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biochimica et biophysica acta-molecular basis of disease影响因子4分无版面费– sci666
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
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease | Vol 1866, Issue 10, 1 October 2020 | ScienceDirect.com by Elsevier
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Biomolecules | Free Full-Text | Type 2 Diabetes and Alzheimer’s Disease: The Emerging Role of Cellular Lipotoxicity
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease | Journal | ScienceDirect.com by Elsevier
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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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Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease | Ubiquitin, Proteasomes, and Disease | ScienceDirect.com by Elsevier
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
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Molecular basis of astrocyte diversity and morphology across the CNS in health and disease | Science
D-Amino acids: Signaling severity in viral infection
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Stroke injury, cognitive impairment and vascular dementia
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Molecular Basis of Disease 1998: Vol 1406 Table of Contents : Free Download, Borrow, and Streaming : Internet Archive
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
