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

Endothelial-to-Mesenchymal Transition in an Hereditary Hemorrhagic Telangiectasia-like Pediatric Case of Multiple Pulmonary Arteriovenous Malformations.

遗传性出血性毛细血管扩张症样儿童多发性肺动静脉畸形中的内皮-间质转化

Lorente-Herraiz Laura, Cuesta Angel M, Recio-Poveda Lucía, Botella Luisa M, Albiñana Virginia

Effect of 5β-dihydrotestosterone on vasodilator function and on cell proliferation

5β-二氢睾酮对血管舒张功能和细胞增殖的影响

Sánchez-Fernández, David; Eguibar, Aritz; López, Cristina; Cuesta, Ángel M; Albiñana, Virginia; Rogers-Ezewuike, Soline; Gómez-Rivas, Juan A; Saldaña, Laura; Botella, Luisa M; Ferrer, Mercedes

Mutation in Chek2 triggers von Hippel-Lindau hemangioblastoma growth

Chek2 突变触发希佩尔-林道血管母细胞瘤生长

Cabrera-Montes, Jorge; Aguirre, Daniel T; Viñas-López, Jesús; Lorente-Herraiz, Laura; Recio-Poveda, Lucía; Albiñana, Virginia; Pérez-Pérez, Julián; Botella, Luisa M; Cuesta, Angel M

Mutation affecting the proximal promoter of Endoglin as the origin of hereditary hemorrhagic telangiectasia type 1

内皮糖蛋白近端启动子突变是遗传性出血性毛细血管扩张症1型的起源

Albiñana, Virginia; Zafra, Ma Paz; Colau, Jorge; Zarrabeitia, Roberto; Recio-Poveda, Lucia; Olavarrieta, Leticia; Pérez-Pérez, Julián; Botella, Luisa M

Vascular injury triggers Krüppel-like factor 6 mobilization and cooperation with specificity protein 1 to promote endothelial activation through upregulation of the activin receptor-like kinase 1 gene

血管损伤会触发 Krüppel 样因子 6 的动员,并与特异性蛋白 1 协同作用,通过上调激活素受体样激酶 1 基因来促进内皮细胞活化。

Garrido-Martín, Eva M; Blanco, Francisco J; Roquè, Mercé; Novensà, Laura; Tarocchi, Mirko; Lang, Ursula E; Suzuki, Toru; Friedman, Scott L; Botella, Luisa M; Bernabéu, Carmelo

BMP9 mutations cause a vascular-anomaly syndrome with phenotypic overlap with hereditary hemorrhagic telangiectasia

BMP9基因突变会导致血管异常综合征,其表型与遗传性出血性毛细血管扩张症有重叠。

Wooderchak-Donahue, Whitney L; McDonald, Jamie; O'Fallon, Brendan; Upton, Paul D; Li, Wei; Roman, Beth L; Young, Sarah; Plant, Parker; Fülöp, Gyula T; Langa, Carmen; Morrell, Nicholas W; Botella, Luisa M; Bernabeu, Carmelo; Stevenson, David A; Runo, James R; Bayrak-Toydemir, Pinar

Copy number variations in endoglin locus: mapping of large deletions in Spanish families with hereditary hemorrhagic telangiectasia type 1

内皮糖蛋白基因座拷贝数变异:西班牙遗传性出血性毛细血管扩张症1型家族中大片段缺失的定位

Fontalba, Ana; Fernández-Luna, Jose L; Zarrabeitia, Roberto; Recio-Poveda, Lucia; Albiñana, Virginia; Ojeda-Fernández, Maria L; Bernabéu, Carmelo; Alcaraz, Luis A; Botella, Luisa M

5'UTR mutations of ENG cause hereditary hemorrhagic telangiectasia.

ENG 基因 5'UTR 突变会导致遗传性出血性毛细血管扩张症

Damjanovich Kristy, Langa Carmen, Blanco Francisco J, McDonald Jamie, Botella Luisa M, Bernabeu Carmelo, Wooderchak-Donahue Whitney, Stevenson David A, Bayrak-Toydemir Pinar

Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia

西班牙遗传性出血性毛细血管扩张症患者的突变研究

Fontalba, Ana; Fernandez-L, Africa; García-Alegria, Eva; Albiñana, Virginia; Garrido-Martin, Eva M; Blanco, Francisco J; Zarrabeitia, Roberto; Perez-Molino, Alfonso; Bernabeu-Herrero, Maria E; Ojeda, Maria-Luisa; Fernandez-Luna, Jose L; Bernabeu, Carmelo; Botella, Luisa M

Hereditary hemorrhagic telangiectasia, a vascular dysplasia affecting the TGF-beta signaling pathway

遗传性出血性毛细血管扩张症,一种影响TGF-β信号通路的血管发育不良

Fernández-L, Africa; Sanz-Rodriguez, Francisco; Blanco, Francisco J; Bernabéu, Carmelo; Botella, Luisa M