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K Mrasek

Showing results (21-30 of 31) with videos related to

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Cytogenetic and Genome Research|February 18, 2006
Different breakage-prone regions on chromosome 1 detected in t(11;14)-positive mantle cell lymphoma cell lines and multiple myeloma cell lines are associated with different tumor progression-related mechanismsC Rudolph, T Liehr, D Steinemann, et al.
Cytogenetic and Genome Research|July 20, 2010
Is there a yet unreported unbalanced chromosomal abnormality without phenotypic consequences in proximal 4p?T Liehr, I Bartels, B Zoll, et al.
Oncogene|February 16, 2010
An HDAC1-binding domain within FATS bridges p21 turnover to radiation-induced tumorigenesisZ Li, Q Zhang, J-H Mao, et al.
Cancer Genetics and Cytogenetics|September 8, 2004
Molecular cytogenetic characterization of the mantle cell lymphoma cell line GRANTA-519C Rudolph, D Steinemann, N Von Neuhoff, et al.
Cytogenetic and Genome Research|September 29, 2007
Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literatureT Liehr, G E Utine, U Trautmann, et al.
Cytogenetic and Genome Research|September 7, 2006
Multicolor fluorescence in situ hybridization (FISH) applied to FISH-bandingT Liehr, H Starke, A Heller, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 9, 2008
Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literatureT Liehr, K Mrasek, S Hinreiner, et al.
Molecular Syndromology|November 1, 2012
Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi AnemiaA Serra, K Eirich, A K Winkler, et al.
Cytogenetic and Genome Research|November 9, 2005
Small supernumerary marker chromosomes--progress towards a genotype-phenotype correlationT Liehr, K Mrasek, A Weise, et al.
Cytogenetic and Genome Research|April 18, 2009
10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequencesT Liehr, M Stumm, R D Wegner, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Cytogenetic and Genome Research|February 18, 2006
Different breakage-prone regions on chromosome 1 detected in t(11;14)-positive mantle cell lymphoma cell lines and multiple myeloma cell lines are associated with different tumor progression-related mechanismsC Rudolph, T Liehr, D Steinemann, et al.
Cytogenetic and Genome Research|July 20, 2010
Is there a yet unreported unbalanced chromosomal abnormality without phenotypic consequences in proximal 4p?T Liehr, I Bartels, B Zoll, et al.
Oncogene|February 16, 2010
An HDAC1-binding domain within FATS bridges p21 turnover to radiation-induced tumorigenesisZ Li, Q Zhang, J-H Mao, et al.
Cancer Genetics and Cytogenetics|September 8, 2004
Molecular cytogenetic characterization of the mantle cell lymphoma cell line GRANTA-519C Rudolph, D Steinemann, N Von Neuhoff, et al.
Cytogenetic and Genome Research|September 29, 2007
Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literatureT Liehr, G E Utine, U Trautmann, et al.
Cytogenetic and Genome Research|September 7, 2006
Multicolor fluorescence in situ hybridization (FISH) applied to FISH-bandingT Liehr, H Starke, A Heller, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 9, 2008
Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literatureT Liehr, K Mrasek, S Hinreiner, et al.
Molecular Syndromology|November 1, 2012
Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi AnemiaA Serra, K Eirich, A K Winkler, et al.
Cytogenetic and Genome Research|November 9, 2005
Small supernumerary marker chromosomes--progress towards a genotype-phenotype correlationT Liehr, K Mrasek, A Weise, et al.
Cytogenetic and Genome Research|April 18, 2009
10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequencesT Liehr, M Stumm, R D Wegner, et al.
Pageof 4