F. Vitelli

发表

Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice.

K. Steel, P. Scambler, K. Devriendt, 2009, The Journal of clinical investigation.

F. Vitelli, X. Swanson, B. Thorne, 2018, Advances in biochemical engineering/biotechnology.

Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1–F3

M. Rocchi, F. Vitelli, S. Fineschi, 2000, Cytogenetic and Genome Research.

TBX1 is required for inner ear morphogenesis.

F. Vitelli, A. Baldini, M. Morishima, 2003, Human molecular genetics.

Assessment of Differentiation States of Hematopoietic Stem Cells Following in Vitro Culture Using Side and Forward Scatter of Flow Cytometry

F. Vitelli, F. Farhangfar, Yu Zhou, 2017 .

Inheritance of a 38‐kb fragment in apparently sporadic facioscapulohumeral muscular dystrophy

F. Vitelli, G. Guazzi, A. Malandrini, 1999, Muscle & nerve.

Gain of function of Tbx1 affects pharyngeal and heart development in the mouse

F. Vitelli, A. Baldini, Tuong Huynh, 2009, Genesis.

Early thyroid development requires a Tbx1-Fgf8 pathway.

F. Vitelli, A. Moon, A. Baldini, 2009, Developmental biology.

Mosaicism in Alport syndrome and genetic counselling

F. Vitelli, G. Mazzucco, A. Renieri, 2000, Journal of medical genetics.

Tbx1 haploinsufficiency identified by functional scanning of the DiGeorge syndrome region is the cause of aortic arch defects in mice.

P. Scambler, A. Bradley, F. Vitelli, 2001 .

Identification and characterization of a highly conserved protein absent in the Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome (AMME).

F. Vitelli, A. Malandrini, A. Renieri, 1999, Genomics.

Microsatellite instability in sporadic mucinous colorectal carcinomas: relationship to clinico‐pathological variables

F. Vitelli, L. Messerini, R. Palmirotta, 1997, The Journal of pathology.

A genetic link between Tbx1 and fibroblast growth factor signaling.

F. Vitelli, A. Baldini, M. Morishima, 2002, Development.

Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice

P. Scambler, A. Bradley, F. Vitelli, 2001, Nature.

KCNE1-like gene is deleted in AMME contiguous gene syndrome: identification and characterization of the human and mouse homologs.

F. Vitelli, S. Banfi, A. Renieri, 1999, Genomics.

Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?

A Ballabio, A. Ballabio, F. Vitelli, 1998, Journal of medical genetics.

FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation.

G. Borsani, A. Ballabio, F. Vitelli, 1998, Genomics.

Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway?

F. Vitelli, A. Baldini, 2003, Trends in genetics : TIG.

Screening for mutations in the neurofibromatosis type 2 (NF2) gene in sporadic meningiomas

F. Vitelli, L. Papi, A. Tedde, 1996, Human Genetics.

Analysis of the neurofibromatosis type 2 gene in different human tumors of neuroectodermal origin

F. Vitelli, P. Radice, P. Grammatico, 1996, Human Genetics.

Alport syndrome and mental retardation: clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR)

F. Vitelli, G. Rizzoni, A. Renieri, 2002, Journal of medical genetics.

Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways.

F. Vitelli, A. Baldini, M. Morishima, 2002, Human molecular genetics.

Genetic dissection of the DiGeorge syndrome phenotype.

F. Vitelli, A. Baldini, E. Lindsay, 2002, Cold Spring Harbor symposia on quantitative biology.

Somatic mutations in the neurofibromatosis type 2 gene in sporadic meningiomas

F. Vitelli, L. Papi, F. Ammannati, 1995, Human Genetics.

Constitutional WT 1 mutations correlate with clinical features in children with progressive nephropathy

F. Vitelli, G. Mazzucco, M. Bruttini, 2000 .

Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development

Joshua W. Vincentz, F. Vitelli, A. Baldini, 2005, Development.

Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants.

F. Vitelli, A. Baldini, Zhen Zhang, 2006, Developmental biology.

Preserved speech variant is allelic of classic Rett syndrome

F. Vitelli, R. Cusano, A. Renieri, 2000, European Journal of Human Genetics.

Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: genetic evidence of impaired tissue response to Fgf8.

F. Vitelli, A. Baldini, Tuong Huynh, 2010, Journal of molecular and cellular cardiology.

Establishment of a scalable manufacturing platform for in-silico-derived ancestral adeno-associated virus vectors

F. Vitelli, W. Dong, Bingnan Gu, 2018, Cell and Gene Therapy Insights.