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Thomas Liehr

Showing results (381-390 of 586) with videos related to

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Molecular Cancer|September 14, 2014
Supraphysiological androgen levels induce cellular senescence in human prostate cancer cells through the Src-Akt pathwayJulia Roediger, Wiebke Hessenkemper, Sophie Bartsch, et al.
International Journal of Molecular Medicine|July 30, 2009
Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogeneticsMarina Manvelyan, Philipp Kempf, Anja Weise, et al.
Molecular Cytogenetics|June 1, 2010
Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pairDilek Aktas, Eda G Utine, Kristin Mrasek, et al.
Medical Microbiology and Immunology|October 7, 2018
Macaca arctoides gammaherpesvirus 1 (strain herpesvirus Macaca arctoides): virus sequence, phylogeny and characterisation of virus-transformed macaque and rabbit cell linesAndi Krumbholz, Janine Roempke, Thomas Liehr, et al.
Cells|April 3, 2021
Evolution of a Multiple Sex-Chromosome System by Three-Sequential Translocations among Potential Sex-Chromosomes in the Taiwanese Frog <i>Odorrana swinhoana</i>Ikuo Miura, Foyez Shams, Si-Min Lin, et al.
European Journal of Human Genetics : EJHG|March 30, 2019
Regarding the rights and duties of Clinical Laboratory Geneticists in genetic healthcare systems; results of a survey in over 50 countriesThomas Liehr, Isabel M Carreira, Zsofia Balogh, et al.
Pakistan Journal of Biological Sciences : PJBS|May 5, 2020
Hypermethylation in Gene Promoters Are Induced by Chronic Exposure to Benzene, Toluene, Ethylbenzene and XylenesRafaele Tavares Silvestre, Maryah Bravo, Fabio Santiago, et al.
Oncology Reports|August 4, 2005
New rearrangement t(3;17)(q26.3;q12) in an AML patient with a poor outcomeMaria Luiza Macedo Silva, Marcelo Land, Anita Heller, et al.
American Journal of Human Genetics|September 12, 2007
The variant inv(2)(p11.2q13) is a genuinely recurrent rearrangement but displays some breakpoint heterogeneityIna Fickelscher, Thomas Liehr, Kathryn Watts, et al.
Cytogenetic and Genome Research|December 19, 2015
Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning DifficultiesMaria Kontodiou, Georgios Daskalakis, Annalisa Vetro, et al.
Pageof 59

Showing results (381-390 of 586) with videos related to

Sort By:
Pageof 59
Molecular Cancer|September 14, 2014
Supraphysiological androgen levels induce cellular senescence in human prostate cancer cells through the Src-Akt pathwayJulia Roediger, Wiebke Hessenkemper, Sophie Bartsch, et al.
International Journal of Molecular Medicine|July 30, 2009
Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogeneticsMarina Manvelyan, Philipp Kempf, Anja Weise, et al.
Molecular Cytogenetics|June 1, 2010
Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pairDilek Aktas, Eda G Utine, Kristin Mrasek, et al.
Medical Microbiology and Immunology|October 7, 2018
Macaca arctoides gammaherpesvirus 1 (strain herpesvirus Macaca arctoides): virus sequence, phylogeny and characterisation of virus-transformed macaque and rabbit cell linesAndi Krumbholz, Janine Roempke, Thomas Liehr, et al.
Cells|April 3, 2021
Evolution of a Multiple Sex-Chromosome System by Three-Sequential Translocations among Potential Sex-Chromosomes in the Taiwanese Frog <i>Odorrana swinhoana</i>Ikuo Miura, Foyez Shams, Si-Min Lin, et al.
European Journal of Human Genetics : EJHG|March 30, 2019
Regarding the rights and duties of Clinical Laboratory Geneticists in genetic healthcare systems; results of a survey in over 50 countriesThomas Liehr, Isabel M Carreira, Zsofia Balogh, et al.
Pakistan Journal of Biological Sciences : PJBS|May 5, 2020
Hypermethylation in Gene Promoters Are Induced by Chronic Exposure to Benzene, Toluene, Ethylbenzene and XylenesRafaele Tavares Silvestre, Maryah Bravo, Fabio Santiago, et al.
Oncology Reports|August 4, 2005
New rearrangement t(3;17)(q26.3;q12) in an AML patient with a poor outcomeMaria Luiza Macedo Silva, Marcelo Land, Anita Heller, et al.
American Journal of Human Genetics|September 12, 2007
The variant inv(2)(p11.2q13) is a genuinely recurrent rearrangement but displays some breakpoint heterogeneityIna Fickelscher, Thomas Liehr, Kathryn Watts, et al.
Cytogenetic and Genome Research|December 19, 2015
Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning DifficultiesMaria Kontodiou, Georgios Daskalakis, Annalisa Vetro, et al.
Pageof 59