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期刊名:Disease models & mechanisms

缩写:DIS MODEL MECH

ISSN:1754-8403

e-ISSN:1754-8411

IF/分区:3.3/Q1

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共收录本刊相关文章索引2568
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Katerina K Yamamoto,Margaret Wan,Rijul S Penkar et al. Katerina K Yamamoto et al.
The Bone Morphogenetic Proteins (BMPs) are secreted peptide ligands of the Transforming Growth Factor beta (TGF-β) family, initially identified for their roles in development and differentiation across animal species. They are now increasi...
Christian E Gonzalez,Rachana S Vaidya,Sade W Clayton et al. Christian E Gonzalez et al.
The chronic inflammation observed during type 2 diabetes (T2D) is associated with spinal pathologies, including intervertebral disc (IVD) degeneration and chronic spine pain. Despite the presence of confounding factors, such as obesity, stu...
F Sanders Pair,Rudradip Pattanayak,James A Mobley et al. F Sanders Pair et al.
14-3-3 proteins impact protein-protein interactions (PPIs) that regulate neuronal functions. The 14-3-3θ isoform is protective in Parkinson's disease (PD) and Dementia with Lewy Bodies (DLB) models. Human PD and DLB brains show increased 1...
Kandas Traore,Damien Seyer,Agnes Mihajlovski et al. Kandas Traore et al.
Antimicrobial resistance represents one of the most serious threats to both public health and economic sustainability. One of the promising approaches to address this problem is phage therapy - treatment of pathogenic bacterial infections u...
Sankalpa Chakraborty,Olivia Sloan,Bryce Dickerson et al. Sankalpa Chakraborty et al.
Heart Failure with preserved Ejection Fraction (HFpEF) is a lethal, heterogeneous, geriatric syndrome. Long noncoding RNAs (lncRNAs) constitute the majority of the functional mammalian transcriptome and are key regulators in complex pathoph...
Robin A Karge,Florian P Fischer,Hannah Schüth et al. Robin A Karge et al.
Genetic defects in AP2M1, which encodes the μ-subunit of the adaptor protein complex 2 (AP-2) essential for clathrin-mediated endocytosis (CME), cause a rare form of developmental and epileptic encephalopathy (DEE). In this study, we model...
Paula Schuster-Winkelmann,Veronika Weß,Marietta Schindler et al. Paula Schuster-Winkelmann et al.
Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by inflammation and joint destruction. Replicating human manifestations of RA in animal models remains challenging, however, due to heterogeneity of the disease. In thi...
Roza H A Masalmeh,John C Dawson,Virginia Alvarez Garcia et al. Roza H A Masalmeh et al.
Glycolysis and the TCA cycle are reprogrammed in cancer cells to meet bioenergetic and biosynthetic demands, including by engagement with the extracellular matrix (ECM). However, the mechanisms by which the ECM engagement reprograms core en...
Dilys Santillo,Evangelos Bellos,Vanessa Sancho-Shimizu Dilys Santillo
Multisystem inflammatory syndrome in children (MIS-C) is a rare condition associated with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and characterised by systemic inflammation and T-cell dysfunction. A subset of ...
Susan M Bello,Anna V Anagnostopoulos,Leigh C Carmody et al. Susan M Bello et al.
The mouse is a premier model system for investigating gene function and modeling human disease. For almost 40 years, Mouse Genome Informatics has worked to capture and integrate the data generated from mouse studies. A critical component of...