Seri M - Search Results

1

Exploration of Tools for the Interpretation of Human Non-Coding Variants.

Tabarini N, Biagi E, Uva P, Iovino E, Pippucci T, Seri M, Cavalli A, Ceccherini I, Rusmini M, Viti F. Tabarini N, et al. Among authors: seri m. Int J Mol Sci. 2022 Oct 26;23(21):12977. doi: 10.3390/ijms232112977. Int J Mol Sci. 2022. PMID: 36361767 Free PMC article. Review.

2

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

3

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: seri m. Oncogene. 1994 Oct;9(10):3025-9. Oncogene. 1994. PMID: 8084609

4

Strategies for the Identification of Intron-Exon Boundaries and Point Mutations: The Example of the RET Proto-Oncogene.

Ceccherini I I, Seri M, Romeo G. Ceccherini I I, et al. Among authors: seri m. Methods. 1996 Feb;9(1):98-105. doi: 10.1006/meth.1996.0013. Methods. 1996. PMID: 9245348

5

Assignment of mouse Gfra1, the homologue of a new human HSCR candidate gene, to the telomeric region of mouse chromosome 19.

Puliti A, Cinti R, Seri M, Ceccherini I, Romeo G. Puliti A, et al. Among authors: seri m. Cytogenet Cell Genet. 1997;78(3-4):291-4. doi: 10.1159/000134675. Cytogenet Cell Genet. 1997. PMID: 9465906

6

Glomerulocystic kidney disease in a family.

Gusmano R, Caridi G, Marini M, Perfumo F, Ghiggeri GM, Piaggio G, Ceccherini I, Seri M. Gusmano R, et al. Among authors: seri m. Nephrol Dial Transplant. 2002 May;17(5):813-8. doi: 10.1093/ndt/17.5.813. Nephrol Dial Transplant. 2002. PMID: 11981068

7

HOX11L1: a promoter study to evaluate possible expression defects in intestinal motility disorders.

Fava M, Borghini S, Cinti R, Cusano R, Seri M, Lerone M, De Giorgio R, Stanghellini V, Martucciello G, Ravazzolo R, Ceccherini I. Fava M, et al. Among authors: seri m. Int J Mol Med. 2002 Jul;10(1):101-6. Int J Mol Med. 2002. PMID: 12060859

8

A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23-q24.

Deglincerti A, De Giorgio R, Cefle K, Devoto M, Pippucci T, Castegnaro G, Panza E, Barbara G, Cogliandro RF, Mungan Z, Palanduz S, Corinaldesi R, Romeo G, Seri M, Stanghellini V. Deglincerti A, et al. Among authors: seri m. Eur J Hum Genet. 2007 Aug;15(8):889-97. doi: 10.1038/sj.ejhg.5201844. Epub 2007 May 9. Eur J Hum Genet. 2007. PMID: 17487221

9

GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease.

Caroli F, Biancheri R, Seri M, Rossi A, Pessagno A, Bugiani M, Corsolini F, Savasta S, Romano S, Antonelli C, Romano A, Pareyson D, Gambero P, Uziel G, Ravazzolo R, Ceccherini I, Filocamo M. Caroli F, et al. Among authors: seri m. Clin Genet. 2007 Nov;72(5):427-33. doi: 10.1111/j.1399-0004.2007.00869.x. Epub 2007 Sep 25. Clin Genet. 2007. PMID: 17894839

10

Garone C, Pippucci T, Cordelli DM, Zuntini R, Castegnaro G, Marconi C, Graziano C, Marchiani V, Verrotti A, Seri M, Franzoni E. Garone C, et al. Among authors: seri m. Dev Med Child Neurol. 2011 Oct;53(10):958-61. doi: 10.1111/j.1469-8749.2011.03993.x. Epub 2011 May 18. Dev Med Child Neurol. 2011. PMID: 21592092 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

309 results

Search Page