DOCSLIB.ORG

Sarvodaya Hospital & Research Centre

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Sarvodaya Hospital & Research Centre 6 38214/2020/ESTT-NE_HRSarvodaya Hospital & Research Centre SOC 2018 - 19 Sno. Department Number of Services 1 Administration 3 2 Audiology 9 3 Blood Bank 10 4 Cardiology 45 5 CTVS 57 6 Dental 163 7 Dermatology 20 8 Diabetci Lab 4 9 ENT 163 10 Gastroentrology 46 11 General Procedure 39 12 General Surgery 226 13 Interventional Radiology 31 14 Laboratory 898 15 Medical Procedure 23 16 Neonatology 15 17 Nephrology 28 18 Neuro Surgery 165 19 Neurology 27 20 Obstetrics & Gynae 110 21 Surgical Oncology 154 22 Medical Oncology 27 23 Radiation Oncology 56 24 Nuclear Medicine 35 25 Opthalmology 108 26 Orthopaedics 278 27 Pain Clinic 14 28 Physiotheraphy 54 29 Plastic Surgery 443 30 Pulmonology 38 31 Radiology 519 32 Urology 219 33 Vaccination 34 Billing Cycle & Policy 1. Room Charge will be charge according to check out time will be 12 Noon. 2. Grace Period will be 2 Hours fof Discharging Patient. 7 3. Patient Bed Transfer - The higher bed category of the bed transfer day will be charged 38214/2020/ESTT-NE_HR4. Post surgery change of bed category - If patient change the bed category from lower to higher after the surgery, then the complete surgery/procedure charges will be applicable as per the higher category. 5. If two or more Surgeries are Performed at same timeon the same area, Then the Frist Surgery will be Charge 100% & Second will Be Charge 60% & Then 50% will be charged for the Third and subsequent surgery (lower charged). 6. All unplanned and emergency surgeries performed from 8 PM to 8 AM Or Any Pubic Holiday shall be charged 25% additional emergency charges on corresponding rates. 7. Day care room charges will be Rs. 1500 applicable up to 8 hours and if stay exceeds more than 8 hours then Full Day Room rent will be charged as per opted room category. 8. If The Patient is in MICU/SICU, Two Visits for the Admitting Doctor as per bed Category and One visit Rs 750 for Intensive Care Team Per day will be charged. 9. Emergency Timing will be 8 PM to 8 AM or Any Public Holiday. 10. If any Surgery Procedure done between Emergency Timing then 25% Extra will be Charge (Normal Procedure Charge + 25% Extra). 11. Emergency Consultation will be charge 100% Extra Charges ( Normal Charges + 100% Extra). Room Tariff Visit Charges Emergency Visit Charges Ward Bed Charge Super Specialist Specialist Super Specialist Specialist General Ward 2700 550 600 1100 1200 Semi Private 4100 650 700 1300 1400 Single Room 6800 700 800 1400 1600 Suite Room 9600 750 800 1500 1600 Presidential Suite 15000 800 900 1600 1800 HDU 4500 650 700 1300 1400 Labour Delivery Room 5500 650 700 1300 1400 PICU 5500 750 800 1500 1600 NICU 5900 750 800 1500 1600 MICU/ CCU 8350 750 800 1500 1600 SICU /CTVS 8350 750 800 1500 1600 Day Care 1500 400 450 800 900 Minimum Advance at The Time Of Admission Sno. Bed Category Advance 1 ICU 30000 2 General Ward 10000 3 Semi Private 15000 4 Single Room 20000 5 Suite Room 25000 6 Elective Surgery 100% of the Estimate / Package rate Administration Charges Service General Twin Single Suite Department Service Name OPD Code Ward Sharing Room Room Administration RC001 File Charges 300 300 300 300 300 Administration RC002 Diet Consultation 300 300 300 300 300 Administration RC003 MLC Charges 1300 1300 1300 1300 1300 Administration RC004 Medical Supervision 350 350 350 350 350 Audiology Department Service Service Name OPD General Twin Single Suite Code Ward Sharing Room Room Audiology AD002 Pure Tone Audiometry ( PTA ) 1058 1058 1219 1380 1541 Audiology AD003 Otoaoustic Emissions (OAE) 1610 1610 1852 2093 2335 Audiology AD004 Speech Therapy (Assessment) 679 679 782 886 989 Audiology AD005 Hearing - Aid Trail 495 495 575 644 725 Audiology AD006 Cochlear Implant - Pre Op Evaluation 8050 8050 9258 10465 11673 Audiology AD007 Neonatal ABR 3163 3163 3646 4117 4589 Audiology AD008 Speech Therapy (Procedure Charges Of 1 Sessions) 3393 3393 3910 4416 4922 Audiology AD009 Speech Therapy Per Session Of 30-40Minutes 633 633 736 828 920 IP Packages Service Length Of Stay Twin Single Suite Department Service Name General Ward Code ICU Ward Sharing Room Room Audiology AD001 Cochlear Implant - Surgery 0 2 73025 84065 94990 105915 Package Includes:- Room Rent as specified , Basic Investigation, Professional Fees of Treating consultant, Ot Charges , Anesthesia Charges & Routine Drugs & consumables. Package excludes:- Extra Stay, Cross consultation, Other Procedure, Professional Fee of other consultant & Cost of Implant. Basic Investigations Include:- CBC, Lft, Kft, Blood Sugar , Chest X - Ray, ECG, HIV, PT, APTT, Hbsag, Hcv, Viral Marker. 8 Note :- The Package Inclusions & Exclusions Will Be Discussed In Detail at The Time Of Patient / Attendant Counselling 38214/2020/ESTT-NE_HR Blood Bank Services Department Service Service Name OPD General Twin Single Suite Code Ward Sharing Room Room Blood Bank BD001 Whole Blood Processing Charges 1500 1500 1500 1500 1500 Blood Bank BD002 Packed Red Blood Cells (PRBC) Processing Charges 1500 1500 1500 1500 1500 Blood Bank BD003 Leukodepleted PRBC Processing Charges 2500 2500 2500 2500 2500 Blood Bank BD004 FFP (Fresh Frozen Plasma) Processing Charges 400 400 400 400 400 Blood Bank BD005 PLC (Platelet Concentrate) Processing Charges 400 400 400 400 400 Blood Bank BD006 Platelet Apheresis (SDPC) Processing Charges 11000 11000 11000 11000 11000 Blood Bank BD007 Blood Letting 700 700 700 700 700 Blood Bank BD008 Donor Grouping 130 130 130 130 130 Blood Bank BD009 Rapid Screening 1100 1100 1100 1100 1100 Blood Bank BD010 Cross Matching 621 621 725 817 909 CARDIOLOGY Department Service Service Name OPD General Twin Single Suite Code Ward Sharing Room Room Cardiology CD030 Pericardial Tapping 12650 14605 16445 18400 Cardiology CD032 Visipaque Charges extra 1725 1725 2070 2300 2530 Cardiology CD033 2D ECHO 2691 2691 3105 3508 3910 Cardiology CD034 2D ECHO for LV function 1610 1610 1852 2093 2335 Cardiology CD035 Neonatal ECHO 3738 3738 4301 4865 5428 Cardiology CD036 Peadiatric ECHO By Consultant In Opd 4025 4025 4635 5233 5842 Cardiology CD037 ECHO Portable 3623 3623 4175 4715 5256 Cardiology CD038 Stress ECHO With TMT 3680 3680 4232 4784 5336 Cardiology CD039 Dobutamine Stress ECHO (DSE) 4485 4485 5164 5831 6509 Cardiology CD040 Trans Oesophagous ECHO Cardiography (TEE) 4485 4485 5164 5831 6509 Cardiology CD041 ECG 345 345 403 449 506 Cardiology CD042 Holter Monitor 24 Hour 2691 2691 3105 3508 3910 Cardiology CD043 Holter Monitor 48 Hour 4485 4485 5164 5831 6509 Cardiology CD044 Ambulatory BP 2530 2530 2910 3289 3669 Cardiology CD045 TMT 2300 2300 2645 2990 3335 IP Packages Length Of Stay General Twin Single Suite Department Item Code Service Name ICU Ward Ward Sharing Room Room Cardiology CD001 Day Care Coronary Angiography 0 Day Care 11500 Cardiology CD002 Coronary Angiography 0 1 14950 17250 19435 21735 Cardiology CD003 Check Angiography 0 1 11500 13225 14950 16675 Cardiology CD004 Angiography Renal 0 1 14950 17250 19435 21735 Cardiology CD005 Angiography Carotid/Peripheral 0 1 14950 17250 19435 21735 Cardiology CD006 Digital Substraction Angiography ( DSA ) 0 1 27025 31165 35190 39215 Cardiology CD007 Coronary Angiography With Coronary Angioplasty 1 2 149500 171925 194350 216775 Cardiology CD008 Coronary Angioplasty 1 2 149500 171925 194350 216775 Cardiology CD009 Second Stage Angioplasty 1 1 69000 79350 89700 100050 Cardiology CD010 POBA (Baloon Angioplasty) 1 1 149500 171925 194350 216775 Cardiology CD011 Angioplasty Peripheral 1 1 143750 165370 186875 208495 Cardiology CD012 Angioplasty Carotid 1 2 115000 132250 149500 166750 Cardiology CD013 Angioplasty Renal 1 1 115000 132250 149500 166750 Cardiology CD014 Coronary Angiography With FFR 0 1 40250 46345 52325 58420 Cardiology CD015 Fractional Flow Rate Study (FFR) 0 1 28750 33120 37375 41745 Cardiology CD016 PTCA With Rotabilation 1 2 212750 244720 276575 308545 Cardiology CD017 Complex PTCA/ Multi Vessel PTCA 1 2 184000 211600 239200 266800 Cardiology CD018 Pacemaker - Single Chamber 1 1 57500 66125 74750 83375 Cardiology CD019 Pacemaker - Double Chamber 1 1 80500 92575 104650 116725 Cardiology CD020 AICD - Single Chamber 1 1 69000 79350 89700 100050 Cardiology CD021 AICD - Double Chamber 1 1 88550 101890 115115 128455 Cardiology CD022 Combo Device CRT -D 1 1 103500 119025 134550 150075 Cardiology CD023 CRT -P 1 1 92000 105800 119600 133400 Cardiology CD024 EPS (Diagnostic) 0 1 34500 39675 44850 50025 Cardiology CD025 EPS with RFA (2D) 1 1 92000 105800 119600 133400 Cardiology CD026 EPS with RFA (3D) 1 1 115000 132250 149500 166750 Cardiology CD027 Device Closar (ASD/VSD/PDA) 0 1 115000 132250 149500 166750 Cardiology CD028 BMV 0 1 115000 132250 149500 166750 Cardiology CD029 IVC Filter 0 1 59455 68425 77395 86250 Cardiology CD031 Temporary Pacemaker Implantation (TPI) 0 1 34500 39675 44850 50025 Package Includes:- Room rent as specified, cath lab charges, Professional fees of cardiologist, basic Investigations , disposables in Cath Lab and Non Ionic Dye , Cost of Aggramed & cost of medicine & consumables. 9 Package excludes:- Stent Cost , implant cost, Gp IIb/ IIIa inhibitor, Other devices like Rota & Atherectomy equipment , additional stay, Professional charges of other 38214/2020/ESTT-NE_HRconsultants, any additional procedure/investigation and consumables. Basic Investigations Include :- CBC, Lft, Kft, Blood Sugar , Chest X - Ray, ECG, HIV, PT, APTT, Hbsag, Hcv, Echo Only One Ecg , One Chest X - Ray & Only One Blood Sugar is Part of Package for CD001 to CD006. Echo is not part of Package for the same. Note :- The Package Inclusions & Exclusions Will Be Discussed
Load more

Recommended publications
  • Functional Impact of Interacting Protein on Kainate Receptors: Necab1 and Neto Proteins
    Instituto de Neurociencias de Alicante Universidad Miguel Hernandez Thesis manuscript for: PhD in Neuroscience Functional impact of interacting protein on kainate receptors: NeCaB1 and NeTo proteins. Jon Palacios Filardo Supervised by: Prof. Juan Lerma Alicante, 2014 Agradecimientos/Acknowledgments Agradecimientos/Acknowledgments Ahora que me encuentro escribiendo los agradecimientos, me doy cuenta que esta es posiblemente la única sección de la tesis que no será corregida. De manera que los escribiré tal como soy, tal vez un poco caótico. En primer lugar debo agradecer al profesor Juan Lerma, por la oportunidad que me brindó al permitirme realizar la tesis en su laboratorio. Más que un jefe ha sido un mentor en todos estos años, 6 exactamente, en los que a menudo al verme decía: “Jonny cogió su fusil”, y al final me entero que es el título de una película de cine… Pero aparte de un montón de anécdotas graciosas, lo que guardaré en la memoria es la figura de un mentor, que de ciencia todo lo sabía y le encantaba compartirlo. Sin duda uno no puede escribir un libro así (la tesis) sin un montón de gente alrededor que te enseña y ayuda. Como ya he dicho han sido 6 años conviviendo con unos maravillosos compañeros, desde julio de 2008 hasta presumiblemente 31 de junio de 2014. De cada uno de ellos he aprendido mucho; técnicamente toda la electrofisiología se la debo a Ana, con una paciencia infinita o casi infinita. La biología molecular me la enseñó Isa. La proteómica la aprendí del trío Esther-Ricado-Izabella. Joana y Ricardo me solventaron mis primeras dudas en el mundo de los kainatos.
    [Show full text]
  • Oliver Von Bohlen Und Halbach.Pdf
    Oliver von Bohlen und Halbach and Rolf Dermietzel Neurotransmitters and Neuromodulators Related Titles Thiel, G. (ed.) Transcription Factors in the Nervous System Development, Brain Function, and Diseases 2006 ISBN 3-527-31285-4 Becker, C.G., Becker, T. (eds.) Model Organisms in Spinal Cord Regeneration 2006 ISBN 3-527-31504-7 Bähr, M. (ed.) Neuroprotection Models, Mechanisms and Therapies 2004 ISBN 3-527-30816-4 Frings, S., Bradley, J. (eds.) Transduction Channels in Sensory Cells 2004 ISBN 3-527-30836-9 Smith, C.U.M. Elements of Molecular Neurobiology 2003 ISBN 0-471-56038-3 Oliver von Bohlen und Halbach and Rolf Dermietzel Neurotransmitters and Neuromodulators Handbook of Receptors and Biological Effects 2nd completely revised and enlarged edition The Authors n All books published by Wiley-VCH are carefully produced. Nevertheless, authors, Dr. Oliver von Bohlen und Halbach editors, and publisher do not warrant the Department of Anatomy and Cell Biology information contained in these books, University of Heidelberg including this book, to be free of errors. Im Neuenheimer Feld 307 Readers are advised to keep in mind that 69120 Heidelberg statements, data, illustrations, procedural Germany details or other items may inadvertently be inaccurate. Prof. Dr. med. Rolf Dermietzel Department of Neuroanatomy and Molecular Brain Research Library of Congress Card No.: applied for University of Bochum British Library Cataloguing-in-Publication Data Universitätsstr. 150 A catalogue record for this book is available 44780 Bochum from the British Library. Germany Bibliographic information published by the Deutsche Nationalbibliothek The Deutsche Nationalbibliothek lists this publica- tion in the Deutsche Nationalbibliografie; detailed bibliographic data are available in the Internet at http://dnb.d-nb.de.
    [Show full text]
  • Molekuláris Bionika És Infobionika Szakok Tananyagának Komplex Fejlesztése Konzorciumi Keretben
    PETER PAZMANY SEMMELWEIS CATHOLIC UNIVERSITY UNIVERSITY Development of Complex Curricula for Molecular Bionics and Infobionics Programs within a consortial* framework** Consortium leader PETER PAZMANY CATHOLIC UNIVERSITY Consortium members SEMMELWEIS UNIVERSITY, DIALOG CAMPUS PUBLISHER The Project has been realised with the support of the European Union and has been co-financed by the European Social Fund *** **Molekuláris bionika és Infobionika Szakok tananyagának komplex fejlesztése konzorciumi keretben ***A projekt az Európai Unió támogatásával, az Európai Szociális Alap társfinanszírozásával valósul meg. 11/25/2011. TÁMOP – 4.1.2-08/2/A/KMR-2009-0006 1 Peter Pazmany Catholic University Faculty of Information Technology www.itk.ppke.hu BASICS OF NEUROBIOLOGY Neurobiológia alapjai IONOTROPIC RECEPTORS (Ionotrop receptorok) ZSOLT LIPOSITS 11/25/2011. TÁMOP – 4.1.2-08/2/A/KMR-2009-0006 2 Basics of Neurobiology: Ionotropic receptors www.itk.ppke.hu TRANSMITTER RECEPTORS WITH THE EXCEPTION OF STEROID SIGNALS AND UNCONVENTIONAL GAS TRANSMIT- TERS (NO, CO), REGULAR NEUROMESSENGERS CAN NOT DIFFUSE THROUGH THE CELL MEMBRANE THEIR EFFECTS ARE MEDIATED BY RECEPTORS THAT ARE EMBEDDED INTO THE POST- SYNAPTIC MEMBRANE RECEPTORS ARE COMPLEX PROTEINS THAT SHOW HIGH-AFFINITY BINDING FOR TRANSMITTER LIGANDS LIGAND BINDING ALTERS THE CONFORMATION OF THE RECEPTOR THAT EVOKES POSTSYNAPTIC RESPONSES THE RESPONSE DEPENDS ON THE AMOUNT OF THE TRANSMITTER, THE NUMBER AND STATE OF THE RECEPTORS TRANSMITTER RECEPTORS BELONG TO TWO CATEGORIES: IONOTROPIC RECEPTORS METABOTROPIC RECEPTORS 11/25/2011. TÁMOP – 4.1.2-08/2/A/KMR-2009-0006 3 Basics of Neurobiology: Ionotropic receptors www.itk.ppke.hu TRANSMITTER RECEPTORS IONOTROPIC RECEPTORS FORM PORES, SPECIFIC ION CHANNELS IN THE MEMBRANE THAT ALLOW THE PASSAGE OF IONS UPON ACTIVATION.
    [Show full text]
  • I. Glur6 Kainate Receptors
    University of Calgary PRISM: University of Calgary's Digital Repository Cumming School of Medicine Cumming School of Medicine Research & Publications 2009-02 Glutamate receptors on myelinated spinal cord axons: I. GluR6 kainate receptors Ouardouz, Mohamed; Basak, Ajoy; Chen, Andrew; Rehak, Renata; Yin, Xinghua; Coderre, Elaine M.; Zamponi, Gerald W.; Hameed, Shahid; Trapp, Bruce D. T.; Stys, Peter K.... Wiley-Liss, Inc. Ouardouz, M., Coderre, E., Basak, A., Chen, A., Zamponi, G. W., Hameed, S., … Stys, P. K. (2009). Glutamate receptors on myelinated spinal cord axons: I. glur6 kainate receptors. Annals of Neurology, 65(2), 151–159. https://doi.org/10.1002/ana.21533 http://hdl.handle.net/1880/106670 unknown https://creativecommons.org/licenses/by/4.0 Downloaded from PRISM: https://prism.ucalgary.ca Glutamate Receptors on Myelinated Spinal Cord Axons: I. GluR6 Kainate Receptors Mohamed Ouardouz, PhD,1 Elaine Coderre,1 Ajoy Basak, PhD,2 Andrew Chen, BSc,2 Gerald W. Zamponi, PhD,3 Shameed Hameed, PhD,3 Renata Rehak, MSc,3 Xinghua Yin, MD,4 Bruce D. Trapp, PhD,4 and Peter K. Stys, MD5 Objective: The deleterious effects of glutamate excitotoxicity are well described for central nervous system gray matter. Although overactivation of glutamate receptors also contributes to axonal injury, the mechanisms are poorly understood. Our goal was to ϩ elucidate the mechanisms of kainate receptor–dependent axonal Ca2 deregulation. ϩ Methods: Dorsal column axons were loaded with a Ca2 indicator and imaged in vitro using confocal laser-scanning micros- copy. ϩ Results: Activation of glutamate receptor 6 (GluR6) kainate receptors promoted a substantial increase in axonal [Ca2 ].
    [Show full text]
  • Inhibitory Effects of Glutamate-Stimulated Astrocytes on Action Potentials Evoked by Bradykinin in Cultured Dorsal Root Ganglion Neurons
    Tokai J Exp Clin Med., Vol. 39, No. 1, pp. 14-24, 2014 Inhibitory Effects of Glutamate-stimulated Astrocytes on Action Potentials Evoked by Bradykinin in Cultured Dorsal Root Ganglion Neurons Kazuo SUZUKI, Minehisa ONO and Kenji TONAKA Department of Biomedical Engineering, Tokai University (Received September 26, 2013; Accepted January 20, 2014) Patch-clamp and Ca2+-imaging techniques have revealed that astrocytes have dynamic properties including ion channel activity and release of neurotransmitters, such as adenosine triphosphate (ATP) and glutamate. Here, we used the patch-clamp technique to determine whether ATP and glutamate is able to modulate the bradykinin (BK) response in neurons cultured with astrocytes in the mouse dorsal root ganglia (DRG) in order to clarify the role of astrocytes in nociceptive signal transmission. Astrocytes were identified using a fluorescent anti-GFAP antibody. The membrane potential of astrocytes was about －39 mV. The application of glutamic acid (GA) to the bath evoked the opening of two types of Cl－ channel in the astrocyte cell membrane with a unit conductance of about 380 pS and 35 pS in the cell-attached mode, respectively. ATP application evoked the opening of two types of astrocyte K+ channel with a unit conductance of about 60 pS and 29 pS, respectively. Application of BK to the neuron evoked an action potential (spike). Concomitant BK application with ATP increased the frequency of BK-evoked neuron spikes when neurons coexisted with astrocytes. Stimulation of BK with GA inhibited the BK-evoked spike under similar conditions. The application of furosemide, a potent cotransporter (Na+-K+-2Cl－) inhibitor, prior to stimulation of BK with GA blocked inhibition of the spike.
    [Show full text]
  • Specificity in Glycosylation of Multiple Flagellins by the Modular and Cell
    RESEARCH ARTICLE Specificity in glycosylation of multiple flagellins by the modular and cell cycle regulated glycosyltransferase FlmG Silvia Ardissone†, Nicolas Kint, Patrick H Viollier* Department of Microbiology & Molecular Medicine, Faculty of Medicine / CMU, University of Geneva, Gene`ve, Switzerland Abstract How specificity is programmed into post-translational modification of proteins by glycosylation is poorly understood, especially for O-linked glycosylation systems. Here we reconstitute and dissect the substrate specificity underpinning the cytoplasmic O-glycosylation pathway that modifies all six flagellins, five structural and one regulatory paralog, in Caulobacter crescentus, a monopolarly flagellated alpha-proteobacterium. We characterize the biosynthetic pathway for the sialic acid-like sugar pseudaminic acid and show its requirement for flagellation, flagellin modification and efficient export. The cognate NeuB enzyme that condenses phosphoenolpyruvate with a hexose into pseudaminic acid is functionally interchangeable with other pseudaminic acid synthases. The previously unknown and cell cycle-regulated FlmG protein, a defining member of a new class of cytoplasmic O-glycosyltransferases, is required and sufficient for flagellin modification. The substrate specificity of FlmG is conferred by its N-terminal flagellin- binding domain. FlmG accumulates before the FlaF secretion chaperone, potentially timing flagellin modification, export, and assembly during the cell division cycle. *For correspondence: [email protected] Present address: †Center for Research on Intracellular Introduction Bacteria, Institute of Post-translational protein modification is essential for various facets in cellular biology, ranging from Microbiology, University Hospital Center and University of gene regulation to the organization of cellular structures. In all cases, biological function underlies Lausanne, Bugnon, Switzerland the capacity to specifically identify and modify the correct target protein.
    [Show full text]
  • Manipulation of Metabotropic and AMPA Glutamate Receptors in the Brain
    Manipulation of Metabotropic and AMPA Glutamate Receptors in the Brain ©Amy G. M. Lam, B.Sc. Hons (University of London) A thesis submitted for the Degree of Doctor of Philosophy to the Faculty of Medicine, University of Glasgow Wellcome Surgical Institute & Hugh Fraser Neuroscience Laboratories, University of Glasgow, Garscube Estate, Bearsden Road, Glasgow G61 1QH March 1999 ProQuest Number: 11007789 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a com plete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. uest ProQuest 11007789 Published by ProQuest LLC(2018). Copyright of the Dissertation is held by the Author. All rights reserved. This work is protected against unauthorized copying under Title 17, United States C ode Microform Edition © ProQuest LLC. ProQuest LLC. 789 East Eisenhower Parkway P.O. Box 1346 Ann Arbor, Ml 48106- 1346 O SGOW b DIVERSITY LIBRARY Co| Declaration I declare that this thesis comprises my own original work and has not been accepted in any previous application for a degree. The work, of which it is a record, has been carried out by myself, except as acknowledged and indicated in the thesis. All sources of information have been specifically referenced. Amy Lam Acknowledgements This thesis would not have been possible without the assistance and support of many people. First and foremost, my greatest thanks go to Professor James McCulloch for his never-failing support over the past few years.
    [Show full text]
  • 7Th International Congress on Amino Acids and Proteins Vienna, Austria
    Amino Acids (2001) 21: 1–90 7th International Congress on Amino Acids and Proteins Vienna, Austria August 6–10, 2001 Abstracts Co-Presidents: Steve Schaffer, Mobilel, AL, U.S.A. Michael Fountoulakis, Basel, Switzerland Gert Lubec, Vienna, Austria Contents Analysis................................................................................ 3 Biology ................................................................................ 10 Proteomics . 14 Medicine . 22 Metabolism/Nutrition . 25 Neurobiology . 35 Neuroscience . 45 Plant Amino Acids . 56 Physiology/Exercise and Sport . 59 Polyamines . 63 Synthesis . 68 Taurine ................................................................................ 74 Amino Acids Transport . 79 Addendum . 86 3 Analysis Fully automated HPLC based analysis of cysteine and related used for calculation of the degree of substitution in case of compounds in plasma using on line microdialysis as sample peptide-conjugates. The results of amino acid analysis were preparation verified by the data of ES mass spectrometry method. [This study was supported by grants from Hungarian E. Bald Research Fund (OTKA) T 030838, T025834, T032425, F034886 Department of Environmental Chemistry, University of ´Lodz´, and from the Ministry of Education (FKFP/0153/2001).] Poland Low molecular weight thiols play important roles in metabolism and homeostasis. While plasma thiols, including Free and bound cysteine in homocystinuria: assessment of metabolically related cysteine, glutathione, and homocysteine, cysteine and glutathione status are being investigated as potential indicators of health status A. Briddon1, I. P. Hargreaves1, and P. J. Lee2 and disease risk, trace levels, poor stability, and the lack of 1 structural properties necessary for the production of signals Department of Clinical Biochemistry, and compatible with common detection methods have hampered 2 Metabolic Unit, The National Hospital for Neurology and their accurate assessment. The facile oxidation of sulfhydryl Neurosurgery, London, U.K.
    [Show full text]
  • The Genus Crataegus: Chemical and Pharmacological Perspectives Dinesh Kumar Et Al
    Revista Brasileira de Farmacognosia Brazilian Journal of Pharmacognosy The genus Crataegus: chemical and 22(5): 1187-1200, Sep./Oct. 2012 pharmacological perspectives Dinesh Kumar,*,1 Vikrant Arya,2 Zulfi qar Ali Bhat,1 Nisar Ahmad Khan,1 Deo Nandan Prasad3 1Department of Pharmaceutical Sciences, University of Kashmir, India, 2ASBASJSM College of Pharmacy, Bela Ropar, Punjab, India, Review 3Shivalik College of Pharmacy, Naya-Nangal, Punjab, India. Abstract: Traditional drugs have become a subject of world importance, with both Received 9 Sep 2011 medicinal and economical implications. A regular and widespread use of herbs Accepted 9 Apr 2012 throughout the world has increased serious concerns over their quality, safety and Available online 16 Aug 2012 efficacy. Thus, a proper scientific evidence or assessment has become the criteria for acceptance of traditional health claims. Plants of the genus Crataegus, Rosaceae, are widely distributed and have long been used in folk medicine for the treatment of Keywords: various ailments such as heart (cardiovascular disorders), central nervous system, Crataegus immune system, eyes, reproductive system, liver, kidney etc. It also exhibits wide flavonoids hawthorn range of cytotoxic, gastroprotective, anti-inflammatory, anti-HIV and antimicrobial maloideae/Rosaceae activities. Phytochemicals like oligomeric procyanidins, flavonoids, triterpenes, thorny bush polysaccharides, catecholamines have been identified in the genus and many of these have been evaluated for biological activities. This review presents comprehensive information on the chemistry and pharmacology of the genus together with the traditional uses of many of its plants. In addition, this review discusses the clinical ISSN 0102-695X trials and regulatory status of various Crataegus plants along with the scope for http://dx.doi.org/10.1590/S0102- future research in this aspect.
    [Show full text]
  • Kainate Receptors and Synaptic Transmission James E
    Progress in Neurobiology 70 (2003) 387–407 Kainate receptors and synaptic transmission James E. Huettner∗ Department of Cell Biology and Physiology, Washington University School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, USA Received 20 February 2003; accepted 25 July 2003 Abstract Excitatory glutamatergic transmission involves a variety of different receptor types, each with distinct properties and functions. Physiolog- ical studies have identified both post- and presynaptic roles for kainate receptors, which are a subtype of the ionotropic glutamate receptors. Kainate receptors contribute to excitatory postsynaptic currents in many regions of the central nervous system including hippocampus, cortex, spinal cord and retina. In some cases, postsynaptic kainate receptors are co-distributed with ␣-amino-3-hydroxy-5-methyl-4- isoxazolepropionic acid (AMPA) and N-methyl-d-aspartate (NMDA) receptors, but there are also synapses where transmission is mediated exclusively by postsynaptic kainate receptors: for example, in the retina at connections made by cones onto off bipolar cells. Modulation of transmitter release by presynaptic kainate receptors can occur at both excitatory and inhibitory synapses. The depolarization of nerve terminals by current flow through ionotropic kainate receptors appears sufficient to account for most examples of presynaptic regulation; however, a number of studies have provided evidence for metabotropic effects on transmitter release that can be initiated by activation of kainate receptors. Recent analysis of knockout mice lacking one or more of the subunits that contribute to kainate receptors, as well as studies with subunit-selective agonists and antagonists, have revealed the important roles that kainate receptors play in short- and long-term synaptic plasticity.
    [Show full text]
  • In Vitro Characterization of NS3763, a Non-Competitive Antagonist of GLUK5 Receptors
    JPET Fast Forward. Published on February 25, 2004 as DOI: 10.1124/jpet.103.062794 JPET FastThis Forward.article has not Published been copyedited on and February formatted. The25, final 2004 version as DOI:10.1124/jpet.103.062794may differ from this version. JPET #62794 1 In vitro characterization of NS3763, a non-competitive antagonist of GLUK5 receptors Jeppe K. Christensen, Thomas Varming, Philip K. Ahring, Tino D. Jørgensen and Elsebet Ø. Nielsen NeuroSearch A/S, 93 Pederstrupvej, DK-2750 Ballerup, Denmark Downloaded from jpet.aspetjournals.org at ASPET Journals on October 1, 2021 Copyright 2004 by the American Society for Pharmacology and Experimental Therapeutics. JPET Fast Forward. Published on February 25, 2004 as DOI: 10.1124/jpet.103.062794 This article has not been copyedited and formatted. The final version may differ from this version. JPET #62794 2 Running title: non-competitive GLUK5 antagonist Corresponding author: Dr. Elsebet Ø. Nielsen Department of Receptor Biochemistry NeuroSearch A/S 93 Pederstrupvej DK-2750 Ballerup Downloaded from Denmark Telephone: (+45) 4460 8000 Direct telephone: (+45) 4460 8237 jpet.aspetjournals.org Fax: (+45) 4460 8080 E-mail: [email protected] at ASPET Journals on October 1, 2021 Tables: 1 Figures: 7 References: 40 Words in Abstract: 159 Words in Introduction: 750 Words in Discussion: 910 Section: Neuropharmacology Non-standard abbreviations: AMPA: α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid ATPA: α-amino-3-hydroxy-5- tertbutylisoxazole-4-propionic acid JPET Fast Forward. Published on February 25, 2004 as DOI: 10.1124/jpet.103.062794 This article has not been copyedited and formatted.
    [Show full text]
  • Nutrition & Supplements
    But wait, there's MORE! We can't publish all our items in one catalog - it takes SIX catalogs! Find details about all the 20212020 catalogs we offer throughout —— the year on page 2. 20222021 AzureStandard.com AzureStandard.com | AZURE STANDARD Nutrition & Supplements 971-200-8350 | 971-200-8350 971-200-8350 CATALOG Delivering supplements and so much more! We seek to make your life easier, healthier, and more fulfilling. Your complete set of When you shop with Azure, you can fill your pantry, your 2021 AZURE CATALOGS Nutrition & Supplements kitchen cabinets, your refrigerator, your freezer, your bathroom includes: THE ITEMS IN THIS CATALOG meet a high threshold for quality. Azure requires transparency from all the companies medicine cabinet, your laundry room, your bedside table, and we work with, and we only choose suppliers that produce foods and products made with only natural ingredients. That means you get even your garden shed with natural and organic products. Nutrition & Supplements nutrient-rich foods and products that are minimally processed with no artificial additives, no preservatives, non-GMO, no MSG, no artificial Publishes in February CT032 colors or flavors. That doesn’t mean every item is organic. Some are made with organic ingredients but are not Certified Organic. Some go Explore all of our products on our website at AzureStandard. Health & Beauty far beyond organic. They all are earth-friendly, non-GMO and meticulously chosen for their healthful qualities. com, or request a specific catalog by Publishes inh April CT033 item number (at right). To receive all of our catalogs and sales Household & Family Azure’s Unacceptable Ingredient List: flyers delivered to your door as they become available, add item Publishes in June CT034 Artificial Colors Certified Colors Shellfish Products CT014 to your order for $19.95.
    [Show full text]