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T Liehr

Showing results (161-170 of 192) with videos related to

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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.
British Journal of Haematology|May 31, 2001
Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative chronic myelogenous leukaemiaH Starke, M Raida, V Trifonov, et al.
Genetics and Molecular Research : GMR|January 15, 2013
Numerical aberrations of chromosome 17 and TP53 in brain metastases derived from breast cancerD S Vasconcelos, F P E da Silva, L G Quintana, et al.
Clinical Genetics|September 5, 2001
Tetrasomy 21 due to a de novo Robertsonian translocation t(14;21) and an additional free trisomy 21T Liehr, V Beensen, H Starke, et al.
Human Genetics|September 10, 1999
Human and mouse RAD17 genes: identification, localization, genomic structure and histological expression pattern in normal testis and seminomaF von Deimling, J M Scharf, T Liehr, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
FISH characterization of a dicentric Yq (p11.32) isochromosome in an azoospermic maleM Codina-Pascual, M Oliver-Bonet, J Navarro, et al.
Gut|November 22, 2008
Hepatocyte differentiation of mesenchymal stem cells from human adipose tissue in vitro promotes hepatic integration in vivoH Aurich, M Sgodda, P Kaltwasser, 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|May 9, 2013
Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four-break rearrangementE Manolakos, A Vetro, E Papadopoulou, et al.
Pageof 20

Showing results (161-170 of 192) with videos related to

Sort By:
Pageof 20
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.
British Journal of Haematology|May 31, 2001
Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative chronic myelogenous leukaemiaH Starke, M Raida, V Trifonov, et al.
Genetics and Molecular Research : GMR|January 15, 2013
Numerical aberrations of chromosome 17 and TP53 in brain metastases derived from breast cancerD S Vasconcelos, F P E da Silva, L G Quintana, et al.
Clinical Genetics|September 5, 2001
Tetrasomy 21 due to a de novo Robertsonian translocation t(14;21) and an additional free trisomy 21T Liehr, V Beensen, H Starke, et al.
Human Genetics|September 10, 1999
Human and mouse RAD17 genes: identification, localization, genomic structure and histological expression pattern in normal testis and seminomaF von Deimling, J M Scharf, T Liehr, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
FISH characterization of a dicentric Yq (p11.32) isochromosome in an azoospermic maleM Codina-Pascual, M Oliver-Bonet, J Navarro, et al.
Gut|November 22, 2008
Hepatocyte differentiation of mesenchymal stem cells from human adipose tissue in vitro promotes hepatic integration in vivoH Aurich, M Sgodda, P Kaltwasser, 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|May 9, 2013
Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four-break rearrangementE Manolakos, A Vetro, E Papadopoulou, et al.
Pageof 20