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

Buiting

Showing results (81-90 of 305) with videos related to

Pageof 31
Sort By:
Journal of Medical Genetics|December 14, 2004
Recurrent deletion of a region containing exon 24 of the RB1 gene caused by non-homologous recombination between a LINE-1HS and MER21B elementP Albrecht, J Bode, K Buiting, et al.
Human Molecular Genetics|March 1, 1997
Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing methodM Zeschnigk, B Schmitz, B Dittrich, et al.
European Journal of Human Genetics : EJHG|April 6, 2006
Identification of cis- and trans-acting factors possibly modifying the risk of epimutations on chromosome 15Corinna Zogel, Stefan Böhringer, Stephanie Gross, et al.
Genomics|March 6, 2007
C15orf2 and a novel noncoding transcript from the Prader-Willi/Angelman syndrome region show monoallelic expression in fetal brainKarin Buiting, Hülya Nazlican, Danuta Galetzka, 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 Human Genetics|April 3, 2001
Disruption of the bipartite imprinting center in a family with Angelman syndromeK Buiting, A Barnicoat, C Lich, et al.
Plos One|September 11, 2013
Human PPP1R26P1 functions as cis-repressive element in mouse Rb1Laura Steenpass, Deniz Kanber, Michaela Hiber, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Mild Angelman syndrome phenotype due to a mosaic methylation imprinting defectLaura C Fairbrother, Cheryl Cytrynbaum, Paula Boutis, et al.
Journal of Clinical Microbiology|June 7, 2003
High percentage of methicillin-resistant Staphylococcus aureus isolates with reduced susceptibility to glycopeptides in The NetherlandsArjanne Van Griethuysen, Annemarie Van 't Veen, Anton Buiting, et al.
Journal of Cellular Physiology|August 1, 1993
Secretion of transforming growth factor-beta isoforms by embryonic stem cells: isoform and latency are dependent on direction of differentiationH G Slager, E Freund, A M Buiting, et al.
Pageof 31

Showing results (81-90 of 305) with videos related to

Sort By:
Pageof 31
Journal of Medical Genetics|December 14, 2004
Recurrent deletion of a region containing exon 24 of the RB1 gene caused by non-homologous recombination between a LINE-1HS and MER21B elementP Albrecht, J Bode, K Buiting, et al.
Human Molecular Genetics|March 1, 1997
Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing methodM Zeschnigk, B Schmitz, B Dittrich, et al.
European Journal of Human Genetics : EJHG|April 6, 2006
Identification of cis- and trans-acting factors possibly modifying the risk of epimutations on chromosome 15Corinna Zogel, Stefan Böhringer, Stephanie Gross, et al.
Genomics|March 6, 2007
C15orf2 and a novel noncoding transcript from the Prader-Willi/Angelman syndrome region show monoallelic expression in fetal brainKarin Buiting, Hülya Nazlican, Danuta Galetzka, 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 Human Genetics|April 3, 2001
Disruption of the bipartite imprinting center in a family with Angelman syndromeK Buiting, A Barnicoat, C Lich, et al.
Plos One|September 11, 2013
Human PPP1R26P1 functions as cis-repressive element in mouse Rb1Laura Steenpass, Deniz Kanber, Michaela Hiber, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Mild Angelman syndrome phenotype due to a mosaic methylation imprinting defectLaura C Fairbrother, Cheryl Cytrynbaum, Paula Boutis, et al.
Journal of Clinical Microbiology|June 7, 2003
High percentage of methicillin-resistant Staphylococcus aureus isolates with reduced susceptibility to glycopeptides in The NetherlandsArjanne Van Griethuysen, Annemarie Van 't Veen, Anton Buiting, et al.
Journal of Cellular Physiology|August 1, 1993
Secretion of transforming growth factor-beta isoforms by embryonic stem cells: isoform and latency are dependent on direction of differentiationH G Slager, E Freund, A M Buiting, et al.
Pageof 31