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

Marcel Karperien

Showing results (171-180 of 194) with videos related to

Pageof 20
Sort By:
The Journal of Endocrinology|February 11, 2011
Genome-wide screening in human growth plates during puberty in one patient suggests a role for RUNX2 in epiphyseal maturationJoyce Emons, Bas E Dutilh, Eva Decker, et al.
Cartilage|June 17, 2017
Molecular Validation of Chondrogenic Differentiation and Hypoxia Responsiveness of Platelet-Lysate Expanded Adipose Tissue-Derived Human Mesenchymal Stromal CellsCatalina Galeano-Garces, Emily T Camilleri, Scott M Riester, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 22, 2010
APC mutations are associated with increased bone mineral density in patients with familial adenomatous polyposisRazvan L Miclea, Marcel Karperien, Alexandra M Langers, et al.
Human Genetics|September 15, 2010
The majority of the genetic risk for Paget's disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genesPui Yan Jenny Chung, Greet Beyens, Steven Boonen, et al.
The American Journal of Pathology|September 4, 2010
No haploinsufficiency but loss of heterozygosity for EXT in multiple osteochondromasChristianne M A Reijnders, Cathelijn J F Waaijer, Andrew Hamilton, et al.
European Journal of Endocrinology|February 9, 2007
Growth hormone secretion and immunological function of a male patient with a homozygous STAT5b mutationMarie J E Walenkamp, Solrun Vidarsdottir, Alberto M Pereira, et al.
Investigative Ophthalmology & Visual Science|April 27, 2005
Whole-body bioluminescent imaging of human uveal melanoma in a new mouse model of local tumor growth and metastasisIrene C Notting, Jeroen T Buijs, Ivo Que, et al.
Gene|July 6, 2016
The synovial microenvironment of osteoarthritic joints alters RNA-seq expression profiles of human primary articular chondrocytesEric A Lewallen, Carolina A Bonin, Xin Li, et al.
Advanced Materials (Deerfield Beach, Fla.)|September 3, 2021
Tethering Cells via Enzymatic Oxidative Crosslinking Enables Mechanotransduction in Non-Cell-Adhesive MaterialsTom Kamperman, Sieger Henke, João F Crispim, et al.
BMC Developmental Biology|April 10, 2009
Adenomatous polyposis coli-mediated control of beta-catenin is essential for both chondrogenic and osteogenic differentiation of skeletal precursorsRazvan L Miclea, Marcel Karperien, Cathy Aj Bosch, et al.
Pageof 20

Showing results (171-180 of 194) with videos related to

Sort By:
Pageof 20
The Journal of Endocrinology|February 11, 2011
Genome-wide screening in human growth plates during puberty in one patient suggests a role for RUNX2 in epiphyseal maturationJoyce Emons, Bas E Dutilh, Eva Decker, et al.
Cartilage|June 17, 2017
Molecular Validation of Chondrogenic Differentiation and Hypoxia Responsiveness of Platelet-Lysate Expanded Adipose Tissue-Derived Human Mesenchymal Stromal CellsCatalina Galeano-Garces, Emily T Camilleri, Scott M Riester, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 22, 2010
APC mutations are associated with increased bone mineral density in patients with familial adenomatous polyposisRazvan L Miclea, Marcel Karperien, Alexandra M Langers, et al.
Human Genetics|September 15, 2010
The majority of the genetic risk for Paget's disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genesPui Yan Jenny Chung, Greet Beyens, Steven Boonen, et al.
The American Journal of Pathology|September 4, 2010
No haploinsufficiency but loss of heterozygosity for EXT in multiple osteochondromasChristianne M A Reijnders, Cathelijn J F Waaijer, Andrew Hamilton, et al.
European Journal of Endocrinology|February 9, 2007
Growth hormone secretion and immunological function of a male patient with a homozygous STAT5b mutationMarie J E Walenkamp, Solrun Vidarsdottir, Alberto M Pereira, et al.
Investigative Ophthalmology & Visual Science|April 27, 2005
Whole-body bioluminescent imaging of human uveal melanoma in a new mouse model of local tumor growth and metastasisIrene C Notting, Jeroen T Buijs, Ivo Que, et al.
Gene|July 6, 2016
The synovial microenvironment of osteoarthritic joints alters RNA-seq expression profiles of human primary articular chondrocytesEric A Lewallen, Carolina A Bonin, Xin Li, et al.
Advanced Materials (Deerfield Beach, Fla.)|September 3, 2021
Tethering Cells via Enzymatic Oxidative Crosslinking Enables Mechanotransduction in Non-Cell-Adhesive MaterialsTom Kamperman, Sieger Henke, João F Crispim, et al.
BMC Developmental Biology|April 10, 2009
Adenomatous polyposis coli-mediated control of beta-catenin is essential for both chondrogenic and osteogenic differentiation of skeletal precursorsRazvan L Miclea, Marcel Karperien, Cathy Aj Bosch, et al.
Pageof 20