Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Natàlia Reixach"'
Autor:
Ricardo Sant’Anna, Pablo Gallego, Lei Z. Robinson, Alda Pereira-Henriques, Nelson Ferreira, Francisca Pinheiro, Sebastian Esperante, Irantzu Pallares, Oscar Huertas, Maria Rosário Almeida, Natàlia Reixach, Raul Insa, Adrian Velazquez-Campoy, David Reverter, Núria Reig, Salvador Ventura
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/e01ea5c5ac0a4bd48c5c5662836b01fd
Autor:
Ricardo Sant'Anna, Pablo Gallego, Lei Z. Robinson, Alda Pereira-Henriques, Nelson Ferreira, Francisca Pinheiro, Sebastian Esperante, Irantzu Pallares, Oscar Huertas, Maria Rosário Almeida, Natàlia Reixach, Raul Insa, Adrian Velazquez-Campoy, David Reverter, Núria Reig, Salvador Ventura
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-13 (2016)
Misfolding of transthyretin can cause amyloid aggregation disorders that can be treated by stabilizing the tetrameric form with tafamidis. Here the authors show that tolcapone, a drug already FDA-approved for Parkinson disease, has strong transthyret
Externí odkaz:
https://doaj.org/article/837ff0b26f1b42a594f1b539d90bcb7c
Autor:
Natàlia Reixach, Martin Lotz, Merissa Olmer, Joel N. Buxbaum, Tokio Matsuzaki, Oscar Alvarez-Garcia, Yukio Akasaki
Publikováno v:
Aging Cell
Summary Deposition of amyloid is a common aging-associated phenomenon in several aging-related diseases. Osteoarthritis (OA) is the most prevalent joint disease, and aging is its major risk factor. Transthyretin (TTR) is an amyloidogenic protein that
Autor:
Martin Lotz, Tokio Matsuzaki, Merissa Olmer, Yukihide Iwamoto, Joel N. Buxbaum, Natàlia Reixach, Oscar Alvarez-Garcia, Yukio Akasaki
Publikováno v:
Arthritis & Rheumatology. 67:2097-2107
Objectives Amyloid deposits are prevalent in osteoarthritis (OA)-affected joints. This study defined the dominant precursor and determined if the deposits affect chondrocyte functions.
Autor:
Natàlia Reixach, Lei Z. Robinson
Publikováno v:
Biochemistry
The quaternary structure stability of proteins is typically studied under conditions that accelerate their aggregation/unfolding processes on convenient laboratory time scales. Such conditions include high temperature or pressure, chaotrope-mediated
Autor:
Lisa M. Ryno, Francesca Cattaneo, Natàlia Reixach, Joel N. Buxbaum, John D. Hulleman, Xin Wang
Publikováno v:
The Journal of Neuroscience. 34:7253-7265
Increased neuronal synthesis of transthyretin (TTR) may favorably impact on Alzheimer's disease (AD) because TTR has been shown to inhibit Aβ aggregation and detoxify cell-damaging conformers. The mechanism whereby hippocampal and cortical neurons f
Publikováno v:
Biochemistry. 52:1913-1926
The transthyretin amyloidoses are diseases of protein misfolding characterized by the extracellular deposition of fibrils and other aggregates of the homotetrameric protein transthyretin (TTR) in peripheral nerves, heart, and other tissues. Age is th
Autor:
Natàlia Reixach, Salvador Ventura, Raul Insa, Ricardo Sant'Anna, Oscar Huertas, David Reverter, Adrián Velázquez-Campoy, Lei Z. Robinson, Sebastian Esperante, Nelson Ferreira, Maria Rosário Almeida, Pablo Gallego, Alda Pereira-Henriques, Irantzu Pallarès, Francisca Pinheiro, Núria Reig
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Nature Communications, Vol 7, Iss 1, Pp 1-13 (2016)
Zaguán. Repositorio Digital de la Universidad de Zaragoza
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Nature Communications
instname
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Nature Communications, Vol 7, Iss 1, Pp 1-13 (2016)
Zaguán. Repositorio Digital de la Universidad de Zaragoza
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Nature Communications
13 pags, 6 figs, 1 tab. -- Supplementary information is available at the Publisher's web
Transthyretin (TTR) is a plasma homotetrameric protein implicated in fatal systemic amyloidoses. TTR tetramer dissociation precedes pathological TTR aggrega
Transthyretin (TTR) is a plasma homotetrameric protein implicated in fatal systemic amyloidoses. TTR tetramer dissociation precedes pathological TTR aggrega
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64234fcfaf7f7adcb8d807ac4da4df1f
http://hdl.handle.net/10261/255695
http://hdl.handle.net/10261/255695
Publikováno v:
The Journal of Neuroscience. 31:12483-12490
Transthyretin (TTR), a systemic amyloid precursor in the human TTR amyloidoses, interacts with β-amyloid (Aβ)in vitro, inhibits Aβ fibril formation, and suppresses the Alzheimer's disease (AD) phenotype in APP23 mice bearing a human APP gene conta
Autor:
Natàlia Reixach, Jeffery W. Kelly, Joel N. Buxbaum, Steve Bourgault, Joshua L. Price, Sungwook Choi
Publikováno v:
Biochemical and Biophysical Research Communications. 410:707-713
The transthyretin amyloidoses are a subset of protein misfolding diseases characterized by the extracellular deposition of aggregates derived from the plasma homotetrameric protein transthyretin (TTR2) in peripheral nerves and the heart. We have esta