By Icon Health Publications
It is a 3-in-1 reference e-book. It provides an entire scientific dictionary overlaying enormous quantities of phrases and expressions when it comes to sickle telephone anemia. It additionally offers huge lists of bibliographic citations. eventually, it presents info to clients on easy methods to replace their wisdom utilizing a variety of net assets. The ebook is designed for physicians, scientific scholars getting ready for Board examinations, scientific researchers, and sufferers who are looking to familiarize yourself with examine devoted to sickle mobile anemia. in case your time is efficacious, this booklet is for you. First, you won't waste time looking out the net whereas lacking loads of suitable info. moment, the booklet additionally saves you time indexing and defining entries. eventually, you won't waste time and cash printing 1000's of websites.
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Extra info for Sickle Cell Anemia - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References
Example text
Senior Associate Dean for Education; Medicine; University of Minnesota Twin Cities 200 Oak Street Se Minneapolis, Mn 554552070 Timing: Fiscal Year 2002; Project Start 01-APR-2001; Project End 31-MAR-2005 Summary: (Investigator's abstract) Sickle cell anemia patients suffer end organ damage due to vaso-occlusion. Over the past two decades investigations of red blood cell/vessel wall interactions have led to a revised paradigm for the understanding of vaso-occlusive phenomena in sickle cell disease.
Concerted efforts are being made to find agents that stimulate fetal hemoglobin synthesis. Hydroxyurea is found to decrease the frequency of painful crisis and hospitalization, and recent studies with butyrates appear to be promising. This program project is a continuation of our research on gene therapy strategies of sickle cell disease. It utilizes several approaches to improve the possibility of gene therapy in sickle cell anemia. From work of the past project years, we have succeeded in building an improved mouse model of sickle cell anemia that may more closely mimic the human condition Because these mice have difficulty in surviving in utero and neonatal period, we are planning various strategies to improve their survival.
Therefore, it is essential to use this model for testing the efficacy and safety of HFV vectors before applying them to clinical studies. Most primates kept in captivity are infected with the simian foamy virus (SFV) which is very similar to HFV. The presence of SFV in HFV vector transduced animals could complicate the interpretation of marking and toxicity results. Therefore, in vitro analysis of HFV effects on SFV will be explored. Transduction protocols from studies in aim 2 will be applied to marking studies of non-human primate hematopoietic progenitor cells.
