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Andrea Haake

Showing results (1-10 of 24) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|December 16, 2015
Quantitative DNA Methylation Profiling in CancerOle Ammerpohl, Andrea Haake, Julia Kolarova, et al.
Expert Opinion on Drug Safety|January 25, 2020
An update on the utility and safety of cholinesterase inhibitors for the treatment of Alzheimer's diseaseAndrea Haake, Kevin Nguyen, Lauren Friedman, et al.
Leukemia & Lymphoma|September 23, 2010
Somatic mutations altering Tyr641 of EZH2 are rare in primary central nervous system lymphomaShoji Pellissery, Julia Richter, Andrea Haake, et al.
Blood|September 24, 2011
A unique case of follicular lymphoma provides insights to the clonal evolution from follicular lymphoma in situ to manifest follicular lymphomaIrina Bonzheim, Itziar Salaverria, Andrea Haake, et al.
European Journal of Medical Genetics|June 25, 2011
A de novo 1.1Mb microdeletion of chromosome 19p13.11 provides indirect evidence for EPS15L1 to be a strong candidate for split hand split foot malformationSusanne Bens, Andrea Haake, Holger Tönnies, et al.
Haematologica|March 20, 2016
Immunohistochemical detection of inhibitor of DNA binding 3 mutational variants in mature aggressive B-cell lymphomaMonika Szczepanowski, Neus Masqué-Soler, Matthias Schlesner, et al.
Molecular Cytogenetics|September 7, 2010
Conflicting results of prenatal FISH with different probes for Down's Syndrome critical regions associated with mosaicism for a de novo del(21)(q22) characterised by molecular karyotyping: Case reportChristel Eckmann-Scholz, Stefan Gesk, Inga Nagel, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|June 17, 2014
The tissue is the issue: improved methylome analysis from paraffin-embedded tissues by application of the HOPE techniqueSebastian Marwitz, Julia Kolarova, Martin Reck, et al.
Hormone Research in Paediatrics|March 30, 2012
Multiplex ligation-dependent probe amplification analysis of the NR0B1(DAX1) locus enables explanation of phenotypic differences in patients with X-linked congenital adrenal hypoplasiaMichela Barbaro, Susanne Bens, Andrea Haake, et al.
European Journal of Human Genetics : EJHG|December 13, 2012
Frequency and characterization of DNA methylation defects in children born SGASusanne Bens, Andrea Haake, Julia Richter, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Methods in Molecular Biology (Clifton, N.J.)|December 16, 2015
Quantitative DNA Methylation Profiling in CancerOle Ammerpohl, Andrea Haake, Julia Kolarova, et al.
Expert Opinion on Drug Safety|January 25, 2020
An update on the utility and safety of cholinesterase inhibitors for the treatment of Alzheimer's diseaseAndrea Haake, Kevin Nguyen, Lauren Friedman, et al.
Leukemia & Lymphoma|September 23, 2010
Somatic mutations altering Tyr641 of EZH2 are rare in primary central nervous system lymphomaShoji Pellissery, Julia Richter, Andrea Haake, et al.
Blood|September 24, 2011
A unique case of follicular lymphoma provides insights to the clonal evolution from follicular lymphoma in situ to manifest follicular lymphomaIrina Bonzheim, Itziar Salaverria, Andrea Haake, et al.
European Journal of Medical Genetics|June 25, 2011
A de novo 1.1Mb microdeletion of chromosome 19p13.11 provides indirect evidence for EPS15L1 to be a strong candidate for split hand split foot malformationSusanne Bens, Andrea Haake, Holger Tönnies, et al.
Haematologica|March 20, 2016
Immunohistochemical detection of inhibitor of DNA binding 3 mutational variants in mature aggressive B-cell lymphomaMonika Szczepanowski, Neus Masqué-Soler, Matthias Schlesner, et al.
Molecular Cytogenetics|September 7, 2010
Conflicting results of prenatal FISH with different probes for Down's Syndrome critical regions associated with mosaicism for a de novo del(21)(q22) characterised by molecular karyotyping: Case reportChristel Eckmann-Scholz, Stefan Gesk, Inga Nagel, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|June 17, 2014
The tissue is the issue: improved methylome analysis from paraffin-embedded tissues by application of the HOPE techniqueSebastian Marwitz, Julia Kolarova, Martin Reck, et al.
Hormone Research in Paediatrics|March 30, 2012
Multiplex ligation-dependent probe amplification analysis of the NR0B1(DAX1) locus enables explanation of phenotypic differences in patients with X-linked congenital adrenal hypoplasiaMichela Barbaro, Susanne Bens, Andrea Haake, et al.
European Journal of Human Genetics : EJHG|December 13, 2012
Frequency and characterization of DNA methylation defects in children born SGASusanne Bens, Andrea Haake, Julia Richter, et al.
Pageof 3