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Recycling of Golgi glycosyltransferases requires direct binding to coatomer

Proceedings of the National Academy of Sciences - PNAS, 2018-09, Vol.115 (36), p.8984-8989

2018

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A weak COPI binding motif in the cytoplasmic tail of SARS‐CoV‐2 spike glycoprotein is necessary for its cleavage, glycosylation, and localization

FEBS letters, 2021-07, Vol.595 (13), p.1758-1767

2021

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The Iminosugar Isofagomine Increases the Activity of N370S Mutant Acid β-Glucosidase in Gaucher Fibroblasts by Several Mechanisms

Proceedings of the National Academy of Sciences - PNAS, 2006-09, Vol.103 (37), p.13813-13818

2006

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Phil Majerus: Champion of low-dose aspirin therapy

Proceedings of the National Academy of Sciences - PNAS, 2016-08, Vol.113 (35), p.9668-9669

Kornfeld, Stuart A.

2016

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Mannose 6-phosphate receptors: new twists in the tale

Nature reviews. Molecular cell biology, 2003-03, Vol.4 (3), p.202-213

2003

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Mislocalization of phosphotransferase as a cause of mucolipidosis III αβ

Proceedings of the National Academy of Sciences - PNAS, 2014-03, Vol.111 (9), p.3532-3537

2014

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Multiple Domains of GlcNAc-1-phosphotransferase Mediate Recognition of Lysosomal Enzymes

The Journal of biological chemistry, 2016-04, Vol.291 (15), p.8295-8307

2016

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DMAP interaction domain of UDP-GlcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase is a substrate recognition module

Proceedings of the National Academy of Sciences - PNAS, 2013-06, Vol.110 (25), p.10246-10251

2013

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A Lifetime of Adventures in Glycobiology

Annual review of biochemistry, 2018-06, Vol.87, p.1

Kornfeld, Stuart

2018

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Analysis of Gga null mice demonstrates a non-redundant role for mammalian GGA2 during development

PloS one, 2012-01, Vol.7 (1), p.e30184

2012

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Structure and Function of the Mannose 6-Phosphate/Insulinlike Growth Factor II Receptors

Annual review of biochemistry, 1992, Vol.61 (1), p.307-330

Kornfeld, Stuart

1992

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Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder

Nature medicine, 2004-05, Vol.10 (5), p.518-523

2004

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AP-1 Binding to Sorting Signals and Release from Clathrin-Coated Vesicles Is Regulated by Phosphorylation

The Journal of cell biology, 2003-03, Vol.160 (5), p.699-708

2003

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Cooperation of GGAs and AP-1 in Packaging MPRs at the Trans-Golgi Network

Science (American Association for the Advancement of Science), 2002-09, Vol.297 (5587), p.1700-1703

2002

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Training the next generation of biomedical investigators in glycosciences

The Journal of clinical investigation, 2016-02, Vol.126 (2), p.405-408

2016

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Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotype

BMC medical genetics, 2013-10, Vol.14 (1), p.106-106, Article 106

2013

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Engineering of GlcNAc-1-Phosphotransferase for Production of Highly Phosphorylated Lysosomal Enzymes for Enzyme Replacement Therapy

Molecular therapy. Methods & clinical development, 2017-06, Vol.5 (C), p.59-65

2017

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Inactivation of the three GGA genes in HeLa cells partially compromises lysosomal enzyme sorting

FEBS open bio, 2021-02, Vol.11 (2), p.367-374

2021

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Disruption of the Man‐6‐P Targeting Pathway in Mice Impairs Osteoclast Secretory Lysosome Biogenesis

Traffic (Copenhagen, Denmark), 2011-07, Vol.12 (7), p.912-924

2011

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Binding of GGA2 to the Lysosomal Enzyme Sorting Motif of the Mannose 6-Phosphate Receptor

Science (American Association for the Advancement of Science), 2001-06, Vol.292 (5522), p.1716-1718

2001

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Asparagine-linked Oligosaccharides Protect Lamp-1 and Lamp-2 from Intracellular Proteolysis

The Journal of biological chemistry, 1999-10, Vol.274 (43), p.31039-31046

1999

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Vacuolization of mucolipidosis type II mouse exocrine gland cells represents accumulation of autolysosomes

Molecular biology of the cell, 2011-04, Vol.22 (8), p.1135-1147

2011

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Glycan Microarray Analysis of P-type Lectins Reveals Distinct Phosphomannose Glycan Recognition

The Journal of biological chemistry, 2009-12, Vol.284 (50), p.35201-35214

2009

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Neurologic abnormalities in mouse models of the lysosomal storage disorders mucolipidosis II and mucolipidosis III γ

PloS one, 2014, Vol.9 (10), p.e109768-e109768

2014

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The GGA proteins: key players in protein sorting at the trans-Golgi network

European journal of cell biology, 2004-07, Vol.83 (6), p.257-262

2004

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Recycling of Golgi glycosyltransferases requires direct binding to coatomer

A weak COPI binding motif in the cytoplasmic tail of SARS‐CoV‐2 spike glycoprotein is necessary for its cleavage, glycosylation, and localization

The Iminosugar Isofagomine Increases the Activity of N370S Mutant Acid β-Glucosidase in Gaucher Fibroblasts by Several Mechanisms

Phil Majerus: Champion of low-dose aspirin therapy

Mannose 6-phosphate receptors: new twists in the tale

Mislocalization of phosphotransferase as a cause of mucolipidosis III αβ

Multiple Domains of GlcNAc-1-phosphotransferase Mediate Recognition of Lysosomal Enzymes

DMAP interaction domain of UDP-GlcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase is a substrate recognition module

A Lifetime of Adventures in Glycobiology

Analysis of Gga null mice demonstrates a non-redundant role for mammalian GGA2 during development

Structure and Function of the Mannose 6-Phosphate/Insulinlike Growth Factor II Receptors

Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder

AP-1 Binding to Sorting Signals and Release from Clathrin-Coated Vesicles Is Regulated by Phosphorylation

Cooperation of GGAs and AP-1 in Packaging MPRs at the Trans-Golgi Network

Training the next generation of biomedical investigators in glycosciences

Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotype

Engineering of GlcNAc-1-Phosphotransferase for Production of Highly Phosphorylated Lysosomal Enzymes for Enzyme Replacement Therapy

Inactivation of the three GGA genes in HeLa cells partially compromises lysosomal enzyme sorting

Disruption of the Man‐6‐P Targeting Pathway in Mice Impairs Osteoclast Secretory Lysosome Biogenesis

Binding of GGA2 to the Lysosomal Enzyme Sorting Motif of the Mannose 6-Phosphate Receptor

Asparagine-linked Oligosaccharides Protect Lamp-1 and Lamp-2 from Intracellular Proteolysis

Vacuolization of mucolipidosis type II mouse exocrine gland cells represents accumulation of autolysosomes

Glycan Microarray Analysis of P-type Lectins Reveals Distinct Phosphomannose Glycan Recognition

Neurologic abnormalities in mouse models of the lysosomal storage disorders mucolipidosis II and mucolipidosis III γ

The GGA proteins: key players in protein sorting at the trans-Golgi network

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