IRIS
PANTALEO, ANTONINO
 Distribuzione geografica
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Continente #
NA - Nord America 81
EU - Europa 50
AS - Asia 2
Totale 133
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Nazione #
US - Stati Uniti d'America 81
IT - Italia 22
SE - Svezia 17
FR - Francia 3
FI - Finlandia 2
GB - Regno Unito 2
IN - India 2
RU - Federazione Russa 2
SI - Slovenia 2
Totale 133
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Città #
Chandler 16
Nyköping 14
Bari 11
Ashburn 9
Fairfield 8
New York 6
Valenzano 4
Cambridge 3
Lawrence 3
Roxbury 3
Wilmington 3
Grottaglie 2
Helsinki 2
Inglewood 2
Ljubljana 2
Pune 2
Altopascio 1
Houston 1
London 1
Napoli 1
Paris 1
Santa Marinella 1
Seattle 1
Stimigliano 1
Woodbridge 1
Totale 99
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Nome #
Beyond BRCA1/2: Homologous Recombination Repair Genetic Profile in a Large Cohort of Apulian Ovarian Cancers 54
The first case of congenital myasthenic syndrome caused by a large homozygous deletion in the cterminal region of colq (Collagen like tail subunit of asymmetric acetylcholinesterase) protein 53
Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants 28
Lateralized overgrowth with vascular malformation caused by a somatic PTPN11 pathogenic variant: another piece added to the puzzle of mosaic RASopathies 5
The chromatin remodeling factors EP300 and TRRAP are novel SMYD3 interactors involved in the emerging 'nonmutational epigenetic reprogramming' cancer hallmark 2
SMYD3 Modulates AMPK-mTOR Signaling Balance in Cancer Cell Response to DNA Damage 2
Understanding the Genetic Landscape of Pancreatic Ductal Adenocarcinoma to Support Personalized Medicine: A Systematic Review 1
SMYD3 Modulates the HGF/MET Signaling Pathway in Gastric Cancer 1
Uncoupling p38α nuclear and cytoplasmic functions and identification of two p38α phosphorylation sites on β-catenin: implications for the Wnt signaling pathway in CRC models 1
Classic Galactosemia: Clinical and Computational Characterization of a Novel GALT Missense Variant (p.A303D) and a Literature Review 1
Clinical Spectrum Associated with Wolfram Syndrome Type 1 and Type 2: A Review on Genotype–Phenotype Correlations 1
The somatic p.T81dup variant in AKT3 gene underlies a mild cerebral phenotype and expands the spectrum including capillary malformation and lateralized overgrowth 1
Tumor Testing and Genetic Analysis to Identify Lynch Syndrome Patients in an Italian Colorectal Cancer Cohort 1
Totale 151
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Categoria #
all - tutte 1.082
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 1.082
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202119 0 0 0 0 0 0 12 1 4 0 2 0
2021/202235 0 1 0 0 0 3 0 3 6 6 12 4
2022/202356 8 9 2 2 4 4 1 8 14 1 1 2
2023/202441 1 3 0 5 6 11 0 3 1 7 4 0
Totale 151