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

Jasmin Beygo

Showing results (1-10 of 45) with videos related to

Pageof 5
Sort By:
European Journal of Human Genetics : EJHG|February 20, 2019
Disruption of KCNQ1 prevents methylation of the ICR2 and supports the hypothesis that its transcription is necessary for imprint establishmentJasmin Beygo, Joachim Bürger, Tim M Strom, et al.
Molecular and Cellular Probes|November 18, 2008
No evidence of an association between polymorphisms in the IRAK-M gene and atopic dermatitis in a German cohortJasmin Beygo, Qumar Parwez, Elisabeth Petrasch-Parwez, et al.
European Journal of Human Genetics : EJHG|March 11, 2020
Common genetic variation in the Angelman syndrome imprinting centre affects the imprinting of chromosome 15Jasmin Beygo, Christian Grosser, Sabine Kaya, et al.
American Journal of Medical Genetics. Part A|November 16, 2020
A boy with Silver-Russell syndrome and Sotos syndromeEva M C Schwaibold, Jasmin Beygo, Katharina Obeid, et al.
European Journal of Human Genetics : EJHG|June 26, 2019
Update of the EMQN/ACGS best practice guidelines for molecular analysis of Prader-Willi and Angelman syndromesJasmin Beygo, Karin Buiting, Simon C Ramsden, et al.
Epigenetics|September 20, 2018
The origin of imprinting defects in Temple syndrome and comparison with other imprinting disordersJasmin Beygo, Claudia Mertel, Sabine Kaya, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 11, 2018
Locus-Specific DNA Methylation Analysis by Targeted Deep Bisulfite SequencingElsa Leitão, Jasmin Beygo, Michael Zeschnigk, et al.
Prenatal Diagnosis|June 21, 2023
Prenatal testing for imprinting disorders: A laboratory perspectiveJasmin Beygo, Silvia Russo, Pierpaola Tannorella, 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.
Orphanet Journal of Rare Diseases|March 26, 2014
Clinical phenotypes of MAGEL2 mutations and deletionsKarin Buiting, Nataliya Di Donato, Jasmin Beygo, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
European Journal of Human Genetics : EJHG|February 20, 2019
Disruption of KCNQ1 prevents methylation of the ICR2 and supports the hypothesis that its transcription is necessary for imprint establishmentJasmin Beygo, Joachim Bürger, Tim M Strom, et al.
Molecular and Cellular Probes|November 18, 2008
No evidence of an association between polymorphisms in the IRAK-M gene and atopic dermatitis in a German cohortJasmin Beygo, Qumar Parwez, Elisabeth Petrasch-Parwez, et al.
European Journal of Human Genetics : EJHG|March 11, 2020
Common genetic variation in the Angelman syndrome imprinting centre affects the imprinting of chromosome 15Jasmin Beygo, Christian Grosser, Sabine Kaya, et al.
American Journal of Medical Genetics. Part A|November 16, 2020
A boy with Silver-Russell syndrome and Sotos syndromeEva M C Schwaibold, Jasmin Beygo, Katharina Obeid, et al.
European Journal of Human Genetics : EJHG|June 26, 2019
Update of the EMQN/ACGS best practice guidelines for molecular analysis of Prader-Willi and Angelman syndromesJasmin Beygo, Karin Buiting, Simon C Ramsden, et al.
Epigenetics|September 20, 2018
The origin of imprinting defects in Temple syndrome and comparison with other imprinting disordersJasmin Beygo, Claudia Mertel, Sabine Kaya, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 11, 2018
Locus-Specific DNA Methylation Analysis by Targeted Deep Bisulfite SequencingElsa Leitão, Jasmin Beygo, Michael Zeschnigk, et al.
Prenatal Diagnosis|June 21, 2023
Prenatal testing for imprinting disorders: A laboratory perspectiveJasmin Beygo, Silvia Russo, Pierpaola Tannorella, 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.
Orphanet Journal of Rare Diseases|March 26, 2014
Clinical phenotypes of MAGEL2 mutations and deletionsKarin Buiting, Nataliya Di Donato, Jasmin Beygo, et al.
Pageof 5