PDF) Guidelines for incorporating scientific knowledge and practice on rare diseases into higher education: neuronal ceroid lipofuscinoses as a model disorder | Sophia Holthaus - Academia.edu
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Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease | Vol 1868, Issue 7, 1 July 2022 | ScienceDirect.com by Elsevier
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease | Journal | ScienceDirect.com by Elsevier
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Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease | Vol 1866, Issue 10, 1 October 2020 | ScienceDirect.com by Elsevier
Biochimica et Biophysica Acta - Molecular Basis of Disease
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Biomolecules | Free Full-Text | Type 2 Diabetes and Alzheimer’s Disease: The Emerging Role of Cellular Lipotoxicity
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Phenylketonuria (PKU) TAM NGUYEN CHEM Introduction PKU is a common inborn metabolic disorder caused by a deficiency of the liver enzyme phenylalanine. - ppt download
MIT Open Access Articles Influence of PDZK1 on lipoprotein metabolism and atherosclerosis
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Physiological and Pathophysiological Roles of Non-Coding RNAs (BBA Collection Otto Warburg 2022) - BBA Collections - Biochimica et Biophysica Acta - Molecular Basis of Disease - Journal - Elsevier
Frontiers | Molecular Basis for the Therapeutic Effects of Exercise on Mitochondrial Defects
D-Amino acids: Signaling severity in viral infection
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
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease | Ubiquitin, Proteasomes, and Disease | ScienceDirect.com by Elsevier
PDF) The effects of frataxin silencing in HeLa cells are rescued by the expression of human mitochondrial ferritin
