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Chemosphere|September 15, 2019
Mass loads, source apportionment, and risk estimation of organic micropollutants from hospital and municipal wastewater in recipient catchmentsMattias Sörengård, Hugo Campos-Pereira, Malin Ullberg, et al.
Journal of Molecular Evolution|April 9, 2020
Exploring Evolutionary Constraints in the Proteomes of Zika, Dengue, and Other Flaviviruses to Find Fitness-Critical SitesJanelle Nunez-Castilla, Jordon Rahaman, Joseph B Ahrens, et al.
Magnetic Resonance in Medicine|September 28, 2007
Fluorine-19 MRI for visualization and quantification of cell migration in a diabetes modelMangala Srinivas, Penelope A Morel, Lauren A Ernst, et al.
The Journal of Physical Chemistry. B|April 28, 2007
The influence of secondary interactions during the formation of polyelectrolyte multilayers: layer thickness, bound water and layer interpenetrationManesh Gopinadhan, Oxana Ivanova, Heiko Ahrens, et al.
Oral Surgery, Oral Medicine, and Oral Pathology|April 1, 1992
Absorbed dose determination for tomographic implant site assessment techniquesD K Kassebaum, N E Stoller, W D McDavid, et al.
Journal of Cancer Research and Clinical Oncology|October 16, 2008
Grade I chondrosarcoma of bone: the Münster experienceArne Streitbürger, Helmut Ahrens, Maurice Balke, et al.
American Journal of Public Health|September 16, 2016
Housing Assistance and Blood Lead Levels: Children in the United States, 2005-2012Katherine A Ahrens, Barbara A Haley, Lauren M Rossen, et al.
Journal of Orthopaedic Surgery and Research|August 27, 2016
Eradication rates, risk factors, and implant selection in two-stage revision knee arthroplasty: a mid-term follow-up studySteffen Hoell, Anna Sieweke, Georg Gosheger, et al.
The Anatomical Record. Part A, Discoveries in Molecular, Cellular, and Evolutionary Biology|October 8, 2005
Anatomical analysis of an aye-aye brain (Daubentonia madagascariensis, primates: Prosimii) combining histology, structural magnetic resonance imaging, and diffusion-tensor imagingJason A Kaufman, Eric T Ahrens, David H Laidlaw, et al.
The Journal of Clinical Endocrinology and Metabolism|February 15, 2007
A disruptive mutation in exon 3 of the GNAS gene with albright hereditary osteodystrophy, normocalcemic pseudohypoparathyroidism, and selective long transcript variant Gsalpha-L deficiencySusanne Thiele, Ralf Werner, Wiebke Ahrens, et al.
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