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

Dirk Hubmacher

Showing results (31-40 of 50) with videos related to

Pageof 5
Sort By:
Laboratory Investigation; a Journal of Technical Methods and Pathology|March 3, 2010
Enhanced fibrillin-2 expression is a general feature of wound healing and sclerosis: potential alteration of cell attachment and storage of TGF-betaJürgen Brinckmann, Nico Hunzelmann, Birgit Kahle, et al.
The Journal of Biological Chemistry|July 26, 2011
Classical and neonatal Marfan syndrome mutations in fibrillin-1 cause differential protease susceptibilities and protein functionRyan Kirschner, Dirk Hubmacher, Garud Iyengar, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|February 11, 2019
Limb- and tendon-specific Adamtsl2 deletion identifies a role for ADAMTSL2 in tendon growth in a mouse model for geleophysic dysplasiaDirk Hubmacher, Nandaraj Taye, Zerina Balic, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|May 15, 2018
Interactions between lysyl oxidases and ADAMTS proteins suggest a novel crosstalk between two extracellular matrix familiesRohtem Aviram, Shelly Zaffryar-Eilot, Dirk Hubmacher, et al.
Scientific Reports|February 9, 2017
Unusual life cycle and impact on microfibril assembly of ADAMTS17, a secreted metalloprotease mutated in genetic eye diseaseDirk Hubmacher, Michael Schneider, Steven J Berardinelli, et al.
Iscience|June 16, 2025
The matricellular protein ADAMTS-like 2 regulates differentiation of skeletal muscle-resident fibro-adipogenic progenitor cellsCharlene Redhead, Nandaraj Taye, Britney Chin-Young, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|November 15, 2019
A novel ADAMTS17 variant that causes Weill-Marchesani syndrome 4 alters fibrillin-1 and collagen type I deposition in the extracellular matrixStylianos Z Karoulias, Aude Beyens, Zerina Balic, et al.
Biochemistry|November 1, 2008
Fibrillins, fibulins, and matrix-associated glycoprotein modulate the kinetics and morphology of in vitro self-assembly of a recombinant elastin-like polypeptideJudith T Cirulis, Catherine M Bellingham, Elaine C Davis, et al.
Molecular Biology of the Cell|November 28, 2008
Fibrillin assembly requires fibronectinLaetitia Sabatier, Daliang Chen, Christine Fagotto-Kaufmann, et al.
The Journal of Biological Chemistry|January 27, 2007
Fibrillin-1 interactions with fibulins depend on the first hybrid domain and provide an adaptor function to tropoelastinEhab El-Hallous, Takako Sasaki, Dirk Hubmacher, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Laboratory Investigation; a Journal of Technical Methods and Pathology|March 3, 2010
Enhanced fibrillin-2 expression is a general feature of wound healing and sclerosis: potential alteration of cell attachment and storage of TGF-betaJürgen Brinckmann, Nico Hunzelmann, Birgit Kahle, et al.
The Journal of Biological Chemistry|July 26, 2011
Classical and neonatal Marfan syndrome mutations in fibrillin-1 cause differential protease susceptibilities and protein functionRyan Kirschner, Dirk Hubmacher, Garud Iyengar, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|February 11, 2019
Limb- and tendon-specific Adamtsl2 deletion identifies a role for ADAMTSL2 in tendon growth in a mouse model for geleophysic dysplasiaDirk Hubmacher, Nandaraj Taye, Zerina Balic, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|May 15, 2018
Interactions between lysyl oxidases and ADAMTS proteins suggest a novel crosstalk between two extracellular matrix familiesRohtem Aviram, Shelly Zaffryar-Eilot, Dirk Hubmacher, et al.
Scientific Reports|February 9, 2017
Unusual life cycle and impact on microfibril assembly of ADAMTS17, a secreted metalloprotease mutated in genetic eye diseaseDirk Hubmacher, Michael Schneider, Steven J Berardinelli, et al.
Iscience|June 16, 2025
The matricellular protein ADAMTS-like 2 regulates differentiation of skeletal muscle-resident fibro-adipogenic progenitor cellsCharlene Redhead, Nandaraj Taye, Britney Chin-Young, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|November 15, 2019
A novel ADAMTS17 variant that causes Weill-Marchesani syndrome 4 alters fibrillin-1 and collagen type I deposition in the extracellular matrixStylianos Z Karoulias, Aude Beyens, Zerina Balic, et al.
Biochemistry|November 1, 2008
Fibrillins, fibulins, and matrix-associated glycoprotein modulate the kinetics and morphology of in vitro self-assembly of a recombinant elastin-like polypeptideJudith T Cirulis, Catherine M Bellingham, Elaine C Davis, et al.
Molecular Biology of the Cell|November 28, 2008
Fibrillin assembly requires fibronectinLaetitia Sabatier, Daliang Chen, Christine Fagotto-Kaufmann, et al.
The Journal of Biological Chemistry|January 27, 2007
Fibrillin-1 interactions with fibulins depend on the first hybrid domain and provide an adaptor function to tropoelastinEhab El-Hallous, Takako Sasaki, Dirk Hubmacher, et al.
Pageof 5