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Romina Ficarella

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Sebastio Perrini; Alessandro Peschechera; Graziano Pesole; Ernesto Picardi; Maria Barbaro; Massimo Carella; Angelo Cignarelli; Michele De Fazio; Romina Ficarella; Luigi Laviola; Annalisa Natalicchio; Pasquale Nigro; Orazio Palumbo; Francesco Giorgino
Differences in gene expression and cytokine release profiles highlight the heterogeneity of distinct subsets of adipose tissue-derived stem cells in the subcutaneous and visceral adipose tissue in humans.
Angelo Cignarelli; Romina Ficarella; Pasquale Nigro; Sebastio Perrini; Alessandro Peschechera; Francesco Giorgino
Human adipose tissue stem cells: relevance in the pathophysiology of obesity and metabolic diseases and therapeutic applications.
Grazia Paola Nicchia; Orazio Nicolotti; F Pisani; A Rossi; Maria Svelto; A Carotti; X Estivill; Romina Ficarella; Paolo Gasparini; I Giangreco; Antonio Frigeri
D184E mutation in aquaporin-4 gene impairs water permeability and links to deafness.

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All Publications

2013: Sebastio Perrini; Alessandro Peschechera; Graziano Pesole; Ernesto Picardi; Maria Barbaro; Massimo Carella; Angelo Cignarelli; Michele De Fazio; Romina Ficarella; Luigi Laviola; Annalisa Natalicchio; Pasquale Nigro; Orazio Palumbo; Francesco Giorgino
Differences in gene expression and cytokine release profiles highlight the heterogeneity of distinct subsets of adipose tissue-derived stem cells in the subcutaneous and visceral adipose tissue in humans.
PloS one 2013;8(3):e57892.
2012: Angelo Cignarelli; Romina Ficarella; Pasquale Nigro; Sebastio Perrini; Alessandro Peschechera; Francesco Giorgino
Human adipose tissue stem cells: relevance in the pathophysiology of obesity and metabolic diseases and therapeutic applications.
Expert reviews in molecular medicine 2012;14():e19.
2011: Grazia Paola Nicchia; Orazio Nicolotti; F Pisani; A Rossi; Maria Svelto; A Carotti; X Estivill; Romina Ficarella; Paolo Gasparini; I Giangreco; Antonio Frigeri
D184E mutation in aquaporin-4 gene impairs water permeability and links to deafness.
Neuroscience 2011;197():80-8.
2009: Sebastio Perrini; Angelo Cignarelli; Romina Ficarella; Luigi Laviola; Francesco Giorgino
Human adipose tissue precursor cells: a new factor linking regulation of fat mass to obesity and type 2 diabetes?
Archives of physiology and biochemistry 2009;115(4):218-26.
2009: Cristina Zadro; Maria Stella Alemanno; Emanuele Bellacchio; Romina Ficarella; Francesca Donaudy; Salvatore Melchionda; Leopoldo Zelante; Raquel Rabionet; Nele Hilgert; Xavier Estivill; Guy Van Camp; Paolo Gasparini; Massimo Carella
Are MYO1C and MYO1F associated with hearing loss?
Biochimica et biophysica acta 2009;1792(1):27-32.
2007: Romina Ficarella; Francesca Di Leva; Mario Bortolozzi; S Ortolano; Francesca Donaudy; Marco Petrillo; Salvatore Melchionda; Andrea Lelli; Teuta Domi; Laura Fedrizzi; D Lim; G E Shull; Paolo Gasparini; Marisa Brini; Fabio Mammano; Ernesto Carafoli
A functional study of plasma-membrane calcium-pump isoform 2 mutants causing digenic deafness.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(5):1516-21.
2006: Francesca Donaudy; L Zheng; Romina Ficarella; Ester Ballana; Massimo Carella; Salvatore Melchionda; Xavier Estivill; J R Bartles; Paolo Gasparini
Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation.
Journal of medical genetics 2006;43(2):157-61.
2005: Lesley J Bruce; Hannah C Robinson; Hélène Guizouarn; Franck Borgese; Penny Harrison; May-Jean King; Jeroen S Goede; Suzanne E Coles; Daniel M Gore; Hans U Lutz; Romina Ficarella; D Mark Layton; Achille Iolascon; J Clive Ellory; Gordon W Stewart
Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1.
Nature genetics 2005;37(11):1258-63.
2005: Claudia Mandato; Stefania Lucariello; Maria Rosaria Licenziati; Adriana Franzese; Maria Immacolata Spagnuolo; Romina Ficarella; Maria Pacilio; Michele Amitrano; Gaetano Capuano; Rosaria Meli; Pietro Vajro
Metabolic, hormonal, oxidative, and inflammatory factors in pediatric obesity-related liver disease.
The Journal of pediatrics 2005;147(1):62-6.
2004: Massimo Carella; Adamo Pio D'Adamo; Sabine Grootenboer-Mignot; Marie C Vantyghem; Laura Esposito; Angela D'Eustacchio; Romina Ficarella; Gordon W Stewart; Paolo Gasparini; Jean Delaunay; Achille Iolascon
A second locus mapping to 2q35-36 for familial pseudohyperkalaemia.
European journal of human genetics : EJHG 2004;12(12):1073-6.
2004: Carmela Lanzara; Antonella Roetto; Filomena Daraio; Sylvain R Rivard; Romina Ficarella; Hervey Simard; Timothy M Cox; Mario Cazzola; Alberto Piperno; Anne-Paule Gimenez-Roqueplo; Paola Grammatico; Stefano Volinia; Paolo Gasparini; Clara Camaschella
Spectrum of hemojuvelin gene mutations in 1q-linked juvenile hemochromatosis.
Blood 2004;103(11):4317-21.
2004: Francesca Donaudy; Rikkert L Snoeckx; Markus Pfister; Hans-Peter Zenner; nikolaus blin; Mariateresa Di Stazio; Antonella Ferrara; Carmela Lanzara; Romina Ficarella; Frank Declau; Carsten M Pusch; Peter Nürnberg; Salvatore Melchionda; Leopoldo Zelante; Ester Ballana; Xavier Estivill; Guy Van Camp; Paolo Gasparini; Anna Savoia
Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4).
American journal of human genetics 2004;74(4):770-6.
2003: Sylvain R Rivard; Carmela Lanzara; Doria Grimard; Massimo Carella; Hervey Simard; Romina Ficarella; Raynald Simard; Adamo Pio D'Adamo; Claude Férec; Clara Camaschella; GIANNI MURA; Antonella Roetto; Marc de Braekeleer; Lucien Bechner; Paolo Gasparini
Juvenile hemochromatosis locus maps to chromosome 1q in a French Canadian population.
European journal of human genetics : EJHG 2003;11(8):585-9.
2003: Sylvain R Rivard; Carmela Lanzara; Doria Grimard; Massimo Carella; Hervey Simard; Romina Ficarella; Raynald Simard; Adamo Pio D'Adamo; Marc de Braekeleer; Paolo Gasparini
Autosomal dominant reticuloendothelial iron overload (HFE type 4) due to a new missense mutation in the FERROPORTIN 1 gene (SLC11A3) in a large French-Canadian family.
Haematologica 2003;88(7):824-6.
2003: Carmela Lanzara; Romina Ficarella; Angela Totaro; Xin Chen; Roberta Roberto; Silverio Perrotta; Carla Lasalandra; Paolo Gasparini; Achille Iolascon; Massimo Carella
Congenital dyserythropoietic anemia type II: exclusion of seven candidate genes.
Blood cells, molecules & diseases 2003;30(1):22-9.