Showing results (211-220 of 512) with videos related to

Sort By:
Pageof 52
Langmuir : the ACS Journal of Surfaces and Colloids|August 29, 2018
Defect-Induced Water Bilayer Growth on Anatase TiO2(101)A Schaefer, V Lanzilotto, U B Cappel, et al.
Clinical Nutrition (Edinburgh, Scotland)|January 29, 2010
An effective lifestyle intervention in overweight children: findings from a randomized controlled trial on "Obeldicks light"T Reinehr, A Schaefer, K Winkel, et al.
Anesthesiology|December 19, 2001
Isoflurane and sevoflurane anesthesia in pigs with a preexistent gas exchange defectA Kleinsasser, K H Lindner, C Hoermann, et al.
Journal of Child and Adolescent Psychopharmacology|March 3, 2005
Treatment with stimulants among youths in a large California health planLaurel A Habel, Catherine A Schaefer, Peter Levine, et al.
The American Journal of Psychiatry|May 2, 2006
Prenatal exposure to maternal genital and reproductive infections and adult schizophreniaVicki Babulas, Pam Factor-Litvak, Raymond Goetz, et al.
Leukemia|August 1, 1992
Induction of differentiation in Friend-erythroleukemia cells by aclacinomycin A: early transient decrease in c-myc and c-myb mRNA levelsA Schaefer, A Dressel, K Lingelbach, et al.
Nuclear Medicine and Biology|February 22, 2001
Preparation and investigation of tumor affinity, uptake kinetic and transport mechanism of iodine-123-labelled amino acid derivatives in human pancreatic carcinoma and glioblastoma cellsS Samnick, A Schaefer, S Siebert, et al.
Arzneimittel-Forschung|December 1, 1988
Mutagenic and antimutagenic effects of 5-substituted 2'-deoxyuridines depending on the nature of the 5-substituentH Marquardt, J Westendorf, A Schaefer, et al.
European Radiology|November 19, 2010
Bilateral contrast-enhanced MR angiography of the hand: diagnostic image quality of accelerated MRI using echo sharing with interleaved stochastic trajectories (TWIST)Jan Thorsten Winterer, P Blanke, A Schaefer, et al.
Biochemistry|July 3, 2010
Structure of the human sulfhydryl oxidase augmenter of liver regeneration and characterization of a human mutation causing an autosomal recessive myopathyVidyadhar N Daithankar, Stephanie A Schaefer, Ming Dong, et al.
Pageof 52