Zobrazeno 1 - 10
of 94
pro vyhledávání: '"Venturini, A."'
Autor:
Mariana Lima Mascarenhas Moreira, Iana Mizumukai de Araújo, Sandra Yasuyo Fukada, Lucas Gabriel R. Venturini, Natalia Rossin Guidorizzi, Carlos Ernesto Garrido, Clifford J. Rosen, Francisco José Albuquerque de Paula
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 17, p 13118 (2023)
Familial partial lipodystrophies (FPLD) are rare diseases characterized by selective loss of subcutaneous adipose tissue at different sites. This cross-sectional observational study aimed to estimate adipose tissue in the bone marrow (BMAT), intra (I
Externí odkaz:
https://doaj.org/article/0c462a56c6884b8980899f3a765f06cb
Autor:
Lucia Giuli, Maria Pallozzi, Giulia Venturini, Antonio Gasbarrini, Francesca Romana Ponziani, Francesco Santopaolo
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 16, p 12754 (2023)
Vascular liver disorders (VLDs) comprise a wide spectrum of clinical-pathological entities that primarily affect the hepatic vascular system of both cirrhotic and non-cirrhotic patients. VLDs more frequently involve the portal and the hepatic veins,
Externí odkaz:
https://doaj.org/article/78c38ab0549349efa8cc6ea732da8307
Autor:
Cayo, Angel1,2 (AUTHOR) acayo@utalca.cl, Venturini, Whitney1,2 (AUTHOR) whitneyventurini@gmail.com, Rebolledo-Mira, Danitza1 (AUTHOR) danitza.rebolledo.ibi@gmail.com, Moore-Carrasco, Rodrigo3 (AUTHOR) rmoore@utalca.cl, Herrada, Andrés A.4 (AUTHOR) andres.herrada@uautonoma.cl, Nova-Lamperti, Estefanía5 (AUTHOR) e.novalamperti@udec.cl, Valenzuela, Claudio1 (AUTHOR) cvalenzuela@utalca.cl, Brown, Nelson E.1 (AUTHOR) cvalenzuela@utalca.cl
Publikováno v:
International Journal of Molecular Sciences. Jun2023, Vol. 24 Issue 11, p9284. 25p.
Autor:
Angel Cayo, Whitney Venturini, Danitza Rebolledo-Mira, Rodrigo Moore-Carrasco, Andrés A. Herrada, Estefanía Nova-Lamperti, Claudio Valenzuela, Nelson E. Brown
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 11, p 9284 (2023)
Despite not dividing, senescent cells acquire the ability to synthesize and secrete a plethora of bioactive molecules, a feature known as the senescence-associated secretory phenotype (SASP). In addition, senescent cells often upregulate autophagy, a
Externí odkaz:
https://doaj.org/article/9563503ffa3e498d91b2483f6abb91d6
Autor:
Jarrod Moore, Jourdan Ewoldt, Gabriela Venturini, Alexandre C. Pereira, Kallyandra Padilha, Matthew Lawton, Weiwei Lin, Raghuveera Goel, Ivan Luptak, Valentina Perissi, Christine E. Seidman, Jonathan Seidman, Michael T. Chin, Christopher Chen, Andrew Emili
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 5, p 4724 (2023)
Hypertrophic cardiomyopathy is one of the most common inherited cardiomyopathies and a leading cause of sudden cardiac death in young adults. Despite profound insights into the genetics, there is imperfect correlation between mutation and clinical pr
Externí odkaz:
https://doaj.org/article/2a6cfd74d9464280bef49900c0d54644
Autor:
Daniele Lavacchi, Giandomenico Roviello, Alessia Guidolin, Silvia Romano, Jacopo Venturini, Enrico Caliman, Agnese Vannini, Elisa Giommoni, Elisa Pellegrini, Marco Brugia, Serena Pillozzi, Lorenzo Antonuzzo
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 6, p 5840 (2023)
The management of patients with metastatic colorectal cancer (mCRC) has the continuum of care as the treatment paradigm. To date, trifluridine/tipiracil, a biochemically modulated fluoropyrimidine, and regorafenib, a multi-kinase inhibitor, remain th
Externí odkaz:
https://doaj.org/article/1ea5422ad7d94ae08facba6e673419bb
Autor:
Michela Casanova, Francesca Pontis, Patrizia Ghidotti, Ilaria Petraroia, Lara Veronica Venturini, Luca Bergamaschi, Stefano Chiaravalli, Loris De Cecco, Maura Massimino, Gabriella Sozzi, Andrea Ferrari, Orazio Fortunato, Patrizia Gasparini
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 22, p 13989 (2022)
Adolescents and young adults (AYA) with rhabdomyosarcoma (RMS) form a subgroup of patients whose optimal clinical management and best possible access to care remain a challenge and whose survival rates lag behind that of children diagnosed with histo
Externí odkaz:
https://doaj.org/article/c8a2bf4286f84afa8c838975129da332
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Akademický článek
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Autor:
Arianna Venturini, Anna Borrelli, Ilaria Musante, Paolo Scudieri, Valeria Capurro, Mario Renda, Nicoletta Pedemonte, Luis J. V. Galietta
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 21, p 11972 (2021)
Cystic fibrosis (CF) is caused by loss of function of the CFTR chloride channel. A substantial number of CF patients carry nonsense mutations in the CFTR gene. These patients cannot directly benefit from pharmacological correctors and potentiators th
Externí odkaz:
https://doaj.org/article/90cee40555d5412c8ee9842eafddf790