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BMC Medical Genetics
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October 10, 2013
Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotype
Eline van Meel, Daniel J Wegner, Paul Cliften, et al.
The Journal of Biological Chemistry
|
October 6, 2009
Glycan microarray analysis of P-type lectins reveals distinct phosphomannose glycan recognition
Xuezheng Song, Yi Lasanajak, Linda J Olson, et al.
Nature Medicine
|
April 27, 2004
Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder
Xiaohua Wu, Richard A Steet, Ognian Bohorov, et al.
Nature Structural & Molecular Biology
|
March 25, 2022
Structure of the human GlcNAc-1-phosphotransferase αβ subunits reveals regulatory mechanism for lysosomal enzyme glycan phosphorylation
Hua Li, Wang-Sik Lee, Xiang Feng, et al.
Biorxiv : the Preprint Server for Biology
|
December 16, 2024
Molecular Insights into the Regulation of GNPTAB by TMEM251
Xi Yang, Balraj Doray, Varsha Venkatarangan, et al.
Nature Communications
|
March 11, 2026
Molecular insights into the regulation of GNPTαβ by LYSET
Xi Yang, Balraj Doray, Danielle Henn, et al.
BBA Advances
|
April 21, 2023
Increased phosphorylation of HexM improves lysosomal uptake and potential for managing GM2 gangliosidoses
Graeme Benzie, Kristen Bouma, Taylor Battellino, et al.
The Journal of Clinical Investigation
|
October 19, 2004
Blasts from the past
Paul A Insel, Stuart Kornfeld, Philip W Majerus, et al.
The Journal of Biological Chemistry
|
April 11, 2013
Structure and function of the DUF2233 domain in bacteria and in the human mannose 6-phosphate uncovering enzyme
Debanu Das, Wang-Sik Lee, Joanna C Grant, et al.
The Journal of Clinical Investigation
|
February 2, 2016
Training the next generation of biomedical investigators in glycosciences
Peter Agre, Carolyn Bertozzi, Mina Bissell, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 61) with videos related to
Sort By:
Page
of 7
BMC Medical Genetics
|
October 10, 2013
Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotype
Eline van Meel, Daniel J Wegner, Paul Cliften, et al.
The Journal of Biological Chemistry
|
October 6, 2009
Glycan microarray analysis of P-type lectins reveals distinct phosphomannose glycan recognition
Xuezheng Song, Yi Lasanajak, Linda J Olson, et al.
Nature Medicine
|
April 27, 2004
Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder
Xiaohua Wu, Richard A Steet, Ognian Bohorov, et al.
Nature Structural & Molecular Biology
|
March 25, 2022
Structure of the human GlcNAc-1-phosphotransferase αβ subunits reveals regulatory mechanism for lysosomal enzyme glycan phosphorylation
Hua Li, Wang-Sik Lee, Xiang Feng, et al.
Biorxiv : the Preprint Server for Biology
|
December 16, 2024
Molecular Insights into the Regulation of GNPTAB by TMEM251
Xi Yang, Balraj Doray, Varsha Venkatarangan, et al.
Nature Communications
|
March 11, 2026
Molecular insights into the regulation of GNPTαβ by LYSET
Xi Yang, Balraj Doray, Danielle Henn, et al.
BBA Advances
|
April 21, 2023
Increased phosphorylation of HexM improves lysosomal uptake and potential for managing GM2 gangliosidoses
Graeme Benzie, Kristen Bouma, Taylor Battellino, et al.
The Journal of Clinical Investigation
|
October 19, 2004
Blasts from the past
Paul A Insel, Stuart Kornfeld, Philip W Majerus, et al.
The Journal of Biological Chemistry
|
April 11, 2013
Structure and function of the DUF2233 domain in bacteria and in the human mannose 6-phosphate uncovering enzyme
Debanu Das, Wang-Sik Lee, Joanna C Grant, et al.
The Journal of Clinical Investigation
|
February 2, 2016
Training the next generation of biomedical investigators in glycosciences
Peter Agre, Carolyn Bertozzi, Mina Bissell, et al.
Page
of 7