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

Liangwu Sun

Showing results (11-20 of 14) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 14 results.
Molecular Genetics and Metabolism|December 28, 2010
Identification of the first COG-CDG patient of Indian originBobby G Ng, Vandana Sharma, Liangwu Sun, et al.
American Journal of Medical Genetics. Part A|May 17, 2007
Expanding spectrum of congenital disorder of glycosylation Ig (CDG-Ig): sibs with a unique skeletal dysplasia, hypogammaglobulinemia, cardiomyopathy, genital malformations, and early lethalityChristian Kranz, Alice A Basinger, Müge Güçsavaş-Calikoğlu, et al.
Human Molecular Genetics|March 3, 2007
COG8 deficiency causes new congenital disorder of glycosylation type IIhChristian Kranz, Bobby G Ng, Liangwu Sun, et al.
Neuron|November 17, 2009
A functional mouse retroposed gene Rps23r1 reduces Alzheimer's beta-amyloid levels and tau phosphorylationYun-wu Zhang, Shijie Liu, Xue Zhang, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Molecular Genetics and Metabolism|December 28, 2010
Identification of the first COG-CDG patient of Indian originBobby G Ng, Vandana Sharma, Liangwu Sun, et al.
American Journal of Medical Genetics. Part A|May 17, 2007
Expanding spectrum of congenital disorder of glycosylation Ig (CDG-Ig): sibs with a unique skeletal dysplasia, hypogammaglobulinemia, cardiomyopathy, genital malformations, and early lethalityChristian Kranz, Alice A Basinger, Müge Güçsavaş-Calikoğlu, et al.
Human Molecular Genetics|March 3, 2007
COG8 deficiency causes new congenital disorder of glycosylation type IIhChristian Kranz, Bobby G Ng, Liangwu Sun, et al.
Neuron|November 17, 2009
A functional mouse retroposed gene Rps23r1 reduces Alzheimer's beta-amyloid levels and tau phosphorylationYun-wu Zhang, Shijie Liu, Xue Zhang, et al.
Pageof 2