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

ADAM12-Generated Basigin Ectodomain Binds β1 Integrin and Enhances the Expression of Cancer-Related Extracellular Matrix Proteins

ADAM12 产生的 Basigin 细胞外结构域与 β1 整合素结合并增强癌症相关细胞外基质蛋白的表达

Kasper J Mygind, Denise Nikodemus, Sebastian Gnosa, Ramya Kweder, Nicolai J Wewer Albrechtsen, Marie Kveiborg, Janine T Erler, Reidar Albrechtsen

SLCO5A1 and synaptic assembly genes contribute to impulsivity in juvenile myoclonic epilepsy

SLCO5A1和突触组装基因与青少年肌阵挛性癫痫的冲动性有关

Roshandel, Delnaz; Sanders, Eric J; Shakeshaft, Amy; Panjwani, Naim; Lin, Fan; Collingwood, Amber; Hall, Anna; Keenan, Katherine; Deneubourg, Celine; Mirabella, Filippo; Topp, Simon; Zarubova, Jana; Thomas, Rhys H; Talvik, Inga; Syvertsen, Marte; Striano, Pasquale; Smith, Anna B; Selmer, Kaja K; Rubboli, Guido; Orsini, Alessandro; Ng, Ching Ching; Møller, Rikke S; Lim, Kheng Seang; Hamandi, Khalid; Greenberg, David A; Gesche, Joanna; Gardella, Elena; Fong, Choong Yi; Beier, Christoph P; Andrade, Danielle M; Jungbluth, Heinz; Richardson, Mark P; Pastore, Annalisa; Fanto, Manolis; Pal, Deb K; Strug, Lisa J

The prognostic value of immune-related genes AZGP1, SLCO5A1, and CTF1 in Uveal melanoma

免疫相关基因AZGP1、SLCO5A1和CTF1在葡萄膜黑色素瘤中的预后价值

Wang, Wanpeng; Wang, Sha

Phenotypic drug screening in a human fibrosis model identified a novel class of antifibrotic therapeutics

在人类纤维化模型中进行表型药物筛选,发现了一类新型抗纤维化疗法。

Michael Gerckens ,Kenji Schorpp ,Francesco Pelizza ,Melanie Wögrath ,Kora Reichau ,Huilong Ma ,Armando-Marco Dworsky ,Arunima Sengupta ,Mircea Gabriel Stoleriu ,Katharina Heinzelmann ,Juliane Merl-Pham ,Martin Irmler ,Hani N Alsafadi ,Eduard Trenkenschuh ,Lenka Sarnova ,Marketa Jirouskova ,Wolfgang Frieß ,Stefanie M Hauck ,Johannes Beckers ,Nikolaus Kneidinger ,Jürgen Behr ,Anne Hilgendorff ,Kamyar Hadian ,Michael Lindner ,Melanie Königshoff ,Oliver Eickelberg ,Martin Gregor ,Oliver Plettenburg ,Ali Önder Yildirim ,Gerald Burgstaller

Mesomelia-synostoses syndrome results from deletion of SULF1 and SLCO5A1 genes at 8q13

肢体中段发育不全-骨性融合综合征是由8q13位点SULF1和SLCO5A1基因缺失引起的。

Isidor, Bertrand; Pichon, Olivier; Redon, Richard; Day-Salvatore, Debra; Hamel, Antoine; Siwicka, Karolina A; Bitner-Glindzicz, Maria; Heymann, Dominique; Kjellén, Lena; Kraus, Cornelia; Leroy, Jules G; Mortier, Geert R; Rauch, Anita; Verloes, Alain; David, Albert; Le Caignec, Cédric