Lorena Di Pietro
Overview
Explore the profile of Lorena Di Pietro including associated specialties, affiliations and a list of published articles.
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Articles
26
Citations
445
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0
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Recent Articles
1.
Tiberio F, Salvati M, Polito L, Tisci G, Vita A, Parolini O, et al.
Mol Ther Nucleic Acids
. 2025 Feb;
36(1):102427.
PMID: 39906733
Crouzon syndrome is a rare genetic craniofacial malformation caused by heterozygous gain-of-function mutations in the gene. The resulting constitutive activation of the FGFR2 signaling causes the premature osteogenic differentiation of...
2.
Masserdotti A, Gasik M, Grillari-Voglauer R, Grillari J, Cargnoni A, Chiodelli P, et al.
Front Cell Dev Biol
. 2024 Aug;
12:1411582.
PMID: 39144254
The intricate interplay between the developing placenta and fetal-maternal interactions is critical for pregnancy outcomes. Despite advancements, gaps persist in understanding biomechanics, transport processes, and blood circulation parameters, all of...
3.
Musolf A, Justice C, Erdogan-Yildirim Z, Goovaerts S, Cuellar A, Shaffer J, et al.
Sci Rep
. 2024 Apr;
14(1):8533.
PMID: 38609424
Craniosynostosis (CS) is a major birth defect resulting from premature fusion of cranial sutures. Nonsyndromic CS occurs more frequently than syndromic CS, with sagittal nonsyndromic craniosynostosis (sNCS) presenting as the...
4.
Panagiotakaki E, Tiziano F, Mikati M, Vijfhuizen L, Nicole S, Lesca G, et al.
Eur J Hum Genet
. 2023 Dec;
32(2):224-231.
PMID: 38097767
Alternating hemiplegia of childhood (AHC) is a rare neurodevelopment disorder that is typically characterized by debilitating episodic attacks of hemiplegia, seizures, and intellectual disability. Over 85% of individuals with AHC...
5.
Ragozzino E, Bortolani S, Di Pietro L, Papait A, Parolini O, Monforte M, et al.
Acta Neuropathol Commun
. 2023 Oct;
11(1):165.
PMID: 37849014
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant epigenetic disorder with highly variable muscle involvement and disease progression. Ongoing clinical trials, aimed at counteracting muscle degeneration and disease progression in...
6.
Di Pietro L, Boroumand M, Lattanzi W, Manconi B, Salvati M, Cabras T, et al.
Int J Mol Sci
. 2023 Oct;
24(19).
PMID: 37834461
Saliva houses over 2000 proteins and peptides with poorly clarified functions, including proline-rich proteins, statherin, P-B peptides, histatins, cystatins, and amylases. Their genes are poorly conserved across related species, reflecting...
7.
Di Pietro L, Giacalone F, Ragozzino E, Saccone V, Tiberio F, De Bardi M, et al.
Cell Death Dis
. 2022 Sep;
13(9):793.
PMID: 36114172
Muscle-resident non-myogenic mesenchymal cells play key roles that drive successful tissue regeneration within the skeletal muscle stem cell niche. These cells have recently emerged as remarkable therapeutic targets for neuromuscular...
8.
Di Pietro L, Palmieri V, Papi M, Lattanzi W
Int J Mol Sci
. 2022 Aug;
23(16).
PMID: 36012749
In the last 20 years, bone regenerative research has experienced exponential growth thanks to the discovery of new nanomaterials and improved manufacturing technologies that have emerged in the biomedical field....
9.
Perini G, Rosa E, Friggeri G, Di Pietro L, Barba M, Parolini O, et al.
Int J Mol Sci
. 2022 Mar;
23(6).
PMID: 35328638
Cancer spheroids are in vitro 3D models that became crucial in nanomaterials science thanks to the possibility of performing high throughput screening of nanoparticles and combined nanoparticle-drug therapies on in...
10.
Di Pietro L, Barba M, Palacios D, Tiberio F, Prampolini C, Baranzini M, et al.
Sci Rep
. 2021 Oct;
11(1):21316.
PMID: 34716352
RUNX2 encodes the master bone transcription factor driving skeletal development in vertebrates, and playing a specific role in craniofacial and skull morphogenesis. The anatomically modern human (AMH) features sequence changes...