RIESS, Olaf: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

Don't use scam websites

1

The cellular and molecular basis of hyperthermia

Bert Hildebrandt, Peter Wust, Olaf Ahlers, Annette Dieing, Geetha Sreenivasa, Thoralf Kerner, Roland Felix, Hanno Riess

Journal:

Critical Reviews in Oncology/Hematology

Year:

2002

Language:

english

File:

PDF, 489 KB

english, 2002

2

A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients

Katharina Rall, Gianmaria Barresi, Michael Walter, Sven Poths, Karina Haebig, Karin Schaeferhoff, Birgitt Schoenfisch, Olaf Riess, Diethelm Wallwiener, Michael Bonin, Sara Brucker

Journal:

Orphanet Journal of Rare Diseases

Year:

2011

Language:

english

File:

PDF, 2.08 MB

english, 2011

3

Spectrum of phenotypes and genotypes in Parkinson's disease

Olaf Riess, Rejko Krüger, Jörg B. Schulz

Journal:

Journal of Neurology

Year:

2002

Language:

english

File:

PDF, 284 KB

english, 2002

4

Dysregulation of coordinated neuronal firing patterns in striatum of freely behaving transgenic rats that model Huntington's disease

Benjamin R. Miller, Adam G. Walker, Stephen C. Fowler, Stephan von Hörsten, Olaf Riess, Michael A. Johnson, George V. Rebec

Journal:

Neurobiology of Disease

Year:

2010

Language:

english

File:

PDF, 886 KB

english, 2010

5

Xq22.3-q23 deletion including ACSL4 in a patient with intellectual disability

Gazou, Anastasia, Riess, Angelika, Grasshoff, Ute, Schäferhoff, Karin, Bonin, Michael, Jauch, Anna, Riess, Olaf, Tzschach, Andreas

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 1.26 MB

english, 2013

6

Improved PCR conditions for the stretch of (CAG) n repeats causing Huntington's disease

Riess, Olaf, Noerremoelle, Anne, Soerensen, Sven Asger, Epplen, Jorg T.

Journal:

Human Molecular Genetics

Year:

1993

Language:

english

File:

PDF, 1.46 MB

english, 1993

7

EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohorts: Table1

Huttenlocher, Johanna, Krüger, Rejko, Capetian, Philipp, Lohmann, Katja, Brockmann, Kathrin, Csoti, Ilona, Klein, Christine, Berg, Daniela, Gasser, Thomas, Bonin, Michael, Riess, Olaf, Bauer, Peter

Journal:

Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 176 KB

english, 2015

8

International Charter of principles for sharing bio-specimens and data

Mascalzoni, Deborah, Dove, Edward S, Rubinstein, Yaffa, Dawkins, Hugh J S, Kole, Anna, McCormack, Pauline, Woods, Simon, Riess, Olaf, Schaefer, Franz, Lochmüller, Hanns, Knoppers, Bartha M, Hansson, M

Journal:

European Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 380 KB

english, 2015

9

Stem Cell Quiescence in the Hippocampal Neurogenic Niche Is Associated With Elevated Transforming Growth Factor-β Signaling in an Animal Model of Huntington Disease

Kandasamy, Mahesh, Couillard-Despres, Sebastien, Raber, Kerstin A., Stephan, Michael, Lehner, Bernadette, Winner, Beate, Kohl, Zacharias, Rivera, Francisco J., Nguyen, Huu Phuc, Riess, Olaf, Bogdahn,

Journal:

Journal of Neuropathology and Experimental Neurology

Year:

2010

Language:

english

File:

PDF, 2.52 MB

english, 2010

10

The BACHD Rat Model of Huntington Disease Shows Signs of Fronto-Striatal Dysfunction in Two Operant Conditioning Tests of Short-Term Memory

Clemensson, Erik Karl Håkan, Clemensson, Laura Emily, Riess, Olaf, Nguyen, Huu Phuc, Li, Xiao-Jiang

Journal:

Year:

2017

Language:

english

File:

PDF, 3.87 MB

english, 2017

11

Intragenic deletions of IL1RAPL1: Report of two cases and review of the literature

Anne Behnecke, Katrin Hinderhofer, Oliver Bartsch, Astrid Nümann, Marie-Luise Ipach, Natalja Damatova, Thomas Haaf, Andreas Dufke, Olaf Riess, Ute Moog

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 437 KB

english, 2011

12

CAG repeats in restless legs syndrome

Markus Konieczny, Peter Bauer, Jürgen Tomiuk, Gabriele Weisser, Jean Haan, Klaus Berger, Olaf Riess, Ludger Schöls

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2006

Language:

english

File:

PDF, 168 KB

english, 2006

13

Protein surveillance machinery in brains with spinocerebellar ataxia type 3: Redistribution and differential recruitment of 26S proteasome subunits and chaperones to neuronal intranuclear inclusions

Thorsten Schmidt, Katrin S. Lindenberg, Antje Krebs, Ludger Schöls, Franco Laccone, Jochen Herms, Martin Rechsteiner, Olaf Riess, G. Bernhard Landwehrmeyer

Journal:

Annals of Neurology

Year:

2002

Language:

english

File:

PDF, 2.69 MB

english, 2002

14

Reply

Daniela Berg, Olaf Riess, Georg Becker

Journal:

Annals of Neurology

Year:

2003

Language:

english

File:

PDF, 50 KB

english, 2003

15

Do CTG expansions at the SCA8 locus cause ataxia?

Ludger Schöls, Ingrid Bauer, Christine Zühlke, Thorsten Schulte, Christina Kölmel, Katrin Bürk, Helge Topka, Peter Bauer, Horst Przuntek, Olaf Riess

Journal:

Annals of Neurology

Year:

2003

Language:

english

File:

PDF, 84 KB

english, 2003

16

Specification of 14-3-3 proteins in Lewy bodies

Daniela Berg, Olaf Riess, Antje Bornemann

Journal:

Annals of Neurology

Year:

2003

Language:

english

File:

PDF, 54 KB

english, 2003

17

Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17)

Arndt Rolfs, Arnulf H. Koeppen, Ingrid Bauer, Peter Bauer, Sven Buhlmann, Helge Topka, Ludger Schöls, Olaf Riess

Journal:

Annals of Neurology

Year:

2003

Language:

english

File:

PDF, 953 KB

english, 2003

18

First appraisal of brain pathology owing to A30P mutant alpha-synuclein

Kay Seidel, Ludger Schöls, Silke Nuber, Elisabeth Petrasch-Parwez, Kristin Gierga, Zbigniew Wszolek, Dennis Dickson, Wei P. Gai, Antje Bornemann, Olaf Riess, Abdelhaq Rami, Wilfried F. A. Den Dunnen,

Journal:

Annals of Neurology

Year:

2010

Language:

english

File:

PDF, 380 KB

english, 2010

19

Errata

Kay Seidel, Ludger Schöls, Silke Nuber, Elisabeth Petrasch-Parwez, Kristin Gierga, Zbigniew Wszolek, Dennis Dickson, Wei P. Gai, Antje Bornemann, Olaf Riess, Abdelhaq Rami, Wilfried F. A. Den Dunnen,

Journal:

Annals of Neurology

Year:

2010

File:

PDF, 25 KB

2010

20

Autosomal dominant cerebellar ataxia: Phenotypic differences in genetically defined subtypes?

Dr. Ludger Schöls, Georgios Amoiridis, Thomas Büttner, Horst Przuntek, Jörg T. Epplen, Olaf Riess

Journal:

Annals of Neurology

Year:

1997

Language:

english

File:

PDF, 903 KB

english, 1997

21

Spectrin mutations in spinocerebellar ataxia (SCA)

Peter Bauer, Ludger Schöls, Olaf Riess

Journal:

Year:

2006

Language:

english

File:

PDF, 81 KB

english, 2006

22

Cellular and subcellular localization of Huntington aggregates in the brain of a rat transgenic for Huntington disease

Elisabeth Petrasch-Parwez, Huu-Phuc Nguyen, Marlen Löbbecke-Schumacher, Hans-Werner Habbes, Stefan Wieczorek, Olaf Riess, Karl-Hermann Andres, Rolf Dermietzel, Stephan Von Hörsten

Journal:

The Journal of Comparative Neurology

Year:

2007

Language:

english

File:

PDF, 2.31 MB

english, 2007

23

Periphilin is strongly expressed in the murine nervous system and is indispensable for murine development

Anne S. Soehn, Thu-Trang Pham, Karin Schaeferhoff, Thomas Floss, Daniela M. Vogt Weisenhorn, Wolfgang Wurst, Michael Bonin, Olaf Riess

Journal:

Year:

2009

Language:

english

File:

PDF, 639 KB

english, 2009

24

Genotype–phenotype relationships in hepatocellular tumors from mice and man

Sabine Stahl, Carina Ittrich, Philip Marx-Stoelting, Christoph Köhle, Özge Altug-Teber, Olaf Riess, Michael Bonin, Jürgen Jobst, Stephan Kaiser, Albrecht Buchmann, Michael Schwarz

Journal:

Year:

2005

Language:

english

File:

PDF, 335 KB

english, 2005

25

Linkage studies and mutation analysis of the PDEB gene in 23 families with leber congenital amaurosis

Olaf Riess, Bernhard Weber, Anne Noeremolle, Rafig A. Shaikh, Michael R. Hayden, Maria A. Musarella

Journal:

Year:

1992

Language:

english

File:

PDF, 688 KB

english, 1992

26

Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits

Denise Horn, Johannes Kapeller, Núria Rivera-Brugués, Ute Moog, Bettina Lorenz-Depiereux, Sebastian Eck, Maja Hempel, Janine Wagenstaller, Alex Gawthrope, Anthony P. Monaco, Michael Bonin, Olaf Riess,

Journal:

Year:

2010

Language:

english

File:

PDF, 207 KB

english, 2010

27

Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early-onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patients

Ana Djarmati, Katja Hedrich, Marina Svetel, Nora Schäfer, Vladislava Juric, Slobodanka Vukosavic, Robert Hering, Olaf Riess, Stanka Romac, Christine Klein, Vladimir Kostic

Journal:

Year:

2004

Language:

english

File:

PDF, 59 KB

english, 2004

28

Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystonias

Kathrin Grundmann, Ulrike Laubis-Herrmann, Dirk Dressler, Juliane Vollmer-Haase, Peter Bauer, Manfred Stuhrmann, Thorsten Schulte, Ludger Schöls, Helge Topka, Olaf Riess

Journal:

Movement Disorders

Year:

2004

Language:

english

File:

PDF, 62 KB

english, 2004

29

Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown cause

Peter Bauer, Friedmar R. Kreuz, Katrin Bürk, Carsten Saft, Jürgen Andrich, Hubert Heilemann, Olaf Riess, Ludger Schöls

Journal:

Movement Disorders

Year:

2006

Language:

english

File:

PDF, 62 KB

english, 2006

30

Prevalence of THAP1 sequence variants in German patients with primary dystonia

Anne S. Söhn, Nicola Glöckle, Andrea Duarte Doetzer, Günther Deuschl, Ute Felbor, Helge R. Topka, Ludger Schöls, Olaf Riess, Peter Bauer, Ulrich Müller, Kathrin Grundmann

Journal:

Movement Disorders

Year:

2010

Language:

english

File:

PDF, 639 KB

english, 2010

31

Localization of sequence variations in PGC-1α influence their modifying effect in Huntington disease

Hong Van B Che, Silke Metzger, Esteban Portal, Carolin Deyle, Olaf Riess, Huu Phuc Nguyen

Journal:

Molecular Neurodegeneration

Year:

2011

Language:

english

File:

PDF, 521 KB

english, 2011

32

Gene expression changes in a transgenic mouse model overexpressing human wildtype and mutant torsinA

Kathrin Grundmann, Jeannette Hübener, Karina Häbig, Bettina Reischmann, Sven Poths, Till-Karsten Hauser, Janine Magg, Olaf Riess, Michael Bonin, Huu Phuc Nguyen

Journal:

PROTEOMICS - Clinical Applications

Year:

2008

Language:

english

File:

PDF, 645 KB

english, 2008

33

Age-dependent gene expression profile and protein expression in a transgenic rat model of Huntington's disease

Huu Phuc Nguyen, Silke Metzger, Carsten Holzmann, Dirk Koczan, Hans-Jürgen Thiesen, Stephan von Hörsten, Olaf Riess, Michael Bonin

Journal:

PROTEOMICS - Clinical Applications

Year:

2008

Language:

english

File:

PDF, 599 KB

english, 2008

34

The codon 408 mutation associated with haplotype 2 is predominant in Polish families with phenylketonuria

Jadwiga Jaruzelska, Karen Friis Henriksen, Flemming Güttler, Olaf Riess, Krzysztof Borski, Nikolaus Blin, Ryszard Slomski

Journal:

Year:

1991

Language:

english

File:

PDF, 382 KB

english, 1991

35

RELP-discordance within the human phenylalanine hydroxylase locus

Olaf Riess, Adelheid Michel, Wolfgang Berger, Peter Nürnberg, Jörg T. Epplen, Astrid Speer, Charles Coutelle

Journal:

Year:

1989

Language:

english

File:

PDF, 538 KB

english, 1989

36

Chromosomal assignment of the human smg GDP dissociation stimulator gene to human chromosome 4q21-q25

Olaf Riess, Cornelia Epplen, Ina Siedlaczck, Jörg T. Epplen

Journal:

Year:

1993

Language:

english

File:

PDF, 222 KB

english, 1993

37

Disturbance of iron metabolism in Parkinson’s disease — ultrasonography as a biomarker

Daniela Berg, Helmine Hochstrasser, Katherine J. Schweitzer, Olaf Riess

Journal:

Neurotoxicity Research

Year:

2006

Language:

english

File:

PDF, 1.59 MB

english, 2006

38

Mutation at the SCA17 locus is not a common cause of primary dystonia

Kathrin Grundmann, Ulrike Laubis-Herrmann, Dirk Dressler, Juliane Vollmer-Haase, Peter Bauer, Manfred Stuhrmann, Thorsten Schulte, Ludger Schöls, Helge Topka, Olaf Riess

Journal:

Journal of Neurology

Year:

2004

Language:

english

File:

PDF, 189 KB

english, 2004

39

Stress induced changes in lymphocyte subpopulations and associated cytokines during whole body hyperthermia of 41.8–42.2°C

Olaf Ahlers, Bert Hildebrandt, Annette Dieing, Maria Deja, Thomas Böhnke, Peter Wust, Hanno Riess, Herwig Gerlach, Thoralf Kerner

Journal:

European Journal of Applied Physiology

Year:

2005

Language:

english

File:

PDF, 305 KB

english, 2005

40

Age at onset in Huntington’s disease is modified by the autophagy pathway: implication of the V471A polymorphism inAtg7

Silke Metzger, Meiju Saukko, Hong Van Che, Liang Tong, Yvonne Puder, Olaf Riess, Huu Phuc Nguyen

Journal:

Year:

2010

Language:

english

File:

PDF, 246 KB

english, 2010

41

Genetic background of apparently idiopathic sporadic cerebellar ataxia

Ludger Schöls, Sandra Szymanski, Sören Peters, Horst Przuntek, Jörg T. Epplen, Cornelia Hardt, Olaf Riess

Journal:

Year:

2000

Language:

english

File:

PDF, 53 KB

english, 2000

42

Transmission distortion of the mutant alleles in spinocerebellar ataxia

Olaf Riess, Jörg T. Epplen, Georgios Amoiridis, Horst Przuntek, L. Schöls

Journal:

Year:

1997

Language:

english

File:

PDF, 27 KB

english, 1997

43

A comprehensive genetic study of the proteasomal subunit S6 ATPase in German Parkinson’s disease patients

Claudia Wahl, Sabine Kautzmann, Guido Krebiehl, Karsten Strauss, Dirk Woitalla, Thomas Müller, Peter Bauer, Olaf Riess, Rejko Krüger

Journal:

Journal of Neural Transmission

Year:

2008

Language:

english

File:

PDF, 405 KB

english, 2008

44

Genetic analysis of coding SNPs in blood-brain barrier transporterMDR1in European Parkinson’s disease patients

Claudia Funke, Anne S. Soehn, Juergen Tomiuk, Olaf Riess, Daniela Berg

Journal:

Journal of Neural Transmission

Year:

2009

Language:

english

File:

PDF, 283 KB

english, 2009

45

Genetic analysis ofheme oxygenase-1(HO-1) in German Parkinson’s disease patients

Claudia Funke, Juergen Tomiuk, Olaf Riess, Daniela Berg, Anne S. Soehn

Journal:

Journal of Neural Transmission

Year:

2009

Language:

english

File:

PDF, 277 KB

english, 2009

46

Whole genome expression analyses of single- and double-knock-out mice implicate partially overlapping functions of alpha- and gamma-synuclein

Melanie Kuhn, Karina Haebig, Michael Bonin, Natalia Ninkina, Vladimir L. Buchman, Sven Poths, Olaf Riess

Journal:

Year:

2007

Language:

english

File:

PDF, 381 KB

english, 2007

47

SCA2trinucleotide expansion in German SCA patients

Olaf Riess, Franco A. Laccone, Suzana Gispert, Ludger Schöls, Christine Zühlke, Ana Maria Menezes Vieira-Saecker, Susanne Herlt, Karl Wessel, Jörg T. Epplen, Bernhard H.F. Weber, Friedmar Kreuz, Sohey

Journal:

Year:

1997

Language:

english

File:

PDF, 102 KB

english, 1997

48

High-throughput resequencing in the diagnosis ofBRCA1/2mutations using oligonucleotide resequencing microarrays

Christopher Schroeder, Fanny Stutzmann, Bernhard H. F. Weber, Olaf Riess, Michael Bonin

Journal:

Breast Cancer Research and Treatment

Year:

2010

Language:

english

File:

PDF, 543 KB

english, 2010

49

SCA3: Neurological features, pathogenesis and animal models

Olaf Riess, Udo Rüb, Annalisa Pastore, Peter Bauer, Ludger Schöls

Journal:

Year:

2008

Language:

english

File:

PDF, 1003 KB

english, 2008

50

The dopamine D2 receptor (DRD2) gene–a genetic risk factor in heavy smoking?

Anil Batra, Gisbert Gelfort, Mathias Bartels, Hanna Smoltczyk, Gerhard Buchkremer, Olaf Riess, Ludger Schöls

Journal:

Addiction Biology

Year:

2000

Language:

english

File:

PDF, 139 KB

english, 2000

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@z-lib.do

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски