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

Alex Henderson

Showing results (51-60 of 98) with videos related to

Pageof 10
Sort By:
Acta Physiologica (Oxford, England)|March 15, 2025
Cold-induced fibrosis and metabolic remodeling in the turtle (Trachemys scripta) ventricleAdam N Keen, James C McConnell, John J Mackrill, et al.
The Journal of Pathology. Clinical Research|May 2, 2019
Breast cancer in patients with germline TP53 pathogenic variants have typical tumour characteristics: the Cohort study of TP53 carrier early onset breast cancer (COPE study)Kate Packwood, Guy Martland, Matthew Sommerlad, et al.
ACS Nano|October 27, 2025
Artificial Intelligence-Powered Raman Spectroscopy through Open Science and FAIR PrinciplesNicolas Coca-Lopez, Victor Alcolea-Rodriguez, Miguel A Bañares, et al.
American Journal of Medical Genetics. Part A|March 29, 2014
Clinical evidence for a mandibular to maxillary transformation in Auriculocondylar syndromeChristopher T Gordon, Christopher M Cunniff, Glenn E Green, et al.
American Journal of Human Genetics|December 27, 2016
De Novo Mutations in EBF3 Cause a Neurodevelopmental SyndromeHannah Sleven, Seth J Welsh, Jing Yu, et al.
American Journal of Human Genetics|April 23, 2005
Heterozygous mutations of OTX2 cause severe ocular malformationsNicola K Ragge, Alison G Brown, Charlotte M Poloschek, et al.
European Journal of Human Genetics : EJHG|March 23, 2017
PUF60 variants cause a syndrome of ID, short stature, microcephaly, coloboma, craniofacial, cardiac, renal and spinal featuresKaren J Low, Morad Ansari, Rami Abou Jamra, et al.
European Journal of Human Genetics : EJHG|July 15, 2018
Expanding the phenotypic spectrum of variants in PDE4D/PRKAR1A: from acrodysostosis to acroscyphodysplasiaCaroline Michot, Carine Le Goff, Edward Blair, et al.
Nature Genetics|May 4, 2010
De novo mutations of SETBP1 cause Schinzel-Giedion syndromeAlexander Hoischen, Bregje W M van Bon, Christian Gilissen, et al.
Frontiers in Neurology|November 30, 2019
Tuberous Sclerosis Complex (TSC): Expert Recommendations for Provision of Coordinated CareNicholas M P Annear, Richard E Appleton, Zahabiyah Bassi, et al.
Pageof 10

Showing results (51-60 of 98) with videos related to

Sort By:
Pageof 10
Acta Physiologica (Oxford, England)|March 15, 2025
Cold-induced fibrosis and metabolic remodeling in the turtle (Trachemys scripta) ventricleAdam N Keen, James C McConnell, John J Mackrill, et al.
The Journal of Pathology. Clinical Research|May 2, 2019
Breast cancer in patients with germline TP53 pathogenic variants have typical tumour characteristics: the Cohort study of TP53 carrier early onset breast cancer (COPE study)Kate Packwood, Guy Martland, Matthew Sommerlad, et al.
ACS Nano|October 27, 2025
Artificial Intelligence-Powered Raman Spectroscopy through Open Science and FAIR PrinciplesNicolas Coca-Lopez, Victor Alcolea-Rodriguez, Miguel A Bañares, et al.
American Journal of Medical Genetics. Part A|March 29, 2014
Clinical evidence for a mandibular to maxillary transformation in Auriculocondylar syndromeChristopher T Gordon, Christopher M Cunniff, Glenn E Green, et al.
American Journal of Human Genetics|December 27, 2016
De Novo Mutations in EBF3 Cause a Neurodevelopmental SyndromeHannah Sleven, Seth J Welsh, Jing Yu, et al.
American Journal of Human Genetics|April 23, 2005
Heterozygous mutations of OTX2 cause severe ocular malformationsNicola K Ragge, Alison G Brown, Charlotte M Poloschek, et al.
European Journal of Human Genetics : EJHG|March 23, 2017
PUF60 variants cause a syndrome of ID, short stature, microcephaly, coloboma, craniofacial, cardiac, renal and spinal featuresKaren J Low, Morad Ansari, Rami Abou Jamra, et al.
European Journal of Human Genetics : EJHG|July 15, 2018
Expanding the phenotypic spectrum of variants in PDE4D/PRKAR1A: from acrodysostosis to acroscyphodysplasiaCaroline Michot, Carine Le Goff, Edward Blair, et al.
Nature Genetics|May 4, 2010
De novo mutations of SETBP1 cause Schinzel-Giedion syndromeAlexander Hoischen, Bregje W M van Bon, Christian Gilissen, et al.
Frontiers in Neurology|November 30, 2019
Tuberous Sclerosis Complex (TSC): Expert Recommendations for Provision of Coordinated CareNicholas M P Annear, Richard E Appleton, Zahabiyah Bassi, et al.
Pageof 10