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

Thomas Haaf

Showing results (121-130 of 190) with videos related to

Pageof 19
Sort By:
European Journal of Human Genetics : EJHG|May 30, 2013
Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6Simone Rost, Elisa Bach, Cordula Neuner, et al.
Scientific Reports|July 30, 2021
A piggyBac-based platform for genome editing and clonal rhesus macaque iPSC line derivationIgnacio Rodriguez-Polo, Sophie Mißbach, Stoyan Petkov, et al.
Scientific Reports|January 22, 2021
A genome-wide transcriptomic analysis of embryos fathered by obese males in a murine model of diet-induced obesityLaura Bernhardt, Marcus Dittrich, Rabih El-Merahbi, et al.
BMC Medical Genetics|May 20, 2018
The conserved p.Arg108 residue in S1PR2 (DFNB68) is fundamental for proper hearing: evidence from a consanguineous Iranian familyMichaela A H Hofrichter, Majid Mojarad, Julia Doll, et al.
Plos One|July 1, 2016
Hypermethylation of FOXP3 Promoter and Premature Aging of the Immune System in Female Patients with Panic Disorder?Martina Prelog, Deborah Hilligardt, Christian A Schmidt, et al.
Epigenetics|January 18, 2014
Widespread differences in cortex DNA methylation of the "language gene" CNTNAP2 between humans and chimpanzeesEberhard Schneider, Nady El Hajj, Steven Richter, et al.
Epigenetics|December 31, 2011
Monozygotic twins discordant for constitutive BRCA1 promoter methylation, childhood cancer and secondary cancerDanuta Galetzka, Tamara Hansmann, Nady El Hajj, et al.
Plos One|October 13, 2011
Reduced mRNA and protein expression of the genomic caretaker RAD9A in primary fibroblasts of individuals with childhood and independent second cancerEva Weis, Holger Schoen, Anja Victor, et al.
Nucleic Acids Research|March 3, 2010
Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patternsEberhard Schneider, Galyna Pliushch, Nady El Hajj, et al.
American Journal of Medical Genetics. Part A|January 19, 2010
Four unrelated patients with Lubs X-linked mental retardation syndrome and different Xq28 duplicationsOliver Bartsch, Konstanze Gebauer, Stanislav Lechno, et al.
Pageof 19

Showing results (121-130 of 190) with videos related to

Sort By:
Pageof 19
European Journal of Human Genetics : EJHG|May 30, 2013
Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6Simone Rost, Elisa Bach, Cordula Neuner, et al.
Scientific Reports|July 30, 2021
A piggyBac-based platform for genome editing and clonal rhesus macaque iPSC line derivationIgnacio Rodriguez-Polo, Sophie Mißbach, Stoyan Petkov, et al.
Scientific Reports|January 22, 2021
A genome-wide transcriptomic analysis of embryos fathered by obese males in a murine model of diet-induced obesityLaura Bernhardt, Marcus Dittrich, Rabih El-Merahbi, et al.
BMC Medical Genetics|May 20, 2018
The conserved p.Arg108 residue in S1PR2 (DFNB68) is fundamental for proper hearing: evidence from a consanguineous Iranian familyMichaela A H Hofrichter, Majid Mojarad, Julia Doll, et al.
Plos One|July 1, 2016
Hypermethylation of FOXP3 Promoter and Premature Aging of the Immune System in Female Patients with Panic Disorder?Martina Prelog, Deborah Hilligardt, Christian A Schmidt, et al.
Epigenetics|January 18, 2014
Widespread differences in cortex DNA methylation of the "language gene" CNTNAP2 between humans and chimpanzeesEberhard Schneider, Nady El Hajj, Steven Richter, et al.
Epigenetics|December 31, 2011
Monozygotic twins discordant for constitutive BRCA1 promoter methylation, childhood cancer and secondary cancerDanuta Galetzka, Tamara Hansmann, Nady El Hajj, et al.
Plos One|October 13, 2011
Reduced mRNA and protein expression of the genomic caretaker RAD9A in primary fibroblasts of individuals with childhood and independent second cancerEva Weis, Holger Schoen, Anja Victor, et al.
Nucleic Acids Research|March 3, 2010
Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patternsEberhard Schneider, Galyna Pliushch, Nady El Hajj, et al.
American Journal of Medical Genetics. Part A|January 19, 2010
Four unrelated patients with Lubs X-linked mental retardation syndrome and different Xq28 duplicationsOliver Bartsch, Konstanze Gebauer, Stanislav Lechno, et al.
Pageof 19