Ceccherini I - Search Results

1

Brosens E, Burns AJ, Brooks AS, Matera I, Borrego S, Ceccherini I, Tam PK, García-Barceló MM, Thapar N, Benninga MA, Hofstra RM, Alves MM. Brosens E, et al. Among authors: ceccherini i. Dev Biol. 2016 Sep 15;417(2):198-208. doi: 10.1016/j.ydbio.2016.07.008. Epub 2016 Jul 15. Dev Biol. 2016. PMID: 27426273 Free article. Review.

2

Radiation hybrids for mapping and cloning DNA sequences of distal 16p.

Ceccherini I, Matera I, Sbrana M, Di Donato A, Yin L, Romeo G. Ceccherini I, et al. Somat Cell Mol Genet. 1992 Jul;18(4):319-24. doi: 10.1007/BF01235755. Somat Cell Mol Genet. 1992. PMID: 1440054

3

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

4

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

5

Interstitial deletion of the endothelin-B receptor gene in the spotting lethal (sl) rat.

Ceccherini I, Zhang AL, Matera I, Yang G, Devoto M, Romeo G, Cass DT. Ceccherini I, et al. Hum Mol Genet. 1995 Nov;4(11):2089-96. doi: 10.1093/hmg/4.11.2089. Hum Mol Genet. 1995. PMID: 8589685

6

Incidence of RET mutations in patients with Hirschsprung's disease.

Sancandi M, Ceccherini I, Costa M, Fava M, Chen B, Wu Y, Hofstra R, Laurie T, Griffths M, Burge D, Tam PK. Sancandi M, et al. Among authors: ceccherini i. J Pediatr Surg. 2000 Jan;35(1):139-42; discussion 142-3. doi: 10.1016/s0022-3468(00)80031-7. J Pediatr Surg. 2000. PMID: 10646792

7

A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease.

Griseri P, Sancandi M, Patrone G, Bocciardi R, Hofstra R, Ravazzolo R, Devoto M, Romeo G, Ceccherini I. Griseri P, et al. Among authors: ceccherini i. Eur J Hum Genet. 2000 Sep;8(9):721-4. doi: 10.1038/sj.ejhg.5200521. Eur J Hum Genet. 2000. PMID: 10980580

8

cDNA sequence and genomic structure of the rat RET proto-oncogene.

Matera I, De Miguel-Rodríguez M, Fernández-Santos JM, Santamaria G, Puliti A, Ravazzolo R, Romeo G, Galera-Davidson H, Ceccherini I. Matera I, et al. Among authors: ceccherini i. DNA Seq. 2000;11(5):405-17. doi: 10.3109/10425170009033991. DNA Seq. 2000. PMID: 11328649

9

Assignment of the HOX11L2 gene to human chromosome band 5q35.1 and of its murine homolog to mouse chromosome bands 11A4-A5 by in situ hybridization.

Cinti R, Fava M, Sancandi M, Matera I, Ravazzolo R, Ceccherini I. Cinti R, et al. Among authors: ceccherini i. Cytogenet Cell Genet. 2001;92(3-4):354-5. doi: 10.1159/000056931. Cytogenet Cell Genet. 2001. PMID: 11435716 No abstract available.

10

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

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