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Pubblicazioni antecedenti il 2004
ANNO 2002
Carinci F, Bodo M, Tosi L, Francioso F, Evangelisti R, Pezzetti
F, Scapoli L, Martinelli M, Baroni T, Stabellini G, Carinci
P, Bellucci C, Lilli C, Volinia S.
Expression profiles of craniosynostosis-derived fibroblasts.
Mol Med. 2002 Oct;8(10):638-44.
Stabellini G, Calastrini C, Scapoli L, Locci P, De Mattei
M, Dellavia C,
Moscheni C, Vertemati M, Bedani PL.
The effect of polyamines and dialysate fluid on extracellular
matrix synthesis in VERO cell cultures.
J Nephrol. 2002 Sep-Oct;15(5):539-46.
Farina A, Wyszynski DF, Pezzetti F, Scapoli L, Martinelli
M, Carinci F, Carls F, Nardelli GB, Tognon M, Carinci P.
Classification of oral clefts by affection site and laterality:
a genotype-phenotype correlation study.
Orthod Craniofac Res. 2002 Aug;5(3):185-91.
Bodo M, Lilli C, Aisa MC, Scapoli L, Bellucci C, Rinaldi
E, Tosi L, Baroni T, Conte C, Bellocchio S, Carinci F, Stabellini
G, Carinci P.
Basic fibroblast growth factor: effects on matrix remodeling,
receptor expression, and transduction pathway in human periosteal
fibroblasts with FGFR2 gene mutation.
J Interferon Cytokine Res. 2002 Jun;22(6):621-30.
Stabellini G, Carinci F, Luigi Bedani P, Calastrini C, De Mattei
M, Scapoli L, Caruso A, Calvitti M, Locci P.
Cyclosporin A and transforming growth factor beta modify the
pattern of extracellular glycosaminoglycans without causing
cytoskeletal changes in human gingival fibroblasts.
Transplantation. 2002 May 27;73(10):1676-9.
Francioso F, Carinci F, Tosi L, Scapoli L, Pezzetti F,
Passerella E, Evangelisti R, Pastore A, Pelucchi S, Piattelli A,
Rubini C, Fioroni M, Carinci P, Volinia S.
Identification of differentially expressed genes in human
salivary gland tumors by DNA microarrays.
Mol Cancer Ther. 2002 May;1(7):533-8.
Scapoli L, Martinelli M, Pezzetti F, Carinci F, Bodo M,
Tognon M, Carinci P.
Linkage disequilibrium between GABRB3 gene and nonsyndromic
familial cleft lip with or without cleft palate.
Hum Genet. 2002 Jan;110(1):15-20. Epub 2001 Nov 10.
ANNO 2001
Martinelli M, Scapoli L, Pezzetti F, Carinci F, Francioso
F, Baciliero U, Padula E, Carinci P, Tognon M.
Linkage analysis of three candidate regions of chromosome 1 in
nonsyndromic familial orofacial cleft.
Ann Hum Genet. 2001 Sep;65(Pt 5):465-71.
Martinelli M, Scapoli L, Pezzetti F, Carinci F, Carinci
P, Stabellini G, Bisceglia L, Gombos F, Tognon M.
C677T variant form at the MTHFR gene and CL/P: a risk factor for
mothers?
Am J Med Genet. 2001 Feb 1;98(4):357-60.
ANNO 2000
Pezzetti F, Scapoli L, Martinelli M, Carinci F, Brunelli
G, Carls FP, Palomba F, Gombos F, Carinci P, Tognon M.
Linkage analysis of candidate endothelin pathway genes in
nonsyndromic familial orofacial cleft.
Ann Hum Genet. 2000 Jul;64(Pt 4):341-7.
Stabellini G, Berti G, Calastrini C, Mariani G, Scapoli
L, Marcucci A, Bedani PL.
Experimental model for studying the effects of
2-ethylhexyl-phthalate and dialysate on connective tissue.
Int J Artif Organs. 2000 May;23(5):305-11.
Ottolenghi C, Veitia R, Quintana-Murci L, Torchard D, Scapoli
L, Souleyreau-Therville N, Beckmann J, Fellous M, McElreavey
K.
The region on 9p associated with 46,XY sex reversal contains
several transcripts expressed in the urogenital system and a novel
doublesex-related domain.
Genomics. 2000 Mar 1;64(2):170-8.
Carinci F, Pezzetti F, Scapoli L, Martinelli M, Carinci
P, Tognon M.
Genetics of nonsyndromic cleft lip and palate: a review of
international studies and data regarding the Italian
population.
Cleft Palate Craniofac J. 2000 Jan;37(1):33-40.
ANNI 1995 -1999
Scapoli C, Collins A, Martinelli M, Pezzetti F, Scapoli
L, Tognon M.
Combined segregation and linkage analysis of nonsyndromic
orofacial cleft in two candidate regions.
Ann Hum Genet. 1999 Jan;63(Pt 1):17-25.
Martinelli M, Scapoli L, Pezzetti F, Carinci F, Carinci
P, Baciliero U, Padula E, Tognon M.
Suggestive linkage between markers on chromosome 19q13.2 and
nonsyndromic orofacial cleft malformation.
Genomics. 1998 Jul 15;51(2):177-81.
Pezzetti F, Scapoli L, Martinelli M, Carinci F, Bodo M,
Carinci P, Tognon M.
A locus in 2p13-p14 (OFC2), in addition to that mapped in 6p23,
is involved in nonsyndromic familial orofacial cleft
malformation.
Genomics. 1998 Jun 15;50(3):299-305.
Scapoli L, Pezzetti F, Carinci F, Martinelli M, Carinci
P, Tognon M.
Lack of linkage disequilibrium between transforming growth
factor alpha Taq I polymorphism and cleft lip with or without cleft
palate in families from Northeastern Italy.
Am J Med Genet. 1998 Jan 13;75(2):203-6.
Scapoli L, Pezzetti F, Carinci F, Martinelli M, Carinci
P, Tognon M.
Evidence of linkage to 6p23 and genetic heterogeneity in
nonsyndromic cleft lip with or without cleft palate.
Genomics. 1997 Jul 15;43(2):216-20.
Carinci F, Pezzetti F, Scapoli L, Padula E, Baciliero U,
Curioni C, Tognon M.
Nonsyndromic cleft lip and palate: evidence of linkage to a
microsatellite marker on 6p23.
Am J Hum Genet. 1995 Jan;56(1):337-9.
