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

Expression of Connexins 37/40 and Pannexin 1 in Early Human and Yotari (Dab1(-/-)) Meninges Development.

人类早期和 Yotari (Dab1(-/-)) 脑膜发育中连接蛋白 37/40 和 Pannexin 1 的表达。

Puljiz Marko, Filipović Natalija, Kelam Nela, Racetin Anita, Katsuyama Yu, Vukojević Katarina

Loss of Dab1 Alters Expression Patterns of Endocytic and Signaling Molecules During Embryonic Lung Development in Mice.

Dab1 的缺失改变了小鼠胚胎肺发育过程中内吞分子和信号分子的表达模式。

Todorović Petar, Maglica Mirko, Kelam Nela, Filipović Natalija, Rizikalo Azer, Perutina Ilija, Mišković Josip, Katsuyama Yu, Vukojević Katarina

Expression Pattern of Dab1, Reelin, PGP9.5 and Sox2 in the Stomach of Yotari (Dab1(-/-)) Mice.

Yotari (Dab1(-/-)) 小鼠胃中 Dab1、Reelin、PGP9.5 和 Sox2 的表达模式。

Todorović Petar, Kelam Nela, Racetin Anita, Filipović Natalija, Katsuyama Yu, Saraga-Babić Mirna, Vukojević Katarina

Herbal Formula Extract Ameliorates Anxiety and Cognitive Impairment via Regulation of the Reelin/Dab-1 Pathway in a Murine Model of Post-Traumatic Stress Disorder

草药配方提取物通过调节创伤后应激障碍小鼠模型中的 Reelin/Dab-1 通路改善焦虑和认知障碍

Hee Ra Park, Mudan Cai, Eun Jin Yang

Resilience to autosomal dominant Alzheimer's disease in a Reelin-COLBOS heterozygous man

Reelin-COLBOS 杂合子男性对常染色体显性阿尔茨海默病的恢复能力

Francisco Lopera #, Claudia Marino #, Anita S Chandrahas #, Michael O'Hare #, Nelson David Villalba-Moreno #, David Aguillon, Ana Baena, Justin S Sanchez, Clara Vila-Castelar, Liliana Ramirez Gomez, Natalia Chmielewska, Gabriel M Oliveira, Jessica Lisa Littau, Kristin Hartmann, Kyungeun Park, Susann

Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18-Year Study

家族性小脑共济失调和肌萎缩侧索硬化症/额颞叶痴呆伴DAB1和C9ORF72重复扩增:一项为期18年的研究

Rosenbohm, Angela; Pott, Hendrik; Thomsen, Mirja; Rafehi, Haloom; Kaya, Sabine; Szymczak, Silke; Volk, Alexander E; Mueller, Kathrin; Silveira, Isabel; Weishaupt, Jochen H; Tönnies, Holger; Seibler, Philip; Zschiedrich, Katja; Schaake, Susen; Westenberger, Ana; Zühlke, Christine; Depienne, Christel; Trinh, Joanne; Ludolph, Albert C; Klein, Christine; Bahlo, Melanie; Lohmann, Katja

Whole genome analysis in APOE4 homozygotes identifies the DAB1-RELN pathway in Alzheimer's disease pathogenesis

对 APOE4 纯合子的全基因组分析揭示了 DAB1-RELN 通路在阿尔茨海默病发病机制中的作用

Bracher-Smith, Matthew; Leonenko, Ganna; Baker, Emily; Crawford, Karen; Graham, Andrew C; Salih, Dervis A; Howell, Brian W; Hardy, John; Escott-Price, Valentina

Individual copy number variation and extensive diversity between major MHC-DAB1 allelic lineages in the European bitterling

欧洲苦鹬中MHC-DAB1主要等位基因谱系间存在个体拷贝数变异和广泛多样性。

Talarico, Lorenzo; Bryjová, Anna; Čížková, Dagmar; Douda, Karel; Reichard, Martin

Mutations in NOTCH3 Gene may Promote the Clinical Presentation of Spinocerebellar Ataxia Type 37 Caused by Mutations in DAB1 Gene

NOTCH3基因突变可能促进由DAB1基因突变引起的37型脊髓小脑性共济失调的临床表现。

Wang, Zhao-Wei; Wang, Li-Ping; Du, Ye; Liu, Qi

Biallelic DAB1 Variants Are Associated With Mild Lissencephaly and Cerebellar Hypoplasia

双等位基因DAB1变异与轻度无脑回畸形和小脑发育不全相关

Smits, Daphne J; Schot, Rachel; Wilke, Martina; van Slegtenhorst, Marjon; de Wit, Marie Claire Y; Dremmen, Marjolein H G; Dobyns, William B; Barkovich, A James; Mancini, Grazia M S