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

A Morcuende

Showing results (101-110 of 111) with videos related to

Pageof 12
Sort By:
Human Genetics|April 17, 2004
SNTG1, the gene encoding gamma1-syntrophin: a candidate gene for idiopathic scoliosisStavros Bashiardes, Rose Veile, Missy Allen, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|February 2, 2006
HOXD10 M319K mutation in a family with isolated congenital vertical talusMatthew B Dobbs, Christina A Gurnett, Brandon Pierce, et al.
The Iowa Orthopaedic Journal|August 16, 2002
Identification and initial characterization of 6,000 expressed sequenced tags (ESTs) from rat normal-growing cartilage and swarm rat chondrosarcoma cDNA librariesJose A Morcuende, Xiao Dong Huang, Jeff Stevens, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 19, 2010
A mouse model of osteochondromagenesis from clonal inactivation of Ext1 in chondrocytesKevin B Jones, Virginia Piombo, Charles Searby, et al.
World Journal of Orthopedics|September 7, 2017
Ponseti method treatment of neglected idiopathic clubfoot: Preliminary results of a multi-center study in NigeriaOlayinka O Adegbehingbe, Adeoye J Adetiloye, Ladipo Adewole, et al.
Human Molecular Genetics|November 15, 2015
A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosisGabe Haller, David Alvarado, Kevin Mccall, et al.
BMC Cancer|September 3, 2010
Microenvironment alters epigenetic and gene expression profiles in Swarm rat chondrosarcoma tumorsChristopher A Hamm, Jeff W Stevens, Hehuang Xie, et al.
Nature Communications|October 11, 2018
A missense variant in SLC39A8 is associated with severe idiopathic scoliosisGabe Haller, Kevin McCall, Supak Jenkitkasemwong, et al.
Neurologia|September 3, 2025
Left atrial appendage closure in patients with prior intracranial bleeding, safety, efficacy, and timingD Gonzalez-Calle, L Nombela-Franco, H Gutierrez-Garcia, et al.
Human Molecular Genetics|May 17, 2014
Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosisJillian G Buchan, David M Alvarado, Gabe E Haller, et al.
Pageof 12

Showing results (101-110 of 111) with videos related to

Sort By:
Pageof 12
Human Genetics|April 17, 2004
SNTG1, the gene encoding gamma1-syntrophin: a candidate gene for idiopathic scoliosisStavros Bashiardes, Rose Veile, Missy Allen, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|February 2, 2006
HOXD10 M319K mutation in a family with isolated congenital vertical talusMatthew B Dobbs, Christina A Gurnett, Brandon Pierce, et al.
The Iowa Orthopaedic Journal|August 16, 2002
Identification and initial characterization of 6,000 expressed sequenced tags (ESTs) from rat normal-growing cartilage and swarm rat chondrosarcoma cDNA librariesJose A Morcuende, Xiao Dong Huang, Jeff Stevens, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 19, 2010
A mouse model of osteochondromagenesis from clonal inactivation of Ext1 in chondrocytesKevin B Jones, Virginia Piombo, Charles Searby, et al.
World Journal of Orthopedics|September 7, 2017
Ponseti method treatment of neglected idiopathic clubfoot: Preliminary results of a multi-center study in NigeriaOlayinka O Adegbehingbe, Adeoye J Adetiloye, Ladipo Adewole, et al.
Human Molecular Genetics|November 15, 2015
A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosisGabe Haller, David Alvarado, Kevin Mccall, et al.
BMC Cancer|September 3, 2010
Microenvironment alters epigenetic and gene expression profiles in Swarm rat chondrosarcoma tumorsChristopher A Hamm, Jeff W Stevens, Hehuang Xie, et al.
Nature Communications|October 11, 2018
A missense variant in SLC39A8 is associated with severe idiopathic scoliosisGabe Haller, Kevin McCall, Supak Jenkitkasemwong, et al.
Neurologia|September 3, 2025
Left atrial appendage closure in patients with prior intracranial bleeding, safety, efficacy, and timingD Gonzalez-Calle, L Nombela-Franco, H Gutierrez-Garcia, et al.
Human Molecular Genetics|May 17, 2014
Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosisJillian G Buchan, David M Alvarado, Gabe E Haller, et al.
Pageof 12