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Harry Schachter

Showing results (31-40 of 41) with videos related to

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Glycoconjugate Journal|June 20, 2003
Two closely related forms of UDP-GlcNAc: alpha6-D-mannoside beta1,2-N-acetylglucosaminyltransferase II occur in the clawed frog Xenopus laevisJan Mucha, Barbara Svoboda, Sonja Kappel, et al.
Plos One|August 18, 2017
The directed migration of gonadal distal tip cells in Caenorhabditis elegans requires NGAT-1, a ß1,4-N-acetylgalactosaminyltransferase enzymeJoseph Veyhl, Robert J Dunn, Wendy L Johnston, et al.
Science (New York, N.Y.)|January 2, 2010
O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin bindingTakako Yoshida-Moriguchi, Liping Yu, Stephanie H Stalnaker, et al.
Neuromuscular Disorders : NMD|January 24, 2006
Carriers and patients with muscle-eye-brain disease can be rapidly diagnosed by enzymatic analysis of fibroblasts and lymphoblastsJiri Vajsar, Wenli Zhang, William B Dobyns, et al.
Clinical Biochemistry|July 10, 2003
Enzymatic diagnostic test for Muscle-Eye-Brain type congenital muscular dystrophy using commercially available reagentsWenli Zhang, Jiri Vajsar, Pinjiang Cao, et al.
Biochemical Society Symposium|March 27, 2003
Functional post-translational proteomics approach to study the role of N-glycans in the development of Caenorhabditis elegansHarry Schachter, Shihao Chen, Wenli Zhang, et al.
Nature Medicine|June 9, 2004
LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophiesRita Barresi, Daniel E Michele, Motoi Kanagawa, et al.
Archives of Neurology|January 16, 2008
Mild POMGnT1 mutations underlie a novel limb-girdle muscular dystrophy variantEmma M Clement, Caroline Godfrey, Jenny Tan, et al.
Plos One|September 8, 2012
Suppression of cancer progression by MGAT1 shRNA knockdownReza Beheshti Zavareh, Mahadeo A Sukhai, Rose Hurren, et al.
Nature Genetics|April 24, 2012
ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndromeTobias Willer, Hane Lee, Mark Lommel, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Glycoconjugate Journal|June 20, 2003
Two closely related forms of UDP-GlcNAc: alpha6-D-mannoside beta1,2-N-acetylglucosaminyltransferase II occur in the clawed frog Xenopus laevisJan Mucha, Barbara Svoboda, Sonja Kappel, et al.
Plos One|August 18, 2017
The directed migration of gonadal distal tip cells in Caenorhabditis elegans requires NGAT-1, a ß1,4-N-acetylgalactosaminyltransferase enzymeJoseph Veyhl, Robert J Dunn, Wendy L Johnston, et al.
Science (New York, N.Y.)|January 2, 2010
O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin bindingTakako Yoshida-Moriguchi, Liping Yu, Stephanie H Stalnaker, et al.
Neuromuscular Disorders : NMD|January 24, 2006
Carriers and patients with muscle-eye-brain disease can be rapidly diagnosed by enzymatic analysis of fibroblasts and lymphoblastsJiri Vajsar, Wenli Zhang, William B Dobyns, et al.
Clinical Biochemistry|July 10, 2003
Enzymatic diagnostic test for Muscle-Eye-Brain type congenital muscular dystrophy using commercially available reagentsWenli Zhang, Jiri Vajsar, Pinjiang Cao, et al.
Biochemical Society Symposium|March 27, 2003
Functional post-translational proteomics approach to study the role of N-glycans in the development of Caenorhabditis elegansHarry Schachter, Shihao Chen, Wenli Zhang, et al.
Nature Medicine|June 9, 2004
LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophiesRita Barresi, Daniel E Michele, Motoi Kanagawa, et al.
Archives of Neurology|January 16, 2008
Mild POMGnT1 mutations underlie a novel limb-girdle muscular dystrophy variantEmma M Clement, Caroline Godfrey, Jenny Tan, et al.
Plos One|September 8, 2012
Suppression of cancer progression by MGAT1 shRNA knockdownReza Beheshti Zavareh, Mahadeo A Sukhai, Rose Hurren, et al.
Nature Genetics|April 24, 2012
ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndromeTobias Willer, Hane Lee, Mark Lommel, et al.
Pageof 5