Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Julia Kolarova

Showing results (1-10 of 26) with videos related to

Pageof 3
Sort By:
Methods in Molecular Biology (Clifton, N.J.)|December 16, 2015
Quantitative DNA Methylation Profiling in CancerOle Ammerpohl, Andrea Haake, Julia Kolarova, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 26, 2016
PLAGL1 epimutation and bladder exstrophy: Coincidence or concurrent etiology?Julia Kolarova, Susanne Bens, Ole Ammerpohl, et al.
Epigenetics|February 19, 2016
Genome-wide methylation analysis of retrocopy-associated CpG islands and their genomic environmentKatrin Grothaus, Deniz Kanber, Alexandra Gellhaus, et al.
Oncology Reports|June 22, 2022
Genome‑wide expression and methylation analyses reveal aberrant cell adhesion signaling in tyrosine kinase inhibitor‑resistant CML cellsMeike Kaehler, Merit Litterst, Julia Kolarova, et al.
Epigenomics|November 7, 2015
The differentially methylated region of MEG8 is hypermethylated in patients with Temple syndromeSusanne Bens, Julia Kolarova, Gabriele Gillessen-Kaesbach, et al.
Clinical Epigenetics|October 20, 2017
Mosaic genome-wide maternal isodiploidy: an extreme form of imprinting disorder presenting as prenatal diagnostic challengeSusanne Bens, Manuel Luedeke, Tanja Richter, et al.
European Journal of Human Genetics : EJHG|February 4, 2016
A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndromeJasmin Beygo, Ivana Joksic, Tim M Strom, et al.
Pediatric Blood & Cancer|October 28, 2016
DNA methylation profiling of pediatric B-cell lymphoblastic leukemia with KMT2A rearrangement identifies hypomethylation at enhancer sitesAnke K Bergmann, Giancarlo Castellano, Julia Alten, et al.
European Journal of Medical Genetics|May 25, 2015
Array-based DNA methylation analysis in individuals with developmental delay/intellectual disability and normal molecular karyotypeJulia Kolarova, Imke Tangen, Susanne Bens, et al.
Plos One|June 23, 2012
DNA-methylation profiling of fetal tissues reveals marked epigenetic differences between chorionic and amniotic samplesChristel Eckmann-Scholz, Susanne Bens, Julia Kolarova, et al.
Pageof 3

Showing results (1-10 of 26) 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.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 26, 2016
PLAGL1 epimutation and bladder exstrophy: Coincidence or concurrent etiology?Julia Kolarova, Susanne Bens, Ole Ammerpohl, et al.
Epigenetics|February 19, 2016
Genome-wide methylation analysis of retrocopy-associated CpG islands and their genomic environmentKatrin Grothaus, Deniz Kanber, Alexandra Gellhaus, et al.
Oncology Reports|June 22, 2022
Genome‑wide expression and methylation analyses reveal aberrant cell adhesion signaling in tyrosine kinase inhibitor‑resistant CML cellsMeike Kaehler, Merit Litterst, Julia Kolarova, et al.
Epigenomics|November 7, 2015
The differentially methylated region of MEG8 is hypermethylated in patients with Temple syndromeSusanne Bens, Julia Kolarova, Gabriele Gillessen-Kaesbach, et al.
Clinical Epigenetics|October 20, 2017
Mosaic genome-wide maternal isodiploidy: an extreme form of imprinting disorder presenting as prenatal diagnostic challengeSusanne Bens, Manuel Luedeke, Tanja Richter, et al.
European Journal of Human Genetics : EJHG|February 4, 2016
A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndromeJasmin Beygo, Ivana Joksic, Tim M Strom, et al.
Pediatric Blood & Cancer|October 28, 2016
DNA methylation profiling of pediatric B-cell lymphoblastic leukemia with KMT2A rearrangement identifies hypomethylation at enhancer sitesAnke K Bergmann, Giancarlo Castellano, Julia Alten, et al.
European Journal of Medical Genetics|May 25, 2015
Array-based DNA methylation analysis in individuals with developmental delay/intellectual disability and normal molecular karyotypeJulia Kolarova, Imke Tangen, Susanne Bens, et al.
Plos One|June 23, 2012
DNA-methylation profiling of fetal tissues reveals marked epigenetic differences between chorionic and amniotic samplesChristel Eckmann-Scholz, Susanne Bens, Julia Kolarova, et al.
Pageof 3