IRISanRaf

FORTUGNO, PAOLA
 Distribuzione geografica
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Continente #
EU - Europa 690
AS - Asia 314
NA - Nord America 165
SA - Sud America 1
Totale 1.170
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Nazione #
CZ - Repubblica Ceca 596
US - Stati Uniti d'America 165
CN - Cina 145
SG - Singapore 106
IT - Italia 57
TR - Turchia 48
DE - Germania 13
FR - Francia 9
HK - Hong Kong 9
GB - Regno Unito 7
FI - Finlandia 4
MY - Malesia 4
MM - Myanmar 2
NL - Olanda 2
AT - Austria 1
BR - Brasile 1
UA - Ucraina 1
Totale 1.170
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Città #
Olomouc 596
Santa Clara 55
Singapore 31
Shanghai 22
North Bergen 21
Rome 17
Assago 16
Dallas 13
Los Angeles 11
Guangzhou 10
West Jordan 10
Hong Kong 9
Frankfurt am Main 7
Montpellier 5
Shenzhen 5
Turin 5
Helsinki 4
Jiaxing 4
Rui'an 4
Seremban 4
Wuhan 4
Beijing 3
Dijon 3
London 3
Milan 3
New York 3
Novara 3
Suffern 3
Trento 3
Ashburn 2
Bologna 2
Bolzano 2
Buglio in Monte 2
Istanbul 2
Jinhua 2
Nanjing 2
Putian 2
Shaoxing 2
Wuxi 2
Xuzhou 2
Yangon 2
Yiwu 2
Zibo 2
Bengbu 1
Buffalo 1
Dongyang 1
Hangzhou 1
Hefei 1
Kunming 1
Maceió 1
Nantong 1
Naples 1
Newport 1
Nuremberg 1
Quanzhou 1
Sanming 1
Taizhou 1
The Dalles 1
Vienna 1
Wuhu 1
Xi'an 1
Xingtai 1
Totale 924
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Nome #
Chemerin expression marks early psoriatic skin lesions and correlates with plasmacytoid dendritic cell recruitment 77
Antigenicity and immunogenicity of phage library-selected peptide mimics of the major surface proteophosphoglycan antigens of Entamoeba histolytica 76
Full sequencing of the FLG gene in Italian patients with atopic eczema: evidence of new mutations, but lack of an association 70
A synonymous mutation in SPINK5 exon 11 causes Netherton syndrome by altering exonic splicing regulatory elements 69
Downregulation of DeltaNp63alpha in keratinocytes by p14ARF-mediated SUMO-conjugation and degradation 69
Colony assay for phage-displayed libraries 69
Betapapillomavirus in multiple non-melanoma skin cancers of Netherton syndrome: Case report and published work review 69
A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in Netherton syndrome 67
Epidermolysis Bullosa (EB) Acquisita in an Adult Patient with Previously Unrecognized Mild Dystrophic EB and Biallelic COL7A1 Mutations 67
Biallelic mutations in RNF220 cause laminopathies featuring leukodystrophy, ataxia and deafness 67
De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway 40
RIPK4 regulates cell-cell adhesion in epidermal development and homeostasis 25
"Affinity maturation" of ligands for HCV-specific serum antibodies 23
Truncating variants in the penultimate exon of TGFBR1 escaping nonsense-mediated mRNA decay cause Loeys-Dietz syndrome 21
The 420K LEKTI variant alters LEKTI proteolytic activation and results in protease deregulation: implications for atopic dermatitis 19
Identification of tumor-associated antigens by screening phage-displayed human cDNA libraries with sera from tumor patients 19
Whole-exome sequencing in patients with ichthyosis reveals modifiers associated with increased IgE levels and allergic sensitizations 14
Genotypic Categorization of Loeys-Dietz Syndrome Based on 24 Novel Families and Literature Data 13
Survivin exists in immunochemically distinct subcellular pools and is involved in spindle microtubule function 13
TFIIH-dependent MMP-1 overexpression in trichothiodystrophy leads to extracellular matrix alterations in patient skin 13
Pathogenic variants in CDH11 impair cell adhesion and cause Teebi hypertelorism syndrome 13
Selection of biologically active peptides by phage display of random peptide libraries 12
Exon-Specific U1s Correct SPINK5 Exon 11 Skipping Caused by a Synonymous Substitution that Affects a Bifunctional Splicing Regulatory Element 12
Long-term follow-up of a spontaneously improving patient with junctional epidermolysis bullosa associated with ITGB4 c.3977-19T>A splicing mutation 12
Multiple Skin Squamous Cell Carcinomas in Junctional Epidermolysis Bullosa Due to Altered Laminin-332 Function 12
Systematic Review and Meta-Analysis of Dietary Interventions and Microbiome in Phenylketonuria 12
Netherton syndrome and its multifaceted defective protein LEKTI 12
A Novel Phenotype of Junctional Epidermolysis Bullosa with Transient Skin Fragility and Predominant Ocular Involvement Responsive to Human Amniotic Membrane Eyedrops 12
Recessive mutations in the neuronal isoforms of DST, encoding dystonin, lead to abnormal actin cytoskeleton organization and HSAN type VI 12
Kindler syndrome with severe mucosal involvement in a large Palestinian pedigree 12
Rational design of shepherdin, a novel anticancer agent 11
p63-dependent and independent mechanisms of nectin-1 and nectin-4 regulation in the epidermis 11
Defining the clinical spectrum of ichthyosis follicularis, atrichia and photophobia clinical association type 1 (IFAP1) 11
Microprocessor-dependent processing of splice site overlapping microRNA exons does not result in changes in alternative splicing 11
ADAM-HCV, a new-concept diagnostic assay for antibodies to hepatitis C virus in serum 11
Reference genes for gene expression analysis in proliferating and differentiating human keratinocytes 11
Early immunopathological diagnosis of ichthyosis with confetti in two sporadic cases with new mutations in keratin 10 11
Nectin-4 mutations causing ectodermal dysplasia with syndactyly perturb the rac1 pathway and the kinetics of adherens junction formation 10
Structural Defects of Laminin β3 N-terminus Underlie Junctional Epidermolysis Bullosa with Altered Granulation Tissue Response 10
Induction of anti-carbohydrate antibodies by phage library-selected peptide mimics 10
Measles skin rash: Infection of lymphoid and myeloid cells in the dermis precedes viral dissemination to the epidermis 10
Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome 10
Regulation of survivin function by Hsp90 10
Chromatin conformation capture in the clinic: 4C-seq/HiC distinguishes pathogenic from neutral duplications at the GPR101 locus 10
Nectinopathies: an emerging group of ectodermal dysplasia syndromes 10
Isolation of phage mimotopes mimicking a protective epitope of GPI-linked proteophosphoglycan antigens of Entamoeba histolytica 10
A truncating mutation in the laminin-332α chain highlights the role of the LG45 proteolytic domain in regulating keratinocyte adhesion and migration 9
Proteolytic activation cascade of the Netherton syndrome-defective protein, LEKTI, in the epidermis: implications for skin homeostasis 9
Lethal Netherton syndrome due to homozygous p.Arg371X mutation in SPINK5 8
Ichthyosis Linearis Circumflexa as the Only Clinical Manifestation of Netherton Syndrome 8
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 8
Intracellular targets of RGDS peptide in melanoma cells 7
RIPK4 regulates cell-cell adhesion in epidermal development and homeostasis 4
null 2
Totale 1.243
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Categoria #
all - tutte 11.522
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 11.522
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2022/202366 0 0 0 0 0 0 12 0 1 0 0 53
2023/2024763 11 1 3 6 3 2 6 9 26 21 305 370
2024/2025414 35 151 12 7 12 78 15 41 55 8 0 0
Totale 1.243