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Annual Report 2014 - 2015 Our Mission
ANNUAL REPORT 2014 - 2015 Our Mission By integrating the fields of medicine, science, engineering and technology into translational knowledge and making the resulting biomedical innovations accessible to public health, to improve the health of the most disadvantaged people in India and throughout the world. Our Vision As a networked organization linking many centers of excellence, THSTI is envisaged as a collective of scientists, engineers and physicians that will effectively enhance the quality of human life through integrating a culture of shared excellence in research, education and translational knowledge with the developing cohorts and studying the pathogenesis and the molecular mechanisms of disease to generate knowledge to complement the processes of designing interventions and technology development. CONTENTS 3 THE ORGANIZATION Society Governing Body Leadership From the Executive Director’s Desk 11 RESEARCH PROGRAMS Vaccine and Infectious Disease Research Centre Pediatric Biology Centre Centre for Biodesign and Diagnostics Policy Center for Biomedical Research Drug Discovery Research Centre Centre for Human Microbial Ecology Population Science Partnership Centre Clinical Development Services Agency 178 ACADEMIA 184 ADMINISTRATION Organization INTRAMURAL CENTRES Vaccine & Infectious Disease Research Centre (VIDRC) Pediatric Biology Centre (PBC) Centre for Biodesign & Diagnostics (CBD) Centre for Human Microbial Ecology (CHME) Policy Centre for Biomedical Research (PCBR) Drug Discovery Research Centre (DDRC) PARTNERSHIP CENTRE Population Science Partnership Centre (PSPC) EXTRAMURAL CENTRE Clinical Development Services Agency (CDSA) THSTI Society 1 2 3 4 5 6 7 8 9 10 11 12 1. Dr. G. Padmanaban 5. Dr. T.S. Rao 9. Dr. J. Gowrishankar Distinguished Professor, Nodal Officer, THSTI, Sr. Advisor, Director, IISc Bangalore Department of Biotechnology, Centre for DNA Fingerprinting President New Delhi & Diagnostics, Member Ex-officio Hyderabad 2. -
Table 2. Significant
Table 2. Significant (Q < 0.05 and |d | > 0.5) transcripts from the meta-analysis Gene Chr Mb Gene Name Affy ProbeSet cDNA_IDs d HAP/LAP d HAP/LAP d d IS Average d Ztest P values Q-value Symbol ID (study #5) 1 2 STS B2m 2 122 beta-2 microglobulin 1452428_a_at AI848245 1.75334941 4 3.2 4 3.2316485 1.07398E-09 5.69E-08 Man2b1 8 84.4 mannosidase 2, alpha B1 1416340_a_at H4049B01 3.75722111 3.87309653 2.1 1.6 2.84852656 5.32443E-07 1.58E-05 1110032A03Rik 9 50.9 RIKEN cDNA 1110032A03 gene 1417211_a_at H4035E05 4 1.66015788 4 1.7 2.82772795 2.94266E-05 0.000527 NA 9 48.5 --- 1456111_at 3.43701477 1.85785922 4 2 2.8237185 9.97969E-08 3.48E-06 Scn4b 9 45.3 Sodium channel, type IV, beta 1434008_at AI844796 3.79536664 1.63774235 3.3 2.3 2.75319499 1.48057E-08 6.21E-07 polypeptide Gadd45gip1 8 84.1 RIKEN cDNA 2310040G17 gene 1417619_at 4 3.38875643 1.4 2 2.69163229 8.84279E-06 0.0001904 BC056474 15 12.1 Mus musculus cDNA clone 1424117_at H3030A06 3.95752801 2.42838452 1.9 2.2 2.62132809 1.3344E-08 5.66E-07 MGC:67360 IMAGE:6823629, complete cds NA 4 153 guanine nucleotide binding protein, 1454696_at -3.46081884 -4 -1.3 -1.6 -2.6026947 8.58458E-05 0.0012617 beta 1 Gnb1 4 153 guanine nucleotide binding protein, 1417432_a_at H3094D02 -3.13334396 -4 -1.6 -1.7 -2.5946297 1.04542E-05 0.0002202 beta 1 Gadd45gip1 8 84.1 RAD23a homolog (S. -
The Ubiquitination Enzymes of Leishmania Mexicana
The ubiquitination enzymes of Leishmania mexicana Rebecca Jayne Burge Doctor of Philosophy University of York Biology October 2020 Abstract Post-translational modifications such as ubiquitination are important for orchestrating the cellular transformations that occur as the Leishmania parasite differentiates between its main morphological forms, the promastigote and amastigote. Although 20 deubiquitinating enzymes (DUBs) have been partially characterised in Leishmania mexicana, little is known about the role of E1 ubiquitin-activating (E1), E2 ubiquitin- conjugating (E2) and E3 ubiquitin ligase (E3) enzymes in this parasite. Using bioinformatic methods, 2 E1, 13 E2 and 79 E3 genes were identified in the L. mexicana genome. Subsequently, bar-seq analysis of 23 E1, E2 and HECT/RBR E3 null mutants generated in promastigotes using CRISPR-Cas9 revealed that the E2s UBC1/CDC34, UBC2 and UEV1 and the HECT E3 ligase HECT2 are required for successful promastigote to amastigote differentiation and UBA1b, UBC9, UBC14, HECT7 and HECT11 are required for normal proliferation during mouse infection. Null mutants could not be generated for the E1 UBA1a or the E2s UBC3, UBC7, UBC12 and UBC13, suggesting these genes are essential in promastigotes. X-ray crystal structure analysis of UBC2 and UEV1, orthologues of human UBE2N and UBE2V1/UBE2V2 respectively, revealed a heterodimer with a highly conserved structure and interface. Furthermore, recombinant L. mexicana UBA1a was found to load ubiquitin onto UBC2, allowing UBC2- UEV1 to form K63-linked di-ubiquitin chains in vitro. UBC2 was also shown to cooperate with human E3s RNF8 and BIRC2 in vitro to form non-K63-linked polyubiquitin chains, but association of UBC2 with UEV1 inhibits this ability. -
Developmental Adaptations of Energy and Lipid Metabolism in Trypanosoma Brucei Insect Forms
Department Biologie I Bereich Genetik Ludwig-Maximilians-Universität München Developmental adaptations of energy and lipid metabolism in Trypanosoma brucei insect forms. Stefan Allmann Dissertation der Fakultät für Biologie, Ludwig-Maximilians-Universität München Eingereicht am 18.09.2014 Erster Gutachter : Prof. Dr. Michael Boshart Biozentrum der Ludwig-Maximilians-Universität München Bereich Genetik Zweiter Gutachter: Prof. Dr. Peter Geigenberger Biozentrum der Ludwig-Maximilians-Universität München Bereich Pflanzenwissenschaften Datum der Abgabe: 18.09.2014 Datum der mündlichen Prüfung: 24.10.2014 Eidesstattliche Erklärung Ich versichere hiermit an Eides statt, dass die vorgelegte Dissertation von mir selbstständig und ohne unerlaubte Hilfe angefertigt wurde. Des Weiteren erkläre ich, dass ich nicht anderweitig ohne Erfolg versucht habe eine Dissertation einzureichen oder mich der Doktorprüfung zu unterziehen. Die folgende Dissertation liegt weder ganz, noch in wesentlichen Teilen einer anderen Prüfungskommission vor. München, 18.09.2014 Statutory declaration I declare that I have authored this thesis independently, that I have not used other than the declared sources/resources. As well I declare, that I have not submitted a dissertation without success and not passed the oral exam. The present dissertation (neither the entire dissertation nor parts) has not been presented to another examination board. Munich, 18.09.2014 III Content Eidesstattliche Erklärung III Statutory declaration III Abbreviations V Publications and Manuscripts Originating from this Thesis VII Contribution to Publications and Manuscripts Presented in this Thesis VIII Summary IX Zusammenfassung X 1. Introduction 11 1.1 Trypanosoma brucei in a nutshell 11 1.2 The parasite’s life cycle 12 1.3 Intermediate and energy metabolism 14 1.4 NADPH balance 17 1.5 Lipid droplets as energy storage 20 2. -
List of Life Members As on 20Th January 2021
LIST OF LIFE MEMBERS AS ON 20TH JANUARY 2021 10. Dr. SAURABH CHANDRA SAXENA(2154) ALIGARH S/O NAGESH CHANDRA SAXENA POST HARDNAGANJ 1. Dr. SAAD TAYYAB DIST ALIGARH 202 125 UP INTERDISCIPLINARY BIOTECHNOLOGY [email protected] UNIT, ALIGARH MUSLIM UNIVERSITY ALIGARH 202 002 11. Dr. SHAGUFTA MOIN (1261) [email protected] DEPT. OF BIOCHEMISTRY J. N. MEDICAL COLLEGE 2. Dr. HAMMAD AHMAD SHADAB G. G.(1454) ALIGARH MUSLIM UNIVERSITY 31 SECTOR OF GENETICS ALIGARH 202 002 DEPT. OF ZOOLOGY ALIGARH MUSLIM UNIVERSITY 12. SHAIK NISAR ALI (3769) ALIGARH 202 002 DEPT. OF BIOCHEMISTRY FACULTY OF LIFE SCIENCE 3. Dr. INDU SAXENA (1838) ALIGARH MUSLIM UNIVERSITY, ALIGARH 202 002 HIG 30, ADA COLONY [email protected] AVANTEKA PHASE I RAMGHAT ROAD, ALIGARH 202 001 13. DR. MAHAMMAD REHAN AJMAL KHAN (4157) 4/570, Z-5, NOOR MANZIL COMPOUND 4. Dr. (MRS) KHUSHTAR ANWAR SALMAN(3332) DIDHPUR, CIVIL LINES DEPT. OF BIOCHEMISTRY ALIGARH UP 202 002 JAWAHARLAL NEHRU MEDICAL COLLEGE [email protected] ALIGARH MUSLIM UNIVERSITY ALIGARH 202 002 14. DR. HINA YOUNUS (4281) [email protected] INTERDISCIPLINARY BIOTECHNOLOGY UNIT ALIGARH MUSLIM UNIVERSITY 5. Dr. MOHAMMAD TABISH (2226) ALIGARH U.P. 202 002 DEPT. OF BIOCHEMISTRY [email protected] FACULTY OF LIFE SCIENCES ALIGARH MUSLIM UNIVERSITY 15. DR. IMTIYAZ YOUSUF (4355) ALIGARH 202 002 DEPT OF CHEMISTRY, [email protected] ALIGARH MUSLIM UNIVERSITY, ALIGARH, UP 202002 6. Dr. MOHAMMAD AFZAL (1101) [email protected] DEPT. OF ZOOLOGY [email protected] ALIGARH MUSLIM UNIVERSITY ALIGARH 202 002 ALLAHABAD 7. Dr. RIAZ AHMAD(1754) SECTION OF GENETICS 16. -
ABSTRACT Title of Dissertation
ABSTRACT Title of Dissertation: COMPARATIVE TRANSCRIPTOME PROFILING OF HUMAN FORESKIN FIBROBLASTS INFECTED WITH THE SYLVIO AND Y STRAINS OF TRYPANOSOMA CRUZI Genevieve Houston-Ludlam, Doctor of Philosophy, 2016 Dissertation Directed by: Professor Najib M. El-Sayed Department of Cell Biology and Molecular Genetics Trypanosoma cruzi, the causative agent of Chagas Disease, is phylogenetically distributed into nearly identical genetic strains which show divergent clinical presentations including differences in rates of cardiomyopathy in humans, different vector species and transmission cycles, and differential congenital transmission in a mouse model. The population structure of these strains divides into two groups, which are geographically and clinically distinct. The aim of this study was to compare the transcriptome of two strains of T. cruzi, Sylvio vs. Y to identify differences in expression that could account for clinical and biochemical differences. We collected and sequenced RNA from T. cruzi-infected and control Human Foreskin Fibroblasts at three timepoints. Differential expression analysis identified gene expression profiles at different timepoints in Sylvio infections, and between Sylvio and Y infections in both parasite and host. The Sylvio strain parasite and the host response to Sylvio infection largely mirrored the host- pathogen interaction seen in our previous Y strain work. IL-8 was more highly expressed in Sylvio-infected HFFs than in Y-infected HFFs. Comparative transcriptome profiling of human foreskin fibroblasts infected with the Sylvio and Y strains of Trypanosoma cruzi By Genevieve Houston-Ludlam Dissertation submitted to the Faculty of the Graduate School of the University of Maryland, College Park, in partial fulfillment of the requirements for the degree of Doctor of Philosophy 2016 Advisory Committee: Professor Najib M. -
Jncasr Annual Report 2013-14 English.Pdf
ISSN.0973-9319 ANNUAL REPORT 2013-14 JAWAHARLAL NEHRU CENTRE FOR ADVANCED SCIENTIFIC RESEARCH (A Deemed to be University) Jakkur, Bangalore – 560 064. Website: http://www.jncasr.ac.in ANNUAL REPORT 2013-14 137 CONTENTS The Centre Page No. Foreword 1 Introduction 2 Objectives 3 Progress 4 Highlights of research and other activities 6 Activities Chart 13 Organisation Chart 14 The Organisation Council of Management 15 Finance Committee 16 Academic Advisory Committee 17 Faculties 18 Administration 18 Units, Centres,Computer Laboratory, Library and Endowed Research Professors 20 Academic Programmes Academic Activities 59 Discussion Meetings 62 Endowment Lectures 62 Silver Jubilee Lectures 63 Special Lectures 63 International Conferences/Workshops / Symposia 63 Seminars / Colloquia 64 Extension Activities Visiting Fellowships 69 Summer Research Fellowship Programme 69 Project Oriented Chemical Education Programme 69 Project Oriented Biological Education Programme 70 JNCASR-CICS Fellowship Programme 70 National Science Day 70 Intellectual Property 71 Research Programmes Research Areas 74 Research Facilities 76 Sponsored Research Projects (Ongoing) 77 New Sponsored Research Projects 83 Publications Research Publications of Units 85 Research Publications of Honorary Faculty/ Endowed Professors 115 Books authored/edited by Honorary Faculty 117 Awards / Distinctions 118 Financial Statements 121 The Centre Foreword I have great pleasure in presenting the Twenty Fifth Annual Report for the year 2013-14. The Centre which is also a Deemed to be University, has been emerging as one of the leading institutions in the country for higher learning and research in frontier areas of science and engineering. There is a steady increase in the number of research students in the Centre pursuing various academic programmes. -
Annual Report 2010 -11
ANNUAL REPORT 2010 -11 INDIAN INSTITUTE OF SCIENCE EDUCATION & RESEARCH CET CAMPUS, THIRUVANANTHAPURAM - 695 016 Publication Committee Dr M.P. Rajan Dr S. Shankaranarayanan Dr Sujith Vijay Mr S Hariharakrishnan Mr B V Ramesh Technical Assistance: Ms. A. S. Aswathy Contact : 0471 2597459, Fax: 0471 2597427 Email : [email protected] CONTENTS Page No. Preface 1 Preamble Introduction 1 IISER Thiruvananthapuram Society 1 Board of Governors and other authorities 2 Academic Advisory Committee 3 2 Human Resource Faculty & their research profile 4 Administrative Support Personnel 20 Students (BS-MS & Ph.D Programme) 20 3 Academic Programmes 22 4 Research Activities Sponsored Projects 23 Fellowships 24 5 Research Publications 24 6 Awards and Honours 28 7 Other Academic Activities Faculty Activities Conferences & Workshops Attended 29 Invited Lectures /Seminars 31 Internship & Outreach Programme 33 Distinguished Visitors 33 Lectures, Colloquia & Seminars organized 34 8 Facilities Research Laboratories 40 Library Resources 40 Computing and Networking Facility 40 9 Sports and Cultural Activities 41 10 Permanent & Transit Campus 41 11 Statement of Audited Annual Account 44 i PREFACE Indian Institute of Science Education and Research Thiruvananthapuram, established by the Ministry of Human Resource Development, Government of India, in 2008 has completed three years. I am happy to present this report of the remarkable progress made by the institute in many fronts during the past year, with the aim of providing high quality education in modern science, integrating it with outstanding research at the undergraduate level itself. During this year we have doubled the faculty strength with one professor and fifteen assistant professors joining us. A brief description of the research interests of the faculty forms a part of this report. -
List of Officers Who Attended Courses at NCRB
List of officers who attened courses at NCRB Sr.No State/Organisation Name Rank YEAR 2000 SQL & RDBMS (INGRES) From 03/04/2000 to 20/04/2000 1 Andhra Pradesh Shri P. GOPALAKRISHNAMURTHY SI 2 Andhra Pradesh Shri P. MURALI KRISHNA INSPECTOR 3 Assam Shri AMULYA KUMAR DEKA SI 4 Delhi Shri SANDEEP KUMAR ASI 5 Gujarat Shri KALPESH DHIRAJLAL BHATT PWSI 6 Gujarat Shri SHRIDHAR NATVARRAO THAKARE PWSI 7 Jammu & Kashmir Shri TAHIR AHMED SI 8 Jammu & Kashmir Shri VIJAY KUMAR SI 9 Maharashtra Shri ABHIMAN SARKAR HEAD CONSTABLE 10 Maharashtra Shri MODAK YASHWANT MOHANIRAJ INSPECTOR 11 Mizoram Shri C. LALCHHUANKIMA ASI 12 Mizoram Shri F. RAMNGHAKLIANA ASI 13 Mizoram Shri MS. LALNUNTHARI HMAR ASI 14 Mizoram Shri R. ROTLUANGA ASI 15 Punjab Shri GURDEV SINGH INSPECTOR 16 Punjab Shri SUKHCHAIN SINGH SI 17 Tamil Nadu Shri JERALD ALEXANDER SI 18 Tamil Nadu Shri S. CHARLES SI 19 Tamil Nadu Shri SMT. C. KALAVATHEY INSPECTOR 20 Uttar Pradesh Shri INDU BHUSHAN NAUTIYAL SI 21 Uttar Pradesh Shri OM PRAKASH ARYA INSPECTOR 22 West Bengal Shri PARTHA PRATIM GUHA ASI 23 West Bengal Shri PURNA CHANDRA DUTTA ASI PC OPERATION & OFFICE AUTOMATION From 01/05/2000 to 12/05/2000 1 Andhra Pradesh Shri LALSAHEB BANDANAPUDI DY.SP 2 Andhra Pradesh Shri V. RUDRA KUMAR DY.SP 3 Border Security Force Shri ASHOK ARJUN PATIL DY.COMDT. 4 Border Security Force Shri DANIEL ADHIKARI DY.COMDT. 5 Border Security Force Shri DR. VINAYA BHARATI CMO 6 CISF Shri JISHNU PRASANNA MUKHERJEE ASST.COMDT. 7 CISF Shri K.K. SHARMA ASST.COMDT. -
Imbim Annual Report 2015
Department of Medical Biochemistry and Microbiology IMBIM ANNUAL REPORT 2015 DEPARTMENT OF MEDICAL BIOCHEMISTRY AND MICROBIOLOGY ANNUAL REPORT 2015 Pictures taken by Helena Öhrvik The role of copper in mast cell granule homeostasis Ctr2 is a protein involved in cellular transport of copper. Upper panels: staining for tryptase, a mast cell granule protease, in tryptase (Mcpt6)-deficient (negative control), Ctr2-/- and wild type (WT) mast cells. Note that the absence of Ctr2 causes upregulated expression of tryptase. Lower panels: staining of Ctr2-/- and WT mast cells with toluidine blue, a proteoglycan- binding dye. Note increased toluidine blue staining of Ctr2-/- mast cells, indicating increased proteoglycan content of granules. Öhrvik, H., Logeman, B., Noguchi, G., Eriksson, I., Kjellén, L., Thiele, D.J., Pejler, G. (2015) Ctr2 regulates mast cell maturation by affecting the storage and expression of tryptase and proteoglycans. J. Immunol. 195, 3654-364. Edited by Veronica Hammar ISBN no 978-91-979531-8-4 PREFACE Another year has passed with both small and large successes for the laboratory. The Department has a stable staff consisting of some 150 people. Including project workers, post doc etc we are around 250 persons that spend our daily work hours at the Department. Fortunately the granting situation for the IMBIM researchers improved considerably during 2015. Many of the small and medium sized research groups received grants that will help them continue to excel during the coming years. In addition Dan Andersson, Leif Andersson, Per Jemth, and a couple of scientists at ICM, received a hefty 47 milj kr grant from “Knut och Alice Wallenbergs Stiftelse” to support their research on the evolution of new genes and proteins. -
Platinum Jubilee Celebrations 2009 Inside
No. 51 March 2010 Newsletter of the Indian Academy of Sciences Platinum Jubilee Celebrations 2009 Inside.... Founded in 1934, the Academy celebrated its Platinum Jubilee 1. Platinum Jubilee year in 2009. A short inaugural function was held on Celebrations – 2009 .................................. 1 1st January, 2009 at the IISc during which the traditional lamp was lit by the President and six former Presidents. 2. Twenty-First Mid-Year Meeting The activities and initiatives for the Platinum year included July 2010 .................................................. 5 monthly lectures, platinum jubilee professorships, special publications, and three meetings and symposia which were 3. 2010 Elections .......................................... 6 held in July, November and December 2009. 4. Special Issues of Journals ......................... 10 PLATINUM JUBILEE MEETING – I The first Meeting was held at Hyderabad during July 2 – 4, 5. Discussion Meeting ...................................13 2009 and was co-hosted by IICT and CCMB. The Welcome Address by the President focused on efforts to mitigate 6. Raman Professor .......................................14 problems of impaired vision. Special lectures were by Lalji Singh and Surendra Prasad. The public lectures were by 7. Academy Public Lectures ..........................14 Narender Luther and W. Selvamurthy. Details of these lectures can be found in 'Patrika' dated September 2009. 8. Summer Research .....................................14 Fellowships Programme PLATINUM JUBILEE MEETING – II 9. Refresher Courses .....................................15 The highlight of the celebrations was the Platinum Jubilee Meeting held at Bangalore during 12 – 14 November 2009, all 10. Lecture Workshops ................................... 18 sessions being arranged at the spacious National Science Seminar Complex of the IISc (J N Tata Auditorium). The 11. Platinum Jubilee Programmes ................... 25 inaugural session was a dignified and ceremonial affair. -
Supplemental Materials
The infection-tolerant mammalian reservoir of Lyme disease and other zoonoses broadly counters the inflammatory effects of endotoxin Supplemental Materials Figures S1-S5 Tables S1-S20 Figure S1. Digital photograph of two adult Peromyscus leucopus with exudative conjunctivitis and huddled together. The animals had received 10 mg/gm body of Escherichia coli lipopolysaccharide intraperitoneally the day before. Figure S2. Species- and tissue-specific responses to LPS. Independent differential gene expression analysis of RNA-seq data were performed for blood, spleen, and liver tissues of P. leucopus and M. musculus collected 4 h after injection with LPS or buffer alsone as control. These are represented as volcano plots with range- adjusted scales for the log2-transformed fold-changes on x-axes and log10-transformed FDR p values on y- axes. Colors of symbols denote the following: red, up-regulated gene with absolute fold-change > 4.0 and p value < 0.05; purple, down-regulated gene with absolute fold-change > 4.0 and p value < 0.05; and gray, all others. Numbers at the top left and right corners in each plot respresent numbers of down- and up-regulated genes, respectively. Figure 3 is same data with constant scales for x- and y-axes across the plots. Numerical values for each gene in the 6 datasets are provided in Tables S4-S9. Figure S3. Correlation of IL-10 and IL-10 P. leucopus and M. musculus from RNA-seq of spleen and of Figure 6B and TaBle S14. The scatter plot is log10 values of normalized unique reads of one coding sequence against another for each of the four groups, as defined in the legend for Figure 6 and indicated By different symBols.