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Nutrients|June 12, 2026
Maternal Methyl-Group Donor Intake and Neonatal Birth Size in Singleton IVF PregnanciesSzilvia Bokor, Regina Felső, Ildikó Csölle, et al.
Scientific Reports|July 19, 2016
Glaucoma related Proteomic Alterations in Human Retina SamplesSebastian Funke, Natarajan Perumal, Sabine Beck, et al.
Deutsche Medizinische Wochenschrift (1946)|January 16, 2004
[Patient classification and analysis of risk profiles for type 2 diabetics as the main focus point in practice. Results of the TEMPO study]B Lippmann-Grob, R A Bierwirth, P Kron, et al.
Human Mutation|January 12, 2005
Characterization of genotype-phenotype relationships and stratification by the CARD15 variant genotype for inflammatory bowel disease susceptibility loci using multiple short tandem repeat genetic markersNigel P S Crawford, Daniel W Colliver, Alisa A Funke, et al.
Plos One|March 8, 2013
Distinct signal transduction pathways downstream of the (P)RR revealed by microarray and ChIP-chip analysesDaniela Zaade, Jennifer Schmitz, Eileen Benke, et al.
Human Mutation|January 1, 1994
Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestriesY Ma, M S Liu, D Chitayat, et al.
Angewandte Chemie (International Ed. in English)|November 6, 2020
Probing Local Electrostatics of Glycine in Aqueous Solution by THz SpectroscopyFederico Sebastiani, Chun Yu Ma, Sarah Funke, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|September 25, 2012
Structural analysis of the pyroglutamate-modified isoform of the Alzheimer's disease-related amyloid-β using NMR spectroscopyNa Sun, Rudolf Hartmann, Justin Lecher, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|July 21, 2015
Pre-transplant arm muscle area: a simple measure to identify patients at riskAna Cláudia Thomaz, Carolline Ilha Silvério, Denise Johnsson Campos, et al.
Human Genetics|December 14, 2006
The glu298asp polymorphism in the nitric oxide synthase 3 gene is associated with the risk of ischemic stroke in two large independent case-control studiesKlaus Berger, Florian Stögbauer, Monika Stoll, et al.
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