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

Base edited skin equivalents with clinical potential for ex vivo correction of recessive dystrophic epidermolysis bullosa

具有临床潜力的基础编辑皮肤等效物,可用于体外矫正隐性营养不良性大疱性表皮松解症

Bassons-Bascuñana, Alex; Duarte, Blanca; Méndez-Jiménez, Estela; Ugalde, Laura; Sanabria-Betrián, Paula; Aussel, Clotilde; Peña-Gutiérrez, Irene; Olalla-Sastre, Beatriz; Ammann, Sandra; Cathomen, Toni; Del Rio, Marcela; Río, Paula; Larcher, Fernando; López-Manzaneda, Sergio

Targeting olfactory receptor OR2AT4: An innovative aptamer-based treatment for hair growth promotion.

靶向嗅觉受体 OR2AT4:一种基于适体的创新型促进头发生长的治疗方法

Mataix Manuel, Illera Nuria, Hidalgo Inés, Arriba Maria Del Carmen de, Martín Elena, Fernández Gerónimo, González Carlos, Larcher Fernando, González Victor M, Rio Marcela Del, Jiménez Francisco, Carretero Marta

Sephardic origins revealed for rare skin disorder, recessive dystrophic epidermolysis bullosa, in individuals carrying the unique c.6527insC mutation

携带独特的 c.6527insC 突变的个体患有罕见的皮肤病——隐性营养不良性大疱性表皮松解症,研究发现其起源于塞法迪犹太人。

Warshauer, Emily Mira; Maier, Paul A; Runfeldt, Goran; Fuentes, Ignacia; Escamez, Maria José; Valinotto, Laura; Natale, Monica; Manzur, Graciela; Illera, Nuria; Garcia, Marta; Del Rio, Marcela; Mencia, Angeles; Holguin, Almudena; Larcher, Fernando; Hellenthal, Garrett; Brown, Adam R; Consuegra, Liliana; Rivera, Carolina; Nogueiro, Inês; Tang, Jean; Oro, Anthony; Marinkovich, Peter; Palisson, Francis; Titeux, Matthias; Hovnanian, Alain A; Sprecher, Eli; Skorecki, Karl; Norris, David; Bruckner, Anna; Kogut, Igor; Bilousova, Ganna; Roop, Dennis

Evaluation of Systemic Gentamicin as Translational Readthrough Therapy for a Patient With Epidermolysis Bullosa Simplex With Muscular Dystrophy Owing to PLEC1 Pathogenic Nonsense Variants

评估全身性庆大霉素作为转化阅读疗法治疗由PLEC1致病性无义变异引起的单纯性大疱性表皮松解症合并肌营养不良症患者的疗效

Martínez-Santamaría, Lucía; Maseda, Rocío; de Arriba, María Del Carmen; Membrilla, Javier A; Sigüenza, Alberto Iglesias; Mascías, Javier; García, Marta; Quintana, Lucía; Esteban-Rodríguez, Isabel; Hernández-Fernández, Carlos Pelayo; Illera, Nuria; Duarte, Blanca; Guerrero-Aspizúa, Sara; Woodley, David T; Del Río, Marcela; de Lucas, Raúl; Larcher, Fernando; Escámez, María José

Clinically Relevant Correction of Recessive Dystrophic Epidermolysis Bullosa by Dual sgRNA CRISPR/Cas9-Mediated Gene Editing

利用双sgRNA CRISPR/Cas9介导的基因编辑技术对隐性营养不良型大疱性表皮松解症进行临床相关矫正

Bonafont, Jose; Mencía, Ángeles; García, Marta; Torres, Raúl; Rodríguez, Sandra; Carretero, Marta; Chacón-Solano, Esteban; Modamio-Høybjør, Silvia; Marinas, Lucía; León, Carlos; Escamez, María J; Hausser, Ingrid; Del Río, Marcela; Murillas, Rodolfo; Larcher, Fernando

COL7A1 Editing via CRISPR/Cas9 in Recessive Dystrophic Epidermolysis Bullosa

通过 CRISPR/Cas9 编辑 COL7A1 治疗隐性营养不良性大疱性表皮松解症

Hainzl, Stefan; Peking, Patricia; Kocher, Thomas; Murauer, Eva M; Larcher, Fernando; Del Rio, Marcela; Duarte, Blanca; Steiner, Markus; Klausegger, Alfred; Bauer, Johann W; Reichelt, Julia; Koller, Ulrich

Classification of skin phenotypes caused by diabetes mellitus using complex scattering parameters in the millimeter-wave frequency range

利用毫米波频率范围内的复杂散射参数对糖尿病引起的皮肤表型进行分类

Dornuf, Fabian; Martín-Mateos, Pedro; Duarte, Blanca; Hils, Bernhard; Bonilla-Manrique, Oscar Elias; Larcher, Fernando; Acedo, Pablo; Krozer, Viktor

Effects of photodynamic therapy on dermal fibroblasts from xeroderma pigmentosum and Gorlin-Goltz syndrome patients

光动力疗法对着色性干皮病和戈林-戈尔茨综合征患者真皮成纤维细胞的影响

Zamarrón, Alicia; García, Marta; Río, Marcela Del; Larcher, Fernando; Juarranz, Ángeles

Gene Editing for the Efficient Correction of a Recurrent COL7A1 Mutation in Recessive Dystrophic Epidermolysis Bullosa Keratinocytes

基因编辑技术高效纠正隐性营养不良性大疱性表皮松解症角质形成细胞中复发的COL7A1突变

Chamorro, Cristina; Mencía, Angeles; Almarza, David; Duarte, Blanca; Büning, Hildegard; Sallach, Jessica; Hausser, Ingrid; Del Río, Marcela; Larcher, Fernando; Murillas, Rodolfo

Feeder Layer Cell Actions and Applications

馈层单元作用及应用

Llames, Sara; García-Pérez, Eva; Meana, Álvaro; Larcher, Fernando; del Río, Marcela