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    Results: 1 to 50 of 97

    1.

    Comparative in silico analyses and experimental validation of novel splice site and missense mutations in the genes MLH1 and MSH2.

    Betz B, Theiss S, Aktas M, Konermann C, Goecke TO, Möslein G, Schaal H, Royer-Pokora B.

    J Cancer Res Clin Oncol. 2009 Aug 8. [Epub ahead of print]PMID: 19669161 [PubMed - as supplied by publisher]Related articles

    2.

    Hyperactivation of the insulin-like growth factor receptor I signaling pathway is an essential event for cisplatin resistance of ovarian cancer cells.

    Eckstein N, Servan K, Hildebrandt B, Pölitz A, von Jonquières G, Wolf-Kümmeth S, Napierski I, Hamacher A, Kassack MU, Budczies J, Beier M, Dietel M, Royer-Pokora B, Denkert C, Royer HD.

    Cancer Res. 2009 Apr 1;69(7):2996-3003. Epub 2009 Mar 24.PMID: 19318572 [PubMed - indexed for MEDLINE]Related articles

    3.

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

    Zhu T, Qin G, Royer-Pokora B.

    Sci China C Life Sci. 2001 Dec;44(6):561-9.PMID: 18763096 [PubMed - in process]Related articles

    4.

    Clinical relevance of mutations in the Wilms tumor suppressor 1 gene WT1 and the cadherin-associated protein beta1 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.

    Royer-Pokora B, Weirich A, Schumacher V, Uschkereit C, Beier M, Leuschner I, Graf N, Autschbach F, Schneider D, von Harrach M.

    Cancer. 2008 Sep 1;113(5):1080-9.PMID: 18618575 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

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

    Neumann F, Markett J, Fenk R, Pooten M, Koch A, Bruennert D, Schimkus N, Wulfert M, Royer-Pokora B, Kronenwett R, Haas R, Gattermann N.

    Hematol Oncol. 2008 Dec;26(4):213-8.PMID: 18449950 [PubMed - indexed for MEDLINE]Related articles

    6.

    Ulna/height ratio as clinical parameter separating EXT1 from EXT2 families?

    Leube B, Hardt K, Portier S, Westhoff B, Jäger M, Krauspe R, Royer-Pokora B.

    Genet Test. 2008 Mar;12(1):129-33.PMID: 18373409 [PubMed - indexed for MEDLINE]Related articles

    7.

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

    Morak M, Schackert HK, Rahner N, Betz B, Ebert M, Walldorf C, Royer-Pokora B, Schulmann K, von Knebel-Doeberitz M, Dietmaier W, Keller G, Kerker B, Leitner G, Holinski-Feder E.

    Eur J Hum Genet. 2008 Jul;16(7):804-11. Epub 2008 Feb 27.PMID: 18301449 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

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

    Steinke V, Rahner N, Morak M, Keller G, Schackert HK, Görgens H, Schmiegel W, Royer-Pokora B, Dietmaier W, Kloor M, Engel C, Propping P, Aretz S; German HNPCC Consortium.

    Eur J Hum Genet. 2008 May;16(5):587-92. Epub 2008 Feb 27.PMID: 18301448 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

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

    Schumacher V, Gueler B, Looijenga LH, Becker JU, Amann K, Engers R, Dotsch J, Stoop H, Schulz W, Royer-Pokora B.

    Mol Reprod Dev. 2008 Sep;75(9):1484-94.PMID: 18271004 [PubMed - indexed for MEDLINE]Related articles

    10.

    Hypomethylation and aberrant expression of the glioma pathogenesis-related 1 gene in Wilms tumors.

    Chilukamarri L, Hancock AL, Malik S, Zabkiewicz J, Baker JA, Greenhough A, Dallosso AR, Huang TH, Royer-Pokora B, Brown KW, Malik K.

    Neoplasia. 2007 Nov;9(11):970-8.PMID: 18030365 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    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.

    Evers C, Beier M, Poelitz A, Hildebrandt B, Servan K, Drechsler M, Germing U, Royer HD, Royer-Pokora B.

    Genes Chromosomes Cancer. 2007 Dec;46(12):1119-28.PMID: 17823930 [PubMed - indexed for MEDLINE]Related articles

    12.

    Clinical outcome and genotype in patients with hereditary multiple exostoses.

    Jäger M, Westhoff B, Portier S, Leube B, Hardt K, Royer-Pokora B, Gossheger G, Krauspe R.

    J Orthop Res. 2007 Dec;25(12):1541-51.PMID: 17676624 [PubMed - indexed for MEDLINE]Related articles

    13.

    Different CTNNB1 mutations as molecular genetic proof for the independent origin of four Wilms tumours in a patient with a novel germ line WT1 mutation.

    Uschkereit C, Perez N, de Torres C, Küff M, Mora J, Royer-Pokora B.

    J Med Genet. 2007 Jun;44(6):393-6.PMID: 17551084 [PubMed - indexed for MEDLINE]Related articles

    14.

    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.

    Leukemia. 2007 May;21(5):1015-25. Epub 2007 Mar 15.PMID: 17361224 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    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.

    Leukemia. 2007 Apr;21(4):836-7. Epub 2007 Feb 1. No abstract available. PMID: 17268524 [PubMed - indexed for MEDLINE]Related articles

    16.

    Impaired glomerular maturation and lack of VEGF165b in Denys-Drash syndrome.

    Schumacher VA, Jeruschke S, Eitner F, Becker JU, Pitschke G, Ince Y, Miner JH, Leuschner I, Engers R, Everding AS, Bulla M, Royer-Pokora B.

    J Am Soc Nephrol. 2007 Mar;18(3):719-29. Epub 2007 Jan 31.PMID: 17267748 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    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.

    Krüger S, Engel C, Bier A, Silber AS, Görgens H, Mangold E, Pagenstecher C, Holinski-Feder E, von Knebel Doeberitz M, Royer-Pokora B, Dechant S, Pox C, Rahner N, Müller A, Schackert HK; German HNPCC Consortium.

    Cancer Lett. 2007 Jul 8;252(1):55-64. Epub 2007 Jan 16.PMID: 17224235 [PubMed - indexed for MEDLINE]Related articles

    18.

    Fusion of H4/D10S170 to PDGFRbeta in a patient with chronic myelomonocytic leukemia and long-term responsiveness to imatinib.

    Drechsler M, Hildebrandt B, Kündgen A, Germing U, Royer-Pokora B.

    Ann Hematol. 2007 May;86(5):353-4. Epub 2007 Jan 9. No abstract available. PMID: 17211520 [PubMed - indexed for MEDLINE]Related articles

    19.

    Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders.

    Hasselbacher K, Wiggins RC, Matejas V, Hinkes BG, Mucha B, Hoskins BE, Ozaltin F, Nürnberg G, Becker C, Hangan D, Pohl M, Kuwertz-Bröking E, Griebel M, Schumacher V, Royer-Pokora B, Bakkaloglu A, Nürnberg P, Zenker M, Hildebrandt F.

    Kidney Int. 2006 Sep;70(6):1008-12. Epub 2006 Aug 16.PMID: 16912710 [PubMed - indexed for MEDLINE]Related articles

    20.

    STK11 status and intussusception risk in Peutz-Jeghers syndrome.

    Hearle N, Schumacher V, Menko FH, Olschwang S, Boardman LA, Gille JJ, Keller JJ, Westerman AM, Scott RJ, Lim W, Trimbath JD, Giardiello FM, Gruber SB, Offerhaus GJ, Rooij FW, Wilson JH, Hansmann A, Möslein G, Royer-Pokora B, Vogel T, Phillips RK, Spigelman AD, Houlston RS.

    J Med Genet. 2006 Aug;43(8):e41.PMID: 16882735 [PubMed - indexed for MEDLINE]Related articlesFree article

    21.

    Frequency and spectrum of cancers in the Peutz-Jeghers syndrome.

    Hearle N, Schumacher V, Menko FH, Olschwang S, Boardman LA, Gille JJ, Keller JJ, Westerman AM, Scott RJ, Lim W, Trimbath JD, Giardiello FM, Gruber SB, Offerhaus GJ, de Rooij FW, Wilson JH, Hansmann A, Möslein G, Royer-Pokora B, Vogel T, Phillips RK, Spigelman AD, Houlston RS.

    Clin Cancer Res. 2006 May 15;12(10):3209-15.PMID: 16707622 [PubMed - indexed for MEDLINE]Related articlesFree article

    22.

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

    Royer-Pokora B, Trost D, Müller N, Hildebrandt B, Germing U, Beier M.

    Cancer Genet Cytogenet. 2006 May;167(1):66-9.PMID: 16682289 [PubMed - indexed for MEDLINE]Related articles

    23.

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

    Trost D, Hildebrandt B, Beier M, Müller N, Germing U, Royer-Pokora B.

    Cancer Genet Cytogenet. 2006 Feb;165(1):51-63.PMID: 16490597 [PubMed - indexed for MEDLINE]Related articles

    24.

    A novel WT1 missense mutation presenting with Denys-Drash syndrome and cortical atrophy.

    Schumacher V, Thumfart J, Drechsler M, Essayie M, Royer-Pokora B, Querfeld U, Müller D.

    Nephrol Dial Transplant. 2006 Feb;21(2):518-21. Epub 2005 Nov 22. No abstract available. PMID: 16303781 [PubMed - indexed for MEDLINE]Related articlesFree article

    25.

    Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.

    Schumacher V, Vogel T, Leube B, Driemel C, Goecke T, Moeslein G, Royer-Pokora B.

    Hum Genet. 2005 May;116(6):541. No abstract available. PMID: 15991322 [PubMed - indexed for MEDLINE]Related articles

    26.

    Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.

    Schumacher V, Vogel T, Leube B, Driemel C, Goecke T, Moeslein G, Royer-Pokora B.

    Hum Genet. 2005 May;116(6):540. No abstract available. PMID: 15991321 [PubMed - indexed for MEDLINE]Related articles

    27.

    Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.

    Schumacher V, Vogel T, Leube B, Driemel C, Goecke T, Moeslein G, Royer-Pokora B.

    Hum Genet. 2005 May;116(6):540. No abstract available. PMID: 15991320 [PubMed - indexed for MEDLINE]Related articles

    28.

    Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.

    Schumacher V, Vogel T, Leube B, Driemel C, Goecke T, Moeslein G, Royer-Pokora B.

    Hum Genet. 2005 May;116(6):540. No abstract available. PMID: 15991319 [PubMed - indexed for MEDLINE]Related articles

    29.

    Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.

    Schumacher V, Vogel T, Leube B, Driemel C, Goecke T, Moeslein G, Royer-Pokora B.

    Hum Genet. 2005 May;116(6):537. No abstract available. PMID: 15991310 [PubMed - indexed for MEDLINE]Related articles

    30.

    Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.

    Schumacher V, Vogel T, Leube B, Driemel C, Goecke T, Moeslein G, Royer-Pokora B.

    Hum Genet. 2005 May;116(6):533. No abstract available. PMID: 15988825 [PubMed - indexed for MEDLINE]Related articles

    31.

    YB-1 provokes breast cancer through the induction of chromosomal instability that emerges from mitotic failure and centrosome amplification.

    Bergmann S, Royer-Pokora B, Fietze E, Jürchott K, Hildebrandt B, Trost D, Leenders F, Claude JC, Theuring F, Bargou R, Dietel M, Royer HD.

    Cancer Res. 2005 May 15;65(10):4078-87.PMID: 15899797 [PubMed - indexed for MEDLINE]Related articlesFree article

    32.

    STK11 genotyping and cancer risk in Peutz-Jeghers syndrome.

    Schumacher V, Vogel T, Leube B, Driemel C, Goecke T, Möslein G, Royer-Pokora B.

    J Med Genet. 2005 May;42(5):428-35. No abstract available. PMID: 15863673 [PubMed - indexed for MEDLINE]Related articlesFree article

    33.

    Gene expression profiling of Philadelphia chromosome (Ph)-negative CD34+ hematopoietic stem and progenitor cells of patients with Ph-positive CML in major molecular remission during therapy with imatinib.

    Neumann F, Teutsch N, Kliszewski S, Bork S, Steidl U, Brors B, Schimkus N, Roes N, Germing U, Hildebrandt B, Royer-Pokora B, Eils R, Gattermann N, Haas R, Kronenwett R.

    Leukemia. 2005 Mar;19(3):458-60. No abstract available. PMID: 15618956 [PubMed - indexed for MEDLINE]Related articles

    34.

    Effective use of high-dose chemotherapy and autologous stem cell rescue for relapsed adult Wilms' tumor and a novel alteration in intron 1 of the WT1 gene.

    Trappe RU, Riess H, Lippek F, Plotkin M, Schumacher V, Royer-Pokora B, Hildebrandt B, Zuber J, Mapara MY, Oertel S, Dörken B.

    J Pediatr Hematol Oncol. 2004 Dec;26(12):820-3.PMID: 15591903 [PubMed - indexed for MEDLINE]Related articles

    35.

    Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities.

    Zenker M, Aigner T, Wendler O, Tralau T, Müntefering H, Fenski R, Pitz S, Schumacher V, Royer-Pokora B, Wühl E, Cochat P, Bouvier R, Kraus C, Mark K, Madlon H, Dötsch J, Rascher W, Maruniak-Chudek I, Lennert T, Neumann LM, Reis A.

    Hum Mol Genet. 2004 Nov 1;13(21):2625-32. Epub 2004 Sep 14.PMID: 15367484 [PubMed - indexed for MEDLINE]Related articlesFree article

    36.

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

    Royer-Pokora B, Beier M, Henzler M, Alam R, Schumacher V, Weirich A, Huff V.

    Am J Med Genet A. 2004 Jun 15;127A(3):249-57.PMID: 15150775 [PubMed - indexed for MEDLINE]Related articles

    37.

    Survival in nephroblastoma treated according to the trial and study SIOP-9/GPOH with respect to relapse and morbidity.

    Weirich A, Ludwig R, Graf N, Abel U, Leuschner I, Vujanic GM, Mehls O, Boos J, Beck J, Royer-Pokora B, Voûte PA.

    Ann Oncol. 2004 May;15(5):808-20.PMID: 15111352 [PubMed - indexed for MEDLINE]Related articlesFree article

    38.

    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.

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

    Clin Genet. 2004 Jan;65(1):61-3. No abstract available. PMID: 15032977 [PubMed - indexed for MEDLINE]Related articles

    39.

    Slow progressive FSGS associated with an F392L WT1 mutation.

    Kaltenis P, Schumacher V, Jankauskiene A, Laurinavicius A, Royer-Pokora B.

    Pediatr Nephrol. 2004 Mar;19(3):353-6. Epub 2004 Jan 27.PMID: 14745636 [PubMed - indexed for MEDLINE]Related articles

    40.

    BASP1 is a transcriptional cosuppressor for the Wilms' tumor suppressor protein WT1.

    Carpenter B, Hill KJ, Charalambous M, Wagner KJ, Lahiri D, James DI, Andersen JS, Schumacher V, Royer-Pokora B, Mann M, Ward A, Roberts SG.

    Mol Cell Biol. 2004 Jan;24(2):537-49.PMID: 14701728 [PubMed - indexed for MEDLINE]Related articlesFree article

    41.

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

    Trost D, Hildebrandt B, Müller N, Germing U, Royer-Pokora B.

    Leuk Res. 2004 Feb;28(2):171-7.PMID: 14654082 [PubMed - indexed for MEDLINE]Related articles

    42.

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

    Leube B, Majewski F, Gebauer J, Royer-Pokora B.

    Am J Med Genet A. 2003 Dec 15;123A(3):296-300.PMID: 14608653 [PubMed - indexed for MEDLINE]Related articles

    43.

    Unbalanced cryptic translocation der(14)t(9;14)(q34.3;q32.33) identified by subtelomeric FISH.

    Leube B, Majewski F, Drechsler M, Royer-Pokora B.

    Clin Dysmorphol. 2003 Oct;12(4):261-5.PMID: 14564215 [PubMed - indexed for MEDLINE]Related articles

    44.

    Two molecular subgroups of Wilms' tumors with or without WT1 mutations.

    Schumacher V, Schuhen S, Sonner S, Weirich A, Leuschner I, Harms D, Licht J, Roberts S, Royer-Pokora B.

    Clin Cancer Res. 2003 Jun;9(6):2005-14.PMID: 12796362 [PubMed - indexed for MEDLINE]Related articlesFree article

    45.

    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.

    Leukemia. 2003 Apr;17(4):807-10. Review. No abstract available. PMID: 12682644 [PubMed - indexed for MEDLINE]Related articles

    46.

    Quantitative real-time reverse-transcription polymerase chain reaction for diagnosis of BCR-ABL positive leukemias and molecular monitoring following allogeneic stem cell transplantation.

    Neumann F, Herold C, Hildebrandt B, Kobbe G, Aivado M, Rong A, Free M, Rössig R, Fenk R, Schneider P, Gattermann N, Royer-Pokora B, Haas R, Kronenwett R.

    Eur J Haematol. 2003 Jan;70(1):1-10.PMID: 12631253 [PubMed - indexed for MEDLINE]Related articles

    47.

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

    Kobbe G, Schneider P, Aivado M, Zohren F, Schubert D, Fenk R, Neumann F, Kronenwett R, Pape H, Rong A, Royer-Pokora B, Hildebrandt B, Germing U, Gattermann N, Heyll A, Haas R.

    Exp Hematol. 2002 Nov;30(11):1346-53.PMID: 12423689 [PubMed - indexed for MEDLINE]Related articles

    48.

    Refined mapping of allele loss at chromosome 10q23-26 in prostate cancer.

    Leube B, Drechsler M, Mühlmann K, Schäfer R, Schulz WA, Santourlidis S, Anastasiadis A, Ackermann R, Visakorpi T, Müller W, Royer-Pokora B.

    Prostate. 2002 Feb 15;50(3):135-44.PMID: 11813205 [PubMed - indexed for MEDLINE]Related articles

    49.

    Germline Wilms tumor suppressor gene (WT1) mutation leading to isolated genital malformation without Wilms tumor or nephropathy.

    Köhler B, Schumacher V, l'Allemand D, Royer-Pokora B, Grüters A.

    J Pediatr. 2001 Mar;138(3):421-4.PMID: 11241055 [PubMed - indexed for MEDLINE]Related articles

    50.

    Par4 is a coactivator for a splice isoform-specific transcriptional activation domain in WT1.

    Richard DJ, Schumacher V, Royer-Pokora B, Roberts SG.

    Genes Dev. 2001 Feb 1;15(3):328-39.PMID: 11159913 [PubMed - indexed for MEDLINE]Related articlesFree article

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