoma: an overview.

Ponzoni M, Bachetti T, Corrias MV, Brignole C, Pastorino F, Calarco E, Bensa V, Giusto E, Ceccherini I, Perri P. Ponzoni M, et al. Among authors: ceccherini i. J Exp Clin Cancer Res. 2022 Mar 11;41(1):92. doi: 10.1186/s13046-022-02281-w. J Exp Clin Cancer Res. 2022. PMID: 35277192 Free PMC article. Review.

2

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

3

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

4

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

5

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

6

Oligogenic inheritance in neuroblastoma.

Longo L, Tonini GP, Ceccherini I, Perri P. Longo L, et al. Among authors: ceccherini i. Cancer Lett. 2005 Oct 18;228(1-2):65-9. doi: 10.1016/j.canlet.2004.12.052. Cancer Lett. 2005. PMID: 15923081

7

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.

8

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

9

The TLX2 homeobox gene is a transcriptional target of PHOX2B in neural-crest-derived cells.

Borghini S, Bachetti T, Fava M, Di Duca M, Cargnin F, Fornasari D, Ravazzolo R, Ceccherini I. Borghini S, et al. Among authors: ceccherini i. Biochem J. 2006 Apr 15;395(2):355-61. doi: 10.1042/BJ20051386. Biochem J. 2006. PMID: 16402914 Free PMC article.

10

Brainstem anomalies in two patients affected by congenital central hypoventilation syndrome.

Bachetti T, Robbiano A, Parodi S, Matera I, Merello E, Capra V, Baglietto MP, Rossi A, Ceccherini I, Ottonello G. Bachetti T, et al. Among authors: ceccherini i. Am J Respir Crit Care Med. 2006 Sep 15;174(6):706-9. doi: 10.1164/rccm.200602-266CR. Epub 2006 Jun 8. Am J Respir Crit Care Med. 2006. PMID: 16763219

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