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

David Tannahill

Showing results (41-50 of 50) with videos related to

Pageof 5
Sort By:
You have reached the last page of results.This site can display upto 50 results.
Proceedings of the National Academy of Sciences of the United States of America|January 11, 2007
The SCL transcriptional network and BMP signaling pathway interact to regulate RUNX1 activityJohn E Pimanda, Ian J Donaldson, Marella F T R de Bruijn, et al.
Nature Genetics|August 5, 2020
Landscape of G-quadruplex DNA structural regions in breast cancerRobert Hänsel-Hertsch, Angela Simeone, Abigail Shea, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 31, 2025
SCoTCH-seq reveals that 5-hydroxymethylcytosine encodes regulatory information across DNA strandsJack S Hardwick, Somdutta Dhir, Angie Kirchner, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 27, 2007
Gata2, Fli1, and Scl form a recursively wired gene-regulatory circuit during early hematopoietic developmentJohn E Pimanda, Katrin Ottersbach, Kathy Knezevic, et al.
Blood|September 23, 2008
Endoglin expression in blood and endothelium is differentially regulated by modular assembly of the Ets/Gata hemangioblast codeJohn E Pimanda, Wan Y I Chan, Nicola K Wilson, et al.
American Journal of Human Genetics|March 9, 2010
Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome)Esther Meyer, Christopher Ricketts, Neil V Morgan, et al.
Plos Genetics|February 9, 2010
Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman diseaseNeil V Morgan, Mark R Morris, Hakan Cangul, et al.
Journal of Medicinal Chemistry|January 23, 2018
Targeting Multiple Effector Pathways in Pancreatic Ductal Adenocarcinoma with a G-Quadruplex-Binding Small MoleculeChiara Marchetti, Katherine G Zyner, Stephan A Ohnmacht, et al.
Cell|July 23, 2013
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genesJacqueline K White, Anna-Karin Gerdin, Natasha A Karp, et al.
Nature Genetics|February 8, 2005
Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndromeIrene A Aligianis, Colin A Johnson, Paul Gissen, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Proceedings of the National Academy of Sciences of the United States of America|January 11, 2007
The SCL transcriptional network and BMP signaling pathway interact to regulate RUNX1 activityJohn E Pimanda, Ian J Donaldson, Marella F T R de Bruijn, et al.
Nature Genetics|August 5, 2020
Landscape of G-quadruplex DNA structural regions in breast cancerRobert Hänsel-Hertsch, Angela Simeone, Abigail Shea, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 31, 2025
SCoTCH-seq reveals that 5-hydroxymethylcytosine encodes regulatory information across DNA strandsJack S Hardwick, Somdutta Dhir, Angie Kirchner, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 27, 2007
Gata2, Fli1, and Scl form a recursively wired gene-regulatory circuit during early hematopoietic developmentJohn E Pimanda, Katrin Ottersbach, Kathy Knezevic, et al.
Blood|September 23, 2008
Endoglin expression in blood and endothelium is differentially regulated by modular assembly of the Ets/Gata hemangioblast codeJohn E Pimanda, Wan Y I Chan, Nicola K Wilson, et al.
American Journal of Human Genetics|March 9, 2010
Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome)Esther Meyer, Christopher Ricketts, Neil V Morgan, et al.
Plos Genetics|February 9, 2010
Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman diseaseNeil V Morgan, Mark R Morris, Hakan Cangul, et al.
Journal of Medicinal Chemistry|January 23, 2018
Targeting Multiple Effector Pathways in Pancreatic Ductal Adenocarcinoma with a G-Quadruplex-Binding Small MoleculeChiara Marchetti, Katherine G Zyner, Stephan A Ohnmacht, et al.
Cell|July 23, 2013
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genesJacqueline K White, Anna-Karin Gerdin, Natasha A Karp, et al.
Nature Genetics|February 8, 2005
Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndromeIrene A Aligianis, Colin A Johnson, Paul Gissen, et al.
Pageof 5