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

Intragenic loss-of-function variants in transcription factors MAZ, FOXP1 and SIN3B in colobomatous microphthalmia

眼裂小眼畸形中转录因子 MAZ、FOXP1 和 SIN3B 的基因内功能缺失变异

Seese, Sarah E; Reis, Linda M; Schneider, Adele; Bardakjian, Tanya; Semina, Elena V

Splicing and frameshift variants in QSER1 may be involved in developmental phenotypes

QSER1中的剪接和移码变异可能与发育表型有关。

Fischer, Megan C; Reis, Linda M; Lenberg, Jerica; Friedman, Jennifer; Seese, Sarah E; Muheisen, Sanaa; Writzl, Karin; Golob, Barbara; Peterlin, Borut; Semina, Elena V

Neuroleptospirosis in patients presenting with primary central nervous system infection: A multicentre study

以原发性中枢神经系统感染为首发症状的神经钩端螺旋体病患者:一项多中心研究

Perera, Nilanka; Gunawardena, Champika; Abeyratne, Varuna; Rajapakse, Parami; Semina, Thisal; Uluwattage, Wimalasiri; Ratnayake, Asanka; Mendis, Suresh; Dickmadugoda, Nandana; Mujaheith, M; Karunanayake, Lilani; Ranawaka, Udaya K

Jellyfish-Inspired Ultrafast and Versatile Magnetic Soft Robots for Biomedical Applications

受水母启发的超高速多功能磁性软体机器人在生物医学领域的应用

Sun, Yuxuan; Liu, Ruiqi; Ma, Chiyuan; Liu, Jingyang; Yi, Semina; Gu, Junnan; Xia, Liangyu; Qing, Haitao; Cai, Kailin; Li, Liang; Yao, Lining; Cao, Quanliang

Heterogeneity-driven phenotypic plasticity and treatment response in branched-organoid models of pancreatic ductal adenocarcinoma.

胰腺导管腺癌分支类器官模型中异质性驱动的表型可塑性和治疗反应

Papargyriou Aristeidis, Najajreh Mulham, Cook David P, Maurer Carlo H, Bärthel Stefanie, Messal Hendrik A, Ravichandran Sakthi K, Richter Till, Knolle Moritz, Metzler Thomas, Shastri Akul R, Öllinger Rupert, Jasper Jacob, Schmidleitner Laura, Wang Surui, Schneeweis Christian, Ishikawa-Ankerhold Hellen, Engleitner Thomas, Mataite Laura, Semina Mariia, Trabulssi Hussein, Lange Sebastian, Ravichandra Aashreya, Schuster Maximilian, Mueller Sebastian, Peschke Katja, Schäfer Arlett, Dobiasch Sophie, Combs Stephanie E, Schmid Roland M, Bausch Andreas R, Braren Rickmer, Heid Irina, Scheel Christina H, Schneider Günter, Zeigerer Anja, Luecken Malte D, Steiger Katja, Kaissis Georgios, van Rheenen Jacco, Theis Fabian J, Saur Dieter, Rad Roland, Reichert Maximilian

T-Cadherin (CDH13) and Non-Coding RNAs: The Crosstalk Between Health and Disease

T-钙黏蛋白(CDH13)和非编码RNA:健康与疾病之间的相互作用

Rubina, Kseniya; Maier, Artem; Klimovich, Polina; Sysoeva, Veronika; Romashin, Daniil; Semina, Ekaterina; Tkachuk, Vsevolod

T-Cadherin Finetunes Proliferation-Differentiation During Adipogenesis via PI3K-AKT Signaling Pathway

T-钙黏蛋白通过PI3K-AKT信号通路微调脂肪生成过程中的增殖-分化

Klimovich, Polina; Brodsky, Ilya; Dzreyan, Valentina; Ivleva, Marianna; Grigorieva, Olga; Meshcheriakov, Mark; Semina, Ekaterina; Sysoeva, Veronika; Tkachuk, Vsevolod; Rubina, Kseniya

Abnormal Splicing in the Final Intron of PRX Results in Dominant Congenital Cataract Without Neurological Phenotype

PRX基因最后一个内含子异常剪接导致显性先天性白内障,但无神经系统表型

Reis, Linda M; Bellingham, James; Motta, Fabiana Louise; Jurkute, Neringa; Raskin, Salmo; Ramos, Fabiana; Mahroo, Omar A; Moosajee, Mariya; Arno, Gavin; Semina, Elena V

Comparison of NSG-Quad and MISTRG-6 humanized mice for modeling circulating and tumor-infiltrating human myeloid cells.

比较 NSG-Quad 和 MISTRG-6 人源化小鼠在模拟循环和肿瘤浸润人类髓系细胞方面的性能

Chen Anna, Knöbl Viktoria, Walzer Oliver, Hauser Jana, Neuwirth Ines, Frank Magdalena, Braun Nina, Duvnjak Semina, Reisecker Johannes, Stecher Carmen, Farr Alex, Brostjan Christine, Herndler-Brandstetter Dietmar

GJA8-associated developmental eye disorders: a new multicentre study highlights mutational hotspots and genotype-phenotype correlations

GJA8相关发育性眼病:一项新的多中心研究揭示了突变热点和基因型-表型相关性

Merepa, Solomon S; Reis, Linda M; Damián, Alejandra; Bardakjian, Tanya; Schneider, Adele; Trujillo-Tiebas, María Jose; Ayuso, Carmen; Galarza, Laura Cortázar; Saez Villaverde, Raquel; Ortiz-Cabrera, Nelmar Valentina; Bax, Dorine A; Holt, Richard; Ceroni, Fabiola; Edery, Patrick; Grelet, Maude; Riccardi, Florence; Maillard, Lauriane; Costakos, Deborah; Plaisancié, Julie; Chassaing, Nicolas; Corton, Marta; Semina, Elena V; Ragge, Nicola K