Now showing items 71-80 of 796
Institutional Experience with Voriconazole Compared with Liposomal Amphotericin B as Empiric Therapy for Febrile Neutropenia
(Blackwell Publishing LtdWiley Periodicals, Inc., 2007-07)
Improving estimates of genetic maps: a meta-analysis-based approach
(Wiley Subscription Services, Inc., A Wiley Company, 2007-07)
Inaccurate genetic ( or linkage ) maps can reduce the power to detect linkage, increase type I error, and distort haplotype and relationship inference. To improve the accuracy of existing maps, I propose a meta-analysis-based ...
An Enu Mutagenesis Screen For Dominant Genetic Modifiers Of Thrombosis In The Factor 5 Leiden Mouse
(Wiley Periodicals, Inc., 2007-07)
The Diagnostic Value of Endoscopic Terminal Ileum Biopsies
(Blackwell Publishing Inc, 2007-05)
Cross-shift peak expiratory flow changes are unassociated with respirable coal dust exposure among South African coal miners Human Subjects Declaration: All participants in this study gave written informed consent, participated voluntarily, and had the right to withdraw at any stage. Ethical approval was obtained from the Institutional Review Board of the University of Michigan and the Ethics Committee of University of KwaZulu-Natal.
(Wiley Subscription Services, Inc., A Wiley Company, 2007-12)
Background The objectives of this study were to determine whether cross-shift changes in peak expiratory flow rate (PEFR) were related to respirable dust exposure in South African coalminers. Methods Fifty workers were ...
Synthesis of the Tetraketide Lactones from the Pikromycin Biosynthetic Pathway
(WILEY-VCH Verlag, 2007-07)
Synthesis of tetraketide lactones 2 and 3 , which are likely to be produced by a model pikromycin polyketide synthase (PKS), has been investigated. The tetraketide lactones with six-membered rings, 2a and 2b , were ...
Treatment Strategies for the Behavioral Symptoms of Alzheimer's Disease: Focus on Early Pharmacologic Intervention
(Wiley Periodicals, Inc.Blackwell Publishing Ltd, 2007-03)
Defects in vestibular sensory epithelia and innervation in mice with loss of Chd7 function: Implications for human CHARGE syndrome
(Wiley Subscription Services, Inc., A Wiley Company, 2007-10-10)
CHD7 is a chromodomain gene mutated in CHARGE syndrome, a multiple anomaly condition characterized by ocular c oloboma, h eart defects, a tresia of the choanae, r etarded growth and development, g enital hypoplasia, ...