Search Results - "Guanti, G"
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1
A novel cell type-specific role of p38α in the control of autophagy and cell death in colorectal cancer cells
Published in Cell death and differentiation (01-04-2007)Get full text
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2
Hereditary Haemorrhagic Telangiectasia (HHT): genetic and molecular aspects
Published in Current pharmaceutical design (01-04-2006)“…Hereditary Haemorrhagic Telangiectasia, or Rendu-Osler-Weber syndrome, is a rare autosomal dominant disorder involving the vascular system and is characterised…”
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3
Cancer risks in LKB1 germline mutation carriers
Published in Gut (01-07-2006)“…Background and aims: Germline mutations in the LKB1 gene are known to cause Peutz-Jeghers syndrome, which is an autosomal dominant disorder characterised by…”
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4
Life expectancy in patients with hereditary haemorrhagic telangiectasia
Published in QJM : An International Journal of Medicine (01-05-2006)“…There are few data on life expectancy in patients with hereditary haemorrhagic telangiectasia (HHT), a disorder with life-threatening complications. Seventy…”
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5
Screening for children from families with Rendu–Osler–Weber disease: from geneticist to clinician
Published in Journal of thrombosis and haemostasis (01-06-2006)“…Background: Rendu–Osler–Weber syndrome, or hereditary hemorrhagic telangiectasia (HHT), is an autosomal dominant vascular disorder. The syndrome is…”
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6
Involvement of PTEN mutations in the genetic pathways of colorectal cancerogenesis
Published in Human molecular genetics (22-01-2000)“…So far, somatic mutations of the PTEN gene have been found in several different neoplasms but not in colorectal tumours. As exons 7 and 8 of the PTEN coding…”
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Germline novel MSH2 deletions and a founder MSH2 deletion associated with anticipation effects in HNPCC
Published in Clinical genetics (01-02-2007)“…Hereditary non‐polyposis colorectal cancer (HNPCC) is caused by inactivating mutations of DNA mismatch repair genes. Large genomic rearrangements in these…”
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Noncolonic cancer stem cells in bone marrow of colorectal cancer patients
Published in Colorectal disease (01-03-2010)“…Objective To investigate whether preoperative noncolonic cancer stem cells in bone marrow (BM) of R0 colorectal cancer (CRC) patients are cancer cells and…”
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Hereditary haemorrhagic telangiectasia: a rare disease as a model for the study of human atherosclerosis
Published in Current pharmaceutical design (01-12-2007)“…Hereditary Haemorrhagic Telangiectasia (HHT) or Rendu-Osler-Weber syndrome is an autosomal dominant disease characterized by local angiodysplasia affecting…”
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10
Functional analysis of LKB1/STK11 mutants and two aberrant isoforms found in Peutz-Jeghers Syndrome patients
Published in Human mutation (01-02-2003)“…Peutz‐Jeghers Syndrome (PJS) is thought to be caused by mutations occurring in the widely expressed serine/threonine protein kinase named LKB1/STK11. Recent…”
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Capillaroscopy of the dorsal skin of the hands in hereditary hemorrhagic telangiectasia
Published in QJM : An International Journal of Medicine (01-10-2005)“…Background: Cutaneous telangiectases are manifestations of hereditary hemorrhagic telangiectasia (HHT), a dominantly inherited disorder. Telangiectases have…”
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12
Genetic testing and surgeon decision
Published in Acta chirurgica Iugoslavica (2004)“…Colorectal cancer is a highly treatable and often curable disease when localized to the bowel. Traditional pathological staging systems have been useful in…”
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13
Site directed mutagenesis of hMLH1 exonic splicing enhancers does not correlate with splicing disruption
Published in Journal of medical genetics (01-06-2004)“…[...]the predictive capacity of the SR protein score matrices may be low in a specific exonic context as suggested by our results or when composite elements…”
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14
A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP family
Published in Journal of medical genetics (01-12-2001)Get full text
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15
Synthesis of a methoxy-substituted lactenediyne
Published in Tetrahedron letters (12-08-2000)“…The novel lactenediyne 12, characterised by a protected 2-hydroxyethyl chain at N-11 and by a methoxy group at C-1 was efficiently prepared by a new strategy…”
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Enzymatic Resolution of Acetoxyalkenylphosphonates and Their Exploitation in the Chemoenzymatic Synthesis of Phosphonic Derivatives of Carbohydrates
Published in Advanced synthesis & catalysis (01-08-2001)“…The resolution of racemic α‐, β‐, and γ‐hydroxy‐ω‐alkenylphosphonates was achieved by enzymatic hydrolysis of the corresponding acetates. The optically active…”
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Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients
Published in Human mutation (01-07-2002)“…Editor's Note: Due to a technical problem in the Editorial Office, the accepted manuscript, which should have been published online during the week of February…”
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The Italian external quality assessment scheme in classical cytogenetics: four years of activity
Published in Community genetics (01-01-2008)“…The Italian external quality assessment scheme in classical cytogenetics was started in 2001 as an activity funded by the National Health System and…”
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Mutational germline analysis of hMSH2 and hMLH1 genes in early onset colorectal cancer patients
Published in Journal of medical genetics (01-07-2000)Get full text
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Cyclin E and chromosome instability in colorectal cancer cell lines
Published in Molecular pathology (01-06-2002)“…Aims/Background: The development of colorectal cancer depends on at least two distinct pathways involving genetic instability, namely: chromosome instability…”
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