Lista de obras - Francesco Claudio Susca - Dominio Público Uruguay

17-alpha-ethinylestradiol and norgestrel in combination induce micronucleus increases and aneuploidy in human lymphocyte and fibroblast cultures

article

A homozygous frameshift mutation in the ESCO2 gene: evidence of intertissue and interindividual variation in Nmd efficiency.

artículo científico publicado en 2006

A novel cell type-specific role of p38α in the control of autophagy and cell death in colorectal cancer cells

artículo científico publicado en 2006

Breakpoint determination of 15 large deletions in Peutz-Jeghers subjects.

artículo científico publicado en 2010

Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study.

artículo científico publicado en 2013

De novo unbalanced translocation leading to monosomy 9p24.3p24.1 and trisomy 19q13.42q13.43 characterized by microarray-based comparative genomic hybridization in a child with partial cortical dysplasia and craniofacial dysmorphisms without trigonoce

artículo científico publicado en 2013

Depressed level of natural killer cells in cancer family syndrome

artículo científico publicado en 1989

Duplication of 9 p11.2-p13.1: a benign cytogenetic variant.

artículo científico publicado en 2004

Effect of prostaglandin E(2) on the proliferation, Ca(2+) mobilization and cAMP in HT-29 human colon adenocarcinoma cells

scientific article published on 01 May 2000

Familial adenomatous polyposis: identification of a new frameshift mutation of the APC gene in an Italian family

artículo científico publicado en 1992

Influence of some detoxification enzyme polymorphisms on cytogenetic biomarkers between individuals exposed to very low doses of 1,3-butadiene.

artículo científico publicado en 2009

Linkage studies in Italian families with familial adenomatous polyposis.

artículo científico publicado en 1993

Molecular and Functional Characterization of Three Different Postzygotic Mutations in PIK3CA-Related Overgrowth Spectrum (PROS) Patients: Effects on PI3K/AKT/mTOR Signaling and Sensitivity to PIK3 Inhibitors.

artículo científico publicado en 2015

SCE frequency measurement could be useful in the prenatal diagnosis of Roberts syndrome.

artículo científico publicado en 2007

Sex chromosome loss, micronuclei, sister chromatid exchange and aging: a study including 16 centenarians

artículo científico publicado en 2001

The Italian external quality assessment scheme in classical cytogenetics: four years of activity.

artículo científico publicado en 2008

The familial adenomatous polyposis region exhibits many different haplotypes

artículo científico publicado en 1998

Translocation of the proto-oncogene Bcl-6 in human glioblastoma multiforme

artículo científico publicado en 2014

Trisomy 13 mosaicism in a phenotypically normal child: Description of cytogenetic and clinical findings from early pregnancy beyond 2 years of age