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Bobby G Ng

Showing results (11-20 of 86) with videos related to

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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 cellsPing 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 glycosylationShiteshu 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 occupancyMarie-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 nosologyBobby 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-CDGPer 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 assayNathanael 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 literatureAli 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 originBobby 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 SignalingZhi-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 glycosylationLyndsay A Harshman, Bobby G Ng, Hudson H Freeze, et al.
Pageof 9

Showing results (11-20 of 86) with videos related to

Sort By:
Pageof 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 cellsPing 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 glycosylationShiteshu 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 occupancyMarie-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 nosologyBobby 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-CDGPer 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 assayNathanael 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 literatureAli 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 originBobby 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 SignalingZhi-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 glycosylationLyndsay A Harshman, Bobby G Ng, Hudson H Freeze, et al.
Pageof 9