Anne S. Olsen

ORCID: 0000-0003-0431-5723
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About
Contact & Profiles
Research Areas
  • Biochemical and Molecular Research
  • Cell Adhesion Molecules Research
  • Cytomegalovirus and herpesvirus research
  • CRISPR and Genetic Engineering
  • RNA and protein synthesis mechanisms
  • Chromosomal and Genetic Variations
  • TGF-β signaling in diseases
  • Sphingolipid Metabolism and Signaling
  • DNA and Nucleic Acid Chemistry
  • HIV/AIDS drug development and treatment
  • Genomics and Chromatin Dynamics
  • Receptor Mechanisms and Signaling
  • DNA Repair Mechanisms
  • Connective tissue disorders research
  • Genomics and Phylogenetic Studies
  • Heat shock proteins research
  • Glycosylation and Glycoproteins Research
  • Animal Genetics and Reproduction
  • Advanced biosensing and bioanalysis techniques
  • Genetics and Neurodevelopmental Disorders
  • RNA Research and Splicing
  • RNA Interference and Gene Delivery
  • Cholinesterase and Neurodegenerative Diseases
  • Physiological and biochemical adaptations
  • Phosphodiesterase function and regulation

Google (United States)
2017

University of Southern Denmark
2014-2015

Norwegian Institute of Bioeconomy Research
2011

Joint Genome Institute
2001-2002

Lawrence Livermore National Laboratory
1991-2001

California State University, Stanislaus
1993

University of Freiburg
1992

Stanford University
1992

Stanford Medicine
1992

University of Oxford
1992

Eric S. Lander Lauren Linton Bruce W. Birren Chad Nusbaum Michael C. Zody and 95 more Jennifer N. Baldwin Keri Devon Ken Dewar Michael P. Doyle William W. Fitzhugh Roel Funke Diane Gage Katrina L. Harris Andrew Heaford John G. Howland Lisa Kann Jessica A. Lehoczky R Paul Levine Paul McEwan Kevin McKernan James C. Meldrim Jill P. Mesirov Cher Miranda William Morris Jerome W. Naylor Christina Raymond Mark Rosetti Ralph Santos Andrew Sheridan Carrie Sougnez Nicole Stange-Thomann Nikola M. Stojanović Aravind Subramanian Dudley Wyman Jane Rogers John Sulston R. Ainscough Stephan Beck David Bentley John H. Burton Christopher Clee Nigel Carter Alan Coulson Rebecca Deadman Panos Deloukas Andrew Dunham Ian Dunham Richard Durbin Lisa French Darren Grafham Simon G. Gregory Tim Hubbard Sean Humphray Adrienne Hunt Matthew C. Jones Christine Lloyd Amanda A. McMurray Lucy Matthews Simon Mercer Sarah Milne James C. Mullikin Andrew J. Mungall R. W. Plumb Mark T. Ross R. Shownkeen Sarah Sims R Waterston Richard K. Wilson LaDeana W. Hillier John D. McPherson Marco A. Marra Elaine R. Mardis Lucinda A. Fulton Asif Chinwalla Kymberlie Pepin Warren Gish Stephanie L. Chissoe Michael C. Wendl Kim D. Delehaunty Tracie L. Miner Andrew Delehaunty Jason Kramer Lisa L. Cook Robert S. Fulton D. Johnson Patrick Minx Sandra W. Clifton Trevor Hawkins Elbert Branscomb Paul Predki Paul Richardson Sarah Wenning Tom Slezak Norman A. Doggett Jan‐Fang Cheng Anne S. Olsen Susan Lucas Christopher J. Elkin Edward C. Uberbacher M.E. Frazier

The human genome holds an extraordinary trove of information about development, physiology, medicine and evolution. Here we report the results international collaboration to produce make freely available a draft sequence genome. We also present initial analysis data, describing some insights that can be gleaned from sequence.

10.1038/35057062 article EN public-domain Nature 2001-02-01
John D. McPherson Marco A. Marra LaDeana Hillier R Waterston Asif Chinwalla and 95 more John Wallis Mandeep Sekhon Kristine M. Wylie Elaine R. Mardis Richard K. Wilson Robert S. Fulton Tamara A. Kucaba Caryn Wagner-McPherson W. Brad Barbazuk Simon G. Gregory Sean Humphray Lisa French Richard S. Evans Graeme Bethel Adam Whittaker Jane L. Holden Owen T McCann Andrew Dunham Carol Soderlund Clare L. Scott David Bentley Gregory D. Schuler Hsiu-Chuan Chen Wonhee Jang Eric D. Green Jacquelyn R. Idol Valerie V. Maduro Kate Montgomery Eunice Lee Ashley Miller Suzanne Emerling Raju Kucherlapati Richard A. Gibbs Stephen W. Scherer James H. Gorrell Erica Sodergren Kerstin P. Clerc-Blankenburg Paul E. Tabor Susan L. Naylor Dawn Garcia Pieter J. de Jong Joseph J. Catanese Norma J. Nowak Kazutoyo Osoegawa Shizhen Qin Lee Rowen Anuradha Madan Monica Dors Leroy Hood Barbara J. Trask Cynthia Friedman Hillary F. Massa Vivian G. Cheung Ilan R. Kirsch Thomas Reid Raluca Yonescu Jean Weissenbach Thomas Brüls Roland Heilig Elbert Branscomb Anne S. Olsen Norman A. Doggett Jan‐Fang Cheng Trevor Hawkins R Myers Jin Shang Lucı́a Ramı́rez Jeremy Schmutz Olivia Velasquez Kami Dixon Nancy Stone David R. Cox David Haussler W. James Kent Terrence S. Furey Sanja Rogić Scot Kennedy Steven J.M. Jones André Rosenthal Gaiping Wen Markus B. Schilhabel Gernot Glöeckner Gerald Nyakatura Reiner Siebert Brigitte Schlegelberger Julie R. Korenberg Xiao–Ning Chen Asao Fujiyama Masahira Hattori Atsushi Toyoda Tetsushi Yada Hong‐Seok Park Yoshiyuki Sakaki Nobuyoshi Shimizu Shuichi Asakawa

10.1038/35057157 article EN Nature 2001-02-15

Hypoxanthine-guanine phosphoribosyltransferase from Chinese hamster brain, liver, and V79 tissue culture cells appears to have identical structural catalytic properties.The enzyme has been purified 540-fold apparent homogeneity brain.The native molecular weight is 78,000 85,000 determined by Sephadex G-100 column chromatography acrylamide gel electrophoresis.The consist of three subunits 25,000 sodium dodecyl sulfate electrophoresis.Electrofocusing electrophoresis demonstrate the presence at...

10.1016/s0021-9258(19)42479-4 article EN cc-by Journal of Biological Chemistry 1974-07-01

Ceramide and its metabolites constitute a diverse group of lipids, which play important roles as structural entities biological membranes well regulators cellular growth, differentiation, development. The C. elegans genome comprises three ceramide synthase genes; hyl-1, hyl-2, lagr-1. HYL-1 function is required for synthesis ceramides sphingolipids containing very long acyl-chains (≥C24), while HYL-2 shorter (≤C22). Here we show that functional loss decreases lifespan, or LAGR-1 does not...

10.1371/journal.pone.0070087 article EN cc-by PLoS ONE 2013-07-19

Abstract. It has recently become apparent that several cytokines and growth factors are capable of modulating fibroblast proliferation biosynthetic activity. To understand the role these in connective tissue regulation, we examined effects simultaneous addition interferon‐γ (IFN‐γ) transforming factor‐β (TGF‐β) on normal human dermal collagen fibronectin production. In addition, vitro transcription rates steady‐state mRNA levels for molecules were determined by nuclear run‐off assays...

10.1111/j.1365-2362.1990.tb01890.x article EN European Journal of Clinical Investigation 1990-10-01

Ceramides are precursors of complex sphingolipids (SLs), which important for normal functioning both the developing and mature brain. Altered SL levels have been associated with many neurodegenerative disorders, including epilepsy, although few direct links identified between genes involved in metabolism epilepsy.We used quantitative real-time PCR, Western blotting, enzymatic assays to determine mRNA, protein, activity ceramide synthase 2 (CERS2) fiibroblasts isolated from parental control...

10.1002/acn3.28 article EN cc-by-nc-nd Annals of Clinical and Translational Neurology 2014-01-13

Abstract. It has recently become apparent that several cytokines and growth factors are capable of modulating fibroblast proliferation biosynthetic activity. To understand the role these in connective tissue regulation, we examined effects simultaneous addition interferon‐γ (IFN‐γ) transforming factor‐β (TGF‐β) on normal human dermal collagen fibronectin production. In addition, vitro transcription rates steady‐state mRNA levels for molecules were determined by nuclear run‐off assays...

10.1111/j.1365-2362.1990.tb01915.x article EN European Journal of Clinical Investigation 1990-10-01

Abstract A minigene version of the human gene for pro alpha(I) chain type I procollagen (COL1A1) was prepared that contained -2.3 kilobases 5'-flanking sequence, first 5 exons and introns, last 6 about 2 3'-flanking sequence. The then used stable transfection experiments with mouse NIH 3T3 fibroblasts. Because products were shorter, it possible to compare expression endogenous alpha 1 (I) by Northern Western blot analyses. results demonstrated construct enough obtain high levels in many...

10.1016/s0021-9258(17)35290-0 article EN cc-by Journal of Biological Chemistry 1991-01-01

Hypoxanthine phosphoribosyltransferase (IMP:pryophosphate phosphoribosyltransferase, EC 2.4.2.8) from human erythrocytes has been purified 13 000-fold to apparent homogeneity. The native enzyme a sedimentation coefficient of 5.9 S, determined by analytical ultracentrifugation, and molecular weight 81 000-83 000, equilibrium centrifugation. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis indicates subunit 26 suggesting that the is trimer. Isoelectric focusing resolves three peaks...

10.1021/bi00630a029 article EN Biochemistry 1977-05-31

To investigate this difference the enzyme was purified from human erythrocytes by method reported to give a 34,500 molecular weight subunit.Although purification produces what appears be single active band on nondenaturing polyacrylamide gels, major protein components observed sodium dodecyl sulfate poly acrylamide gels are not derived enzyme.Instead, activity is associated with minor component of subunit 26,000.Heating at 85' in presence phosphoribosylpyrophosphate yields complete recovery...

10.1016/s0021-9258(19)42480-0 article EN cc-by Journal of Biological Chemistry 1974-07-01

The HSPDE4A gene spans 50 kb, consists of at least 17 exons and is orientated 5´–3´, telomere to centromere. It located chromosome 19p13.2, being 350 kb proximal the encoding TYK2 850 distal low-density lipoprotein receptor. Its structure consistent with production active ‘long ’ ‘short isoenzymes as result alternative mRNA splicing two splice junctions. Identified single alternatively spliced 5´ exon unique N-terminal region long isoenzyme HSPDE4A4B (pde46). upstream conserved regions, UCR1...

10.1042/bj3330693 article EN Biochemical Journal 1998-08-01

A basic ribosomal phosphoprotein of 30,000 molecular weight was rapidly dephosphorylated in cultured Drosophila melanogaster cells heat shocked at 37 degrees C. The protein associated with the 40S subunit and had an electrophoretic mobility similar to that purified rat liver S6 on two-dimensional polyacrylamide gels as well a partial proteolysis peptide map. In logarithmically growing cultures, this D. appeared have single phosphorylated species consisting 30 40% total cellular S6. Thus,...

10.1128/mcb.3.11.2017 article EN Molecular and Cellular Biology 1983-11-01

The carcinoembryonic antigen (CEA)-like genes are members of a large gene family which Is part the immunoglobulln superfamily.The CEA is divided into two major subgroups, CEA-subgroup and pregnancy-specific glycoprotein (PSG)-subgroup.In course an effort to develop set overlapping cosmlds spanning human chromosome 19, we identified 245 cosmids In 19 cosmid library (6 -7X redundant) by hybridization with IgC-like domain fragment gene.A fluorescence-based restriction enzyme digest...

10.1093/nar/20.7.1629 article EN Nucleic Acids Research 1992-01-01

Hypoxanthine phosphoribosyltransferase (HPRT, IMP:pyrophosphate phosphoribosyltransferase, EC 2.4.2.8) can be purified 5-to 10,000-fold from extracts of HeLa (human) cells by a three-step procedure consisting high-speed centrifugation, adsorption to Sepharose-conjugated HPRT antibody, and sodium dodecyl sulfate/polyacrylamide gel electrophoresis. Purified enzyme labeled in vivo with radioactive lysine, arginine, or methionine was digested trypsin the tryptic peptides were separated column...

10.1073/pnas.74.3.926 article EN Proceedings of the National Academy of Sciences 1977-03-01

We have developed an in vitro translation system from heat-shocked and normal Drosophila cultured cells.The lysates retain regulation of typical the whble cells which they were prepared, both when programmed by endogenous mRNA RNA-dependent.These systems been used to investigate mechanism shutdown protein synthesis selection heat shock mRNAs for Drosophila.Supplementation intact RNA-dependent with separated ribosome or supernatant fractions showed fraction cou1d"rescue" a lysate.Normal...

10.1016/s0021-9258(17)35916-1 article EN cc-by Journal of Biological Chemistry 1986-02-01

10.1016/s0076-6879(78)51076-8 article EN Methods in enzymology on CD-ROM/Methods in enzymology 1978-01-01
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