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Advances in Experimental Medicine and Biology|January 1, 1995
Dendritic cells differentiated from human monocytes through a combination of IL-4, GM-CSF and IFN-gamma exhibit phenotype and function of blood dendritic cellsH Xu, M Krämer, H P Spengler, et al.
Scandinavian Journal of Immunology|December 1, 1993
1,25-Dihydroxyvitamin D3 exerts opposing effects to IL-4 on MHC class-II antigen expression, accessory activity, and phagocytosis of human monocytesH Xu, A Soruri, R K Gieseler, et al.
JBR-BTR : Organe De La Societe Royale Belge De Radiologie (SRBR) = Orgaan Van De Koninklijke Belgische Vereniging Voor Radiologie (KBVR)|March 29, 2005
Small bowel obstruction secondary to disseminated candidiasis in an immunocompromised patient: radiologic-pathologic correlationD Bielen, K Mortelé, H Peters, et al.
The Journal of Chemical Physics|December 5, 2012
Diffusion of water and selected atoms in DMPC lipid bilayer membranesF Y Hansen, G H Peters, H Taub, et al.
Psicologia, Reflexao E Critica : Revista Semestral Do Departamento De Psicologia Da UFRGS|February 7, 2020
Planning theory- and evidence-based behavior change interventions: a conceptual review of the intervention mapping protocolGerjo Kok, Louk W H Peters, Robert A C Ruiter
Scientific Reports|November 4, 2016
Few Ramachandran Angle Changes Provide Interaction Strength Increase in Aβ42 versus Aβ40 Amyloid FibrilsOscar H Bastidas, Benjamin Green, Mary Sprague, et al.
Optics Express|May 4, 2026
Monolithic excitable photonic neuronOdhran Liston, Robert N Sheehan, Frank H Peters, et al.
Biology of Reproduction|May 23, 2001
A highly conserved sequence essential for translational repression of the protamine 1 messenger rna in murine spermatidsJ Zhong, A H Peters, K Kafer, et al.
Journal of Reproduction and Fertility|January 1, 1976
Follicular atresia in the infant human ovaryR Himelstein-Braw, A G Byskov, H Peters, et al.
Human Mutation|March 25, 1999
Mutation screening of neurofibromatosis type 1 (NF1) exons 28 and 29 with single strand conformation polymorphism (SSCP): five novel mutations, one recurrent transition and two polymorphisms in a panel of 118 unrelated NF1 patients. Mutations in brief no. 229. OnlineH Peters, A Lüder, A Harder, et al.
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