Search research articles
Contact Us
Filters
Showing results (11-20 of 86) with videos related to
Page
of 9
Sort By:
The Journal of Biological Chemistry
|
April 13, 2012
Identification of intercellular cell adhesion molecule 1 (ICAM-1) as a hypoglycosylation marker in congenital disorders of glycosylation cells
Ping He, Bobby G Ng, Marie-Estelle Losfeld, et al.
Human Molecular Genetics
|
July 12, 2013
Mutations in STT3A and STT3B cause two congenital disorders of glycosylation
Shiteshu Shrimal, Bobby G Ng, Marie-Estelle Losfeld, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
June 14, 2012
A sensitive green fluorescent protein biomarker of N-glycosylation site occupancy
Marie-Estelle Losfeld, Francesca Soncin, Bobby G Ng, et al.
Molecular Genetics and Metabolism
|
April 23, 2024
Clinical and biochemical footprints of congenital disorders of glycosylation: Proposed nosology
Bobby G Ng, Hudson H Freeze, Nastassja Himmelreich, et al.
Journal of Inherited Metabolic Disease
|
September 4, 2015
Serum transferrin carrying the xeno-tetrasaccharide NeuAc-Gal-GlcNAc2 is a biomarker of ALG1-CDG
Per Bengtson, Bobby G Ng, Jaak Jaeken, et al.
Traffic (Copenhagen, Denmark)
|
October 10, 2013
Dissecting functions of the conserved oligomeric Golgi tethering complex using a cell-free assay
Nathanael P Cottam, Katherine M Wilson, Bobby G Ng, et al.
Molecular Genetics and Metabolism Reports
|
March 4, 2022
Uridine monophosphate (UMP)-responsive developmental and epileptic encephalopathy: A case report of two siblings and a review of literature
Ali Al-Otaibi, Alaa AlAyed, Asma Al Madhi, et al.
Molecular Genetics and Metabolism
|
December 28, 2010
Identification of the first COG-CDG patient of Indian origin
Bobby G Ng, Vandana Sharma, Liangwu Sun, et al.
Frontiers in Cell and Developmental Biology
|
October 1, 2021
A Dominant Heterozygous Mutation in <i>COG4</i> Causes Saul-Wilson Syndrome, a Primordial Dwarfism, and Disrupts Zebrafish Development via Wnt Signaling
Zhi-Jie Xia, Xin-Xin I Zeng, Mitali Tambe, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
June 22, 2016
Congenital nephrotic syndrome in an infant with ALG1-congenital disorder of glycosylation
Lyndsay A Harshman, Bobby G Ng, Hudson H Freeze, et al.
Page
of 9
Search research articles
Search
Showing results (11-20 of 86) with videos related to
Sort By:
Page
of 9
The Journal of Biological Chemistry
|
April 13, 2012
Identification of intercellular cell adhesion molecule 1 (ICAM-1) as a hypoglycosylation marker in congenital disorders of glycosylation cells
Ping He, Bobby G Ng, Marie-Estelle Losfeld, et al.
Human Molecular Genetics
|
July 12, 2013
Mutations in STT3A and STT3B cause two congenital disorders of glycosylation
Shiteshu Shrimal, Bobby G Ng, Marie-Estelle Losfeld, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
June 14, 2012
A sensitive green fluorescent protein biomarker of N-glycosylation site occupancy
Marie-Estelle Losfeld, Francesca Soncin, Bobby G Ng, et al.
Molecular Genetics and Metabolism
|
April 23, 2024
Clinical and biochemical footprints of congenital disorders of glycosylation: Proposed nosology
Bobby G Ng, Hudson H Freeze, Nastassja Himmelreich, et al.
Journal of Inherited Metabolic Disease
|
September 4, 2015
Serum transferrin carrying the xeno-tetrasaccharide NeuAc-Gal-GlcNAc2 is a biomarker of ALG1-CDG
Per Bengtson, Bobby G Ng, Jaak Jaeken, et al.
Traffic (Copenhagen, Denmark)
|
October 10, 2013
Dissecting functions of the conserved oligomeric Golgi tethering complex using a cell-free assay
Nathanael P Cottam, Katherine M Wilson, Bobby G Ng, et al.
Molecular Genetics and Metabolism Reports
|
March 4, 2022
Uridine monophosphate (UMP)-responsive developmental and epileptic encephalopathy: A case report of two siblings and a review of literature
Ali Al-Otaibi, Alaa AlAyed, Asma Al Madhi, et al.
Molecular Genetics and Metabolism
|
December 28, 2010
Identification of the first COG-CDG patient of Indian origin
Bobby G Ng, Vandana Sharma, Liangwu Sun, et al.
Frontiers in Cell and Developmental Biology
|
October 1, 2021
A Dominant Heterozygous Mutation in <i>COG4</i> Causes Saul-Wilson Syndrome, a Primordial Dwarfism, and Disrupts Zebrafish Development via Wnt Signaling
Zhi-Jie Xia, Xin-Xin I Zeng, Mitali Tambe, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
June 22, 2016
Congenital nephrotic syndrome in an infant with ALG1-congenital disorder of glycosylation
Lyndsay A Harshman, Bobby G Ng, Hudson H Freeze, et al.
Page
of 9