Royer-Pokora B - Search Results

1

Comparative performance analysis of human iPSC-derived and primary neural progenitor cells (NPC) grown as neurospheres in vitro.

Hofrichter M, Nimtz L, Tigges J, Kabiri Y, Schröter F, Royer-Pokora B, Hildebrandt B, Schmuck M, Epanchintsev A, Theiss S, Adjaye J, Egly JM, Krutmann J, Fritsche E. Hofrichter M, et al. Among authors: royer pokora b. Stem Cell Res. 2017 Dec;25:72-82. doi: 10.1016/j.scr.2017.10.013. Epub 2017 Oct 26. Stem Cell Res. 2017. PMID: 29112887 Free article.

2

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. Neumann F, et al. Eur J Haematol. 2003 Jan;70(1):1-10. doi: 10.1034/j.1600-0609.2003.02811.x. Eur J Haematol. 2003. PMID: 12631253

3

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. Trost D, et al. Leuk Res. 2004 Feb;28(2):171-7. doi: 10.1016/s0145-2126(03)00221-2. Leuk Res. 2004. PMID: 14654082

4

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. Trost D, et al. Cancer Genet Cytogenet. 2006 Feb;165(1):51-63. doi: 10.1016/j.cancergencyto.2005.09.007. Cancer Genet Cytogenet. 2006. PMID: 16490597

5

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. Royer-Pokora B, et al. Cancer Genet Cytogenet. 2006 May;167(1):66-9. doi: 10.1016/j.cancergencyto.2005.08.003. Cancer Genet Cytogenet. 2006. PMID: 16682289

6

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. Evers C, et al. Genes Chromosomes Cancer. 2007 Dec;46(12):1119-28. doi: 10.1002/gcc.20498. Genes Chromosomes Cancer. 2007. PMID: 17823930

7

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. Betz B, et al. J Cancer Res Clin Oncol. 2010 Jan;136(1):123-34. doi: 10.1007/s00432-009-0643-z. J Cancer Res Clin Oncol. 2010. PMID: 19669161

8

Spontaneous in vitro transformation of primary human osteoblast-like cells.

Magdolen U, Schmitt M, Hildebrandt B, Diehl P, Schauwecker J, Saldamli B, Burgkart R, Tübel J, Gradinger R, Royer-Pokora B. Magdolen U, et al. Cancer Genomics Proteomics. 2010 Mar-Apr;7(2):61-6. Cancer Genomics Proteomics. 2010. PMID: 20335519

9

Comprehensive array CGH of normal karyotype myelodysplastic syndromes reveals hidden recurrent and individual genomic copy number alterations with prognostic relevance.

Thiel A, Beier M, Ingenhag D, Servan K, Hein M, Moeller V, Betz B, Hildebrandt B, Evers C, Germing U, Royer-Pokora B. Thiel A, et al. Leukemia. 2011 Mar;25(3):387-99. doi: 10.1038/leu.2010.293. Epub 2011 Jan 28. Leukemia. 2011. PMID: 21274003

10

Structural chromosome abnormalities, increased DNA strand breaks and DNA strand break repair deficiency in dermal fibroblasts from old female human donors.

Kalfalah F, Seggewiß S, Walter R, Tigges J, Moreno-Villanueva M, Bürkle A, Ohse S, Busch H, Boerries M, Hildebrandt B, Royer-Pokora B, Boege F. Kalfalah F, et al. Aging (Albany NY). 2015 Feb;7(2):110-22. doi: 10.18632/aging.100723. Aging (Albany NY). 2015. PMID: 25678531 Free PMC article.

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