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Chemically modified β-glucuronidase crosses blood-brain barrier and clears neuronal storage in murine mucopolysaccharidosis VII

Proceedings of the National Academy of Sciences - PNAS, 2008-02, Vol.105 (7), p.2616-2621

2008

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Pharmacologic manipulation of lysosomal enzyme transport across the blood–brain barrier

Journal of cerebral blood flow and metabolism, 2016-03, Vol.36 (3), p.476-486

2016

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Overcoming the Blood-Brain Barrier with High-Dose Enzyme Replacement Therapy in Murine Mucopolysaccharidosis VII

Proceedings of the National Academy of Sciences - PNAS, 2005-10, Vol.102 (41), p.14777-14782

2005

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Assessment of bone dysplasia by micro-CT and glycosaminoglycan levels in mouse models for mucopolysaccharidosis type I, IIIA, IVA, and VII

Journal of inherited metabolic disease, 2013-03, Vol.36 (2), p.235-246

2013

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Biochemical evidence for superior correction of neuronal storage by chemically modified enzyme in murine mucopolysaccharidosis VII

Proceedings of the National Academy of Sciences - PNAS, 2012-10, Vol.109 (42), p.17022-17027

2012

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Developmentally Regulated Mannose 6-Phosphate Receptor-Mediated Transport of a Lysosomal Enzyme across the Blood-Brain Barrier

Proceedings of the National Academy of Sciences - PNAS, 2004-08, Vol.101 (34), p.12658-12663

2004

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Epinephrine enhances lysosomal enzyme delivery across the blood-brain barrier by up-regulation of the mannose 6-phosphate receptor

Proceedings of the National Academy of Sciences - PNAS, 2007-07, Vol.104 (31), p.12873-12878

2007

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Glycosylation-Independent Targeting Enhances Enzyme Delivery to Lysosomes and Decreases Storage in Mucopolysaccharidosis Type VII Mice

Proceedings of the National Academy of Sciences - PNAS, 2004-03, Vol.101 (9), p.3083-3088

2004

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Vestronidase alfa: Recombinant human β-glucuronidase as an enzyme replacement therapy for MPS VII

Molecular genetics and metabolism, 2020-05, Vol.130 (1), p.65-76

2020

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Infused Fc-tagged β-glucuronidase crosses the placenta and produces clearance of storage in utero in mucopolysaccharidosis VII mice

Proceedings of the National Academy of Sciences - PNAS, 2008-06, Vol.105 (24), p.8375-8380

2008

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Enzyme Therapy in Mannose Receptor-Null Mucopolysaccharidosis VII Mice Defines Roles for the Mannose 6-Phosphate and Mannose Receptors

Proceedings of the National Academy of Sciences - PNAS, 2006-10, Vol.103 (41), p.15172-15177

2006

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Carbonic Anhydrase XIV Is Enriched in Specific Membrane Domains of Retinal Pigment Epithelium, Müller Cells, and Astrocytes

Proceedings of the National Academy of Sciences - PNAS, 2005-05, Vol.102 (22), p.8030-8035

2005

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Regulation of Transferrin-Mediated Iron Uptake by HFE, The Protein Defective in Hereditary Hemochromatosis

Proceedings of the National Academy of Sciences - PNAS, 2002-03, Vol.99 (5), p.3117-3122

2002

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Expression of a Novel Transmembrane Carbonic Anhydrase Isozyme XII in Normal Human Gut and Colorectal Tumors

The American journal of pathology, 2000-02, Vol.156 (2), p.577-584

2000

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Mannose 6-Phosphate Receptor–mediated Transport of Sulfamidase Across the Blood–brain Barrier in the Newborn Mouse

Molecular therapy, 2008-07, Vol.16 (7), p.1261-1266

2008

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Mutations and polymorphisms in GUSB gene in mucopolysaccharidosis VII (Sly Syndrome)

Human mutation, 2009-04, Vol.30 (4), p.511-519

2009

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Development and testing of new screening method for keratan sulfate in mucopolysaccharidosis IVA

Pediatric research, 2004-04, Vol.55 (4), p.592-597

2004

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New strategies for enzyme replacement therapy for lysosomal storage diseases

Rejuvenation research, 2010-04, Vol.13 (2-3), p.229-236

2010

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Localization of Carbonic Anhydrase XII to the Basolateral Membrane of H+-secreting Cells of Mouse and Rat Kidney

The journal of histochemistry and cytochemistry, 2003-09, Vol.51 (9), p.1217-1224

2003

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Mitochondrial Carbonic Anhydrase CA VB: Differences in Tissue Distribution and Pattern of Evolution from Those of CA VA Suggest Distinct Physiological Roles

Proceedings of the National Academy of Sciences - PNAS, 2000-02, Vol.97 (4), p.1677-1682

2000

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Purification and Kinetic Analysis of Recombinant CA XII, a Membrane Carbonic Anhydrase Overexpressed in Certain Cancers

Proceedings of the National Academy of Sciences - PNAS, 2000-12, Vol.97 (26), p.14212-14217

2000

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Crystal Structure of the Dimeric Extracellular Domain of Human Carbonic Anhydrase XII, A Bitopic Membrane Protein Overexpressed in Certain Cancer Tumor Cells

Proceedings of the National Academy of Sciences - PNAS, 2001-08, Vol.98 (17), p.9545-9550

2001

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Identification of N-Glycans Displaying Mannose-6-Phosphate and their Site of Attachment on Therapeutic Enzymes for Lysosomal Storage Disorder Treatment

Analytical chemistry (Washington), 2011-07, Vol.83 (13), p.5344-5352

2011

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Long circulating enzyme replacement therapy rescues bone pathology in mucopolysaccharidosis VII murine model

Molecular genetics and metabolism, 2012-09, Vol.107 (1-2), p.161-172

2012

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Active Site Mutant Transgene Confers Tolerance to Human β-Glucuronidase without Affecting the Phenotype of MPS VII Mice

Proceedings of the National Academy of Sciences - PNAS, 2001-02, Vol.98 (5), p.2205-2210

2001

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Chemically modified β-glucuronidase crosses blood-brain barrier and clears neuronal storage in murine mucopolysaccharidosis VII

Pharmacologic manipulation of lysosomal enzyme transport across the blood–brain barrier

Overcoming the Blood-Brain Barrier with High-Dose Enzyme Replacement Therapy in Murine Mucopolysaccharidosis VII

Assessment of bone dysplasia by micro-CT and glycosaminoglycan levels in mouse models for mucopolysaccharidosis type I, IIIA, IVA, and VII

Biochemical evidence for superior correction of neuronal storage by chemically modified enzyme in murine mucopolysaccharidosis VII

Developmentally Regulated Mannose 6-Phosphate Receptor-Mediated Transport of a Lysosomal Enzyme across the Blood-Brain Barrier

Epinephrine enhances lysosomal enzyme delivery across the blood-brain barrier by up-regulation of the mannose 6-phosphate receptor

Glycosylation-Independent Targeting Enhances Enzyme Delivery to Lysosomes and Decreases Storage in Mucopolysaccharidosis Type VII Mice

Vestronidase alfa: Recombinant human β-glucuronidase as an enzyme replacement therapy for MPS VII

Infused Fc-tagged β-glucuronidase crosses the placenta and produces clearance of storage in utero in mucopolysaccharidosis VII mice

Enzyme Therapy in Mannose Receptor-Null Mucopolysaccharidosis VII Mice Defines Roles for the Mannose 6-Phosphate and Mannose Receptors

Carbonic Anhydrase XIV Is Enriched in Specific Membrane Domains of Retinal Pigment Epithelium, Müller Cells, and Astrocytes

Regulation of Transferrin-Mediated Iron Uptake by HFE, The Protein Defective in Hereditary Hemochromatosis

Expression of a Novel Transmembrane Carbonic Anhydrase Isozyme XII in Normal Human Gut and Colorectal Tumors

Mannose 6-Phosphate Receptor–mediated Transport of Sulfamidase Across the Blood–brain Barrier in the Newborn Mouse

Mutations and polymorphisms in GUSB gene in mucopolysaccharidosis VII (Sly Syndrome)

Development and testing of new screening method for keratan sulfate in mucopolysaccharidosis IVA

New strategies for enzyme replacement therapy for lysosomal storage diseases

Localization of Carbonic Anhydrase XII to the Basolateral Membrane of H+-secreting Cells of Mouse and Rat Kidney

Mitochondrial Carbonic Anhydrase CA VB: Differences in Tissue Distribution and Pattern of Evolution from Those of CA VA Suggest Distinct Physiological Roles

Purification and Kinetic Analysis of Recombinant CA XII, a Membrane Carbonic Anhydrase Overexpressed in Certain Cancers

Crystal Structure of the Dimeric Extracellular Domain of Human Carbonic Anhydrase XII, A Bitopic Membrane Protein Overexpressed in Certain Cancer Tumor Cells

Identification of N-Glycans Displaying Mannose-6-Phosphate and their Site of Attachment on Therapeutic Enzymes for Lysosomal Storage Disorder Treatment

Long circulating enzyme replacement therapy rescues bone pathology in mucopolysaccharidosis VII murine model

Active Site Mutant Transgene Confers Tolerance to Human β-Glucuronidase without Affecting the Phenotype of MPS VII Mice

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