Zobrazeno 1 - 10 of 39 pro vyhledávání: '"Ricard López"'
1
Akademický článek
Assessment of the Correlation and Diagnostic Accuracy between Cerebrospinal Fluid and Plasma Alzheimer’s Disease Biomarkers: A Comparison of the Lumipulse and Simoa Platforms
Autor: Farida Dakterzada, Raffaela Cipriani, Ricard López-Ortega, Alfonso Arias, Iolanda Riba-Llena, Maria Ruiz-Julián, Raquel Huerto, Nuria Tahan, Carlos Matute, Estibaliz Capetillo-Zarate, Gerard Piñol-Ripoll
Publikováno v: International Journal of Molecular Sciences, Vol 25, Iss 9, p 4594 (2024)
We compared the clinical and analytical performance of Alzheimer’s disease (AD) plasma biomarkers measured using the single-molecule array (Simoa) and Lumipulse platforms. We quantified the plasma levels of amyloid beta 42 (Aβ42), Aβ40, phosphory
Externí odkaz: https://doaj.org/article/da57d8b1deb548eb80bccb47d09ca2c9
Zobrazit plný text záznamu
2
Akademický článek
Assessment of the Concordance and Diagnostic Accuracy Between Elecsys and Lumipulse Fully Automated Platforms and Innotest
Autor: Farida Dakterzada, Ricard López-Ortega, Alfonso Arias, Iolanda Riba-Llena, Maria Ruiz-Julián, Raquel Huerto, Nuria Tahan, Gerard Piñol-Ripoll
Publikováno v: Frontiers in Aging Neuroscience, Vol 13 (2021)
Manual ELISA assays are the most commonly used methods for quantification of biomarkers; however, they often show inter- and intra-laboratory variability that limits their wide use. Here, we compared the Innotest ELISA method with two fully automated
Externí odkaz: https://doaj.org/article/ba6bd2c6e0fe4ea4ac853900520d16b8
Zobrazit plný text záznamu
3
Akademický článek
Absence of Substantial Copy Number Differences in a Pair of Monozygotic Twins Discordant for Features of Autism Spectrum Disorder
Autor: Marina Laplana, José Luis Royo, Anton Aluja, Ricard López, Damiàn Heine-Sunyer, Joan Fibla
Publikováno v: Case Reports in Genetics, Vol 2014 (2014)
Autism spectrum disorder (ASD) is a highly heritable disease (~0.9) with a complex genetic etiology. It is initially characterized by altered cognitive ability which commonly includes impaired language and communication skills as well as fundamental
Externí odkaz: https://doaj.org/article/1aa28984da02497cb94f43edde21f6a1
Zobrazit plný text záznamu
6
Data from T-Type Cav3.1 Channels Mediate Progression and Chemotherapeutic Resistance in Glioblastoma
Autor: Carles Cantí, Judit Herreros, Maria Santacana, Ricard López-Ortega, Elisabet Talavera, Lía Alza, Oscar Maiques, Marta C. Sallán, Anna Visa
T-type Ca2+ channels (TTCC) have been identified as key regulators of cancer cell cycle and survival. In vivo studies in glioblastoma (GBM) murine xenografts have shown that drugs able to block TTCC in vitro (such as tetralol derivatives mibefradil/N
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46fb94ca4f627a90b66a67da6ce4a451
https://doi.org/10.1158/0008-5472.c.6511353.v1
Zobrazit plný text záznamu
7
Enantioselective molecular recognition in a flexible self-folding cavitand
Autor: Rubén Álvarez-Yebra, Ricard López-Coll, Pere Galán-Masferrer, Agustí Lledó
We report a chiral deep cavitand receptor based on calix[5]arene stabilized by a cooperative network of hydrogen bonds and having a highly flexible structure. The dynamic features of the host have been studied by 1H NMR spectroscopy, revealing a bowl
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c60144faf27593192d2093ddb7fa5c4
https://doi.org/10.26434/chemrxiv-2022-tpf8w
Zobrazit plný text záznamu
8
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
9
The efficacy of combining topiramate and 4-aminopyridine to reduce relapses and interictal progression in two cases of episodic ataxia type 2
Autor: Cristina, González-Mingot, Ricard, López-Ortega, Luis, Brieva-Ruiz
Publikováno v: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 43(8)
Episodic ataxia type 2 is an autosomal dominant channelopathy, caused by genetic variants in the voltage-dependent calcium channel a-1 subunit (CACNA1A), which is characterized by intermittent episodes of vertigo and ataxia. A slow progression of cer
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5208bbb46cd1fb4fb9fc84be1f911cb1
https://pubmed.ncbi.nlm.nih.gov/35595874
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje