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The lncRNAMALAT1-WTAP axis: a novel layer of EMT regulation in hypoxic triple-negative breast cancer.
- Published in:
- Cell Death Discovery, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41420-024-02058-4
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- Publication type:
- Article
Daily Fructose Traces Intake and Liver Injury in Children with Hereditary Fructose Intolerance.
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- Nutrients, 2019, v. 11, n. 10, p. 2397, doi. 10.3390/nu11102397
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- Publication type:
- Article
A Collaborative Approach for Triggering Environmental Awareness: The 3Rs for Sustainable Use of Natural Resources in Ulaanbaatar (3R4UB).
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- Sustainability (2071-1050), 2023, v. 15, n. 18, p. 13846, doi. 10.3390/su151813846
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- Publication type:
- Article
Peripheral, Marginal, or Non-Core Areas? Setting the Context to Deal with Territorial Inequalities through a Systematic Literature Review.
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- Sustainability (2071-1050), 2023, v. 15, n. 13, p. 10401, doi. 10.3390/su151310401
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- Publication type:
- Article
The first two-year follow-up in a patient with isolated sensory neuronopathy due to biallelic expansion in RFC1 gene.
- Published in:
- 2023
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- Publication type:
- Letter
Do It Yourself! Collaborative Processes for Inclusive Design and Capacity Building in Louisiana (USA).
- Published in:
- Urban Science, 2024, v. 8, n. 2, p. 32, doi. 10.3390/urbansci8020032
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- Publication type:
- Article
Crosstalk between 14-3-3θ and AF4 enhances MLL-AF4 activity and promotes leukemia cell proliferation.
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- Cellular Oncology (2211-3428), 2019, v. 42, n. 6, p. 829, doi. 10.1007/s13402-019-00468-6
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- Publication type:
- Article
SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing loss.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2016, v. 54, n. 9, p. e259, doi. 10.1515/cclm-2015-1216
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- Publication type:
- Article
Prenatal molecular diagnosis of inherited neuromuscular diseases: Duchenne/Becker muscular dystrophy, myotonic dystrophy type 1 and spinal muscular atrophy.
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- Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 12, p. 2239, doi. 10.1515/cclm-2013-0209
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- Publication type:
- Article
NOX Dependent ROS Generation and Cell Metabolism.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 3, p. 2086, doi. 10.3390/ijms24032086
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- Publication type:
- Article
Nuclear FGFR2 Interacts with the MLL-AF4 Oncogenic Chimera and Positively Regulates HOXA9 Gene Expression in t(4;11) Leukemia Cells.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 9, p. 4623, doi. 10.3390/ijms22094623
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- Publication type:
- Article
Phosphorylation Sites in Protein Kinases and Phosphatases Regulated by Formyl Peptide Receptor 2 Signaling.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 11, p. 3818, doi. 10.3390/ijms21113818
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- Publication type:
- Article
Genetic characterization of Italian patients with Bardet-Biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: identification of eleven novel pathogenic sequence variants.
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- BMC Medical Genetics, 2017, v. 18, p. 1, doi. 10.1186/s12881-017-0372-0
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- Publication type:
- Article
Molecular Characterization of Choroideremia-Associated Deletions Reveals an Unexpected Regulation of CHM Gene Transcription.
- Published in:
- Genes, 2021, v. 12, n. 8, p. 1111, doi. 10.3390/genes12081111
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- Publication type:
- Article
The TNFRSF13C H159Y Variant Is Associated with Severe COVID-19: A Retrospective Study of 500 Patients from Southern Italy.
- Published in:
- Genes, 2021, v. 13, n. 6, p. 881, doi. 10.3390/genes12060881
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- Publication type:
- Article
NOX2-Dependent Reactive Oxygen Species Regulate Formyl-Peptide Receptor 1-Mediated TrkA Transactivation in SH-SY5Y Cells.
- Published in:
- Oxidative Medicine & Cellular Longevity, 2019, p. 1, doi. 10.1155/2019/2051235
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- Publication type:
- Article
Transglutaminase 1 Gene Mutations in Italian Patients with Autosomal Recessive Lamellar Ichthyosis.
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- Journal of Investigative Dermatology, 2001, v. 116, n. 5, p. 809, doi. 10.1046/j.1523-1747.2001.01314.x
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- Publication type:
- Article
Intrapresa femminile e cura dei contesti: verso una mappa delle pratiche di genere a Napol.
- Published in:
- Scienze del Territorio, 2023, v. 11, n. 1, p. 51, doi. 10.36253/sdt-14479
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- Publication type:
- Article
MALAT1-dependent hsa_circ_0076611 regulates translation rate in triple-negative breast cancer.
- Published in:
- Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-03539-x
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- Publication type:
- Article
Design for Resilient Post-Disaster Wood Waste Upcycling: The Katrina Furniture Project Experience and Its "Legacy" in a Digital Perspective.
- Published in:
- Buildings (2075-5309), 2024, v. 14, n. 7, p. 2065, doi. 10.3390/buildings14072065
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- Publication type:
- Article
Phosphoproteomic analysis sheds light on intracellular signaling cascades triggered by Formyl-Peptide Receptor 2.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-54502-6
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- Publication type:
- Article
De Novo Large Deletions in the PHEX Gene Caused X-Linked Hypophosphataemic Rickets in Two Italian Female Infants Successfully Treated with Burosumab.
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- Diagnostics (2075-4418), 2023, v. 13, n. 15, p. 2552, doi. 10.3390/diagnostics13152552
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- Publication type:
- Article
Comprehensive Molecular Analysis of DMD Gene Increases the Diagnostic Value of Dystrophinopathies: A Pilot Study in a Southern Italy Cohort of Patients.
- Published in:
- Diagnostics (2075-4418), 2021, v. 11, n. 10, p. 1910, doi. 10.3390/diagnostics11101910
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- Publication type:
- Article
Multi-Gene Next-Generation Sequencing for Molecular Diagnosis of Autosomal Recessive Congenital Ichthyosis: A Genotype-Phenotype Study of Four Italian Patients.
- Published in:
- Diagnostics (2075-4418), 2020, v. 10, n. 12, p. 995, doi. 10.3390/diagnostics10120995
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- Publication type:
- Article
Formyl Peptide Receptor 1 Modulates Endothelial Cell Functions by NADPH Oxidase-Dependent VEGFR2 Transactivation.
- Published in:
- Oxidative Medicine & Cellular Longevity, 2018, p. 1, doi. 10.1155/2018/2609847
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- Publication type:
- Article
RP1 Dominant p.Ser740* Pathogenic Variant in 20 Knowingly Unrelated Families Affected by Rod–Cone Dystrophy: Potential Founder Effect in Western Sicily.
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- Medicina (1010660X), 2024, v. 60, n. 2, p. 254, doi. 10.3390/medicina60020254
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- Publication type:
- Article
MiR‐27a downregulates 14‐3‐3θ, RUNX1, AF4, and MLL‐AF4, crucial drivers of blast transformation in t(4;11) leukemia cells.
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- Cell Biochemistry & Function, 2022, v. 40, n. 7, p. 706, doi. 10.1002/cbf.3736
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- Publication type:
- Article
Lamellar ichthyosis and arthrogryposis in a premature neonate.
- Published in:
- 2015
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- Publication type:
- Case Study
Six novel alleles identified in Italian hereditary fructose intolerance patients enlarge the mutation spectrum of the aldolase B gene.
- Published in:
- Human Mutation, 2004, v. 24, n. 6, p. 534, doi. 10.1002/humu.9290
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- Publication type:
- Article
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-24636-1
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- Publication type:
- Article
New Molecular Mechanisms and Clinical Impact of circRNAs in Human Cancer.
- Published in:
- Cancers, 2021, v. 13, n. 13, p. 3154, doi. 10.3390/cancers13133154
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- Publication type:
- Article
Aminotransferases and muscular diseases: A disregarded lesson. Case reports and review of the literature.
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- Journal of Paediatrics & Child Health, 2012, v. 48, n. 10, p. 886, doi. 10.1111/j.1440-1754.2010.01730.x
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- Publication type:
- Article
Comprehensive mutation analysis (20 families) of the choroideremia gene reveals a missense variant that prevents the binding of REP1 with rab geranylgeranyl transferase.
- Published in:
- Human Mutation, 2011, v. 32, n. 12, p. 1460, doi. 10.1002/humu.21591
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- Publication type:
- Article
Hereditary fructose intolerance: functional study of two novel ALDOB natural variants and characterization of a partial gene deletion.
- Published in:
- Human Mutation, 2010, v. 31, n. 12, p. 1294, doi. 10.1002/humu.21359
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- Publication type:
- Article
Metabolic Alterations in Cardiomyocytes of Patients with Duchenne and Becker Muscular Dystrophies.
- Published in:
- Journal of Clinical Medicine, 2019, v. 8, n. 12, p. 2151, doi. 10.3390/jcm8122151
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- Publication type:
- Article
Prioritization of putatively detrimental variants in euploid miscarriages.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-05737-3
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- Publication type:
- Article
Regulation of Inflammation and Oxidative Stress by Formyl Peptide Receptors in Cardiovascular Disease Progression.
- Published in:
- Life (2075-1729), 2021, v. 11, n. 3, p. 243, doi. 10.3390/life11030243
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- Publication type:
- Article
The Molecular Basis of Hereditary Fructose Intolerance in Italian Children.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 1993, v. 31, n. 10, p. 675
- By:
- Publication type:
- Article
Urban Commons between Ostrom's and Neo-Materialist Approaches: The Case of Lido Pola in Naples, Southern Italy.
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- Land (2012), 2023, v. 12, n. 3, p. 524, doi. 10.3390/land12030524
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- Publication type:
- Article
Formyl-Peptide Receptor 2 Signaling Modulates SLC7A11/xCT Expression and Activity in Tumor Cells.
- Published in:
- Antioxidants, 2024, v. 13, n. 5, p. 552, doi. 10.3390/antiox13050552
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- Publication type:
- Article
Formyl Peptide Receptor 2-Dependent cPLA2 and 5-LOX Activation Requires a Functional NADPH Oxidase.
- Published in:
- Antioxidants, 2024, v. 13, n. 2, p. 220, doi. 10.3390/antiox13020220
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- Publication type:
- Article
Formyl-Peptide Receptor 2 Signaling Redirects Glucose and Glutamine into Anabolic Pathways in Metabolic Reprogramming of Lung Cancer Cells.
- Published in:
- Antioxidants, 2022, v. 11, n. 9, p. 1692, doi. 10.3390/antiox11091692
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- Publication type:
- Article
Pro-Resolving FPR2 Agonists Regulate NADPH Oxidase-Dependent Phosphorylation of HSP27, OSR1, and MARCKS and Activation of the Respective Upstream Kinases.
- Published in:
- Antioxidants, 2021, v. 10, n. 1, p. 134, doi. 10.3390/antiox10010134
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- Publication type:
- Article
A putative frameshift variant in the CHM gene is associated with an unexpected splicing alteration in a choroideremia patient.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 11, p. 1, doi. 10.1002/mgg3.1490
- By:
- Publication type:
- Article
Structural and functional analysis of aldolase B mutants related to hereditary fructose intolerance
- Published in:
- FEBS Letters, 2002, v. 531, n. 2, p. 152, doi. 10.1016/S0014-5793(02)03451-8
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- Publication type:
- Article