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Thomas Liehr

Showing results (391-400 of 586) with videos related to

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Scientific Reports|July 2, 2025
Barleria extracts containing barlerin and verbascoside boost immunity and regulate CYP450 gene in prostate cancerSanit Kaewdaungdee, Zi Wei Sham, Hao Xuan Ho, et al.
Oncology Letters|March 22, 2016
A novel <i>IGH@</i> gene rearrangement associated with <i>CDKN2A</i>/<i>B</i> deletion in young adult B-cell acute lymphoblastic leukemiaMoneeb A K Othman, Beata Grygalewicz, Barbara Pienkowska-Grela, et al.
Cytogenetic and Genome Research|April 16, 2014
An interstitial 4q31.21q31.22 microdeletion associated with developmental delay: case report and literature reviewAngeliki-Maria Vlaikou, Emmanouil Manolakos, Dimitrios Noutsopoulos, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|October 19, 2012
Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?Roberta Santos Guilherme, Elisabeth Klein, Claudia Venner, et al.
Prenatal Diagnosis|May 21, 2009
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGHEmmanouil Manolakos, Annalisa Vetro, Stylianos Kitmirides, et al.
Molecular Cytogenetics|February 24, 2009
Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal maleSofia Kitsiou-Tzeli, Emmanouil Manolakos, Magdalini Lagou, et al.
Clinical Dysmorphology|March 7, 2012
Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literatureEmmanouil Manolakos, Stavros Sifakis, Sotirios Sotiriou, et al.
Molecular Cytogenetics|June 13, 2012
Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case reportMilene Vianna Mulatinho, Cassio Luiz de Carvalho Serao, Fernanda Scalco, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|June 28, 2007
Three unusual but cytogenetically similar cases with up to five different cell lines involving structural and numerical abnormalities of chromosome 18Isabel M Carreira, Alexandra Mascarenhas, Eunice Matoso, et al.
Animals : an Open Access Journal From MDPI|August 26, 2022
Genomic Organization of Microsatellites and <i>LINE-1-</i>like Retrotransposons: Evolutionary Implications for <i>Ctenomys minutus</i> (Rodentia: Ctenomyidae) CytotypesThays Duarte de Oliveira, Natasha Avila Bertocchi, Rafael Kretschmer, et al.
Pageof 59

Showing results (391-400 of 586) with videos related to

Sort By:
Pageof 59
Scientific Reports|July 2, 2025
Barleria extracts containing barlerin and verbascoside boost immunity and regulate CYP450 gene in prostate cancerSanit Kaewdaungdee, Zi Wei Sham, Hao Xuan Ho, et al.
Oncology Letters|March 22, 2016
A novel <i>IGH@</i> gene rearrangement associated with <i>CDKN2A</i>/<i>B</i> deletion in young adult B-cell acute lymphoblastic leukemiaMoneeb A K Othman, Beata Grygalewicz, Barbara Pienkowska-Grela, et al.
Cytogenetic and Genome Research|April 16, 2014
An interstitial 4q31.21q31.22 microdeletion associated with developmental delay: case report and literature reviewAngeliki-Maria Vlaikou, Emmanouil Manolakos, Dimitrios Noutsopoulos, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|October 19, 2012
Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?Roberta Santos Guilherme, Elisabeth Klein, Claudia Venner, et al.
Prenatal Diagnosis|May 21, 2009
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGHEmmanouil Manolakos, Annalisa Vetro, Stylianos Kitmirides, et al.
Molecular Cytogenetics|February 24, 2009
Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal maleSofia Kitsiou-Tzeli, Emmanouil Manolakos, Magdalini Lagou, et al.
Clinical Dysmorphology|March 7, 2012
Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literatureEmmanouil Manolakos, Stavros Sifakis, Sotirios Sotiriou, et al.
Molecular Cytogenetics|June 13, 2012
Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case reportMilene Vianna Mulatinho, Cassio Luiz de Carvalho Serao, Fernanda Scalco, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|June 28, 2007
Three unusual but cytogenetically similar cases with up to five different cell lines involving structural and numerical abnormalities of chromosome 18Isabel M Carreira, Alexandra Mascarenhas, Eunice Matoso, et al.
Animals : an Open Access Journal From MDPI|August 26, 2022
Genomic Organization of Microsatellites and <i>LINE-1-</i>like Retrotransposons: Evolutionary Implications for <i>Ctenomys minutus</i> (Rodentia: Ctenomyidae) CytotypesThays Duarte de Oliveira, Natasha Avila Bertocchi, Rafael Kretschmer, et al.
Pageof 59