Sancandi M - Search Results

1

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: sancandi m. Eur J Hum Genet. 2000 Sep;8(9):721-4. doi: 10.1038/sj.ejhg.5200521. Eur J Hum Genet. 2000. PMID: 10980580

2

A rare haplotype of the RET proto-oncogene is a risk-modifying allele in hirschsprung disease.

Griseri P, Pesce B, Patrone G, Osinga J, Puppo F, Sancandi M, Hofstra R, Romeo G, Ravazzolo R, Devoto M, Ceccherini I. Griseri P, et al. Among authors: sancandi m. Am J Hum Genet. 2002 Oct;71(4):969-74. doi: 10.1086/342774. Epub 2002 Sep 4. Am J Hum Genet. 2002. PMID: 12214285 Free PMC article.

3

Single nucleotide polymorphic alleles in the 5' region of the RET proto-oncogene define a risk haplotype in Hirschsprung's disease.

Sancandi M, Griseri P, Pesce B, Patrone G, Puppo F, Lerone M, Martucciello G, Romeo G, Ravazzolo R, Devoto M, Ceccherini I. Sancandi M, et al. J Med Genet. 2003 Sep;40(9):714-8. doi: 10.1136/jmg.40.9.714. J Med Genet. 2003. PMID: 12960220 Free PMC article. No abstract available.

4

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. 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

5

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: sancandi m. Cytogenet Cell Genet. 2001;92(3-4):354-5. doi: 10.1159/000056931. Cytogenet Cell Genet. 2001. PMID: 11435716 No abstract available.

6

Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervation.

Costa M, Fava M, Seri M, Cusano R, Sancandi M, Forabosco P, Lerone M, Martucciello G, Romeo G, Ceccherini I. Costa M, et al. Among authors: sancandi m. J Med Genet. 2000 Jul;37(7):E9. doi: 10.1136/jmg.37.7.e9. J Med Genet. 2000. PMID: 10882761 Free PMC article. No abstract available.

7

A heterozygous endothelin 3 mutation in Waardenburg-Hirschsprung disease: is there a dosage effect of EDN3/EDNRB gene mutations on neurocristopathy phenotypes?

Pingault V, Bondurand N, Lemort N, Sancandi M, Ceccherini I, Hugot JP, Jouk PS, Goossens M. Pingault V, et al. Among authors: sancandi m. J Med Genet. 2001 Mar;38(3):205-9. doi: 10.1136/jmg.38.3.205. J Med Genet. 2001. PMID: 11303518 Free PMC article. No abstract available.

8

Differential behaviour of normal, transformed and Fanconi's anemia lymphoblastoid cells to modeled microgravity.

Cuccarolo P, Barbieri F, Sancandi M, Viaggi S, Degan P. Cuccarolo P, et al. Among authors: sancandi m. J Biomed Sci. 2010 Jul 28;17(1):63. doi: 10.1186/1423-0127-17-63. J Biomed Sci. 2010. PMID: 20667080 Free PMC article.

9

Brain-Region-Specific Differences in Protein Citrullination/Deimination in a Pre-Motor Parkinson's Disease Rat Model.

Mercer A, Sancandi M, Maclatchy A, Lange S. Mercer A, et al. Among authors: sancandi m. Int J Mol Sci. 2024 Oct 17;25(20):11168. doi: 10.3390/ijms252011168. Int J Mol Sci. 2024. PMID: 39456949 Free PMC article.

10

Effects of a probiotic suspension Symprove™ on a rat early-stage Parkinson's disease model.

Sancandi M, De Caro C, Cypaite N, Marascio N, Avagliano C, De Marco C, Russo E, Constanti A, Mercer A. Sancandi M, et al. Front Aging Neurosci. 2023 Jan 18;14:986127. doi: 10.3389/fnagi.2022.986127. eCollection 2022. Front Aging Neurosci. 2023. PMID: 36742204 Free PMC article.

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