日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Molecular Changes Induced by Carbon Dioxide Laser in Hailey-Hailey Disease: A Potential Mechanism Underlying Treatment Efficacy

二氧化碳激光治疗海利-海利病引起的分子变化:一种潜在的治疗疗效机制

Antoñanzas, Javier; España, Agustín; Gorostidi, Ana; Patiño-García, Ana; Araúzo-Bravo, Marcos J; Gerovska, Daniela; Salido-Vallejo, Rafael; Aguado-Gil, Leyre

A More Homogeneous Phenotype in Parkinson's Disease Related to R1441G Mutation in the LRRK2 Gene

LRRK2基因R1441G突变与帕金森病表型更加同质化相关

Vinagre-Aragón, Ana; Campo-Caballero, David; Mondragón-Rezola, Elisabet; Pardina-Vilella, Lara; Hernandez Eguiazu, Haizea; Gorostidi, Ana; Croitoru, Ioana; Bergareche, Alberto; Ruiz-Martinez, Javier

The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight

西班牙帕金森病遗传结构:表征人群特异性风险、差异性单倍型结构并提供病因学见解

Bandres-Ciga, Sara; Ahmed, Sarah; Sabir, Marya S; Blauwendraat, Cornelis; Adarmes-Gómez, Astrid D; Bernal-Bernal, Inmaculada; Bonilla-Toribio, Marta; Buiza-Rueda, Dolores; Carrillo, Fátima; Carrión-Claro, Mario; Gómez-Garre, Pilar; Jesús, Silvia; Labrador-Espinosa, Miguel A; Macias, Daniel; Méndez-Del-Barrio, Carlota; Periñán-Tocino, Teresa; Tejera-Parrado, Cristina; Vargas-González, Laura; Diez-Fairen, Monica; Alvarez, Ignacio; Tartari, Juan Pablo; Buongiorno, Mariateresa; Aguilar, Miquel; Gorostidi, Ana; Bergareche, Jesús Alberto; Mondragon, Elisabet; Vinagre-Aragon, Ana; Croitoru, Ioana; Ruiz-Martínez, Javier; Dols-Icardo, Oriol; Kulisevsky, Jaime; Marín-Lahoz, Juan; Pagonabarraga, Javier; Pascual-Sedano, Berta; Ezquerra, Mario; Cámara, Ana; Compta, Yaroslau; Fernández, Manel; Fernández-Santiago, Rubén; Muñoz, Esteban; Tolosa, Eduard; Valldeoriola, Francesc; Gonzalez-Aramburu, Isabel; Sanchez Rodriguez, Antonio; Sierra, María; Menéndez-González, Manuel; Blazquez, Marta; Garcia, Ciara; Suarez-San Martin, Esther; García-Ruiz, Pedro; Martínez-Castrillo, Juan Carlos; Vela-Desojo, Lydia; Ruz, Clara; Barrero, Francisco Javier; Escamilla-Sevilla, Francisco; Mínguez-Castellanos, Adolfo; Cerdan, Debora; Tabernero, Cesar; Gomez Heredia, Maria Jose; Perez Errazquin, Francisco; Romero-Acebal, Manolo; Feliz, Cici; Lopez-Sendon, Jose Luis; Mata, Marina; Martínez Torres, Irene; Kim, Jonggeol Jeffrey; Dalgard, Clifton L; Brooks, Janet; Saez-Atienzar, Sara; Gibbs, J Raphael; Jorda, Rafael; Botia, Juan A; Bonet-Ponce, Luis; Morrison, Karen E; Clarke, Carl; Tan, Manuela; Morris, Huw; Edsall, Connor; Hernandez, Dena; Simon-Sanchez, Javier; Nalls, Mike A; Scholz, Sonja W; Jimenez-Escrig, Adriano; Duarte, Jacinto; Vives, Francisco; Duran, Raquel; Hoenicka, Janet; Alvarez, Victoria; Infante, Jon; Marti, Maria José; Clarimón, Jordi; López de Munain, Adolfo; Pastor, Pau; Mir, Pablo; Singleton, Andrew

Alzheimer's disease cerebrospinal fluid biomarker in cognitively normal subjects

认知功能正常受试者的阿尔茨海默病脑脊液生物标志物

Toledo, Jon B; Zetterberg, Henrik; van Harten, Argonde C; Glodzik, Lidia; Martinez-Lage, Pablo; Bocchio-Chiavetto, Luisella; Rami, Lorena; Hansson, Oskar; Sperling, Reisa; Engelborghs, Sebastiaan; Osorio, Ricardo S; Vanderstichele, Hugo; Vandijck, Manu; Hampel, Harald; Teipl, Stefan; Moghekar, Abhay; Albert, Marilyn; Hu, William T; Monge Argilés, Jose A; Gorostidi, Ana; Teunissen, Charlotte E; De Deyn, Peter P; Hyman, Bradley T; Molinuevo, Jose L; Frisoni, Giovanni B; Linazasoro, Gurutz; de Leon, Mony J; van der Flier, Wiesje M; Scheltens, Philip; Blennow, Kaj; Shaw, Leslie M; Trojanowski, John Q

Beyond asexual development: modifications in the gene expression profile caused by the absence of the Aspergillus nidulans transcription factor FlbB

无性发育之外:构巢曲霉转录因子FlbB缺失引起的基因表达谱改变

Oiartzabal-Arano, Elixabet; Garzia, Aitor; Gorostidi, Ana; Ugalde, Unai; Espeso, Eduardo A; Etxebeste, Oier

SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy

SCN4A孔道突变是常染色体显性遗传性特发性震颤的致病因素之一,并可能增加癫痫的易感性。

Bergareche, Alberto; Bednarz, Marcin; Sánchez, Elena; Krebs, Catharine E; Ruiz-Martinez, Javier; De La Riva, Patricia; Makarov, Vladimir; Gorostidi, Ana; Jurkat-Rott, Karin; Marti-Masso, Jose Felix; Paisán-Ruiz, Coro

GIGYF2 mutation in late-onset Parkinson's disease with cognitive impairment

GIGYF2 基因突变与晚发性帕金森病伴认知障碍相关

Ruiz-Martinez, Javier; Krebs, Catharine E; Makarov, Vladimir; Gorostidi, Ana; Martí-Massó, Jose Félix; Paisán-Ruiz, Coro

Epitope Mapping of Antibodies to Alpha-Synuclein in LRRK2 Mutation Carriers, Idiopathic Parkinson Disease Patients, and Healthy Controls.

LRRK2 突变携带者、特发性帕金森病患者和健康对照者中抗 α-突触核蛋白抗体的表位定位

Alvarez-Castelao Beatriz, Gorostidi Ana, Ruíz-Martínez Javier, López de Munain Adolfo, Castaño José G

The LRRK2 G2019S mutant exacerbates basal autophagy through activation of the MEK/ERK pathway

LRRK2 G2019S突变体通过激活MEK/ERK通路加剧基础自噬。

Bravo-San Pedro, José M; Niso-Santano, Mireia; Gómez-Sánchez, Rubén; Pizarro-Estrella, Elisa; Aiastui-Pujana, Ana; Gorostidi, Ana; Climent, Vicente; López de Maturana, Rakel; Sanchez-Pernaute, Rosario; López de Munain, Adolfo; Fuentes, José M; González-Polo, Rosa A