Следене
Roberto D. Fanganiello
Roberto D. Fanganiello
Faculté de Médecine Dentaire, Université Laval
Потвърден имейл адрес: ulaval.ca - Начална страница
Заглавие
Позовавания
Позовавания
Година
Reconstruction of large cranial defects in nonimmunosuppressed experimental design with human dental pulp stem cells
A de Mendonça Costa, DF Bueno, MT Martins, I Kerkis, A Kerkis, ...
Journal of Craniofacial Surgery 19 (1), 204-210, 2008
2812008
Genetics of craniosynostosis: genes, syndromes, mutations and genotype-phenotype correlations
M Passos-Bueno, A Serti├®, F Jehee, R Fanganiello, E Yeh
Frontiers of oral biology 12, 107, 2008
1902008
Syndromes of the first and second pharyngeal arches: a review
MR Passos‐Bueno, CC Ornelas, RD Fanganiello
American Journal of Medical Genetics Part A 149 (8), 1853-1859, 2009
1372009
New source of muscle-derived stem cells with potential for alveolar bone reconstruction in cleft lip and/or palate patients
DF Bueno, I Kerkis, AM Costa, MT Martins, GS Kobayashi, E Zucconi, ...
Tissue Engineering Part A 15 (2), 427-435, 2009
1102009
Craniofacial sutures: development, disease and treatment
DP Rice, PT Sharpe
Karger Medical and Scientific Publishers, 2008
852008
Optimization of parameters for a more efficient use of adipose‐derived stem cells in regenerative medicine therapies
M Aguena, R Dalto Fanganiello, LAL Tissiani, FAA Ishiy, R Atique, ...
Stem Cells International 2012 (1), 303610, 2012
632012
Is bone transplantation the gold standard for repair of alveolar bone defects?
CE Raposo-Amaral, DF Bueno, AB Almeida, V Jorgetti, CC Costa, ...
Journal of tissue engineering 5, 2041731413519352, 2014
552014
TCOF1 mutation database: Novel mutation in the alternatively spliced exon 6A and update in mutation nomenclature
A Splendore, RD Fanganiello, C Masotti, LSC Morganti, ...
Human mutation 25 (5), 429-434, 2005
532005
Apert p. Ser252Trp mutation in FGFR2 alters osteogenic potential and gene expression of cranial periosteal cells
RD Fanganiello, AL Sertié, EM Reis, E Yeh, NAJ Oliveira, DF Bueno, ...
Molecular Medicine 13, 422-442, 2007
492007
Multisystem Proteinopathy Due to VCP Mutations: A Review of Clinical Heterogeneity and Genetic Diagnosis
G Pfeffer, G Lee, CS Pontifex, RD Fanganiello, A Peck, CC Weihl, ...
Genes 13 (6), 963, 2022
452022
A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia
RD Fanganiello, VE Kimonis, CC Corte, R Nitrini, MR Passos-Bueno
Brazilian Journal of Medical and Biological Research 44, 374-380, 2011
382011
Cnbp ameliorates Treacher Collins Syndrome craniofacial anomalies through a pathway that involves redox-responsive genes
MSP De Peralta, VS Mouguelar, MA Sdrigotti, FAA Ishiy, RD Fanganiello, ...
Cell death & disease 7 (10), e2397-e2397, 2016
372016
Improvement of In Vitro Osteogenic Potential through Differentiation of Induced Pluripotent Stem Cells from Human Exfoliated Dental Tissue towards Mesenchymal …
FAA Ishiy, RD Fanganiello, K Griesi-Oliveira, AM Suzuki, GS Kobayashi, ...
Stem Cells International 2015 (1), 249098, 2015
362015
Craniosynostoses: molecular genetics, principles of diagnosis and treatment
M Muenke, W Kress, H Collmann, B Solomon
Karger Medical and Scientific Publishers, 2011
342011
Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy
M Korb, A Peck, LN Alfano, KI Berger, MK James, N Ghoshal, E Healzer, ...
Orphanet journal of rare diseases 17 (1), 23, 2022
262022
Increased In Vitro Osteopotential in SHED Associated with Higher IGF2 Expression When Compared with hASCs
RD Fanganiello, FAA Ishiy, GS Kobayashi, L Alvizi, DY Sunaga, ...
Stem Cell Reviews and Reports 11, 635-644, 2015
262015
CD105 is regulated by hsa-miR-1287 and its expression is inversely correlated with osteopotential in SHED
FAA Ishiy, RD Fanganiello, GS Kobayashi, E Kague, PS Kuriki, ...
Bone 106, 112-120, 2018
232018
Further evidence of association between mutations in FGFR2 and syndromic craniosynostosis with sacrococcygeal eversion
NAJ Oliveira, LG Alonso, RD Fanganiello, MR Passos‐Bueno
Birth Defects Research Part A: Clinical and Molecular Teratology 76 (8), 629-633, 2006
232006
Novel molecular pathways elicited by mutant FGFR2 may account for brain abnormalities in Apert syndrome
E Yeh, RD Fanganiello, DY Sunaga, X Zhou, G Holmes, KM Rocha, ...
PloS one 8 (4), e60439, 2013
192013
Scientific principles of adipose stem cells
L Kokai, K Marra, JP Rubin
Academic Press, 2021
162021
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