Zobrazeno 1 - 10
of 136
pro vyhledávání: '"José Bragança"'
Autor:
Mohammad Mehdi Heidari, Mehri Khatami, Akram Kamalipour, Mustafa Kalantari, Mahsa Movahed, Mohammad Hayet Emmamy, Mehdi Hadadzadeh, José Bragança, Mohsen Namnabat, Bahareh Mazrouei
Publikováno v:
EXCLI Journal : Experimental and Clinical Sciences, Vol 21, Pp 1306-1330 (2022)
Most studies aiming at unraveling the molecular events associated with cardiac congenital heart disease (CHD) have focused on the effect of mutations occurring in the nuclear genome. In recent years, a significant role has been attributed to mitochon
Externí odkaz:
https://doaj.org/article/9b7d30ec94a346bfaa0661d7f4b899df
Autor:
José Bragança, Sónia Figueiredo, Carla Alexandra Rego, Filomena dos Reis Conceição, Saúl Neves de Jesus
Publikováno v:
BioChem, Vol 2, Iss 1, Pp 93-103 (2022)
Researchers at Universities generate and convey the knowledge acquired through communications in specialized (inter)national journals and congresses. An effort to share the scientific achievements with the general public is extremely important. For t
Externí odkaz:
https://doaj.org/article/d7438a702e4a48158f153998d7de55d7
Autor:
Mónica T. Fernandes, Victor Yassuda, José Bragança, Wolfgang Link, Bibiana I. Ferreira, Ana Luísa De Sousa-Coelho
Publikováno v:
Gastrointestinal Disorders, Vol 3, Iss 4, Pp 218-236 (2021)
Colorectal cancer (CRC) is the third most common cancer and the second leading cause of death due to cancer in the world. Therefore, the identification of novel druggable targets is urgently needed. Tribbles proteins belong to a pseudokinase family,
Externí odkaz:
https://doaj.org/article/4b7eddd73718442fb80be4be470c2766
Autor:
Cátia D. Correia, Anita Ferreira, Mónica T. Fernandes, Bárbara M. Silva, Filipa Esteves, Helena S. Leitão, José Bragança, Sofia M. Calado
Publikováno v:
Cells, Vol 12, Iss 13, p 1727 (2023)
Cardiovascular diseases (CVDs) are pointed out by the World Health Organization (WHO) as the leading cause of death, contributing to a significant and growing global health and economic burden. Despite advancements in clinical approaches, there is a
Externí odkaz:
https://doaj.org/article/bb134f253db54345ac35519a3a72a601
Autor:
Anabela Malho Guedes, Roberto Calças Marques, Brigitte Ribeiro, Mónica T. Fernandes, Marília Faísca, Ana Paula Silva, José Bragança, Anabela Rodrigues
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Peritoneal protein loss (PPL) has been correlated with mortality, malnutrition and inflammation. More recently overhydration was brought to the equation. This study aims to review classic and recent factors associated with PPL. Prevalent and incident
Externí odkaz:
https://doaj.org/article/06a0e40e90504dbbbc19e85cbf017179
Publikováno v:
Stem Cell Research, Vol 55, Iss , Pp 102462- (2021)
Left Ventricular Noncompaction Cardiomyopathy (LVNC) is characterized by abnormal number and prominence of trabeculations of the left ventricle of the heart. Although LVNC has been associated with mutations in several genes encoding for transcription
Externí odkaz:
https://doaj.org/article/66ce82d9d2404321b55cf9f86ba0bbf2
Autor:
Sofia M. Calado, Dina Bento, David Justino, Leonardo Mendes-Silva, Nuno Marques, José Bragança
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102302- (2021)
Left Ventricular Noncompaction Cardiomyopathy (LVNC) is characterized by excessive trabeculation of the left ventricle. To date, mutations in more than 40 genes have been associated with LVNC, however the exact mechanisms underlying the disease remai
Externí odkaz:
https://doaj.org/article/dfda4fcf8c6e47888841752b46f567b0
Publikováno v:
Stem Cell Research, Vol 45, Iss , Pp - (2020)
Fabry Disease (FD) is a multisystemic X-linked disorder that belongs to the group of lysosomal storage disorders (LSDs). Causal mutations on alpha-galactosidase A (α-Gal A) commonly lead to abnormal protein and consequently to FD. Since it is an X-l
Externí odkaz:
https://doaj.org/article/34a55bcc820b4ad0b3b3e9669c052f97
Publikováno v:
Stem Cell Research, Vol 41, Iss , Pp - (2019)
Gaucher Disease (GD) type 3 is a neurological form of a multisystemic autosomal recessive disorder belonging to the group of lysosomal storage diseases. Causal mutations in the glucocerebrosidase 1 (GBA1) commonly lead to abnormal protein and GD, het
Externí odkaz:
https://doaj.org/article/07d9889b90434447a9d672045d0a04dd
Autor:
Sara Xapelli, Fabienne Agasse, Laura Sardà-Arroyo, Liliana Bernardino, Tiago Santos, Filipa F Ribeiro, Jorge Valero, José Bragança, Clarissa Schitine, Ricardo A de Melo Reis, Ana M Sebastião, João O Malva
Publikováno v:
PLoS ONE, Vol 8, Iss 5, p e63529 (2013)
The endocannabinoid system has been implicated in the modulation of adult neurogenesis. Here, we describe the effect of type 1 cannabinoid receptor (CB1R) activation on self-renewal, proliferation and neuronal differentiation in mouse neonatal subven
Externí odkaz:
https://doaj.org/article/204615273e6c44b1a58e63b392407849