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

Harris Morrison

Showing results (11-20 of 20) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 20 results.
Science (New York, N.Y.)|September 6, 2008
Human-specific gain of function in a developmental enhancerShyam Prabhakar, Axel Visel, Jennifer A Akiyama, et al.
Chromosoma|June 19, 2002
Heterochromatin, HP1 and methylation at lysine 9 of histone H3 in animalsIan G Cowell, Rebecca Aucott, Shantha K Mahadevaiah, et al.
Plos Genetics|April 26, 2014
FRA2A is a CGG repeat expansion associated with silencing of AFF3Sofie Metsu, Liesbeth Rooms, Jacqueline Rainger, et al.
Disease Models & Mechanisms|April 26, 2014
A novel mouse model of Warburg Micro syndrome reveals roles for RAB18 in eye development and organisation of the neuronal cytoskeletonSarah M Carpanini, Lisa McKie, Derek Thomson, et al.
Human Molecular Genetics|April 19, 2013
Glucocorticoid receptor is required for foetal heart maturationEva A Rog-Zielinska, Adrian Thomson, Christopher J Kenyon, et al.
Science (New York, N.Y.)|October 26, 2013
Fine tuning of craniofacial morphology by distant-acting enhancersCatia Attanasio, Alex S Nord, Yiwen Zhu, et al.
Human Molecular Genetics|June 14, 2012
Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODHJoe Rainger, Hemant Bengani, Leigh Campbell, et al.
Plos Genetics|March 12, 2019
ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathyMark T Handley, Kaalak Reddy, Jimi Wills, et al.
Plos Genetics|July 14, 2011
Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and miceJoe Rainger, Ellen van Beusekom, Jacqueline K Ramsay, et al.
Plos Genetics|December 27, 2018
Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and MiceJoe Rainger, Ellen van Beusekom, Jacqueline K Ramsay, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Science (New York, N.Y.)|September 6, 2008
Human-specific gain of function in a developmental enhancerShyam Prabhakar, Axel Visel, Jennifer A Akiyama, et al.
Chromosoma|June 19, 2002
Heterochromatin, HP1 and methylation at lysine 9 of histone H3 in animalsIan G Cowell, Rebecca Aucott, Shantha K Mahadevaiah, et al.
Plos Genetics|April 26, 2014
FRA2A is a CGG repeat expansion associated with silencing of AFF3Sofie Metsu, Liesbeth Rooms, Jacqueline Rainger, et al.
Disease Models & Mechanisms|April 26, 2014
A novel mouse model of Warburg Micro syndrome reveals roles for RAB18 in eye development and organisation of the neuronal cytoskeletonSarah M Carpanini, Lisa McKie, Derek Thomson, et al.
Human Molecular Genetics|April 19, 2013
Glucocorticoid receptor is required for foetal heart maturationEva A Rog-Zielinska, Adrian Thomson, Christopher J Kenyon, et al.
Science (New York, N.Y.)|October 26, 2013
Fine tuning of craniofacial morphology by distant-acting enhancersCatia Attanasio, Alex S Nord, Yiwen Zhu, et al.
Human Molecular Genetics|June 14, 2012
Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODHJoe Rainger, Hemant Bengani, Leigh Campbell, et al.
Plos Genetics|March 12, 2019
ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathyMark T Handley, Kaalak Reddy, Jimi Wills, et al.
Plos Genetics|July 14, 2011
Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and miceJoe Rainger, Ellen van Beusekom, Jacqueline K Ramsay, et al.
Plos Genetics|December 27, 2018
Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and MiceJoe Rainger, Ellen van Beusekom, Jacqueline K Ramsay, et al.
Pageof 2