BMB Reports : eISSN 1976-670X

Cited by CrossRef (15)

  1. Merel O. Mol, Suzanne S. M. Miedema, John C. van Swieten, Jeroen G. J. van Rooij, Elise G. P. Dopper. Molecular Pathways Involved in Frontotemporal Lobar Degeneration with TDP-43 Proteinopathy: What Can We Learn from Proteomics?. IJMS 2021;22:10298
    https://doi.org/10.3390/ijms221910298
  2. Shweta Goyal, Rajnish Kumar Chaturvedi. Mitochondrial Protein Import Dysfunction in Pathogenesis of Neurodegenerative Diseases. Mol Neurobiol 2021;58:1418
    https://doi.org/10.1007/s12035-020-02200-0
  3. Dalia A. Mandour, M. A. Bendary, Amira E. Alsemeh. Histological and imunohistochemical alterations of hippocampus and prefrontal cortex in a rat model of Alzheimer like-disease with a preferential role of the flavonoid “hesperidin”. J Mol Histol 2021;52:1043
    https://doi.org/10.1007/s10735-021-09998-6
  4. Joanna Bons, Jacob Rose, Ran Zhang, Jordan B Burton, Christopher Carrico, Eric Verdin, Birgit Schilling. In‐depth analysis of the Sirtuin 5‐regulated mouse brain malonylome and succinylome using library‐free data‐independent acquisitions. Proteomics 2023;23
    https://doi.org/10.1002/pmic.202100371
  5. Amanda Cano, Patric Turowski, Miren Ettcheto, Jason Thomas Duskey, Giovanni Tosi, Elena Sánchez-López, Maria Luisa García, Antonio Camins, Eliana B. Souto, Agustín Ruiz, Marta Marquié, Mercè Boada. Nanomedicine-based technologies and novel biomarkers for the diagnosis and treatment of Alzheimer’s disease: from current to future challenges. J Nanobiotechnol 2021;19
    https://doi.org/10.1186/s12951-021-00864-x
  6. Wen Chen, Huakan Zhao, Yongsheng Li. Mitochondrial dynamics in health and disease: mechanisms and potential targets. Sig Transduct Target Ther 2023;8
    https://doi.org/10.1038/s41392-023-01547-9
  7. Runjiao Zhang, Yizhou Zhang, Fangzhen Guo, Sha Li, Huixian Cui. RNA N6-Methyladenosine Modifications and Its Roles in Alzheimer’s Disease. Front. Cell. Neurosci. 2022;16
    https://doi.org/10.3389/fncel.2022.820378
  8. Zhen Lan, Yanting Chen, Jiali Jin, Yun Xu, Xiaolei Zhu. Long Non-coding RNA: Insight Into Mechanisms of Alzheimer's Disease. Front. Mol. Neurosci. 2022;14
    https://doi.org/10.3389/fnmol.2021.821002
  9. Anna Atlante, Daniela Valenti, Valentina Latina, Giuseppina Amadoro. Dysfunction of Mitochondria in Alzheimer’s Disease: ANT and VDAC Interact with Toxic Proteins and Aid to Determine the Fate of Brain Cells. IJMS 2022;23:7722
    https://doi.org/10.3390/ijms23147722
  10. Jasvinder Singh Bhatti, Kavya Tamarai, Ramesh Kandimalla, Maria Manczak, Xiangling Yin, Bhagavathi Ramasubramanian, Neha Sawant, Jangampalli Adi Pradeepkiran, Murali Vijayan, Subodh Kumar, P. Hemachandra Reddy. Protective effects of a mitochondria-targeted small peptide SS31 against hyperglycemia-induced mitochondrial abnormalities in the liver tissues of diabetic mice, Tallyho/JngJ mice. Mitochondrion 2021;58:49
    https://doi.org/10.1016/j.mito.2021.02.007
  11. Xue-Ying He, Carl Dobkin, W.Ted Brown, Song-Yu Yang. 3-Hydroxyacyl-CoA and Alcohol Dehydrogenase Activities of Mitochondrial Type 10 17β-Hydroxysteroid Dehydrogenase in Neurodegeneration Study. JAD 2022;88:1487
    https://doi.org/10.3233/JAD-220481
  12. Roger Mullins, Dimitrios Kapogiannis. Alzheimer’s Disease-Related Genes Identified by Linking Spatial Patterns of Pathology and Gene Expression. Front. Neurosci. 2022;16
    https://doi.org/10.3389/fnins.2022.908650
  13. Seulki Park, Kidae Kim, Keeok Haam, Hyun Seung Ban, Jung-Ae Kim, Byoung Chul Park, Sung Goo Park, Sunhong Kim, Jeong-Hoon Kim. Long-term depletion of cereblon induces mitochondrial dysfunction in cancer cells. BMB Rep 2021;54:305
    https://doi.org/10.5483/BMBRep.2021.54.6.218
  14. Haiyang Du, Xiaoyu Meng, Yu Yao, Jun Xu. The mechanism and efficacy of GLP-1 receptor agonists in the treatment of Alzheimer’s disease. Front. Endocrinol. 2022;13
    https://doi.org/10.3389/fendo.2022.1033479
  15. Cagri Yalgin, Bohdana Rovenko, Ana Andjelković, Margot Neefjes, Burak Oymak, Eric Dufour, Ville Hietakangas, Howard T. Jacobs. Effects on Dopaminergic Neurons Are Secondary in COX-Deficient Locomotor Dysfunction in Drosophila. iScience 2020;23:101362
    https://doi.org/10.1016/j.isci.2020.101362