Tuesday, March 3, 2009 Daily Program Summary
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2012 Annual Report
Memorial Sloan-Kettering Cancer Center 2012 ANNUAL REPORT A SHARED VISION A SINGULAR MISSION Nurse practitioner Naomi Cazeau, of the Adult Bone Marrow Transplant Service. PING CHI PHYSICIAN-SCIENTIST 10 STEPHEN SOLOMON ALEXANDER RUDENSKY INTERVENTIONAL IMMUNOLOGIST RADIOLOGIST 16 12 VIVIANE TABAR The clinicians and scientists of NEUROSURGEON Memorial Sloan-Kettering share a vision and 18 a singular mission — to conquer cancer. STEPHEN LONG STRUCTURAL BIOLOGIST They are experts united against a 20 SIMON POWELL complex disease. Each type of cancer R ADIATION ONCOLOGIST 24 ETHEL LAW is different, each tumor is unique. Set free NURSE PRACTITIONER in surroundings that invite the sharing of 26 ideas and resources, they attack the CHRISTINA LESLIE complexity of cancer from every angle COMPUTATIONAL BIOLOGIST and every discipline. 34 SCOTT ARMSTRONG PEDIATRIC ONCOLOGIST 30 TO JORGE REIS-FILHO EXPERIMENTAL PATHOLOGIST CONQUER 38 CANCER 04 Letter from the Chairman and the President A complete version of this report — 42 Statistical Profile which includes lists of our donors, 44 Financial Summary doctors, and scientists — 46 Boards of Overseers and Managers is available on our website at 49 The Campaign for Memorial Sloan-Kettering www.mskcc.org/annualreport. 4 5 Letter from the Chairman In 2012 the leadership of Memorial Sloan-Kettering endorsed Douglas A. Warner III These programmatic investments require leadership and and the President a $2.2 billion investment in a clinical expansion that will set vision. Our new Physician-in-Chief, José Baselga, joined the stage for a changing care paradigm into the next decade us on January 1, 2013. An internationally recognized and beyond. -
2011 Annual Report
Memorial Sloan-Kettering Cancer Center 2011 Annual Report 10 steps closer 10 steps closer Letter from the Chairman and the President 1 1 | First effective treatments for advanced melanoma 5 2 Genomic analysis offers clues to most common | type of ovarian cancer 7 3 Breast cancer surgery: practice-changing | findings for some patients 9 4 New drugs offer survival benefit for men | with metastatic prostate cancer 11 5 | Insights into DNA damage and repair 13 6 Novel stem cell technique shows promise | in treating disease 15 7 Combination therapy may prevent spread | of nasopharyngeal tumors 17 8 Algorithm can predict shape of proteins, | speeding basic cancer research 19 9 Two of 2011’s top five advances in cancer | research led by MSKCC physician-scientists 21 10 | The Josie Robertson Surgery Center 23 The Campaign for Memorial Sloan-Kettering 25 Statistical Profile 27 Financial Summary 29 Boards of Overseers and Managers 31 www.mskcc.org/annualreport Letter from the Chairman and the President The year 2011 was a strong one at Memorial Sloan-Kettering. We continued to lead across “Our success as an institution is due in the spectrum of patient care, research, and training, and laid the groundwork for important progress in the years ahead. great measure to our remarkable staff… We want to begin by saying that our success as an institution is due in great measure to our remarkable staff. On a daily basis, we are inspired by their dedication and compassion, and We are inspired by their dedication Douglas A. Warner III are grateful for the work they do in the service of our patients and our mission. -
Science & Policy Meeting Jennifer Lippincott-Schwartz Science in The
SUMMER 2014 ISSUE 27 encounters page 9 Science in the desert EMBO | EMBL Anniversary Science & Policy Meeting pageS 2 – 3 ANNIVERSARY TH page 8 Interview Jennifer E M B O 50 Lippincott-Schwartz H ©NI Membership expansion EMBO News New funding for senior postdoctoral In perspective Georgina Ferry’s enlarges its membership into evolution, researchers. EMBO Advanced Fellowships book tells the story of the growth and ecology and neurosciences on the offer an additional two years of financial expansion of EMBO since 1964. occasion of its 50th anniversary. support to former and current EMBO Fellows. PAGES 4 – 6 PAGE 11 PAGES 16 www.embo.org HIGHLIGHTS FROM THE EMBO|EMBL ANNIVERSARY SCIENCE AND POLICY MEETING transmissible cancer: the Tasmanian devil facial Science meets policy and politics tumour disease and the canine transmissible venereal tumour. After a ceremony to unveil the 2014 marks the 50th anniversary of EMBO, the 45th anniversary of the ScienceTree (see box), an oak tree planted in soil European Molecular Biology Conference (EMBC), the organization of obtained from countries throughout the European member states who fund EMBO, and the 40th anniversary of the European Union to symbolize the importance of European integration, representatives from the govern- Molecular Biology Laboratory (EMBL). EMBO, EMBC, and EMBL recently ments of France, Luxembourg, Malta, Spain combined their efforts to put together a joint event at the EMBL Advanced and Switzerland took part in a panel discussion Training Centre in Heidelberg, Germany, on 2 and 3 July 2014. The moderated by Marja Makarow, Vice President for Research of the Academy of Finland. -
Dual Recognition of H3k4me3 and H3k27me3 by a Plant Histone Reader SHL
ARTICLE DOI: 10.1038/s41467-018-04836-y OPEN Dual recognition of H3K4me3 and H3K27me3 by a plant histone reader SHL Shuiming Qian1,2, Xinchen Lv3,4, Ray N. Scheid1,2,LiLu1,2, Zhenlin Yang3,4, Wei Chen3, Rui Liu3, Melissa D. Boersma2, John M. Denu2,5,6, Xuehua Zhong 1,2 & Jiamu Du 3 The ability of a cell to dynamically switch its chromatin between different functional states constitutes a key mechanism regulating gene expression. Histone mark “readers” display 1234567890():,; distinct binding specificity to different histone modifications and play critical roles in reg- ulating chromatin states. Here, we show a plant-specific histone reader SHORT LIFE (SHL) capable of recognizing both H3K27me3 and H3K4me3 via its bromo-adjacent homology (BAH) and plant homeodomain (PHD) domains, respectively. Detailed biochemical and structural studies suggest a binding mechanism that is mutually exclusive for either H3K4me3 or H3K27me3. Furthermore, we show a genome-wide co-localization of SHL with H3K27me3 and H3K4me3, and that BAH-H3K27me3 and PHD-H3K4me3 interactions are important for SHL-mediated floral repression. Together, our study establishes BAH-PHD cassette as a dual histone methyl-lysine binding module that is distinct from others in recognizing both active and repressive histone marks. 1 Laboratory of Genetics, University of Wisconsin-Madison, Madison, WI 53706, USA. 2 Wisconsin Institute for Discovery, University of Wisconsin-Madison, Madison, WI 53706, USA. 3 National Key Laboratory of Plant Molecular Genetics, CAS Center for Excellence in Molecular Plant Sciences, Shanghai Center for Plant Stress Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 201602, China. -
The Astbury Centre for Structural Molecular Biology Annual Report
Front cover illustration Comparison of joint FRET efficiency and fluorescence lifetime histograms for closed SecYEG:SecA:ADP (left) and translocating complex in the presence of proSpy1 substrate and ATP (right). Top and right sides of each histogram show distribution of lifetimes and FRET efficiencies, respectively. This investigation was a collaboration between Roman Tuma, Joel Crossley, Matthew Watson, Sheena Radford (University of Leeds), and Ian Collinson, Dan Watkins (University of Bristol) and Tomas Fessl (University of South Bohemia).More details can be found on pg 93 of this report. i Mission Statement The Astbury Centre for Structural Molecular Biology will promote interdisciplinary research of the highest standard on the structure and function of biological molecules, biomolecular assemblies and complexes using physico-chemical, molecular biological and computational approaches. ii Introduction Welcome to the Annual Report of the Astbury Centre for Structural Molecular Biology 2018. I hope you enjoy reading its contents. It has been yet another busy and successful year for the Centre. The reports in the pages that follow highlight just some of our scientific successes of the last year of our members. We are proud of the strength of our community and our collaborations both locally within the Astbury Centre and University as well as with colleagues from across the globe. I would like to thank every member of the Centre for their hard work over the year: our Support staff, Technicians, Facility Managers, Students, Post-docs, Fellows and Academic staff and, of course, Lucy Gray for her excellent organisation and administrative support. Thank you all. During 2018 the Astbury Centre continued in its mission to “Understand Life in Molecular Detail” through multiple different activities, including some exciting research discoveries. -
Spring 2015 BCH Sem Sched
Spring 2015 Seminar Schedule Name Title Host STEVEN MCKNIGHT UT SOUTHWESTERN MEDICAL CENTER GREENLEAF/ JANUARY 9 “DISCOVERY, OPTIMIZATION AND MECHANISTIC BRENNAN CHARACTERIZATION OF A NEUROPROTECTIVE CHEMICAL” *HANDLER MEMORIAL LECTURE – 103 BRYAN RESEARCH BUILDING AT 1:30 PM HOWARD CHANG STANFORD UNIVERSITY SCHOOL OF MEDICINE HARGROVE NOTE: WED., JANUARY 21 “GENOME REGULATION BY LONG NONCODING RNAS” JOHN HANOVER NIDDK, NIH BOYCE JANUARY 30 “A LITTLE SUGAR GOES A LONG WAY: O-GLCNAC AND DISEASE EPIGENETICS” CRAIG THOMPSON MEMORIAL SLOAN KETTERING CANCER CENTER COGGINS FEBRUARY 6 TITLE TBA **KAMIN MEMORIAL LECTURE – 103 BRYAN RESEARCH BUILDING AT 1:30 PM PETER BURGERS WASHINGTON UNIVERSITY SCHOOL OF MEDICINE MODRICH FEBRUARY 20 (TENTATIVE) “CONNECTING DNA DAMAGE TO CHECKPOINT INITIATION” JONATHAN STAMLER CASE WESTERN RESERVE UNIVERSITY FRIDOVICH FEBRUARY 27 TITLE TBA DINSHAW PATEL MEMORIAL SLOAN KETTERING CANCER CENTER AL-HASHIMI MARCH 6 "STRUCTURAL BIOLOGY OF RNA-MEDIATED GENE REGULATION AND HISTONE MARK-MEDIATED EPIGENETIC REGULATION" RONALD BREAKER YALE UNIVERSITY AL-HASHIMI MARCH 13 TITLE TBA FRANCES BRODSKY UCSF/UNIVERSITY COLLEGE LONDON BOYCE MARCH 20 "DIVERSITY OF CLATHRIN FUNCTION IN METABOLISM, MEMBRANE TRAFFIC AND BEYOND " BEN LUISI UNIVERSITY OF CAMBRIDGE BEESE APRIL 3 TITLE TBA CATHY DRENNAN MASSACHUSETTS INSTITUTE OF TECHNOLOGY BONNIE APRIL 10 "SHAKE, RATTLE, & ROLL: CAPTURING SNAPSHOTS OF CUTHBERT/ METALLOENZYMES IN ACTION" STUDENTS STUDENT-SPONSORED LECTURESHIP SERIES REBECCA BUTCHER UNIVERSITY OF FLORIDA ZHOU APRIL 17 “CHEMICAL COMMUNICATION IN C. ELEGANS” BRUCE TIDOR MASSACHUSETTS INSTITUTE OF TECHNOLOGY DONALD APRIL 24 (TENTATIVE) TITLE TBA AMY KEATING MASSACHUSETTS INSTITUTE OF TECHNOLOGY DONALD MAY 1 (TENTATIVE) "MEASURING AND MODELING THE BINDING SPECIFICITY OF STRUCTURALLY CONSERVED PROTEIN INTERACTION DOMAINS" RALF MENDEL JOINT SEMINAR WITH CHEMISTRY DEPARTMENT THIELE/ MAY 8 TITLE TBA YOKOYAMA ~ seminars are held on Fridays in Room 147, Nanaline Duke Building at 12:OO noon ~ *Handler Memorial Lecture at 1:30 p.m. -
Describing the Elephant the Three-Dimensional Structures of Rnas Are Notoriously Difficult to Determine
SCOTT BASKERVILLE AND ANDREW D. ELLINGTON RNA STRUCTURE Describing the elephant The three-dimensional structures of RNAs are notoriously difficult to determine. Functional comparisons of variant molecules and cross-linking experiments are providing new information for structural modeling. The old fable of the blind men trying to describe the in vitro selection is the Rev-binding element (RBE) of shape of an elephant seems aptly to describe the present HIV-1. RBE is a 30-base sequence of the HIV-1 genome state of RNA structural analysis. Until recently, the crys- that can fold into a 'stem-internal-loop-stem' secondary tal structure of only one large RNA, tRNA, was known, structure and that interacts with the Rev protein, and and other non-crystallographic approaches to RNA regulates the splicing and transport of viral mRNAs. structure determination had not been particularly fruit- From a population of partially randomized sequences, ful. Low-resolution electron micrographs are at best able Bartel and Szostak [3] selected RBE variants that could to identify the global structure of the ribosome, but can- bind the Rev protein, whereas Giver et al. [4] selected not provide three-dimensional structural details. The binding variants from a population of completely random nuclear magnetic resonance (NMR) spectra of most sequences. These experiments revealed numerous se- RNAs are so complex that this method of structure quence co-variations that were used by Leclerc et al. [5] determination is limited to molecules of molecular mass 10 000 daltons or less. But new methods now provide at least partial insights into RNA structures. -
Women Physiologists
Women physiologists: Centenary celebrations and beyond physiologists: celebrations Centenary Women Hodgkin Huxley House 30 Farringdon Lane London EC1R 3AW T +44 (0)20 7269 5718 www.physoc.org • journals.physoc.org Women physiologists: Centenary celebrations and beyond Edited by Susan Wray and Tilli Tansey Forewords by Dame Julia Higgins DBE FRS FREng and Baroness Susan Greenfield CBE HonFRCP Published in 2015 by The Physiological Society At Hodgkin Huxley House, 30 Farringdon Lane, London EC1R 3AW Copyright © 2015 The Physiological Society Foreword copyright © 2015 by Dame Julia Higgins Foreword copyright © 2015 by Baroness Susan Greenfield All rights reserved ISBN 978-0-9933410-0-7 Contents Foreword 6 Centenary celebrations Women in physiology: Centenary celebrations and beyond 8 The landscape for women 25 years on 12 "To dine with ladies smelling of dog"? A brief history of women and The Physiological Society 16 Obituaries Alison Brading (1939-2011) 34 Gertrude Falk (1925-2008) 37 Marianne Fillenz (1924-2012) 39 Olga Hudlická (1926-2014) 42 Shelagh Morrissey (1916-1990) 46 Anne Warner (1940–2012) 48 Maureen Young (1915-2013) 51 Women physiologists Frances Mary Ashcroft 56 Heidi de Wet 58 Susan D Brain 60 Aisah A Aubdool 62 Andrea H. Brand 64 Irene Miguel-Aliaga 66 Barbara Casadei 68 Svetlana Reilly 70 Shamshad Cockcroft 72 Kathryn Garner 74 Dame Kay Davies 76 Lisa Heather 78 Annette Dolphin 80 Claudia Bauer 82 Kim Dora 84 Pooneh Bagher 86 Maria Fitzgerald 88 Stephanie Koch 90 Abigail L. Fowden 92 Amanda Sferruzzi-Perri 94 Christine Holt 96 Paloma T. Gonzalez-Bellido 98 Anne King 100 Ilona Obara 102 Bridget Lumb 104 Emma C Hart 106 Margaret (Mandy) R MacLean 108 Kirsty Mair 110 Eleanor A. -
Research Report 2009 Max Planck Institute for Molecular Genetics, Berlin Imprint | Research Report 2009
Research Report 2009 Max Planck Institute for Molecular Genetics, Berlin Imprint | Research Report 2009 Published by the Max Planck Institute for Molecular Genetics (MPIMG), Berlin, Germany, December 2009 Editorial Board: B.G. Herrmann, H. Lehrach, H.-H. Ropers, M. Vingron Conception & coordination: Patricia Marquardt Photography: Katrin Ullrich, MPIMG; David Ausserhofer Scientific Illustrations: MPIMG Production: Thomas Didier, Meta Data Contact: Max Planck Institute for Molecular Genetics Ihnestr. 63 – 73 14195 Berlin Germany Phone: +49 (0)30 8413-0 Fax: +49 (0)30 8413-1207 Email: [email protected] For further information about the MPIMG, please visit http://www.molgen.mpg.de MPI for Molecular Genetics Research Report 2009 Research Report 2009 1 Max Planck Institute for Molecular Genetics Berlin, December 2009 The Max Planck Institute for Molecular Genetics 2 MPI for Molecular Genetics Research Report 2009 Table of contents Organisational structure . 6 The Max Planck Institute for Molecular Genetics . 7 Mission . 7 Development of the Institute. 7 Research Concept . 8 Department of Developmental Genetics (Bernhard Herrmann) . 9 Transmission ratio distortion (H. Bauer) . 13 Regulatory Networks of Mesoderm Formation & Somitogenesis (B. Herrmann) . 17 Signal Transduction in Embryogenesis and Tumour Progression (M. Morkel) . 22 Organogenesis (H. Schrewe) . 26 General information about the whole Department . 29 Department of Vertebrate Genomics (Hans Lehrach) . 33 Molecular Embryology and Aging (J. Adjaye) . 40 Neuropsychiatric Genetics (L. Bertram) . 46 Automation (A. Dahl, W. Nietfeld, H. Seitz) . 49 Nucleic Acid-based Technologies (J. Glökler) . 55 Bioinformatics (R. Herwig) . 60 Comparative and Functional Genomics (H. Himmelbauer) . .65 Genetic Variation, Haplotypes & Genetics of Complex Diseases (M. Hoehe) . 69 3 in vitro Ligand Screening (Z. -
Australian Biochemist the Magazine of the Australian Society for Biochemistry and Molecular Biology Inc
ISSN 1443-0193 Australian Biochemist The Magazine of the Australian Society for Biochemistry and Molecular Biology Inc. Volume 47 AUGUST 2016 No.2 SHOWCASE ON RESEARCH Protein Misfolding and Proteostasis THIS ISSUE INCLUDES Showcase on Research Regular Departments A Short History of Amyloid SDS (Students) Page Molecular Chaperones: The Cutting Edge Guardians of the Proteome Off the Beaten Track When Proteostasis Goes Bad: Intellectual Property Protein Aggregation in the Cell Our Sustaining Members Extracellular Chaperones and Forthcoming Meetings Proteostasis Directory INSIDE ComBio2016 International Speaker Profiles Vol 47 No 2 August 2016 AUSTRALIAN BIOCHEMIST Page 1 ‘OSE’ Fill-in Puzzle We have another competition for the readers of the Australian Biochemist. All correct entries received by the Editor (email [email protected]) before 3 October 2016 will enter the draw to receive a gift voucher. With thanks to Rebecca Lew. The purpOSE is to choOSE from thOSE words listed and transpOSE them into the grid. So, clOSE your door, repOSE in a chair, and diagnOSE the answers – you don’t want to lOSE! 6 letters 8 letters ALDOSE FRUCTOSE FUCOSE FURANOSE HEXOSE PYRANOSE KETOSE RIBOSE 9 letters XYLOSE CELLULOSE GALACTOSE 7 letters RAFFINOSE AMYLOSE TREHALOSE GLUCOSE LACTOSE 11 letters MALTOSE DEOXYRIBOSE PENTOSE Australian Biochemist – Editor Chu Kong Liew, Editorial Officer Liana Friedman © 2016 Australian Society for Biochemistry and Molecular Biology Inc. All rights reserved. Page 2 AUSTRALIAN BIOCHEMIST Vol 47 No 2 August 2016 SHOWCASE ON RESEARCH EDITORIAL Molecular Origami: the Importance of Managing Protein Folding In my humble opinion, the most important biological transcription, RNA processing and transport, translation, molecule is the protein. -
Annual Report 2004
Astbury Centre for Structural Molecular Biology University of Leeds Annual Report 2004 © The University of Leeds, 2005 Front cover illustration: A collage of pictures illustrating the work of the Astbury Centre. Upper left: The contribution of the charge state ions to the folded (red), partially folded (yellow) and unfolded (green) β2-microglobulin conformers determined by ESI-Mass Spectrometry (see page 9); Upper right: Mechanical unfolding of proteins: a contour plot showing the difference in distance between every pair of amino-acids in protein L after pulling the protein apart by extensions of 1.6 Å before, and 1.6 Å after, the mechanical unfolding event. Pairs of residues that move further apart from each other during unfolding are coloured purple to green (-10 to 0Å), those that become closer to one another are shown in green to red (0 to 10 Å) (see page 23); Lower right: Dynamics on the ps-ns timescales for the backbone of apo-MS2W82R as detected by {1H} -15N Heteronculear nOe experiments. The image shows a tubes representation of the backbone of MS2W82R [PDB code 1MSC] with {1H}-15N heteronuclear nOe intensity shown by shading from white to black. White indicates little mobility [nOe ~ 0.8-0.9] and black indicates significant mobility [minimum nOe = 0.13] (see page 107); Lower left: Ribbon diagram of an AB coat protein dimer from the MS2 phage (subunit A in blue, B in green) complexed with the wild-type MS2 RNA stem-loop operator (shown in stick format) (see page 95). Acknowledgement The Astbury Centre for Structural Molecular Biology thanks its many sponsors for support of the work and its members for writing these reports. -
BIOLOGY 639 SCIENCE ONLINE the Unexpected Brains Behind Blood Vessel Growth 641 THIS WEEK in SCIENCE 668 U.K
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