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Morphological and functional analyses of skeletal muscles from an immunodeficient animal model of limb-girdle muscular dystrophy type 2E.

Muscle & nerve

Giovannelli G, Giacomazzi G, Grosemans H, Sampaolesi M.
PMID: 29476695
Muscle Nerve. 2018 Feb 24; doi: 10.1002/mus.26112. Epub 2018 Feb 24.

INTRODUCTION: Limb-girdle muscular dystrophy type 2E (LGMD2E) is caused by mutations in the β-sarcoglycan gene, which is expressed in skeletal, cardiac, and smooth muscles. β-Sarcoglycan-deficient (Sgcb-null) mice develop severe muscular dystrophy and cardiomyopathy with focal areas of necrosis.METHODS: In...

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Giovannelli G, Giacomazzi G, Grosemans H, et al. Morphological and functional analyses of skeletal muscles from an immunodeficient animal model of limb-girdle muscular dystrophy type 2E. Muscle Nerve. 2018;doi: 10.1002/mus.26112.
Giovannelli, G., Giacomazzi, G., Grosemans, H., & Sampaolesi, M. (2018). Morphological and functional analyses of skeletal muscles from an immunodeficient animal model of limb-girdle muscular dystrophy type 2E. Muscle & nerve, . https://doi.org/10.1002/mus.26112
Giovannelli, Gaia, et al. "Morphological and functional analyses of skeletal muscles from an immunodeficient animal model of limb-girdle muscular dystrophy type 2E." Muscle & nerve vol. (2018). doi: https://doi.org/10.1002/mus.26112
Giovannelli G, Giacomazzi G, Grosemans H, Sampaolesi M. Morphological and functional analyses of skeletal muscles from an immunodeficient animal model of limb-girdle muscular dystrophy type 2E. Muscle Nerve. 2018 Feb 24; doi: 10.1002/mus.26112. Epub 2018 Feb 24. PMID: 29476695; PMCID: PMC6099247.
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Exploring Wound-Healing Genomic Machinery with a Network-Based Approach.

Pharmaceuticals (Basel, Switzerland)

Vitali F, Marini S, Balli M, Grosemans H, Sampaolesi M, Lussier YA, Cusella De Angelis MG, Bellazzi R.
PMID: 28635674
Pharmaceuticals (Basel). 2017 Jun 21;10(2). doi: 10.3390/ph10020055.

The molecular mechanisms underlying tissue regeneration and wound healing are still poorly understood despite their importance. In this paper we develop a bioinformatics approach, combining biology and network theory to drive experiments for better understanding the genetic underpinnings of...

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Vitali F, Marini S, Balli M, et al. Exploring Wound-Healing Genomic Machinery with a Network-Based Approach. Pharmaceuticals (Basel). 2017;10(2)doi: 10.3390/ph10020055.
Vitali, F., Marini, S., Balli, M., Grosemans, H., Sampaolesi, M., Lussier, Y. A., Cusella De Angelis, M. G., & Bellazzi, R. (2017). Exploring Wound-Healing Genomic Machinery with a Network-Based Approach. Pharmaceuticals (Basel, Switzerland), 10(2), . https://doi.org/10.3390/ph10020055
Vitali, Francesca, et al. "Exploring Wound-Healing Genomic Machinery with a Network-Based Approach." Pharmaceuticals (Basel, Switzerland) vol. 10,2 (2017). doi: https://doi.org/10.3390/ph10020055
Vitali F, Marini S, Balli M, Grosemans H, Sampaolesi M, Lussier YA, Cusella De Angelis MG, Bellazzi R. Exploring Wound-Healing Genomic Machinery with a Network-Based Approach. Pharmaceuticals (Basel). 2017 Jun 21;10(2). doi: 10.3390/ph10020055. PMID: 28635674; PMCID: PMC5490412.
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Cardiac Niche Influences the Direct Reprogramming of Canine Fibroblasts into Cardiomyocyte-Like Cells.

Stem cells international

Palazzolo G, Quattrocelli M, Toelen J, Dominici R, Anastasia L, Tettamenti G, Barthelemy I, Blot S, Gijsbers R, Cassano M, Sampaolesi M.
PMID: 26681949
Stem Cells Int. 2016;2016:4969430. doi: 10.1155/2016/4969430. Epub 2015 Nov 23.

The Duchenne and Becker muscular dystrophies are caused by mutation of dystrophin gene and primarily affect skeletal and cardiac muscles. Cardiac involvement in dystrophic GRMD dogs has been demonstrated by electrocardiographic studies with the onset of a progressive cardiomyopathy...

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Palazzolo G, Quattrocelli M, Toelen J, et al. Cardiac Niche Influences the Direct Reprogramming of Canine Fibroblasts into Cardiomyocyte-Like Cells. Stem Cells Int. 2015;2016:4969430doi: 10.1155/2016/4969430.
Palazzolo, G., Quattrocelli, M., Toelen, J., Dominici, R., Anastasia, L., Tettamenti, G., Barthelemy, I., Blot, S., Gijsbers, R., Cassano, M., & Sampaolesi, M. (2016). Cardiac Niche Influences the Direct Reprogramming of Canine Fibroblasts into Cardiomyocyte-Like Cells. Stem cells international, 20164969430. https://doi.org/10.1155/2016/4969430
Palazzolo, Giacomo, et al. "Cardiac Niche Influences the Direct Reprogramming of Canine Fibroblasts into Cardiomyocyte-Like Cells." Stem cells international vol. 2016 (2016): 4969430. doi: https://doi.org/10.1155/2016/4969430
Palazzolo G, Quattrocelli M, Toelen J, Dominici R, Anastasia L, Tettamenti G, Barthelemy I, Blot S, Gijsbers R, Cassano M, Sampaolesi M. Cardiac Niche Influences the Direct Reprogramming of Canine Fibroblasts into Cardiomyocyte-Like Cells. Stem Cells Int. 2016;2016:4969430. doi: 10.1155/2016/4969430. Epub 2015 Nov 23. PMID: 26681949; PMCID: PMC4670879.
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Generation and selection of anti-flagellin monoclonal antibodies useful for serotyping Salmonella enterica.

SpringerPlus

Hiriart Y, Serradell M, Martínez A, Sampaolesi S, Maciel DG, Chabalgoity JA, Yim L, Algorta G, Rumbo M.
PMID: 24349948
Springerplus. 2013 Nov 28;2:640. doi: 10.1186/2193-1801-2-640. eCollection 2013.

In developing countries, bacterial acute gastroenteritis continues to be an important cause of morbidity and mortality among young children. Salmonellosis constitutes a major cause of infectious enteritis worldwide, most of them associated to the consumption of contaminated food products....

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Hiriart Y, Serradell M, Martínez A, et al. Generation and selection of anti-flagellin monoclonal antibodies useful for serotyping Salmonella enterica. Springerplus. 2013;2:640doi: 10.1186/2193-1801-2-640.
Hiriart, Y., Serradell, M., Martínez, A., Sampaolesi, S., Maciel, D. G., Chabalgoity, J. A., Yim, L., Algorta, G., & Rumbo, M. (2013). Generation and selection of anti-flagellin monoclonal antibodies useful for serotyping Salmonella enterica. SpringerPlus, 2640. https://doi.org/10.1186/2193-1801-2-640
Hiriart, Yanina, et al. "Generation and selection of anti-flagellin monoclonal antibodies useful for serotyping Salmonella enterica." SpringerPlus vol. 2 (2013): 640. doi: https://doi.org/10.1186/2193-1801-2-640
Hiriart Y, Serradell M, Martínez A, Sampaolesi S, Maciel DG, Chabalgoity JA, Yim L, Algorta G, Rumbo M. Generation and selection of anti-flagellin monoclonal antibodies useful for serotyping Salmonella enterica. Springerplus. 2013 Nov 28;2:640. doi: 10.1186/2193-1801-2-640. eCollection 2013. PMID: 24349948; PMCID: PMC3862864.
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Myogenic potential of canine craniofacial satellite cells.

Frontiers in aging neuroscience

La Rovere RM, Quattrocelli M, Pietrangelo T, Di Filippo ES, Maccatrozzo L, Cassano M, Mascarello F, Barthélémy I, Blot S, Sampaolesi M, Fulle S.
PMID: 24860499
Front Aging Neurosci. 2014 May 13;6:90. doi: 10.3389/fnagi.2014.00090. eCollection 2014.

The skeletal fibers have different embryological origin; the extraocular and jaw-closer muscles develop from prechordal mesoderm while the limb and trunk muscles from somites. These different origins characterize also the adult muscle stem cells, known as satellite cells (SCs)...

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La Rovere RM, Quattrocelli M, Pietrangelo T, et al. Myogenic potential of canine craniofacial satellite cells. Front Aging Neurosci. 2014;6:90doi: 10.3389/fnagi.2014.00090.
La Rovere, R. M., Quattrocelli, M., Pietrangelo, T., Di Filippo, E. S., Maccatrozzo, L., Cassano, M., Mascarello, F., Barthélémy, I., Blot, S., Sampaolesi, M., & Fulle, S. (2014). Myogenic potential of canine craniofacial satellite cells. Frontiers in aging neuroscience, 690. https://doi.org/10.3389/fnagi.2014.00090
La Rovere, Rita Maria Laura, et al. "Myogenic potential of canine craniofacial satellite cells." Frontiers in aging neuroscience vol. 6 (2014): 90. doi: https://doi.org/10.3389/fnagi.2014.00090
La Rovere RM, Quattrocelli M, Pietrangelo T, Di Filippo ES, Maccatrozzo L, Cassano M, Mascarello F, Barthélémy I, Blot S, Sampaolesi M, Fulle S. Myogenic potential of canine craniofacial satellite cells. Front Aging Neurosci. 2014 May 13;6:90. doi: 10.3389/fnagi.2014.00090. eCollection 2014. PMID: 24860499; PMCID: PMC4026742.
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Development of a New Tool for 3D Modeling for Regenerative Medicine.

International journal of biomedical imaging

Mattoli F, Tiribuzi R, D'Angelo F, di Girolamo I, Quattrocelli M, Montesano S, Crispoltoni L, Oikonomou V, Cusella De Angelis MG, Marconi P, Orlacchio A, Sampaolesi M, Martino S, Orlacchio A.
PMID: 21776249
Int J Biomed Imaging. 2011;2011:236854. doi: 10.1155/2011/236854. Epub 2011 Jun 13.

The effectiveness of therapeutic treatment based on regenerative medicine for degenerative diseases (i.e., neurodegenerative or cardiac diseases) requires tools allowing the visualization and analysis of the three-dimensional (3D) distribution of target drugs within the tissue. Here, we present a...

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Mattoli F, Tiribuzi R, D'Angelo F, et al. Development of a New Tool for 3D Modeling for Regenerative Medicine. Int J Biomed Imaging. 2011;2011:236854doi: 10.1155/2011/236854.
Mattoli, F., Tiribuzi, R., D'Angelo, F., di Girolamo, I., Quattrocelli, M., Montesano, S., Crispoltoni, L., Oikonomou, V., Cusella De Angelis, M. G., Marconi, P., Orlacchio, A., Sampaolesi, M., Martino, S., & Orlacchio, A. (2011). Development of a New Tool for 3D Modeling for Regenerative Medicine. International journal of biomedical imaging, 2011236854. https://doi.org/10.1155/2011/236854
Mattoli, Filippo, et al. "Development of a New Tool for 3D Modeling for Regenerative Medicine." International journal of biomedical imaging vol. 2011 (2011): 236854. doi: https://doi.org/10.1155/2011/236854
Mattoli F, Tiribuzi R, D'Angelo F, di Girolamo I, Quattrocelli M, Montesano S, Crispoltoni L, Oikonomou V, Cusella De Angelis MG, Marconi P, Orlacchio A, Sampaolesi M, Martino S, Orlacchio A. Development of a New Tool for 3D Modeling for Regenerative Medicine. Int J Biomed Imaging. 2011;2011:236854. doi: 10.1155/2011/236854. Epub 2011 Jun 13. PMID: 21776249; PMCID: PMC3132439.
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Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs.

Nature

Sampaolesi M, Blot S, D'Antona G, Granger N, Tonlorenzi R, Innocenzi A, Mognol P, Thibaud JL, Galvez BG, Barthélémy I, Perani L, Mantero S, Guttinger M, Pansarasa O, Rinaldi C, De Angelis MG, Torrente Y, Bordignon C, Bottinelli R, Cossu G.
PMID: 23426261
Nature. 2013 Feb 20;494(7438):506. doi: 10.1038/nature11976. Epub 2013 Feb 20.

No abstract available.

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Sampaolesi M, Blot S, D'Antona G, et al. Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs. Nature. 2013;494(7438):506doi: 10.1038/nature11976.
Sampaolesi, M., Blot, S., D'Antona, G., Granger, N., Tonlorenzi, R., Innocenzi, A., Mognol, P., Thibaud, J. L., Galvez, B. G., Barthélémy, I., Perani, L., Mantero, S., Guttinger, M., Pansarasa, O., Rinaldi, C., De Angelis, M. G., Torrente, Y., Bordignon, C., Bottinelli, R., & Cossu, G. (2013). Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs. Nature, 494(7438), 506. https://doi.org/10.1038/nature11976
Sampaolesi, Maurilio, et al. "Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs." Nature vol. 494,7438 (2013): 506. doi: https://doi.org/10.1038/nature11976
Sampaolesi M, Blot S, D'Antona G, Granger N, Tonlorenzi R, Innocenzi A, Mognol P, Thibaud JL, Galvez BG, Barthélémy I, Perani L, Mantero S, Guttinger M, Pansarasa O, Rinaldi C, De Angelis MG, Torrente Y, Bordignon C, Bottinelli R, Cossu G. Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs. Nature. 2013 Feb 20;494(7438):506. doi: 10.1038/nature11976. Epub 2013 Feb 20. PMID: 23426261.
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Activin A Modulates CRIPTO-1/HNF4.

Stem cells international

Duelen R, Gilbert G, Patel A, de Schaetzen N, De Waele L, Roderick L, Sipido KR, Verfaillie CM, Buyse GM, Thorrez L, Sampaolesi M.
PMID: 28163723
Stem Cells Int. 2017;2017:4651238. doi: 10.1155/2017/4651238. Epub 2017 Jan 09.

The use of human pluripotent stem cells in basic and translational cardiac research requires efficient differentiation protocols towards cardiomyocytes. In vitro differentiation yields heterogeneous populations of ventricular-, atrial-, and nodal-like cells hindering their potential applications in regenerative therapies. We...

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Duelen R, Gilbert G, Patel A, et al. Activin A Modulates CRIPTO-1/HNF4. Stem Cells Int. 2017;2017:4651238doi: 10.1155/2017/4651238.
Duelen, R., Gilbert, G., Patel, A., de Schaetzen, N., De Waele, L., Roderick, L., Sipido, K. R., Verfaillie, C. M., Buyse, G. M., Thorrez, L., & Sampaolesi, M. (2017). Activin A Modulates CRIPTO-1/HNF4. Stem cells international, 20174651238. https://doi.org/10.1155/2017/4651238
Duelen, Robin, et al. "Activin A Modulates CRIPTO-1/HNF4." Stem cells international vol. 2017 (2017): 4651238. doi: https://doi.org/10.1155/2017/4651238
Duelen R, Gilbert G, Patel A, de Schaetzen N, De Waele L, Roderick L, Sipido KR, Verfaillie CM, Buyse GM, Thorrez L, Sampaolesi M. Activin A Modulates CRIPTO-1/HNF4. Stem Cells Int. 2017;2017:4651238. doi: 10.1155/2017/4651238. Epub 2017 Jan 09. PMID: 28163723; PMCID: PMC5253508.
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Gender Differences and Outcomes in Melanoma Patients.

Oncology and therapy

Morgese F, Sampaolesi C, Torniai M, Conti A, Ranallo N, Giacchetti A, Serresi S, Onofri A, Burattini M, Ricotti G, Berardi R.
PMID: 32700073
Oncol Ther. 2020 Jun;8(1):103-114. doi: 10.1007/s40487-020-00109-1. Epub 2020 Feb 04.

INTRODUCTION: Melanoma is one of the most common cancers in younger people. The incidence of cutaneous melanoma is increasing in patients of both sexes, with female patients generally living longer than their male counterparts. The aim of this retrospective...

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Morgese F, Sampaolesi C, Torniai M, et al. Gender Differences and Outcomes in Melanoma Patients. Oncol Ther. 2020;8(1):103-114doi: 10.1007/s40487-020-00109-1.
Morgese, F., Sampaolesi, C., Torniai, M., Conti, A., Ranallo, N., Giacchetti, A., Serresi, S., Onofri, A., Burattini, M., Ricotti, G., & Berardi, R. (2020). Gender Differences and Outcomes in Melanoma Patients. Oncology and therapy, 8(1), 103-114. https://doi.org/10.1007/s40487-020-00109-1
Morgese, Francesca, et al. "Gender Differences and Outcomes in Melanoma Patients." Oncology and therapy vol. 8,1 (2020): 103-114. doi: https://doi.org/10.1007/s40487-020-00109-1
Morgese F, Sampaolesi C, Torniai M, Conti A, Ranallo N, Giacchetti A, Serresi S, Onofri A, Burattini M, Ricotti G, Berardi R. Gender Differences and Outcomes in Melanoma Patients. Oncol Ther. 2020 Jun;8(1):103-114. doi: 10.1007/s40487-020-00109-1. Epub 2020 Feb 04. PMID: 32700073; PMCID: PMC7359998.
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Cytoprotective Effects of Punicalagin on Hydrogen-Peroxide-Mediated Oxidative Stress and Mitochondrial Dysfunction in Retinal Pigment Epithelium Cells.

Antioxidants (Basel, Switzerland)

Clementi ME, Maulucci G, Bianchetti G, Pizzoferrato M, Sampaolese B, Tringali G.
PMID: 33572785
Antioxidants (Basel). 2021 Jan 29;10(2). doi: 10.3390/antiox10020192.

The retinal pigment epithelium (RPE) is a densely pigmented, monostratified epithelium that provides metabolic and functional support to the outer segments of photoreceptors. Endogenous or exogenous oxidative stimuli determine a switch from physiological to pathological conditions, characterized by an...

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Clementi ME, Maulucci G, Bianchetti G, et al. Cytoprotective Effects of Punicalagin on Hydrogen-Peroxide-Mediated Oxidative Stress and Mitochondrial Dysfunction in Retinal Pigment Epithelium Cells. Antioxidants (Basel). 2021;10(2)doi: 10.3390/antiox10020192.
Clementi, M. E., Maulucci, G., Bianchetti, G., Pizzoferrato, M., Sampaolese, B., & Tringali, G. (2021). Cytoprotective Effects of Punicalagin on Hydrogen-Peroxide-Mediated Oxidative Stress and Mitochondrial Dysfunction in Retinal Pigment Epithelium Cells. Antioxidants (Basel, Switzerland), 10(2), . https://doi.org/10.3390/antiox10020192
Clementi, Maria Elisabetta, et al. "Cytoprotective Effects of Punicalagin on Hydrogen-Peroxide-Mediated Oxidative Stress and Mitochondrial Dysfunction in Retinal Pigment Epithelium Cells." Antioxidants (Basel, Switzerland) vol. 10,2 (2021). doi: https://doi.org/10.3390/antiox10020192
Clementi ME, Maulucci G, Bianchetti G, Pizzoferrato M, Sampaolese B, Tringali G. Cytoprotective Effects of Punicalagin on Hydrogen-Peroxide-Mediated Oxidative Stress and Mitochondrial Dysfunction in Retinal Pigment Epithelium Cells. Antioxidants (Basel). 2021 Jan 29;10(2). doi: 10.3390/antiox10020192. PMID: 33572785; PMCID: PMC7911437.
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Tocilizumab or glucocorticoids treatment for patients with SARS-CoV-2 pneumonia: An observational study.

The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases

Dolci G, Cassone G, Besutti G, Corsini R, Sampaolesi F, Iotti V, Galli E, Palermo A, Fontana M, Mancuso P.
PMID: 34963560
Braz J Infect Dis. 2021 Dec 21;101702. doi: 10.1016/j.bjid.2021.101702. Epub 2021 Dec 21.

OBJECTIVE: To estimate the effect of tocilizumab or glucocorticoids in preventing death and intubation in patients hospitalized with SARS-CoV-2 pneumonia.METHODS: This was a retrospective cohort study enrolling all consecutive patients hospitalized at Reggio Emilia AUSL between February the 11RESULTS...

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Dolci G, Cassone G, Besutti G, et al. Tocilizumab or glucocorticoids treatment for patients with SARS-CoV-2 pneumonia: An observational study. Braz J Infect Dis. 2021;101702doi: 10.1016/j.bjid.2021.101702.
Dolci, G., Cassone, G., Besutti, G., Corsini, R., Sampaolesi, F., Iotti, V., Galli, E., Palermo, A., Fontana, M., Mancuso, P. (2021). Tocilizumab or glucocorticoids treatment for patients with SARS-CoV-2 pneumonia: An observational study. The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases, 101702. https://doi.org/10.1016/j.bjid.2021.101702
Dolci, Giovanni, et al. "Tocilizumab or glucocorticoids treatment for patients with SARS-CoV-2 pneumonia: An observational study." The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases vol. (2021): 101702. doi: https://doi.org/10.1016/j.bjid.2021.101702
Dolci G, Cassone G, Besutti G, Corsini R, Sampaolesi F, Iotti V, Galli E, Palermo A, Fontana M, Mancuso P. Tocilizumab or glucocorticoids treatment for patients with SARS-CoV-2 pneumonia: An observational study. Braz J Infect Dis. 2021 Dec 21;101702. doi: 10.1016/j.bjid.2021.101702. Epub 2021 Dec 21. PMID: 34963560; PMCID: PMC8687752.
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Upregulation of miR181a/miR212 Improves Myogenic Commitment in Murine Fusion-Negative Rhabdomyosarcoma.

Frontiers in physiology

Pozzo E, Giarratana N, Sassi G, Elmastas M, Killian T, Wang CC, Marini V, Ronzoni F, Yustein J, Uyttebroeck A, Sampaolesi M.
PMID: 34421639
Front Physiol. 2021 Aug 06;12:701354. doi: 10.3389/fphys.2021.701354. eCollection 2021.

Fusion-negative rhabdomyosarcoma (FN-RMS) is the most common soft tissue sarcoma of childhood arising from undifferentiated skeletal muscle cells from uncertain origin. Currently used therapies are poorly tumor-specific and fail to tackle the molecular machinery underlying the tumorigenicity and uncontrolled...

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Pozzo E, Giarratana N, Sassi G, et al. Upregulation of miR181a/miR212 Improves Myogenic Commitment in Murine Fusion-Negative Rhabdomyosarcoma. Front Physiol. 2021;12:701354doi: 10.3389/fphys.2021.701354.
Pozzo, E., Giarratana, N., Sassi, G., Elmastas, M., Killian, T., Wang, C. C., Marini, V., Ronzoni, F., Yustein, J., Uyttebroeck, A., & Sampaolesi, M. (2021). Upregulation of miR181a/miR212 Improves Myogenic Commitment in Murine Fusion-Negative Rhabdomyosarcoma. Frontiers in physiology, 12701354. https://doi.org/10.3389/fphys.2021.701354
Pozzo, Enrico, et al. "Upregulation of miR181a/miR212 Improves Myogenic Commitment in Murine Fusion-Negative Rhabdomyosarcoma." Frontiers in physiology vol. 12 (2021): 701354. doi: https://doi.org/10.3389/fphys.2021.701354
Pozzo E, Giarratana N, Sassi G, Elmastas M, Killian T, Wang CC, Marini V, Ronzoni F, Yustein J, Uyttebroeck A, Sampaolesi M. Upregulation of miR181a/miR212 Improves Myogenic Commitment in Murine Fusion-Negative Rhabdomyosarcoma. Front Physiol. 2021 Aug 06;12:701354. doi: 10.3389/fphys.2021.701354. eCollection 2021. PMID: 34421639; PMCID: PMC8378536.
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