PDF) The effects of frataxin silencing in HeLa cells are rescued by the expression of human mitochondrial ferritin
Soluble epoxide hydrolase and TRPC3 channels jointly contribute to homocysteine-induced cardiac hypertrophy: Interrelation and regulation by C/EBPβ,Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease - X-MOL
Stroke injury, cognitive impairment and vascular dementia
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MIT Open Access Articles Influence of PDZK1 on lipoprotein metabolism and atherosclerosis
Phenylketonuria (PKU) TAM NGUYEN CHEM Introduction PKU is a common inborn metabolic disorder caused by a deficiency of the liver enzyme phenylalanine. - ppt download
Angiopoietin-like protein 8 deficiency attenuates thoracic aortic aneurysm/dissection development in β-aminopropionitrile monofumarate-induced model mice,Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease - X-MOL
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AbuMweis, S, S Jew, R Tayyem, and L Agraib. 2018. "Eicosapentaenoic acid and docosahexaenoic acid containing supplements mo
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Titel Academic Radiology Acta Biomaterialia Acta Materialia Advanced Powder Technology Advances in Colloid and Interface Science
Synapse - Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
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Evolutionary artificial intelligence based peptide discoveries for effective Covid-19 therapeutics,Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease - X-MOL
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Molecular basis of astrocyte diversity and morphology across the CNS in health and disease | Science
Elsevier Genetics & Genomics - BBA Molecular Basis of Disease invites papers for the forthcoming Special Issue. Submission deadline December 31st, 2021. Find out more: http://spkl.io/618843EX8 | Facebook
Frontiers | Molecular Basis for the Therapeutic Effects of Exercise on Mitochondrial Defects
