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Orario:
17.00-19.30
Mercoledì 3
luglio 2011
1) Scientific report of PhD students in Oncology and
Genetics
- Creatine Transporter
Defect Diagnosed by Proton NMR Spectroscopy in Males With Intellectual
Disability (30’, Mencarelli MA. – Medical
Genetics section)
-
Incidence of cancer in ultracentenarians,
in elderly with Alzheimer's disease and in subjects with Werner Syndrome
(30', Guercio V. - Hepatobiliopancreatic Diseases and Multitumoral
Syndromes)
- Prostate cancer: the
influence of STAT3 and the presence of Human Polyomavirus BK in
cells (30', Mischitelli M. – Oncological
Genetics section)
2) Communications
-
Submission of the manuscript “Epigenetic
and copy number variation analysis in retinoblastoma by MS-MLPA”
to Cancer Science (15’, Livide G.)
- Proposals for the
reorganization of University Departments (15’, Ariani F.)
Mercoledì 1
giugno 2011
- Monica
Mischitelli “Prostate
cancer: the influence of STAT3 and the presence of Human Polyomavirus BK
in cells”
- Valeria
Rizzo “Title to define”
- Nadia Casini
“Title to define”
- Valentina
Guercio “PM chemical characterization and differences in cytotoxicity
versus pro-inflammatory potency of different PM fractions in human
epithelial lung cells”
- Bruccheri Maria
Grazia “Title to define”
Mercoledì 4
maggio 2011
1) Scientific report of PhD students in Oncology and
Genetics
- Detection of
constitutional epigenetic changes in colorectal cancer and multiple
primitive tumors (30', Crucianelli F. – Colorectal and
gastroesophageal diseases)
- Identification of the regulatory mechanisms of
Cdk2/CyclinA inhibition by pRb2/p130 protein (30', Conti D. -
Oncological Genetics section)
- Outcome of surgical treatment of colorectal cancer
in the elderly (30', Fontani A. - Colorectal and gastroesophageal
diseases)
- Prenatal diagnosis by standard karyotype (30’,
Parri V. – Medical Genetics section)
2) Communications
- Submission of the manuscript “p53
Arg72Pro SNP influences the risk of hereditary retinoblastoma”
to the Journal of Human Genetics in collaboration with the University of
Torino (15’, Disciglio V.)
- Results of Doctoral School
evaluation by the “Nucleo di Valutazione di Ateneo” (15’, Renieri A.)
Mercoledì 6
aprile 2011
1) Scientific report of PhD students in Oncology and
Genetics
- New small molecule
inhibitors of Src as potential candidates for cancer therapy
(30', Cozzi M. - Oncological Genetics section)
- Involvement of ERK8 in autophagy (30', Colecchia D.
- Medical Genetics section)
- Decipher database as a tool for genomic imbalances
analysis (30', Mucciolo M. - Medical Genetics section)
- Bioinformatics approach to the pRb pathway in
cancer initiation and progression (30’conference call from USA, Olayinka
O. - Oncological Genetics section)
2) Communications
- Acceptance with revisions of
the paper “Investigation of modifier genes within copy number variations
in Rett syndrome” by the Journal of Human Genetics (15’, Artuso R.)
- Results of Doctoral School
evaluation by the Scientific Committee (15’, Ariani F.)
Mercoledì 2
marzo 2011
- Forte Iris
“Gastric cancer and cell cycle regulation”
- Zangari
Rosalia “The impact of traffic pollution on antioxidant system of two
populations exposed to different levels of pollutants”
- De Filippis
Roberta “Induced pluripotent stem cells as a human model to study Rett
syndrome: FOXG1”
- Amenduni
Mariangela “Induced pluripotent stem cells as a human model to study
Rett syndrome: CDKL5”
-
Martellucci Jacopo
“Title to define”
Mercoledì 2
febbraio 2011
- Lorenzi Bruno
“Evaluation of anorectal function after radiotherapy in patients treated
for rectal cancer”
- La Montagna
Raffaele “Androgen
receptor and PIN1 in prostate cancer”,
- Disciglio
Vittoria “Deletions and duplications on 16p11.2”
- Livide
Gabriella “Role of MDM2 T309G and TP53 R72P polymorphisms in modulation
of variable phenotypic expression of retinoblastoma”
-
Pacifici Marco
“Title to define”
Mercoledì
15 dicembre 2010
- Mari Francesca,
“Report of the American Society of Human Genetics meeting”
- Mirella Bruttini
and Rosangela Artuso “Next Generation Sequencing: preliminary results”
- Fallerini Chiara
“Mutation analysis in COL4A5 gene”
-
Grillo Elisa “Mutation analysis in patients with Rett syndrome”
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