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

Izabela Harabula

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
Current Opinion in Genetics & Development|January 9, 2021
The dynamics of chromatin architecture in brain development and functionIzabela Harabula, Ana Pombo
Current Opinion in Cell Biology|May 31, 2020
Evolving methodologies and concepts in 4D nucleome researchThomas M Sparks, Izabela Harabula, Ana Pombo
Journal of Medical Genetics|August 6, 2017
Mutations in <i>MYO1H</i> cause a recessive form of central hypoventilation with autonomic dysfunctionMalte Spielmann, Luis R Hernandez-Miranda, Isabella Ceccherini, et al.
Development (Cambridge, England)|July 31, 2023
Induction of kidney-related gene programs through co-option of SALL1 in mole ovotestesMagdalena Schindler, Marco Osterwalder, Izabela Harabula, et al.
Cell Reports|February 10, 2015
Deletions, Inversions, Duplications: Engineering of Structural Variants using CRISPR/Cas in MiceKaterina Kraft, Sinje Geuer, Anja J Will, et al.
Biorxiv : the Preprint Server for Biology|August 20, 2025
Specialised super-enhancer networks in stem cells and neuronsIzabela Harabula, Liam Speakman, Francesco Musella, et al.
Genome Research|January 13, 2016
Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and miceMalte Spielmann, Naseebullah Kakar, Naeimeh Tayebi, et al.
Nature Genetics|September 29, 2018
Dynamic 3D chromatin architecture contributes to enhancer specificity and limb morphogenesisBjørt K Kragesteen, Malte Spielmann, Christina Paliou, et al.
American Journal of Human Genetics|December 7, 2014
Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndromeNadja Ehmke, Almuth Caliebe, Rainer Koenig, et al.
Science (New York, N.Y.)|October 9, 2020
The mole genome reveals regulatory rearrangements associated with adaptive intersexualityFrancisca M Real, Stefan A Haas, Paolo Franchini, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Current Opinion in Genetics & Development|January 9, 2021
The dynamics of chromatin architecture in brain development and functionIzabela Harabula, Ana Pombo
Current Opinion in Cell Biology|May 31, 2020
Evolving methodologies and concepts in 4D nucleome researchThomas M Sparks, Izabela Harabula, Ana Pombo
Journal of Medical Genetics|August 6, 2017
Mutations in <i>MYO1H</i> cause a recessive form of central hypoventilation with autonomic dysfunctionMalte Spielmann, Luis R Hernandez-Miranda, Isabella Ceccherini, et al.
Development (Cambridge, England)|July 31, 2023
Induction of kidney-related gene programs through co-option of SALL1 in mole ovotestesMagdalena Schindler, Marco Osterwalder, Izabela Harabula, et al.
Cell Reports|February 10, 2015
Deletions, Inversions, Duplications: Engineering of Structural Variants using CRISPR/Cas in MiceKaterina Kraft, Sinje Geuer, Anja J Will, et al.
Biorxiv : the Preprint Server for Biology|August 20, 2025
Specialised super-enhancer networks in stem cells and neuronsIzabela Harabula, Liam Speakman, Francesco Musella, et al.
Genome Research|January 13, 2016
Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and miceMalte Spielmann, Naseebullah Kakar, Naeimeh Tayebi, et al.
Nature Genetics|September 29, 2018
Dynamic 3D chromatin architecture contributes to enhancer specificity and limb morphogenesisBjørt K Kragesteen, Malte Spielmann, Christina Paliou, et al.
American Journal of Human Genetics|December 7, 2014
Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndromeNadja Ehmke, Almuth Caliebe, Rainer Koenig, et al.
Science (New York, N.Y.)|October 9, 2020
The mole genome reveals regulatory rearrangements associated with adaptive intersexualityFrancisca M Real, Stefan A Haas, Paolo Franchini, et al.
Pageof 2