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Disease Models and Mechanisms 封面图

Disease Models and Mechanisms

IF3.3
论文数2579
被引数7703
期刊论文 2579
发表时间
Infectious Disease: Evolution, Mechanism and Global Health传染病:进化、机制与全球健康
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deleteHackett, Rachel; Allen, Judith E.; Sanyal, Sumana; Tobin, David M.; Vance, Russell
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Characterization of a humanized mouse model of Duchenne muscular dystrophy to support the development of genetic medicines对杜氏肌营养不良人源化小鼠模型的表征,以支持基因药物的开发
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deleteBraunreiter, Kara; Kempton, Amber; Mejia-Guerra, Maria Katherine; Murray, Andrew; Baine, Stephen; Adegboye, Kaitlin; Haile, Alex; Ahuja, Suruchi Jai Kumar; Fedoce, Alessandra; Liu, Chang; Burch, Peter; Kabadi, Ami Meda
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Retinopathy-associated inosine monophosphate dehydrogenase 1 mutations cause metabolic and filament defects in cones视网膜病变相关的次黄嘌呤单核苷酸脱氢酶1突变导致视锥细胞的代谢和原纤维缺陷
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deleteRutter, Kaitlyn M.; Giarmarco, Michelle M.; Truong, Vivian; Wang, Yekai; Eminhizer, Mark; Xiang, Yinxiao; Cleghorn, Whitney M.; Sanchez, Gardenia; Burrell, Anika L.; Kollman, Justin M.; Du, Jianhai; Brockerhoff, Susan E.
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Interleukin-1 regulates myeloid cell trafficking and cerebral blood flow following intracerebral haemorrhage白细胞介素-1调节髓系细胞迁移和颅内出血后的脑血流
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deleteBarrington, Jack; Rivers-Auty, Jack; Strangward, Patrick; Tamburrano, Sabrina; Lenart, Nikolett; Swanton, Tessa; Lemarchand, Eloise; Parry-Jones, Adrian R.; Denes, Adam; Brough, David; Allan, Stuart M.
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Generation and characterization of a mouse model of Becker muscular dystrophy with a deletion of Dmd exons 52 to 55生成了带有Dmd基因外显子52至55缺失的小鼠型贝克肌营养不良模型,并对其进行了表征。
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PREAI
deletePerillat, Lucie O. M.; Wong, Tatianna W. Y.; Maino, Eleonora; Ahmed, Abdalla; Scott, Ori; Hyatt, Elzbieta; Delgado-Olguin, Paul; Visuvanathan, Shagana; Ivakine, Evgueni A.; Cohn, Ronald D.
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Models of Bosch-Boonstra-Schaaf optic atrophy syndrome reveal genotype-phenotype correlations in brain structure and behavior博世-博恩斯特-肖аф视神经萎缩综合征的模型揭示了基因型-表型相关性在脑结构和行为中的作用。
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deleteMaass, Johann G.; Kamionek, Dominik; Mantilleri, Annabelle; Theiss, Susanne; Dotsch, Laura; Franke, Felix; Schubert, Tim; Scheck, Jonas G.; Pitzer, Claudia; Piovani, Paolo; Bertacchi, Michele; Deschaux, Olivier; Singh, Anubhav; Chen, Chun-An; Frohlich, Henning; Studer, Michele; Schaaf, Christian P.
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Advocating for automation in animal research: using home cage monitoring to advance welfare, reproducibility and scientific openness倡导动物研究中的自动化:利用笼内监测来促进福利、可重复性和科学开放性
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deleteWells, Sara; Abelson, Klas; Armstrong, J. Douglas; Bains, Sonia; Bikovski, Lior; Bleich, Andre; Bronstad, Aurora; Dennison, Ngaire; Dickson, Suzanne L.; Forrest, Hamish; Gates, Hilary; Guzhva, Oleksiy; Hamed, Adam; Harris, Kate; Hartley, Matthew; Holter, Sabine M.; Ike, Kevin G. O.; Lewejohann, Lars; Mathis, Alexander; Nielsen, Thomas Svava; Norton, Tomas; Peirson, Stuart; Potschka, Heidrun; Prins, Jan-Bas; Rosati, Giorgio; Rozman, Jan; Russig, Holger; Schneltzer, Elida; Seebeck, Petra; Stiedl, Oliver; Talbot, Steven R.; Tremoleda, Jordi L.; Witham, Claire; Wohr, Markus; Voikar, Vootele
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A subset of neutrophil phagosomes is characterised by pulses of Class I PI3K activity (vol 18, dmm052042, 2025)中性粒细胞吞噬体中的一个子集,其特征是具有Class I PI3K活性的脉冲(vol 18, dmm052042, 2025)。
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deleteMuir, Clare F.; Reyes-Aldasoro, Constantino Carlos; Prajsnar, Tomasz K.; Michno, Bartosz J.; Cholewa-Waclaw, Justyna; Ho, Yin X.; Bernut, Audrey; Loynes, Catherine A.; Elworthy, Stone; Bowden, Kieran A.; Cadby, Ashley J.; Prince, Lynne R.; King, Jason S.; Ellett, Felix; Condliffe, Alison M.; Renshaw, Stephen A.
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Expanding and refining the Mammalian Phenotype Ontology to enhance disease model discovery扩展和完善哺乳动物表型本体论,以增强疾病模型发现
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deleteBello, Susan M.; V. Anagnostopoulos, Anna; Carmody, Leigh C.; Matentzoglu, Nicolas; Smith, Cynthia L.
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Generation of human induced pluripotent stem cell lines from patients with FGFR2-linked syndromic craniosynostosis从FGFR2相关综合征性颅缝早闭患者中生成人类诱导多能干细胞系
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deleteGijsbertsen, Max; Mathijssen, Irene M. J.; Madancos, Ana F. Duarte; van Leeuwen, Johannes P. T. M.; van de Peppel, Jeroen
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HTRA1-dependent proteolysis induces age-related retinal degeneration and exacerbates choroidal neovascularizationHTRA1依赖性蛋白酶解诱导年龄相关性视网膜变性并加剧脉络膜新生血管形成
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deleteKatschke, Kenneth J.; Truong, Tom; Pham, Victoria; Xi, Hongkang; Tang, Wanjian; Gu, Xiaowu; Teotia, Pooja; Hofmann, Jeffrey W.; Chaney, Shawnta Y.; Kirchhofer, Daniel; Campagne, Menno Van Lookeren; Jeanne, Marion
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GABAergic neuronal dysfunction underlies tremor in spinocerebellar ataxia 3GABAergic神经元功能障碍是脊髓小脑共济失调3型震颤的病理基础。
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deleteBanerjee, Animesh; Chatterjee, Moumita; Tan, Kah Junn; Tay, Shermaine; Duan, Kaibo; Andiappan, Anand Kumar; Howland, Shanshan Wu; Aso, Yoshinori; Aw, Sherry Shiying
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Establishment of a second-generation transgenic marmoset with germline transmission that models polyglutamine disease建立具有种系传递的第二代转基因狨猴,以模拟多聚谷氨酰胺疾病
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deleteMinakawa, Eiko N.; Owari, Kensuke; Nogami, Naotake; Nakatani, Terumi; Koizumi, Masashi; Kawanobe, Akiyo; Saga, Yosuke; Kudo, Moeko; Noguchi, Satoru; Hanakawa, Takashi; Hori, Yuki; Numazawa, Hidemi; Takeuchi, Toshihide; Katakai, Yuko; Saito, Ryoichi; Nagai, Yoshitaka; Saito, Yuko; Tomioka, Ikuo; Seki, Kazuhiko
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