Royer-Pokora, B: search on Z-Library

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1

Clinical relevance of mutations in the Wilms tumor suppressor 1 gene WT1 and the cadherin-associated protein β1 gene CTNNB1 for patients with Wilms tumors : Results of long-term surveillance of 71 patients from International Society of Pediatric Oncology Study 9/Society for Pediatric Oncology

Brigitte Royer-Pokora, Angela Weirich, Valerie Schumacher, Constanze Uschkereit, Manfred Beier, Ivo Leuschner, Norbert Graf, Frank Autschbach, Dominique Schneider, Melissa von Harrach

Journal:

Year:

2008

Language:

english

File:

PDF, 229 KB

english, 2008

2

Früher neonataler Tod bei Drash-Syndrom

M. Guschmann, M. Vogel, V. Schumacher, B. Royer-Pokora, H. Neitzel, T. Lennert

Journal:

Monatsschrift Kinderheilkunde

Year:

1998

Language:

german

File:

PDF, 230 KB

german, 1998

3

Characteristics of testicular dysgenesis syndrome and decreased expression of SRY and SOX9 in Frasier syndrome

Valérie Schumacher, Banu Gueler, Leendert H.J. Looijenga, Jan Ulrich Becker, Kerstin Amann, Rainer Engers, Joerg Dotsch, Hans Stoop, Wolfgang Schulz, Brigitte Royer-Pokora

Journal:

Molecular Reproduction and Development

Year:

2008

Language:

english

File:

PDF, 836 KB

english, 2008

4

The additive effect of p53 Arg72Pro and RNASEL Arg462Gln genotypes on age of disease onset in Lynch syndrome patients with pathogenic germline mutations in MSH2 or MLH1

Stefan Krüger, Christoph Engel, Andrea Bier, Ann-Sophie Silber, Heike Görgens, Elisabeth Mangold, Constanze Pagenstecher, Elke Holinski-Feder, Magnus von Knebel Doeberitz, Brigitte Royer-Pokora, Stefa

Journal:

Year:

2007

Language:

english

File:

PDF, 349 KB

english, 2007

5

Hypomethylation and Aberrant Expression of the Glioma Pathogenesis-Related 1 Gene in Wilms Tumors

Chilukamarri, Laxmi, Hancock, Anne L., Malik, Sally, Zabkiewicz, Joanna, Baker, Jenny A., Greenhough, Alexander, Dallosso, Anthony R., Huang, Tim Hui-Ming, Royer-Pokora, Brigitte, Brown, Keith W., Mal

Journal:

Year:

2007

Language:

english

File:

PDF, 1.20 MB

english, 2007

6

Wilms tumor cells with WT1 mutations have characteristic features of mesenchymal stem cells and express molecular markers of paraxial mesoderm

Royer-Pokora, B., Busch, M., Beier, M., Duhme, C., de Torres, C., Mora, J., Brandt, A., Royer, H. D.

Journal:

Human Molecular Genetics

Year:

2010

Language:

english

File:

PDF, 738 KB

english, 2010

7

Ten novel mutations found in aniridia

Matthias T. F. Wolf, B Lorenz, A Winterpacht, M Drechsler, V Schumacher, B Royer-Pokora, A Blankenagel, B Zabel, G Wildhardt

Journal:

Year:

1998

Language:

english

File:

PDF, 450 KB

english, 1998

8

Promoter 1 of LMO2, a master gene for hematopoiesis, is regulated by the erythroid specific transcription factor GATA1

Maik Martin Pruess, Matthias Drechsler, Brigitte Royer-Pokora

Journal:

Gene Function & Disease

Year:

2000

Language:

english

File:

PDF, 269 KB

english, 2000

9

A subtelomeric cryptic unbalanced translocation der (1)t(1;18)(q44;q23) in a severely retarded girl: similarities and differences to the deletion 1q42/43-ter syndrome

Matthias Drechsler, Frank Majewski, Barbara Leube, Vera M. Kalscheuer, Hans Hilger Ropers, Brigitte Royer-Pokora

Journal:

Gene Function & Disease

Year:

2001

Language:

english

File:

PDF, 616 KB

english, 2001

10

Clinical, cytogenetic, and molecular observations in a patient with Pallister-Killian-syndrome with an unusual karyotype

Barbara Leube, Frank Majewski, Jürgen Gebauer, Brigitte Royer-Pokora

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 161 KB

english, 2003

11

Twenty-four new cases of WT1 germline mutations and review of the literature: Genotype/phenotype correlations for Wilms tumor development

Brigitte Royer-Pokora, Manfred Beier, Markus Henzler, Rita Alam, Valérie Schumacher, Angela Weirich, Vicki Huff

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 201 KB

english, 2004

12

Molecular definition of chromosome arm 5q deletion end points and detection of hidden aberrations in patients with myelodysplastic syndromes and isolated del(5q) using oligonucleotide array CGH

Christina Evers, Manfred Beier, Anne Poelitz, Barbara Hildebrandt, Kati Servan, Matthias Drechsler, Ulrich Germing, Hans-Dieter Royer, Brigitte Royer-Pokora

Journal:

Genes, Chromosomes and Cancer

Year:

2007

Language:

english

File:

PDF, 424 KB

english, 2007

13

Direct pulsed field gel electrophoresis of Wilms' tumors shows that dna deletions in 11 p 13 are rare

Brigitte Royer-Pokora, Susanne Ragg, Brigitte Heckl-Östreicher, Manuela Held, Ursula Loos, Katherine Call, Tom Glaser, David Housman, Grady Saunders, Bernhard Zabel, Bryan Williams, Annemarie Poustka

Journal:

Genes, Chromosomes and Cancer

Year:

1991

Language:

english

File:

PDF, 2.90 MB

english, 1991

14

Wilms' tumor-specific methylation pattern in 11p13 detected by PFGE

Dr. Brigitte Royer-Pokora, Susanne Schneider

Journal:

Genes, Chromosomes and Cancer

Year:

1992

Language:

english

File:

PDF, 777 KB

english, 1992

15

Therapy adapted to molecular response in patients with chronic myelogenous leukaemia in first chronic phase: results of the Duesseldorf study

Frank Neumann, Judith Markett, Roland Fenk, Monika Pooten, Anne Koch, Daniela Bruennert, Nadine Schimkus, Michael Wulfert, Brigitte Royer-Pokora, Ralf Kronenwett, Rainer Haas, Norbert Gattermann

Journal:

Hematological Oncology

Year:

2008

Language:

english

File:

PDF, 118 KB

english, 2008

16

Expression of resistance-related proteins in nephroblastoma after chemotherapy

Manfred Volm, Jürgen Mattern, Gerd Stammler, Brigitte Royer-Pokora, Susanne Schneider, Angela Weirich, Rolf Ludwig

Journal:

International Journal of Cancer

Year:

1995

Language:

english

File:

PDF, 820 KB

english, 1995

17

Clinical outcome and genotype in patients with hereditary multiple exostoses

Marcus Jäger, Bettina Westhoff, Sebastian Portier, Barbara Leube, Karin Hardt, Brigitte Royer-Pokora, Georg Goßheger, Rüdiger Krauspe

Journal:

Journal of Orthopaedic Research

Year:

2007

Language:

english

File:

PDF, 362 KB

english, 2007

18

Hidden chromosomal aberrations are rare in primary myelodysplastic syndromes with evolution to acute myeloid leukaemia and normal cytogenetics

Detlef Trost, Barbara Hildebrandt, Nicola Müller, Ulrich Germing, Brigitte Royer-Pokora

Journal:

Leukemia Research

Year:

2004

Language:

english

File:

PDF, 127 KB

english, 2004

19

P-67 Hyperdiploidy in MDS and AML is associated with poor prognosis

S. Balleisen, S. Knipp, A. Kuendgen, B. Hildebrandt, N. Gattermann, R. Haas, B. Royer-Pokora, U. Genning

Journal:

Leukemia Research

Year:

2005

Language:

english

File:

PDF, 80 KB

english, 2005

20

134 Hidden genomic abnormalities detected in MDS patients with a normal karyotype have prognostic relevance

B. Royer-Pokora, A. Thiel, M. Beier, D. Ingenhag, K. Servan, M. Hein, U. Germing, B. Hildebrandt

Journal:

Leukemia Research

Year:

2011

Language:

english

File:

PDF, 54 KB

english, 2011

21

Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene

M. Drechsler, E. J. Meijers-Heijboer, S. Schneider, B. Schurich, C. Grond-Ginsbach, G. Tariverdian, G. Kantner, A. Blankenagel, D. Kaps, T. Schroeder-Kurth, B. Royer-Pokora

Journal:

Year:

1994

Language:

english

File:

PDF, 1015 KB

english, 1994

22

Exon skipping due to a mutation in a donor splice site in theWT-1gene is associated with Wilms' tumor and severe genital malformations

Susanne Schneider, Gabi Wildhardt, Rolf Ludwig, Brigitte Royer-Pokora

Journal:

Year:

1993

Language:

english

File:

PDF, 871 KB

english, 1993

23

Molecular cloning of the translocation breakpoint in T-ALL 11;14 (p13;q11): genomic map of TCR alpha and delta region on chromosome 14q11 and long-range map of region 11p13

Brigitte Royer-Pokora, Brigitte Fleischer, Susanne Ragg, Uschi Loos, Dorothea Williams

Journal:

Year:

1989

Language:

english

File:

PDF, 1.07 MB

english, 1989

24

Tumor specificity of acute avian leukemia viruses reflected by their transformation target cell specificity in vitro

T. Graf, B. Royer-Pokora, W. Meyer-Glauner, H. Beug

Journal:

Medical Microbiology and Immunology

Year:

1977

Language:

english

File:

PDF, 2.99 MB

english, 1977

25

Plasmids controlling synthesis of hemolysin inEscherichia coli

Brigitte Royer-Pokora, Werner Goebel

Journal:

Molecular Genetics and Genomics

Year:

1976

Language:

english

File:

PDF, 653 KB

english, 1976

26

A novel post-transcriptional splicing form of the acute T cell leukemia proto-oncogeneLmo2

Tianhui Zhu, Gang Qin, Brigitte Royer-Pokora

Journal:

SCIENCE CHINA Life Sciences

Year:

2001

Language:

english

File:

PDF, 793 KB

english, 2001

27

Fusion ofH4/D10S170toPDGFRβin a patient with chronic myelomonocytic leukemia and long-term responsiveness to imatinib

Matthias Drechsler, Barbara Hildebrandt, Andrea Kündgen, Ulrich Germing, Brigitte Royer-Pokora

Journal:

Annals of Hematology

Year:

2007

Language:

english

File:

PDF, 88 KB

english, 2007

28

Comparativein silicoanalyses and experimental validation of novel splice site and missense mutations in the genesMLH1andMSH2

Beate Betz, Stephan Theiss, Murat Aktas, Carolin Konermann, Timm O. Goecke, Gabriela Möslein, Heiner Schaal, Brigitte Royer-Pokora

Journal:

Journal of Cancer Research and Clinical Oncology

Year:

2010

Language:

english

File:

PDF, 618 KB

english, 2010

29

A LINE element is present at the site of a 300-kb deletion starting in intron 10 of thePAX6gene in a case of familial aniridia

Matthias Drechsler, B. Royer-Pokora

Journal:

Year:

1996

Language:

english

File:

PDF, 125 KB

english, 1996

30

A high proportion of mutations in the BRCA1 gene in German breast/ovarian cancer families with clustering of mutations in the 3′ third of the gene

Juan Dong, Jenny Chang-Claude, Yixin Wu, Valérie Schumacher, Irmgard Debatin, Patricia Tonin, Brigitte Royer-Pokora

Journal:

Year:

1998

Language:

english

File:

PDF, 95 KB

english, 1998

31

Slow progressive FSGS associated with an F392LWT1mutation

Petras Kaltenis, Valérie Schumacher, Augustina Jankauskienė, Arvydas Laurinavičius, Brigitte Royer-Pokora

Journal:

Pediatric Nephrology

Year:

2004

Language:

english

File:

PDF, 171 KB

english, 2004

32

Genetische Prädisposition für Wilms-Tumor

B. Royer-Pokora

Journal:

medizinische genetik

Year:

2007

Language:

german

File:

PDF, 835 KB

german, 2007

33

SDHD mutation analysis in seven German patients with sporadic carotid body paraganglioma: one novel mutation, no Dutch founder mutation and further evidence that G12S is a polymorphism

B Leube, R Huber, TO Goecke, W Sandmann, B Royer-Pokora

Journal:

Clinical Genetics

Year:

2004

Language:

english

File:

PDF, 67 KB

english, 2004

34

Mutant avian erythroblastosis virus with restricted target cell specificity

Royer-Pokora, Brigitte, Grieser, Sigrid, Beug, Hartmut, Graf, Thomas

Journal:

Year:

1979

File:

PDF, 443 KB

1979

35

Isolation of UV-resistant revertants from a xeroderma pigmentosum complementation group A cell line

Royer-Pokora, Brigitte, Haseltine, William A.

Journal:

Year:

1984

File:

PDF, 347 KB

1984

36

Cloning the gene for an inherited human disorder—chronic granulomatous disease—on the basis of its chromosomal location

Royer-Pokora, Brigitte, Kunkel, Louis M., Monaco, Anthony P., Goff, Sabra C., Newburger, Peter E., Baehner, Robert L., Cole, F. Sessions, Curnutte, John T., Orkin, Stuart H.

Journal:

Year:

1986

File:

PDF, 876 KB

1986

37

No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients

Steinke, Verena, Rahner, Nils, Morak, Monika, Keller, Gisela, Schackert, Hans K, Görgens, Heike, Schmiegel, Wolff, Royer-Pokora, Brigitte, Dietmaier, Wolfgang, Kloor, Matthias

Journal:

European Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 110 KB

english, 2008

38

Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCC

Morak, Monika, Schackert, Hans Konrad, Rahner, Nils, Betz, Beate, Ebert, Matthias, Walldorf, Constanze, Royer-Pokora, Brigitte, Schulmann, Karsten, von Knebel-Doeberitz, Magnus, Dietmaier, Wolfgang

Journal:

European Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 267 KB

english, 2008

39

Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK)

Reis, André, Hennies, Hans-Christian, Langbein, Lutz, Digweed, Martin, Mischke, Dietmar, Drechsler, Matthias, Schröck, Evelin, Royer-Pokora, Brigitte, Franke, Werner W., Sperling, Karl

Journal:

Nature Genetics

Year:

1994

File:

PDF, 768 KB

1994

40

Simultaneous occurrence of a t(9;22) (Ph) with a t(2;11) in a patient with CML and emergence of a new clone with the t(2;11) alone after imatinib mesylate treatment

Royer-Pokora, B, Hildebrandt, B, Redmann, A, Herold, C, Kronenwett, R, Haas, R, Drechsler, M, Wieland, C

Journal:

Year:

2003

Language:

english

File:

PDF, 109 KB

english, 2003

41

The tyrosine-kinase inhibitor imatinib induces long-term remission in a patient with chronic myelogenous leukemia with translocation t(4;22)

Neumann, F, Poelitz, A, Hildebrandt, B, Fenk, R, Haas, R, Royer-Pokora, B, Germing, U

Journal:

Year:

2007

Language:

english

File:

PDF, 88 KB

english, 2007

42

A novel transcript of the LMO2 gene, LMO2-c, is regulated by GATA-1 and PU.1 and encodes an antagonist of LMO2

Wang, Q, Zhang, M, Wang, X, Yuan, W, Chen, D, Royer-Pokora, B, Zhu, T

Journal:

Year:

2007

Language:

english

File:

PDF, 507 KB

english, 2007

43

Analysis of native WT1 protein from frozen human kidney and Wilms' tumors

Iben, Sebastian, Royer-Pokora, Brigitte

Journal:

Year:

1999

Language:

english

File:

PDF, 117 KB

english, 1999

44

TTG-2, a lim-domaine protein with a possible role in protein-protein interaction

E. Keppel, G. Wildhardt, M. Blüthner, W. Kaelin, B. Royer-Pokora

Journal:

Journal of Cancer Research and Clinical Oncology

Year:

1995

Language:

english

File:

PDF, 163 KB

english, 1995

45

WT1mutations in patients with Denys-Drash syndrome and wilms’ tumor

V. Schumacher, S. Schneider, B. Royer-Pokora

Journal:

Journal of Cancer Research and Clinical Oncology

Year:

1995

Language:

english

File:

PDF, 147 KB

english, 1995

46

Delineation by molecular cytogenetics of 5q deletion breakpoints in myelodyplastic syndromes and acute myeloid leukemia

Brigitte Royer-Pokora, Detlef Trost, Nicola Müller, Barbara Hildebrandt, Ulrich Germing, Manfred Beier

Journal:

Cancer Genetics and Cytogenetics

Year:

2006

Language:

english

File:

PDF, 138 KB

english, 2006

47

Molecular cytogenetic profiling of complex karyotypes in primary myelodysplastic syndromes and acute myeloid leukemia

Detlef Trost, Barbara Hildebrandt, Manfred Beier, Nicola Müller, Ulrich Germing, Brigitte Royer-Pokora

Journal:

Cancer Genetics and Cytogenetics

Year:

2006

Language:

english

File:

PDF, 493 KB

english, 2006

48

Reliable engraftment, low toxicity, and durable remissions following allogeneic blood stem cell transplantation with minimal conditioning

Guido Kobbe, Peter Schneider, Manuel Aivado, Fabian Zohren, Dominique Schubert, Roland Fenk, Frank Neumann, Ralf Kronenwett, Hildegard Pape, Astrid Rong, Brigitte Royer-Pokora, Barbara Hildebrandt, Ul

Journal:

Experimental Hematology

Year:

2002

Language:

english

File:

PDF, 91 KB

english, 2002

49

Determination of Functional Domains of the Human Transcription Factor PAX8 Responsible for its Nuclear Localization and Transactivating Potential

Andrej Poleev, Olga Okladnova, Anna-Maria Musti, Susanne Schneider, Brigitta Royer-Pokora, Dimitrij Plachov

Journal:

Year:

1997

Language:

english

File:

PDF, 1.14 MB

english, 1997

50

Pathological assessment of mismatch repair gene variants in Lynch syndrome: Past, present, and future

Lene Juel Rasmussen, Christopher D. Heinen, Brigitte Royer-Pokora, Mark Drost, Sean Tavtigian, Robert M.W. Hofstra, Niels de Wind

Journal:

Year:

2012

Language:

english

File:

PDF, 282 KB

english, 2012