Netherton syndrome and its multifaceted defective protein LEKTI
2013-01-01 D'Alessio, M; Fortugno, P; Zambruno, G; Hovnanian, A
Nectinopathies: an emerging group of ectodermal dysplasia syndromes
2013-01-01 Brancati, F; Agolini, E; Fortugno, P
A truncating mutation in the laminin-332α chain highlights the role of the LG45 proteolytic domain in regulating keratinocyte adhesion and migration
2014-01-01 Di Zenzo, G; El Hachem, M; Diociaiuti, A; Boldrini, R; Calabresi, V; Cianfarani, F; Fortugno, P; Piccinni, E; Zambruno, G; Castiglia, D
Nectin-4 mutations causing ectodermal dysplasia with syndactyly perturb the rac1 pathway and the kinetics of adherens junction formation
2014-01-01 Fortugno, Paola; Josselin, Emmanuelle; Tsiakas, Konstantinos; Agolini, Emanuele; Cestra, Gianluca; Teson, Massimo; Santer, René; Castiglia, Daniele; Novelli, Giuseppe; Dallapiccola, Bruno; Kurth, Ingo; Lopez, Marc; Zambruno, Giovanna; Brancati, Francesco
Early immunopathological diagnosis of ichthyosis with confetti in two sporadic cases with new mutations in keratin 10
2014-01-01 Diociaiuti, Andrea; Fortugno, Paola; El Hachem, May; Angelo, Corrado; Proto, Vittoria; De Luca, Naomi; Martinelli, Diego; Boldrini, Renata; Castiglia, Daniele; Zambruno, Giovanna
p63-dependent and independent mechanisms of nectin-1 and nectin-4 regulation in the epidermis
2015-01-01 Mollo, Maria Rosaria; Antonini, Dario; Mitchell, Karen; Fortugno, Paola; Costanzo, Antonio; Dixon, Jill; Brancati, Francesco; Missero, Caterina
Whole-exome sequencing in patients with ichthyosis reveals modifiers associated with increased IgE levels and allergic sensitizations
2015-01-01 Kiritsi, Dimitra; Valari, Manthoula; Fortugno, Paola; Hausser, Ingrid; Lykopoulou, Lilia; Zambruno, Giovanna; Fischer, Judith; Bruckner-Tuderman, Leena; Jakob, Thilo; Has, Cristina
Kindler syndrome with severe mucosal involvement in a large Palestinian pedigree
2015-01-01 El Hachem, May; Diociaiuti, Andrea; Proto, Vittoria; Fortugno, Paola; Zambruno, Giovanna; Castiglia, Daniele; Naim, Majdy
TFIIH-dependent MMP-1 overexpression in trichothiodystrophy leads to extracellular matrix alterations in patient skin
2015-01-01 Arseni, Lavinia; Lanzafame, Manuela; Compe, Emmanuel; Fortugno, Paola; Afonso-Barroso, António; Peverali, Fiorenzo A; Lehmann, Alan R; Zambruno, Giovanna; Egly, Jean-Marc; Stefanini, Miria; Orioli, Donata
Reference genes for gene expression analysis in proliferating and differentiating human keratinocytes
2015-01-01 Lanzafame, Manuela; Botta, Elena; Teson, Massimo; Fortugno, Paola; Zambruno, Giovanna; Stefanini, Miria; Orioli, Donata
Exon-Specific U1s Correct SPINK5 Exon 11 Skipping Caused by a Synonymous Substitution that Affects a Bifunctional Splicing Regulatory Element
2015-01-01 Dal Mas, Andrea; Fortugno, Paola; Donadon, Irving; Levati, Lauretta; Castiglia, Daniele; Pagani, Franco
Ichthyosis Linearis Circumflexa as the Only Clinical Manifestation of Netherton Syndrome
2015-01-01 Guerra, Liliana; Fortugno, Paola; Pedicelli, Cristina; Mazzanti, Cinzia; Proto, Vittoria; Zambruno, Giovanna; Castiglia, Daniele
Betapapillomavirus in multiple non-melanoma skin cancers of Netherton syndrome: Case report and published work review
2015-01-01 Guerra, Liliana; Fortugno, Paola; Sinistro, Anna; Proto, Vittoria; Zambruno, Giovanna; Didona, Biagio; Castiglia, Daniele
A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in Netherton syndrome
2016-01-01 Numata, Sanae; Teye, Kwesi; Krol, Rafal P; Okamatsu, Yuki; Hashikawa, Keiko; Matsuda, Mitsuhiro; Fortugno, Paola; Di Zenzo, Giovanni; Castiglia, Daniele; Zambruno, Giovanna; Hamada, Takahiro; Hashimoto, Takashi
Structural Defects of Laminin β3 N-terminus Underlie Junctional Epidermolysis Bullosa with Altered Granulation Tissue Response
2016-01-01 El Hachem, Maya; Fortugno, Paola; Palmeri, Antonio; Helmer-Citterich, Manuela; Diociaiuti, Andrea; Proto, Vittoria; Boldrini, Renata; Zambruno, Giovanna; Castiglia, Daniele
Lack of K140 immunoreactivity in junctional epidermolysis bullosa skin and keratinocytes associates with misfolded laminin epidermal growth factor-like motif 2 of the β3 short arm
2018-01-01 Condorelli, A G; Fortugno, P; Cianfarani, F; Proto, V; Di Zenzo, G; Didona, B; Zambruno, G; Castiglia, D
Epidermolysis Bullosa (EB) Acquisita in an Adult Patient with Previously Unrecognized Mild Dystrophic EB and Biallelic COL7A1 Mutations
2018-01-01 Guerra, Liliana; Condorelli, Angelo Giuseppe; Fortugno, Paola; Calabresi, Valentina; Pedicelli, Cristina; Di Zenzo, Giovanni; Castiglia, Daniele
Microprocessor-dependent processing of splice site overlapping microRNA exons does not result in changes in alternative splicing
2018-01-01 Pianigiani, Giulia; Licastro, Danilo; Fortugno, Paola; Castiglia, Daniele; Petrovic, Ivana; Pagani, Franco
Recessive mutations in the neuronal isoforms of DST, encoding dystonin, lead to abnormal actin cytoskeleton organization and HSAN type VI
2019-01-01 Fortugno, Paola; Angelucci, Francesco; Cestra, Gianluca; Camerota, Letizia; Ferraro, Angelo Salvatore; Cordisco, Sonia; Uccioli, Luigi; Castiglia, Daniele; De Angelis, Barbara; Kurth, Ingo; Kornak, Uwe; Brancati, Francesco
Genotypic Categorization of Loeys-Dietz Syndrome Based on 24 Novel Families and Literature Data
2019-01-01 Camerota, Letizia; Ritelli, Marco; Wischmeijer, Anita; Majore, Silvia; Cinquina, Valeria; Fortugno, Paola; Monetta, Rosanna; Gigante, Laura; Marfan Syndrome Study Group Tor Vergata University Hospital, Null; Sangiuolo, Federica Carla; Novelli, Giuseppe; Colombi, Marina; Brancati, Francesco
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Netherton syndrome and its multifaceted defective protein LEKTI | 1-gen-2013 | D'Alessio, M; Fortugno, P; Zambruno, G; Hovnanian, A | |
| Nectinopathies: an emerging group of ectodermal dysplasia syndromes | 1-gen-2013 | Brancati, F; Agolini, E; Fortugno, P | |
| A truncating mutation in the laminin-332α chain highlights the role of the LG45 proteolytic domain in regulating keratinocyte adhesion and migration | 1-gen-2014 | Di Zenzo, G; El Hachem, M; Diociaiuti, A; Boldrini, R; Calabresi, V; Cianfarani, F; Fortugno, P; Piccinni, E; Zambruno, G; Castiglia, D | |
| Nectin-4 mutations causing ectodermal dysplasia with syndactyly perturb the rac1 pathway and the kinetics of adherens junction formation | 1-gen-2014 | Fortugno, Paola; Josselin, Emmanuelle; Tsiakas, Konstantinos; Agolini, Emanuele; Cestra, Gianluca; Teson, Massimo; Santer, René; Castiglia, Daniele; Novelli, Giuseppe; Dallapiccola, Bruno; Kurth, Ingo; Lopez, Marc; Zambruno, Giovanna; Brancati, Francesco | |
| Early immunopathological diagnosis of ichthyosis with confetti in two sporadic cases with new mutations in keratin 10 | 1-gen-2014 | Diociaiuti, Andrea; Fortugno, Paola; El Hachem, May; Angelo, Corrado; Proto, Vittoria; De Luca, Naomi; Martinelli, Diego; Boldrini, Renata; Castiglia, Daniele; Zambruno, Giovanna | |
| p63-dependent and independent mechanisms of nectin-1 and nectin-4 regulation in the epidermis | 1-gen-2015 | Mollo, Maria Rosaria; Antonini, Dario; Mitchell, Karen; Fortugno, Paola; Costanzo, Antonio; Dixon, Jill; Brancati, Francesco; Missero, Caterina | |
| Whole-exome sequencing in patients with ichthyosis reveals modifiers associated with increased IgE levels and allergic sensitizations | 1-gen-2015 | Kiritsi, Dimitra; Valari, Manthoula; Fortugno, Paola; Hausser, Ingrid; Lykopoulou, Lilia; Zambruno, Giovanna; Fischer, Judith; Bruckner-Tuderman, Leena; Jakob, Thilo; Has, Cristina | |
| Kindler syndrome with severe mucosal involvement in a large Palestinian pedigree | 1-gen-2015 | El Hachem, May; Diociaiuti, Andrea; Proto, Vittoria; Fortugno, Paola; Zambruno, Giovanna; Castiglia, Daniele; Naim, Majdy | |
| TFIIH-dependent MMP-1 overexpression in trichothiodystrophy leads to extracellular matrix alterations in patient skin | 1-gen-2015 | Arseni, Lavinia; Lanzafame, Manuela; Compe, Emmanuel; Fortugno, Paola; Afonso-Barroso, António; Peverali, Fiorenzo A; Lehmann, Alan R; Zambruno, Giovanna; Egly, Jean-Marc; Stefanini, Miria; Orioli, Donata | |
| Reference genes for gene expression analysis in proliferating and differentiating human keratinocytes | 1-gen-2015 | Lanzafame, Manuela; Botta, Elena; Teson, Massimo; Fortugno, Paola; Zambruno, Giovanna; Stefanini, Miria; Orioli, Donata | |
| Exon-Specific U1s Correct SPINK5 Exon 11 Skipping Caused by a Synonymous Substitution that Affects a Bifunctional Splicing Regulatory Element | 1-gen-2015 | Dal Mas, Andrea; Fortugno, Paola; Donadon, Irving; Levati, Lauretta; Castiglia, Daniele; Pagani, Franco | |
| Ichthyosis Linearis Circumflexa as the Only Clinical Manifestation of Netherton Syndrome | 1-gen-2015 | Guerra, Liliana; Fortugno, Paola; Pedicelli, Cristina; Mazzanti, Cinzia; Proto, Vittoria; Zambruno, Giovanna; Castiglia, Daniele | |
| Betapapillomavirus in multiple non-melanoma skin cancers of Netherton syndrome: Case report and published work review | 1-gen-2015 | Guerra, Liliana; Fortugno, Paola; Sinistro, Anna; Proto, Vittoria; Zambruno, Giovanna; Didona, Biagio; Castiglia, Daniele | |
| A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in Netherton syndrome | 1-gen-2016 | Numata, Sanae; Teye, Kwesi; Krol, Rafal P; Okamatsu, Yuki; Hashikawa, Keiko; Matsuda, Mitsuhiro; Fortugno, Paola; Di Zenzo, Giovanni; Castiglia, Daniele; Zambruno, Giovanna; Hamada, Takahiro; Hashimoto, Takashi | |
| Structural Defects of Laminin β3 N-terminus Underlie Junctional Epidermolysis Bullosa with Altered Granulation Tissue Response | 1-gen-2016 | El Hachem, Maya; Fortugno, Paola; Palmeri, Antonio; Helmer-Citterich, Manuela; Diociaiuti, Andrea; Proto, Vittoria; Boldrini, Renata; Zambruno, Giovanna; Castiglia, Daniele | |
| Lack of K140 immunoreactivity in junctional epidermolysis bullosa skin and keratinocytes associates with misfolded laminin epidermal growth factor-like motif 2 of the β3 short arm | 1-gen-2018 | Condorelli, A G; Fortugno, P; Cianfarani, F; Proto, V; Di Zenzo, G; Didona, B; Zambruno, G; Castiglia, D | |
| Epidermolysis Bullosa (EB) Acquisita in an Adult Patient with Previously Unrecognized Mild Dystrophic EB and Biallelic COL7A1 Mutations | 1-gen-2018 | Guerra, Liliana; Condorelli, Angelo Giuseppe; Fortugno, Paola; Calabresi, Valentina; Pedicelli, Cristina; Di Zenzo, Giovanni; Castiglia, Daniele | |
| Microprocessor-dependent processing of splice site overlapping microRNA exons does not result in changes in alternative splicing | 1-gen-2018 | Pianigiani, Giulia; Licastro, Danilo; Fortugno, Paola; Castiglia, Daniele; Petrovic, Ivana; Pagani, Franco | |
| Recessive mutations in the neuronal isoforms of DST, encoding dystonin, lead to abnormal actin cytoskeleton organization and HSAN type VI | 1-gen-2019 | Fortugno, Paola; Angelucci, Francesco; Cestra, Gianluca; Camerota, Letizia; Ferraro, Angelo Salvatore; Cordisco, Sonia; Uccioli, Luigi; Castiglia, Daniele; De Angelis, Barbara; Kurth, Ingo; Kornak, Uwe; Brancati, Francesco | |
| Genotypic Categorization of Loeys-Dietz Syndrome Based on 24 Novel Families and Literature Data | 1-gen-2019 | Camerota, Letizia; Ritelli, Marco; Wischmeijer, Anita; Majore, Silvia; Cinquina, Valeria; Fortugno, Paola; Monetta, Rosanna; Gigante, Laura; Marfan Syndrome Study Group Tor Vergata University Hospital, Null; Sangiuolo, Federica Carla; Novelli, Giuseppe; Colombi, Marina; Brancati, Francesco |
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