Works matching AU Botta, Annalisa

Results: 42

The long pentraxin PTX3: a novel serum marker to improve the prediction of osteoporosis and osteoarthritis bone-related phenotypes.

Published in:

Journal of Orthopaedic Surgery & Research, 2021, v. 16, n. 1, p. 1, doi. 10.1186/s13018-021-02440-3

By:

Visconti, Virginia Veronica;
Greggi, Chiara;
Fittipaldi, Simona;
Casamassima, Donato;
Tallarico, Mariagrazia;
Romano, Francesco;
Botta, Annalisa;
Tarantino, Umberto

Publication type:

Article

Correction to: The long pentraxin PTX3: a novel serum marker to improve the prediction of osteoporosis and osteoarthritis bonerelated phenotypes.

Published in:

2021

By:

Visconti, Virginia Veronica;
Greggi, Chiara;
Fittipaldi, Simona;
Casamassima, Donato;
Tallarico, Mariagrazia;
Romano, Francesco;
Botta, Annalisa;
Tarantino, Umberto

Publication type:

Correction Notice

The long pentraxin PTX3: a novel serum marker to improve the prediction of osteoporosis and osteoarthritis bone-related phenotypes.

Published in:

Journal of Orthopaedic Surgery & Research, 2021, v. 16, n. 1, p. 1, doi. 10.1186/s13018-021-02440-3

By:

Visconti, Virginia Veronica;
Greggi, Chiara;
Fittipaldi, Simona;
Casamassima, Donato;
Tallarico, Mariagrazia;
Romano, Francesco;
Botta, Annalisa;
Tarantino, Umberto

Publication type:

Article

The long pentraxin PTX3: a novel serum marker to improve the prediction of osteoporosis and osteoarthritis bone-related phenotypes.

Published in:

Journal of Orthopaedic Surgery & Research, 2021, v. 16, n. 1, p. 1, doi. 10.1186/s13018-021-02440-3

By:

Visconti, Virginia Veronica;
Greggi, Chiara;
Fittipaldi, Simona;
Casamassima, Donato;
Tallarico, Maria Grazia;
Romano, Francesco;
Botta, Annalisa;
Tarantino, Umberto

Publication type:

Article

Mutated sigma-1R disrupts cell homeostasis in dHMN patient cells.

Published in:

Cellular & Molecular Life Sciences, 2025, v. 82, n. 1, p. 1, doi. 10.1007/s00018-025-05676-y

By:

Zanin, Sofia;
Ciscato, Francesco;
Petrucci, Antonio;
Botta, Annalisa;
Chiossi, Federico;
Vazza, Giovanni;
Rizzuto, Rosario;
Pallafacchina, Giorgia

Publication type:

Article

Altered Expression of Cell Cycle Regulators and Factors Released by Aged Cells in Skeletal Muscle of Patients with Bone Fragility: A Pilot Study on the Potential Role of SIRT1 in Muscle Atrophy.

Published in:

Biomedicines, 2025, v. 13, n. 6, p. 1350, doi. 10.3390/biomedicines13061350

By:

Falvino, Angela;
Bonanni, Roberto;
Gasperini, Beatrice;
Cariati, Ida;
Chiavoghilefu, Angela;
Smakaj, Amarildo;
Visconti, Virginia Veronica;
Botta, Annalisa;
Iundusi, Riccardo;
Gasbarra, Elena;
Tancredi, Virginia;
Tarantino, Umberto

Publication type:

Article

Cellular Senescence: The Driving Force of Musculoskeletal Diseases.

Published in:

Biomedicines, 2024, v. 12, n. 9, p. 1948, doi. 10.3390/biomedicines12091948

By:

Falvino, Angela;
Gasperini, Beatrice;
Cariati, Ida;
Bonanni, Roberto;
Chiavoghilefu, Angela;
Gasbarra, Elena;
Botta, Annalisa;
Tancredi, Virginia;
Tarantino, Umberto

Publication type:

Article

Identification of Aberrantly-Expressed Long Non-Coding RNAs in Osteoblastic Cells from Osteoporotic Patients.

Published in:

Biomedicines, 2020, v. 8, n. 3, p. 65, doi. 10.3390/biomedicines8030065

By:

Centofanti, Federica;
Santoro, Massimo;
Marini, Mario;
Visconti, Virginia Veronica;
Rinaldi, Anna Maria;
Celi, Monica;
D'Arcangelo, Giovanna;
Novelli, Giuseppe;
Orlandi, Augusto;
Tancredi, Virginia;
Tarantino, Umberto;
Botta, Annalisa

Publication type:

Article

Carrier frequency of CFTR variants in the non‐Caucasian populations by genome aggregation database (gnomAD)‐based analysis.

Published in:

Annals of Human Genetics, 2020, v. 84, n. 6, p. 463, doi. 10.1111/ahg.12396

By:

Nappo, Stefania;
Mannucci, Liliana;
Novelli, Giuseppe;
Sangiuolo, Federica;
D'Apice, Maria Rosaria;
Botta, Annalisa

Publication type:

Article

Role of the Vitamin D Receptor (VDR) in the Pathogenesis of Osteoporosis: A Genetic, Epigenetic and Molecular Pilot Study.

Published in:

Genes, 2023, v. 14, n. 3, p. 542, doi. 10.3390/genes14030542

By:

Gasperini, Beatrice;
Visconti, Virginia Veronica;
Ciccacci, Cinzia;
Falvino, Angela;
Gasbarra, Elena;
Iundusi, Riccardo;
Brandi, Maria Luisa;
Botta, Annalisa;
Tarantino, Umberto

Publication type:

Article

Deregulated Clusterin as a Marker of Bone Fragility: New Insights into the Pathophysiology of Osteoporosis.

Published in:

Genes, 2022, v. 13, n. 4, p. 652, doi. 10.3390/genes13040652

By:

Visconti, Virginia Veronica;
Greggi, Chiara;
Cariati, Ida;
Gasperini, Beatrice;
Mastrogregori, Ambra;
Botta, Annalisa;
Tarantino, Umberto

Publication type:

Article

Altered Ca<sup>2+</sup> Homeostasis and Endoplasmic Reticulum Stress in Myotonic Dystrophy Type 1 Muscle Cells.

Published in:

Genes, 2013, v. 4, n. 2, p. 275, doi. 10.3390/genes4020275

By:

Botta, Annalisa;
Malena, Adriana;
Loro, Emanuele;
Moro, Giulia Del;
Suman, Matteo;
Pantic, Boris;
Szabadkai, Gyorgy;
Vergani, Lodovica

Publication type:

Article

Methylation of the Vitamin D Receptor Gene in Human Disorders.

Published in:

International Journal of Molecular Sciences, 2024, v. 25, n. 1, p. 107, doi. 10.3390/ijms25010107

By:

Gasperini, Beatrice;
Falvino, Angela;
Piccirilli, Eleonora;
Tarantino, Umberto;
Botta, Annalisa;
Visconti, Virginia Veronica

Publication type:

Article

In Cis Effect of DMPK Expanded Alleles in Myotonic Dystrophy Type 1 Patients Carrying Variant Repeats at 5′ and 3′ Ends of the CTG Array.

Published in:

International Journal of Molecular Sciences, 2023, v. 24, n. 12, p. 10129, doi. 10.3390/ijms241210129

By:

Visconti, Virginia Veronica;
Macrì, Elisa;
D'Apice, Maria Rosaria;
Centofanti, Federica;
Massa, Roberto;
Novelli, Giuseppe;
Botta, Annalisa

Publication type:

Article

Epigenetics of Myotonic Dystrophies: A Minireview.

Published in:

International Journal of Molecular Sciences, 2021, v. 22, n. 22, p. 12594, doi. 10.3390/ijms222212594

By:

Visconti, Virginia Veronica;
Centofanti, Federica;
Fittipaldi, Simona;
Macrì, Elisa;
Novelli, Giuseppe;
Botta, Annalisa

Publication type:

Article

DNA Methylation Signatures of Bone Metabolism in Osteoporosis and Osteoarthritis Aging-Related Diseases: An Updated Review.

Published in:

International Journal of Molecular Sciences, 2021, v. 22, n. 8, p. 4244, doi. 10.3390/ijms22084244

By:

Visconti, Virginia Veronica;
Cariati, Ida;
Fittipaldi, Simona;
Iundusi, Riccardo;
Gasbarra, Elena;
Tarantino, Umberto;
Botta, Annalisa

Publication type:

Article

Circulating Long Non-Coding RNA GAS5 Is Overexpressed in Serum from Osteoporotic Patients and Is Associated with Increased Risk of Bone Fragility.

Published in:

International Journal of Molecular Sciences, 2020, v. 21, n. 18, p. 6930, doi. 10.3390/ijms21186930

By:

Visconti, Virginia Veronica;
Fittipaldi, Simona;
Ciuffi, Simone;
Marini, Francesca;
Isaia, Giancarlo;
D'Amelio, Patrizia;
Migliaccio, Silvia;
Marcocci, Claudio;
Minisola, Salvatore;
Nuti, Ranuccio;
Novelli, Giuseppe;
Brandi, Maria Luisa;
Botta, Annalisa;
Tarantino, Umberto

Publication type:

Article

A 34-year longitudinal study on long-term cardiac outcomes in DM1 patients with normal ECG at baseline at an Italian clinical centre.

Published in:

Journal of Neurology, 2018, v. 265, n. 4, p. 885, doi. 10.1007/s00415-018-8773-3

By:

Bucci, Elisabetta;
Testa, Marco;
Licchelli, Loretta;
Frattari, Alessandra;
El Halabieh, Nadia Attalla;
Gabriele, Erica;
Pignatelli, Giulia;
De Santis, Tiziana;
Fionda, Laura;
Vanoli, Fiammetta;
Morino, Stefania;
Garibaldi, Matteo;
Di Pasquale, Antonella;
Vanacore, Nicola;
Botta, Annalisa;
Antonini, Giovanni

Publication type:

Article

Erratum to: Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factors.

Published in:

2016

By:

Bianchi, Maria;
Leoncini, Emanuele;
Masciullo, Marcella;
Modoni, Anna;
Gadalla, Shahinaz;
Massa, Roberto;
Botta, Annalisa;
Rastelli, Emanuele;
Terracciano, Chiara;
Antonini, Giovanni;
Bucci, Elisabetta;
Petrucci, Antonio;
Costanzi, Sandro;
Santoro, Massimo;
Boccia, Stefania;
Silvestri, Gabriella

Publication type:

Erratum

Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2.

Published in:

Journal of Neurology, 2012, v. 259, n. 10, p. 2090, doi. 10.1007/s00415-012-6462-1

By:

Cardani, Rosanna;
Giagnacovo, Marzia;
Botta, Annalisa;
Rinaldi, Fabrizio;
Morgante, Alessandra;
Udd, Bjarne;
Raheem, Olayinka;
Penttilä, Sini;
Suominen, Tiina;
Renna, Laura;
Sansone, Valeria;
Bugiardini, Enrico;
Novelli, Giuseppe;
Meola, Giovanni

Publication type:

Article

An Age-Standardized Prevalence Estimate and a Sex and Age Distribution of Myotonic Dystrophy Types 1 and 2 in the Rome Province, Italy.

Published in:

Neuroepidemiology, 2016, v. 46, n. 3, p. 191, doi. 10.1159/000444018

By:

Vanacore, Nicola;
Rastelli, Emanuele;
antonini, Giovanni;
Bianchi, Maria Laura Ester;
Botta, annalisa;
Bucci, Elisabetta;
Casali, Carlo;
Costanzi-Porrini, Sandro;
Giacanelli, Manlio;
Gibellini, Manuela;
Modoni, anna;
Novelli, Giuseppe;
Pennisi, Elena Maria;
Petrucci, antonio;
Piantadosi, Carlo;
Silvestri, Gabriella;
Terracciano, Chiara;
Massa, Roberto

Publication type:

Article

Characterization of FMR1 Repeat Expansion and Intragenic Variants by Indirect Sequence Capture.

Published in:

Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.743230

By:

Grosso, Valentina;
Marcolungo, Luca;
Maestri, Simone;
Alfano, Massimiliano;
Lavezzari, Denise;
Iadarola, Barbara;
Salviati, Alessandro;
Mariotti, Barbara;
Botta, Annalisa;
D'Apice, Maria Rosaria;
Novelli, Giuseppe;
Delledonne, Massimo;
Rossato, Marzia

Publication type:

Article

A 14-Year Italian Experience in DM2 Genetic Testing: Frequency and Distribution of Normal and Premutated CNBP Alleles.

Published in:

Frontiers in Genetics, 2021, v. 11, p. 1, doi. 10.3389/fgene.2021.668094

By:

Botta, Annalisa;
Visconti, Virginia Veronica;
Fontana, Luana;
Bisceglia, Paola;
Bengala, Mario;
Massa, Roberto;
Bagni, Ilaria;
Cardani, Rosanna;
Sangiuolo, Federica;
Meola, Giovanni;
Antonini, Giovanni;
Petrucci, Antonio;
Pegoraro, Elena;
D'Apice, Maria Rosaria;
Novelli, Giuseppe

Publication type:

Article

Vitamin D Receptor in Muscle Atrophy of Elderly Patients: A Key Element of Osteoporosis-Sarcopenia Connection.

Published in:

Aging & Disease, 2018, v. 9, n. 6, p. 952, doi. 10.14336/AD.2018.0215

By:

Scimeca, Manuel;
Centofanti, Federica;
Celi, Monica;
Gasbarra, Elena;
Novelli, Giuseppe;
Botta, Annalisa;
Tarantino, Umberto

Publication type:

Article

Searching for Psoriasis Susceptibility Genes in Italy: Genome Scan and Evidence for a New Locus on Chromosome 1.

Published in:

Journal of Investigative Dermatology, 1999, v. 112, n. 1, p. 32, doi. 10.1046/j.1523-1747.1999.00471.x

By:

Capon, Francesca;
Novelli, Giuseppe;
Semprini, Sabrina;
Clementi, Maurizio;
Nudo, Maurizio;
Vultaggio, Pietro;
Mazzanti, Cinzia;
Gobello, Tommaso;
Botta, Annalisa;
Fabrizi, Giuseppe;
Dallapiccola, Bruno

Publication type:

Article

SCN4A as modifier gene in patients with myotonic dystrophy type 2.

Published in:

Scientific Reports, 2018, v. 8, n. 1, p. N.PAG, doi. 10.1038/s41598-018-29302-z

By:

Binda, Anna;
Renna, Laura V.;
Bosè, Francesca;
Brigonzi, Elisa;
Botta, Annalisa;
Valaperta, Rea;
Fossati, Barbara;
Rivolta, Ilaria;
Meola, Giovanni;
Cardani, Rosanna

Publication type:

Article

Epstein- Barr virus infection induces miR-21 in terminally differentiated malignant B cells.

Published in:

International Journal of Cancer, 2015, v. 137, n. 6, p. 1491, doi. 10.1002/ijc.29489

By:

Anastasiadou, Eleni;
Garg, Neha;
Bigi, Rachele;
Yadav, Shivangi;
Campese, Antonio Francesco;
Lapenta, Caterina;
Spada, Massimo;
Cuomo, Laura;
Botta, Annalisa;
Belardelli, Filippo;
Frati, Luigi;
Ferretti, Elisabetta;
Faggioni, Alberto;
Trivedi, Pankaj

Publication type:

Article

The Role of Motor System in Mental Rotation: New Insights from Myotonic Dystrophy Type 1.

Published in:

Journal of the International Neuropsychological Society, 2020, v. 26, n. 5, p. 492, doi. 10.1017/S1355617719001383

By:

Cona, Giorgia;
Casagrande, Arianna;
Lenzoni, Sabrina;
Pegoraro, Elena;
Bozzoni, Virginia;
Bello, Luca;
Sorarù, Gianni;
Botta, Annalisa;
Semenza, Carlo

Publication type:

Article

Workload measurement for molecular genetics laboratory: A survey study.

Published in:

PLoS ONE, 2018, v. 13, n. 11, p. 1, doi. 10.1371/journal.pone.0206855

By:

Tagliafico, Enrico;
Bernardis, Isabella;
Grasso, Marina;
D’Apice, Maria Rosaria;
Lapucci, Cristina;
Botta, Annalisa;
Giachino, Daniela Francesca;
Marinelli, Maria;
Primignani, Paola;
Russo, Silvia;
Sani, Ilaria;
Seia, Manuela;
Fini, Sergio;
Rimessi, Paola;
Tenedini, Elena;
Ravani, Anna;
Genuardi, Maurizio;
Ferlini, Alessandra;
null, null

Publication type:

Article

Cutaneous and metabolic defects associated with nuclear abnormalities in a transgenic mouse model expressing R527H lamin A mutation causing mandibuloacral dysplasia type A (MADA) syndrome.

Published in:

Acta Myologica, 2020, v. 39, n. 4, p. 320, doi. 10.36185/2532-1900-036

By:

Rosaria D'Apice, Maria;
De Dominicis, Angela;
Murdocca, Michela;
Amati, Francesca;
Botta, Annalisa;
Sangiuolo, Federica;
Lattanzi, Giovanna;
Federici, Massimo;
Novelli, Giuseppe

Publication type:

Article

Identification, molecular characterization and segregation analysis of a variant DMPK pre-mutation allele in a three-generation Italian family.

Published in:

Acta Myologica, 2020, v. 39, n. 1, p. 13, doi. 10.36185/2532-1900-002

By:

Fontana, Luana;
Santoro, Massimo;
D'Apice, Maria Rosaria;
Peluso, Francesca;
Gori, Giulia;
Morrone, Amelia;
Novelli, Giuseppe;
Dosa, Laura;
Botta, Annalisa

Publication type:

Article

Evidence for differential S100 gene over-expression in psoriatic patients from genetically heterogeneous pedigrees.

Published in:

Human Genetics, 2002, v. 111, n. 4/5, p. 310, doi. 10.1007/s00439-002-0812-5

By:

Semprini, Sabrina;
Capon, Francesca;
Tacconelli, Alessandra;
Giardina, Emiliano;
Orecchia, Angela;
Mingarelli, Rita;
Gobello, Tommaso;
Zambruno, Giovanna;
Botta, Annalisa;
Fabrizi, Giuseppe;
Novelli, Giuseppe

Publication type:

Article

The Role of PTX3 in Mineralization Processes and Aging-Related Bone Diseases.

Published in:

Frontiers in Immunology, 2021, v. 11, p. N.PAG, doi. 10.3389/fimmu.2020.622772

By:

Tarantino, Umberto;
Greggi, Chiara;
Cariati, Ida;
Visconti, Virginia Veronica;
Gasparini, Monica;
Cateni, Marco;
Gasbarra, Elena;
Botta, Annalisa;
Salustri, Antonietta;
Scimeca, Manuel

Publication type:

Article

Congenital heart disease in mice deficient for the DiGeorge syndrome region.

Published in:

Nature, 1999, v. 401, n. 6751, p. 379, doi. 10.1038/43903

By:

Lindsay, Elizabeth A.;
Botta, Annalisa;
Jurecic, Vesna;
Carattini-Rivera, Sandra;
Cheah, Yin-Chai;
Rosenblatt, Howard M.;
Bradley, Allan;
Baldini, Antonio

Publication type:

Article

Characterization of full-length CNBP expanded alleles in myotonic dystrophy type 2 patients by Cas9-mediated enrichment and nanopore sequencing.

Published in:

eLife, 2022, p. 1, doi. 10.7554/eLife.80229

By:

Alfano, Massimiliano;
De Antoni, Luca;
Centofanti, Federica;
Visconti, Virginia Veronica;
Maestri, Simone;
Esposti, Chiara Degli;
Massa, Roberto;
D'Apice, Maria Rosaria;
Novelli, Giuseppe;
Delledonne, Massimo;
Botta, Annalisa;
Rossato, Marzia

Publication type:

Article

TNNT2 Missplicing in Skeletal Muscle as a Cardiac Biomarker in Myotonic Dystrophy Type 1 but Not in Myotonic Dystrophy Type 2.

Published in:

Frontiers in Neurology, 2019, p. 1, doi. 10.3389/fneur.2019.00992

By:

Bosè, Francesca;
Renna, Laura Valentina;
Fossati, Barbara;
Arpa, Giovanni;
Labate, Valentina;
Milani, Valentina;
Botta, Annalisa;
Micaglio, Emanuele;
Meola, Giovanni;
Cardani, Rosanna

Publication type:

Article

Overexpression of CUGBP1 in Skeletal Muscle from Adult Classic Myotonic Dystrophy Type 1 but Not from Myotonic Dystrophy Type 2.

Published in:

PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0083777

By:

Cardani, Rosanna;
Bugiardini, Enrico;
Renna, Laura V.;
Rossi, Giulia;
Colombo, Graziano;
Valaperta, Rea;
Novelli, Giuseppe;
Botta, Annalisa;
Meola, Giovanni

Publication type:

Article

Overexpression of microRNA-206 in the skeletal muscle from myotonic dystrophy type 1 patients.

Published in:

2010

By:

Gambardella S;
Rinaldi F;
Lepore SM;
Viola A;
Loro E;
Angelini C;
Vergani L;
Novelli G;
Botta A;
Gambardella, Stefano;
Rinaldi, Fabrizio;
Lepore, Saverio M;
Viola, Antonella;
Loro, Emanuele;
Angelini, Corrado;
Vergani, Lodovica;
Novelli, Giuseppe;
Botta, Annalisa

Publication type:

journal article

Overexpression to microRNA-206 in the skeletal muscle from myotonic dystrophy type 1 patients.

Published in:

Journal of Translational Medicine, 2010, v. 8, p. 48, doi. 10.1186/1479-5876-8-48

By:

Gambardella, Stefano;
Rinaldi, Fabrizio;
Lepore, Saverio M.;
Viola, Antonella;
Loro, Emanuele;
Angelini, Corrado;
Vergani, Lodovica;
Novelli, Giuseppe;
Botta, Annalisa

Publication type:

Article

Functional characterization of the 5′ flanking region of human ubiquitin fusion degradation 1 like gene ( UFD1L).

Published in:

Cell Biochemistry & Function, 2002, v. 20, n. 2, p. 163, doi. 10.1002/cbf.966

By:

Amati, Francesca;
Conti, Emanuela;
Botta, Annalisa;
Amicucci, Paola;
Dallapiccola, Bruno;
Novelli, Giuseppe

Publication type:

Article

Activation of the interferon type I response rather than autophagy contributes to myogenesis inhibition in congenital DM1 myoblasts.

Published in:

Cell Death & Disease, 2018, v. 9, n. 11, p. 1, doi. 10.1038/s41419-018-1080-1

By:

Rizzo, Milena;
Beffy, Pascale;
Del Carratore, Renata;
Falleni, Alessandra;
Pretini, Virginia;
D’Aurizio, Romina;
Botta, Annalisa;
Evangelista, Monica;
Stoccoro, Andrea;
Coppedè, Fabio;
Furling, Denis;
Simili, Marcella

Publication type:

Article

Circulating MicroRNAs as Biomarkers of Osteoporosis and Fragility Fractures.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 8, p. 2267, doi. 10.1210/clinem/dgac293

By:

Ciuffi, Simone;
Marini, Francesca;
Fossi, Caterina;
Donati, Simone;
Giusti, Francesca;
Botta, Annalisa;
Masi, Laura;
Isaia, Giancarlo;
Marcocci, Claudio;
Migliaccio, Silvia;
Minisola, Salvatore;
Nuti, Ranuccio;
Tarantino, Umberto;
Iantomasi, Teresa;
Brandi, Maria Luisa

Publication type:

Article