in leukapheresis 10. Specific gravity of copper sulfate for Hgb screening 11. Antigens belonging to KELL except: Lutheran‚ Cellano‚ Penney‚ Sutter 12. Next to ABO‚ what blood group system is tested prior to transfusion 13. How to test in vivo sensitization of RBCs 14. Sugar responsible for Grp B blood group specificity 15. Rh-Hr nomenclature is introduced by? 16. CRP indicates what? 17. Qualitative VDRL is interpreted by: titration‚ naked eye‚ spectrophotometer‚ microscopically
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Synthetic‚ Structural‚ theoretical and biological study of triorganotin(IV) Schiff base complexes derived from amino acids Abstract A new series of triorganotin(IV) complexes of monofunctional bidentate Schiff base have been synthesized and characterized through elemental analysis‚ conductance measurements‚ molecular weight determinations‚ UV-visible‚ multinuclear (1H‚ 13C‚ 119Sn) NMR spectroscopy‚ FT-IR‚ X-ray powder diffraction and theoretical calculations. On the basis of these techniques‚ it
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in dissolution velocity is because of increase in surface area going beyond that of micronized products. Fine powders/particles retain an increased adhesiveness very well known from powder technology. These features enhance bioavailability. Much in vivo data generated with drug nanoparticles by NanoSystems confirm this [22]. However‚ there are two more remarkable features of drug nanoparticles (i.e.‚ DissoCubes): (a) an increase in saturation solubility and (b) structural changes inside the particles
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Aldehyde and Ketone 1. ALDEHYDE Definition: An aldehyde is an organic compound containing a formyl group. This functional group‚ with the structure R-CHO‚ consists of a carbonyl center (a carbon double bonded to oxygen) bonded to hydrogen and an R group‚ which is any generic alkyl or side chain. The group without R is called the aldehyde group or formyl group. Aldehydes differ from ketones in that the carbonyl is placed at the end of a carbon skeleton rather than between two carbon atoms
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transplantation using a collagen bilayer matrix for cartilage repair. J Bone Jt Surg Br 1997;79(5):831–6. [34] Minas T‚ Nehrer S. Current concepts in the treatment of articular cartilage defects. Orthopedics 1997;20(6):525–38. [35] LeBaron RG‚ Athanasiou KA. Ex vivo synthesis of articular cartilage. Biomaterials 2000;21(24):2575–87. [36] Lee DA‚ Bader DL. Compressive strains at physiological frequencies influence the metabolism of chondrocytes seeded in agarose. J Orthop Res 1997;15(2):181–8. [37] Webb K‚ Hlady
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Hindawi Publishing Corporation International Journal of Surgical Oncology Volume 2012‚ Article ID 861257‚ 12 pages doi:10.1155/2012/861257 Research Article Assessing Breast CancerMargins Ex Vivo Using Aqueous Quantum-Dot-Molecular Probes Giang H. T. Au‚1 Wan Y. Shih‚1 Wei-Heng Shih‚2 LinetteMejias‚3 Vanlila K. Swami‚3 KimberlyWasko‚4 and Ari D. Brooks4 1 School of Biomedical Engineering‚ Science and Health Systems‚ Drexel University‚ 3141 Chestnut Street‚ Philadelphia‚ PA 19104‚ USA 2Department
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94-98. 20. Basu S.‚ Hazra B.‚ "Evaluation of nitric oxide scavenging activity of selected medicinal plants used in inflammatory diseases"‚ Phytotherapy research‚ vol. 20(10)‚ 2006‚ pp. 896-900. 22. Adhiraj N.‚ Ravikumar T.‚ Shanmugasundaram N.‚ "In vivo and in vitro evaluation of hair growth potential of Shoe flower"‚ Jr. of ethanopharmacology‚ vol. 88(2-3)‚ 2003‚ pp. 235-239. 25. Palani V.‚ Senthilkumaran R.K.‚ "Biochemical evaluation in antitumour effect of Muthu Marunthu on experimental fibrosarcoma
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Causes and Treatment of Panic Attacks Rosendo Rodriguez Liberty University Abstract It is necessary to first understand what anxiety disorder is in order to understand more easily what and how panic attacks occur in an individual. Anxiety is a normal reaction to different situations of life. However‚ when it comes as chronic or excessive it becomes a disease that prevents the normal functioning of a person. The anxiety symptoms are a response to a situation that is interpreted
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tumour watch and disease profiling studies for the Tel-AML1 mouse project in Chapter 4. This work was a collaboration with Dr. Louise van der Weyden‚ my colleague in the lab and Dr. Brian Huntly in MRCCIMR Cambridge. I have included some of their in vivo work to prove that this mouse model has been successful for modelling cALL (childhood Acute Lymphoblastic Leukemia) in human‚ and is included in Figure 4-9. None of the material presented herein has been submitted previously for the purpose of obtaining
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CHAPTER 1 Introduction and Its Background Introduction Infectious diseases are one of the main contributors to global mortality and morbidity. Infectious diseases are caused by pathogenic microorganisms‚ such as bacteria‚ viruses‚ parasites or fungi. These diseases can be spread‚ directly or indirectly‚ from one person to another. Vaccines‚ antibiotics‚ and many other advances have lessened the impact of infectious diseases. Unfortunately‚ this has not been true everywhere. It has not been true in
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