Zobrazeno 1 - 10
of 42
pro vyhledávání: '"I Seixas"'
Publikováno v:
Acta Médica Portuguesa, Vol 11, Iss 1 (1998)
The thoracic outlet syndrome is a changeable clinical syndrome caused by compression of the neurovascular bundle of the upper extremity, within the cervicoaxillary channel. From April 1980 through May 1995, 24 patients with clinical thoracic outlet s
Externí odkaz:
https://doaj.org/article/fb1356d8aca94a7eb1438c0d7bb928b8
Publikováno v:
Acta Médica Portuguesa, Vol 10, Iss 1 (1997)
Externí odkaz:
https://doaj.org/article/d6b80f24dc524b368367d24bb030fa46
Control of cortical cytoskeleton-membrane interaction by RhoA regulates peripheral nerve myelination
Bidirectional transmission of mechanical and biochemical signals is integral to cell-environment communication and underlies the function of Schwann cells, the myelinating glia of the peripheral nervous system. As major integrators of “outside-in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4c76a8e2de46b34a2c078807dde20e0
https://doi.org/10.1101/2021.11.09.467948
https://doi.org/10.1101/2021.11.09.467948
Autor:
Lopes E, Franklin Rjm, de Faria Jp, Damaris Bausch-Fluck, Chao Zhao, Azevedo Mm, Montani L, João B. Relvas, Bernd Wollscheid, Rui Loja Fernandes, Ana I. Seixas, Monteiro Ma, Patrick G. A. Pedrioli, Helena S. Domingues
Loss of myelin underlies the pathology of several neurological disorders of diverse etiology. CNS remyelination by adult oligodendrocyte progenitor cells (OPCs) can occur but it differs from developmental myelination carried out by neonatal OPCs. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93104dca1c4769be5fa76fd542601fc0
https://doi.org/10.1101/2021.03.24.436006
https://doi.org/10.1101/2021.03.24.436006
Autor:
Inês Mendes Pinto, Joana Faria, Diogo Fernandes, João B. Relvas, Maria M. Azevedo, Ana I. Seixas
Publikováno v:
Cellular and Molecular Life Sciences. 76:1-11
The organization of actin filaments into a wide range of subcellular structures is a defining feature of cell shape and dynamics, important for tissue development and homeostasis. Nervous system function requires morphological and functional plastici
Autor:
Helena S. Domingues, João B. Relvas, Fabrice P. Cordelières, Paula Sampaio, Ana I. Seixas, Maria M. Azevedo
Publikováno v:
Glia. 66:1826-1844
During central nervous system development, oligodendrocytes form structurally and functionally distinct actin-rich protrusions that contact and wrap around axons to assemble myelin sheaths. Establishment of axonal contact is a limiting step in myelin
Autor:
R. N., Cunha, E., Vieira-Sousa, N., Khmelinskii, P., Ávila-Ribeiro, M., Couto, M. I., Seixas, N., Martins, M., Bernardes, A., Martins, A. B., da Silva, M. H., Lourenço, C., Miguel, V., Tavares, P., Valente, J., Costa, J., Rovisco, R., Aguiar, V., Afreixo, A., Barcelos
Publikováno v:
ARP Rheumatology; Jan-Mar2022, Vol. 47 Issue 1, p42-48, 7p
Autor:
Andréia Rangel-Santos, Érica Pereira-Costa, Elaine Raniero-Fernandes, Magaly Arrais-Santos, Jefferson Russo Victor, Luiz C. Bento-de-Souza, Alberto José da Silva Duarte, Luciana Bento-de-Souza, Maria I. Seixas-Duarte, João B. Oliveira-Filho
Publikováno v:
Results in Immunology
The thymus is the site of T cell maturation. Notch receptors (Notch1-4) and ligands (DLL1-3 and Jagged1-2) constitute one of several pathways involved in this process. Our data revealed differential constitutive expression of Notch genes and ligands
Autor:
Elizabeth O'Hearn, Olga Pletnikova, Daniel W. Chung, Ana I. Seixas, Hyon S. Hwang, Christopher A. Ross, Rachael L. Cohen, Russell L. Margolis, Juan C. Troncoso, Dobrila D. Rudnicki, Susan E. Holmes, John Q. Trojanowski
Publikováno v:
Movement Disorders. 30:1813-1824
Objective SCA12 is a progressive autosomal-dominant disorder, caused by a CAG/CTG repeat expansion in PPP2R2B on chromosome 5q32, and characterized by tremor, gait ataxia, hyperreflexia, dysmetria, abnormal eye movements, anxiety, depression, and som
Autor:
Ashutosh Dhingra, Joana R. Loureiro, Patrizia Rizzu, Vítor Tedim Cruz, Angela Timóteo, Claudia L. Oliveira, Guy A. Rouleau, Jorge Sequeiros, Andrés Ordóñez-Ugalde, José Bessa, Beatriz Quintáns, María Jesús Sobrido, Cristina Costa, Hugo Marcelino, Ana I. Seixas, Eva Brandão, Angel Carracedo, Paula Coutinho, Peter Heutink, Isabel Silveira, José Leal Loureiro
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
The American journal of human genetics 101(1), 87-103 (2017). doi:10.1016/j.ajhg.2017.06.007
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
The American journal of human genetics 101(1), 87-103 (2017). doi:10.1016/j.ajhg.2017.06.007
Advances in human genetics in recent years have largely been driven by next-generation sequencing (NGS); however, the discovery of disease-related gene mutations has been biased toward the exome because the large and very repetitive regions that char