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

Mon-Li Chu

Showing results (21-30 of 39) with videos related to

Pageof 4
Sort By:
Matrix Biology : Journal of the International Society for Matrix Biology|December 23, 2015
Loss of fibulin-4 results in abnormal collagen fibril assembly in bone, caused by impaired lysyl oxidase processing and collagen cross-linkingTakako Sasaki, Reinout Stoop, Takao Sakai, et al.
Cell and Tissue Research|December 30, 2015
Forelimb contractures and abnormal tendon collagen fibrillogenesis in fibulin-4 null miceDessislava Z Markova, Te-Cheng Pan, Rui-Zhu Zhang, et al.
Human Genetics|August 3, 2005
A homozygous COL6A2 intron mutation causes in-frame triple-helical deletion and nonsense-mediated mRNA decay in a patient with Ullrich congenital muscular dystrophyLaura Lucarini, Betti Giusti, Rui-Zhu Zhang, et al.
Surgery|July 2, 2011
Tumor-specific expression and alternative splicing of the COL6A3 gene in pancreatic cancerHwyda Arafat, Melissa Lazar, Khalifa Salem, et al.
Muscle & Nerve|April 5, 2002
Novel COL6A1 splicing mutation in a family affected by mild Bethlem myopathyOlga Camacho Vanegas, Rui-Zhu Zhang, Patrizia Sabatelli, et al.
Annals of Neurology|November 10, 2005
COL6A1 genomic deletions in Bethlem myopathy and Ullrich muscular dystrophyGuglielmina Pepe, Laura Lucarini, Rui-Zhu Zhang, et al.
The Journal of Biological Chemistry|April 9, 2013
COL6A3 protein deficiency in mice leads to muscle and tendon defects similar to human collagen VI congenital muscular dystrophyTe-Cheng Pan, Rui-Zhu Zhang, Dessislava Markova, et al.
Molecular and Cellular Biology|December 12, 2007
Fibulin-2 is dispensable for mouse development and elastic fiber formationFrancois-Xavier Sicot, Takeshi Tsuda, Dessislava Markova, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|June 25, 2016
Functional consequence of fibulin-4 missense mutations associated with vascular and skeletal abnormalities and cutis laxaTakako Sasaki, Franz-Georg Hanisch, Rainer Deutzmann, et al.
The Journal of Biological Chemistry|July 17, 2015
Fibulin-4 E57K Knock-in Mice Recapitulate Cutaneous, Vascular and Skeletal Defects of Recessive Cutis Laxa 1B with both Elastic Fiber and Collagen Fibril AbnormalitiesOlga Igoucheva, Vitali Alexeev, Carmen M Halabi, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Matrix Biology : Journal of the International Society for Matrix Biology|December 23, 2015
Loss of fibulin-4 results in abnormal collagen fibril assembly in bone, caused by impaired lysyl oxidase processing and collagen cross-linkingTakako Sasaki, Reinout Stoop, Takao Sakai, et al.
Cell and Tissue Research|December 30, 2015
Forelimb contractures and abnormal tendon collagen fibrillogenesis in fibulin-4 null miceDessislava Z Markova, Te-Cheng Pan, Rui-Zhu Zhang, et al.
Human Genetics|August 3, 2005
A homozygous COL6A2 intron mutation causes in-frame triple-helical deletion and nonsense-mediated mRNA decay in a patient with Ullrich congenital muscular dystrophyLaura Lucarini, Betti Giusti, Rui-Zhu Zhang, et al.
Surgery|July 2, 2011
Tumor-specific expression and alternative splicing of the COL6A3 gene in pancreatic cancerHwyda Arafat, Melissa Lazar, Khalifa Salem, et al.
Muscle & Nerve|April 5, 2002
Novel COL6A1 splicing mutation in a family affected by mild Bethlem myopathyOlga Camacho Vanegas, Rui-Zhu Zhang, Patrizia Sabatelli, et al.
Annals of Neurology|November 10, 2005
COL6A1 genomic deletions in Bethlem myopathy and Ullrich muscular dystrophyGuglielmina Pepe, Laura Lucarini, Rui-Zhu Zhang, et al.
The Journal of Biological Chemistry|April 9, 2013
COL6A3 protein deficiency in mice leads to muscle and tendon defects similar to human collagen VI congenital muscular dystrophyTe-Cheng Pan, Rui-Zhu Zhang, Dessislava Markova, et al.
Molecular and Cellular Biology|December 12, 2007
Fibulin-2 is dispensable for mouse development and elastic fiber formationFrancois-Xavier Sicot, Takeshi Tsuda, Dessislava Markova, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|June 25, 2016
Functional consequence of fibulin-4 missense mutations associated with vascular and skeletal abnormalities and cutis laxaTakako Sasaki, Franz-Georg Hanisch, Rainer Deutzmann, et al.
The Journal of Biological Chemistry|July 17, 2015
Fibulin-4 E57K Knock-in Mice Recapitulate Cutaneous, Vascular and Skeletal Defects of Recessive Cutis Laxa 1B with both Elastic Fiber and Collagen Fibril AbnormalitiesOlga Igoucheva, Vitali Alexeev, Carmen M Halabi, et al.
Pageof 4