The University of Siena PhD Course in
Genetics, Oncology and Clinical Medicine
Genetics, Oncology and Clinical Medicine
PhD Graduate
Elisa LANDUCCI
PhD Program years: 2014-2017
PUBLICATIONS DURING THE PHD PROGRAM
- Altered expression of neuropeptides in FoxG1-null heterozygous mutant mice.
Frullanti E, Amabile S, Lolli MG, Bartolini A, Livide G, Landucci E, Mari F, Vaccarino FM, Ariani F, Massimino L, Renieri A, Meloni I..
Eur J Hum Genet. 2016 Feb;24(2):252-7.
ABSTRACTS OF CONFERENCE DURING THE PHD PROGRAM
1. Further evidence for digenic inheritance in Alport syndrome: combined mutations in collagen IV and slit diaphragm genes.
A. M Pinto, M. Baldassarri, M. Grohmann, K. Dahan, H. Storey, E. Landucci, C. Fallerini, L. Bianciardi, E. Lazzeri, P. Romagnani, A. Provenzano, S. Giglio, M. D'Amico, C. Pecoraro, I. Meloni, C. Bergmann, M. Nagel, F. Ariani, F. Mari, A. Renieri.
ESHG meeting, June 2015
2. Imbalance of excitatory/inhibitory synaptic expression in Rett syndrome iPSC-based neuronal models.
I. Meloni, S. Amabile, E. Landucci, T. Patriarchi, E. Frullanti, AM. Pinto, C. Lo Rizzo, F. Ariani, F. Mari, MA. Mencarelli, JW. Hell, A. Renieri.
ESHG meeting, Glasgow June 2015
3. Further evidence for digenic inheritance in Alport syndrome: combined mutations in collagen IV and slit diaphragm genes.
F. Ariani, A. M. Pinto, M. Baldassarri, M. Grohmann, K. Dahan, H. Storey, E. Landucci, C. Fallerini, L. Bianciardi, E. Lazzeri, P. Romagnani, A. Provenzano, S. Giglio, M. D'Amico, C. Pecoraro, I. Meloni, C. Bergmann, M. Nagel, F. Mari, A. Renieri.
Alport society meeting, Gottingen, September 2015
A. M Pinto, M. Baldassarri, M. Grohmann, K. Dahan, H. Storey, E. Landucci, C. Fallerini, L. Bianciardi, E. Lazzeri, P. Romagnani, A. Provenzano, S. Giglio, M. D'Amico, C. Pecoraro, I. Meloni, C. Bergmann, M. Nagel, F. Ariani, F. Mari, A. Renieri.
ESHG meeting, June 2015
2. Imbalance of excitatory/inhibitory synaptic expression in Rett syndrome iPSC-based neuronal models.
I. Meloni, S. Amabile, E. Landucci, T. Patriarchi, E. Frullanti, AM. Pinto, C. Lo Rizzo, F. Ariani, F. Mari, MA. Mencarelli, JW. Hell, A. Renieri.
ESHG meeting, Glasgow June 2015
3. Further evidence for digenic inheritance in Alport syndrome: combined mutations in collagen IV and slit diaphragm genes.
F. Ariani, A. M. Pinto, M. Baldassarri, M. Grohmann, K. Dahan, H. Storey, E. Landucci, C. Fallerini, L. Bianciardi, E. Lazzeri, P. Romagnani, A. Provenzano, S. Giglio, M. D'Amico, C. Pecoraro, I. Meloni, C. Bergmann, M. Nagel, F. Mari, A. Renieri.
Alport society meeting, Gottingen, September 2015
ACTIVITY DURING THE PHD PROGRAM
- 1st YEAR (a.a. 2014-15)
- 2nd YEAR (a.a. 2015-16)
- 3rd YEAR (a.a. 2016-17)
TRAINING PERIOD ABROAD
-
Hosting Institution Name
Location
Period dates
-
Hosting Institution Name
Location
Period dates
