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Histamine induces ATP release from human subcutaneous fibroblasts via pannexin-...

Pinheiro, Ana Rita; Paramos-de-Carvalho, Diogo; Certal, Mariana; Costa, M. Adelina; Costa, Cristina; Magalhães-Cardoso, Maria Teresa

Changes in the regulation of connective tissue ATP-mediated mechano-transduction and remodeling may be an important link to the pathogenesis of chronic pain. It has been demonstrated that mast cell-derived histamine plays an important role in painful fibrotic diseases. Here we analyzed the involvement of ATP in the response of human subcutaneous fibroblasts to histamine. Acute histamine application caused a ris...


Bradykinin-induced Ca2+ signaling in human subcutaneous fibroblasts involves AT...

Pinheiro, Ana Rita; Paramos-de-Carvalho, Diogo; Certal, Mariana; Costa, Cristina; Magalhães-Cardoso, Maria Teresa; Ferreirinha, Fátima

Background: Chronic musculoskeletal pain involves connective tissue remodeling triggered by inflammatory mediators, such as bradykinin. Fibroblast cells signaling involve changes in intracellular Ca2+ ([Ca2+]i). ATP has been related to connective tissue mechanotransduction, remodeling and chronic inflammatory pain, via P2 purinoceptors activation. Here, we investigated the involvement of ATP in bradykinin-induc...


Ataxias espinocerebelares em 114 famílias do sul do Brasil : achados clínicos e...

Kieling, Christian Costa; Trott, Alexis; Jardim, Laura Bannach; Wanderley, Héctor Yuri Conti; Ludwig, Henrique Tschoepke; Saute, Jonas Alex Morales

Data: 2008   |   Origem: OASIS br

Molecular diagnosis of Huntington disease in Portugal : implications for geneti...

Costa, Maria do Carmo; Magalhães, Paula; Ferreirinha, Fátima; Guimarães, Laura; Januário, Cristina; Gaspar, Isabel; Loureiro, Leal; Vale, José

Huntington disease (HD) is a eurodegenerative, autosomal dominant disorder of late-onset, caused by the expansion of a CAG repeat in the coding region of the gene. Ours is the reference laboratory for genetic testing in HD, in Portugal, since 1998; 90.1% of all 158 families known were identified for the first time, including patients with unusual presentation or without family history. A total of 338 genetic te...


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Fundação para a Ciência e a Tecnologia Universidade do Minho   Governo Português Ministério da Educação e Ciência Programa Operacional da Sociedade do Conhecimento União Europeia