Publications by authors named "Lorena Di Pietro"

15 Publications

GLI1 and AXIN2 Are Distinctive Markers of Human Calvarial Mesenchymal Stromal Cells in Nonsyndromic Craniosynostosis.

Authors:

Lorena Di Pietro Marta Barba Chiara Prampolini Sabrina Ceccariglia Paolo Frassanito Alessia Vita Enrico Guadagni Davide Bonvissuto Luca Massimi Gianpiero Tamburrini Ornella Parolini Wanda Lattanzi

Int J Mol Sci 2020 Jun 19;21(12). Epub 2020 Jun 19.

Dipartimento Scienze della Vita e Sanità Pubblica, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.

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June 2020

Graphene Oxide Nano-Concentrators Selectively Modulate RNA Trapping According to Metal Cations in Solution.

Authors:

Valentina Palmieri Lorena Di Pietro Giordano Perini Marta Barba Ornella Parolini Marco De Spirito Wanda Lattanzi Massimiliano Papi

Front Bioeng Biotechnol 2020 25;8:421. Epub 2020 May 25.

Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Rome, Italy.

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May 2020

Rising Roles of Small Noncoding RNAs in Cotranscriptional Regulation: In Silico Study of miRNA and piRNA Regulatory Network in Humans.

Authors:

Massimiliano Chetta Lorena Di Pietro Nenad Bukvic Wanda Lattanzi

Genes (Basel) 2020 04 29;11(5). Epub 2020 Apr 29.

Dipartimento Scienze della Vita e Sanità Pubblica, Sezione di Biologia Applicata, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.

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April 2020

Gain-of-function variants and overexpression of RUNX2 in patients with nonsyndromic midline craniosynostosis.

Authors:

Araceli Cuellar Krithi Bala Lorena Di Pietro Marta Barba Garima Yagnik Jia Lie Liu Christina Stevens David J Hur Roxann G Ingersoll Cristina M Justice Hicham Drissi Jinoh Kim Wanda Lattanzi Simeon A Boyadjiev

Bone 2020 08 30;137:115395. Epub 2020 Apr 30.

Department of Pediatrics, University of California Davis School of Medicine, Sacramento, CA, USA. Electronic address:

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August 2020

Corrigendum to "BBS9 gene in nonsyndromic craniosynostosis: Role of the primary cilium in the aberrant ossification of the suture osteogenic niche" [Bone 112 (July 2018) 58-70].

Authors:

Marta Barba Lorena Di Pietro Luca Massimi Maria Concetta Geloso Paolo Frassanito Massimo Caldarelli Fabrizio Michetti Stefano Della Longa Paul A Romitti Concezio Di Rocco Alessandro Arcovito Ornella Parolini Gianpiero Tamburrini Camilla Bernardini Simeon Antonov Boyadjiev Wanda Lattanzi

Bone 2019 Apr 15;121:293. Epub 2019 Feb 15.

Istituto di Anatomia Umana e Biologia Cellulare, Università Cattolica del Sacro Cuore, 00168 Rome, Italy; Fondazione Policlinico Universitario "Agostino Gemelli", 00168 Rome, Italy. Electronic address:

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April 2019

Longitudinal evaluation of SMN levels as biomarker for spinal muscular atrophy: results of a phase IIb double-blind study of salbutamol.

J Med Genet 2019 05 28;56(5):293-300. Epub 2018 Dec 28.

Muscle Pathology and Neuroimmunology Unit, Neurological Institute Carlo Besta, Milano, Italy.

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May 2019

Graphene Oxide Induced Osteogenesis Quantification by In-Situ 2D-Fluorescence Spectroscopy.

Authors:

Valentina Palmieri Marta Barba Lorena Di Pietro Claudio Conti Marco De Spirito Wanda Lattanzi Massimiliano Papi

Int J Mol Sci 2018 Oct 26;19(11). Epub 2018 Oct 26.

Institute of Physics, Fondazione Policlinico Universitario A. Gemelli-IRCCS, Università Cattolica del Sacro Cuore, Largo Francesco Vito 1, 00168 Rome, Italy.

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October 2018

Skeletal Muscle MicroRNAs as Key Players in the Pathogenesis of Amyotrophic Lateral Sclerosis.

Authors:

Lorena Di Pietro Wanda Lattanzi Camilla Bernardini

Int J Mol Sci 2018 May 22;19(5). Epub 2018 May 22.

Istituto di Anatomia Umana e Biologia Cellulare, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.

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May 2018

BBS9 gene in nonsyndromic craniosynostosis: Role of the primary cilium in the aberrant ossification of the suture osteogenic niche.

Authors:

Marta Barba Lorena Di Pietro Luca Massimi Maria Concetta Geloso Paolo Frassanito Massimo Caldarelli Fabrizio Michetti Stefano Della Longa Paul A Romitti Concezio Di Rocco Alessandro Arcovito Ornella Parolini Gianpiero Tamburrini Camilla Bernardini Simeon A Boyadjiev Wanda Lattanzi

Bone 2018 07 17;112:58-70. Epub 2018 Apr 17.

Istituto di Anatomia Umana e Biologia Cellulare, Università Cattolica del Sacro Cuore, 00168 Rome, Italy; Fondazione Policlinico Universitario "Agostino Gemelli", 00168 Rome, Italy. Electronic address:

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July 2018

Effects of Class II-Selective Histone Deacetylase Inhibitor on Neuromuscular Function and Disease Progression in SOD1-ALS Mice.

Authors:

Daniela Buonvicino Roberta Felici Giuseppe Ranieri Riccardo Caramelli Andrea Lapucci Leonardo Cavone Mirko Muzzi Lorena Di Pietro Camilla Bernardini Clemens Zwergel Sergio Valente Antonello Mai Alberto Chiarugi

Neuroscience 2018 05 26;379:228-238. Epub 2018 Mar 26.

Department of Health Sciences, Section of Clinical Pharmacology and Oncology, University of Florence, Italy.

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May 2018

Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients.

Authors:

Lorena Di Pietro Mirko Baranzini Maria Grazia Berardinelli Wanda Lattanzi Mauro Monforte Giorgio Tasca Amelia Conte Giandomenico Logroscino Fabrizio Michetti Enzo Ricci Mario Sabatelli Camilla Bernardini

Sci Rep 2017 08 25;7(1):9538. Epub 2017 Aug 25.

Institute of Anatomy and Cell Biology, Università Cattolica del Sacro Cuore, 00168, Rome, Italy.

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August 2017

Schizophrenia and Human Self-Domestication: An Evolutionary Linguistics Approach.

Authors:

Antonio Benítez-Burraco Lorena Di Pietro Marta Barba Wanda Lattanzi

Brain Behav Evol 2017 3;89(3):162-184. Epub 2017 May 3.

Department of Philology, Faculty of Humanities, University of Huelva, Huelva, Spain.

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March 2018

Genetic advances in craniosynostosis.

Authors:

Wanda Lattanzi Marta Barba Lorena Di Pietro Simeon A Boyadjiev

Am J Med Genet A 2017 May 4;173(5):1406-1429. Epub 2017 Feb 4.

Division of Genomic Medicine, Department of Pediatrics, Davis Medical Center, University of California, Sacramento, California.

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May 2017

Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study.

Eur J Hum Genet 2013 Jun 17;21(6):630-6. Epub 2012 Oct 17.

Medical Genetics Institute, Catholic University, Rome, Italy.

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June 2013

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.

Nat Genet 2012 Sep 29;44(9):1030-4. Epub 2012 Jul 29.

Center for Human Genome Variation, Duke University School of Medicine, Durham, North Carolina, USA.

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September 2012