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The Journal of Biological Chemistry|December 2, 2004
Proteomic analysis of in vivo phosphorylated synaptic proteinsMark O Collins, Lu Yu, Marcelo P Coba, et al.Proteomics. Clinical Applications|February 4, 2015
Programmed cell death 6 interacting protein (PDCD6IP) and Rabenosyn-5 (ZFYVE20) are potential urinary biomarkers for upper gastrointestinal cancerHolger Husi, Richard J E Skipworth, Andrew Cronshaw, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 13, 2018
MAGE genes in the kidney: identification of MAGED2 as upregulated during kidney injury and in stressed tubular cellsLara Valiño-Rivas, Leticia Cuarental, Mateo Agustin, et al.Clinical Chemistry and Laboratory Medicine|January 16, 2020
The influence of hypoxia on the prostate cancer proteomeJames A Ross, Johannes P C Vissers, Jyoti Nanda, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 6, 2014
Habitual Myofibrillar Protein Synthesis Is Normal in Patients with Upper GI Cancer CachexiaAlisdair J MacDonald, Neil Johns, Nathan Stephens, et al.Journal of Biomedical Science|January 5, 2020
Bile and urine peptide marker profiles: access keys to molecular pathways and biological processes in cholangiocarcinomaTorsten Voigtländer, Jochen Metzger, Holger Husi, et al.Journal of Neurochemistry|April 26, 2006
Molecular characterization and comparison of the components and multiprotein complexes in the postsynaptic proteomeMark O Collins, Holger Husi, Lu Yu, et al.Neuromuscular Disorders : NMD|May 4, 2020
A late-onset congenital myasthenic syndrome due to a heterozygous DOK7 mutationPaulo Bastos, Raquel Barbosa, Marco Fernandes, et al.Clinics and Practice|April 3, 2021
Mitral Valve Subacute Endocarditis Caused by Abiotrophia Defectiva: A Case ReportCatarina Faria, Renato Guerreiro, Sofia Cruz, et al.Clinical Neurology and Neurosurgery|July 31, 2021
Characterization of a Portuguese family with Charcot-Marie-Tooth disease type 1E due to a novel point mutation in the PMP22 geneMarco Fernandes, André Caetano, Luís Castelhano, et al.Pageof 12