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Potential Climate and Human Water-Use Effects on Water-Quality Trends in a Semiarid, Western U.S. Watershed: Fountain Creek, Colorado, USA

Water (Basel), 2024-05, Vol.16 (10), p.1343

2024

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Function and Change with Aging of α-Klotho in the Kidney

Vitamins and hormones, 2016, Vol.101, p.239

2016

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Structural and biochemical characterization of O-mannose-linked human natural killer-1 glycan expressed on phosphacan in developing mouse brains

Glycobiology (Oxford), 2014-03, Vol.24 (3), p.314-324

2014

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Protein O-mannosylation is necessary for normal embryonic development in zebrafish

Glycobiology (Oxford), 2010-09, Vol.20 (9), p.1089-1102

2010

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Identification of a post-translational modification with ribitol-phosphate and its defect in muscular dystrophy

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S90-S90

2016

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Hepatitis C virus among blood donors in Lubumbashi, DRC: Seroprevalence and molecular characterisation

Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine, 2023-05, Vol.30 (2), p.272-278

2023

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G.P.11 Fukutin-related protein (FKRP) is involved in the post-phosphoryl modification of α -dystroglycan

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.815-815

2012

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Protective effect of N-glycan bisecting GlcNAc residues on -amyloid production in Alzheimer's disease

Glycobiology (Oxford), 2010-01, Vol.20 (1), p.99-106

2010

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FP.37 CDP-ribitol prodrug treatment ameliorates ISPD-deficient muscular dystrophy mouse model

Neuromuscular disorders : NMD, 2022-10, Vol.32, p.S120

2022

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Demonstration of Mammalian Protein O-Mannosyltransferase Activity: Coexpression of POMT1 and POMT2 Required for Enzymatic Activity

Proceedings of the National Academy of Sciences - PNAS, 2004-01, Vol.101 (2), p.500-505

2004

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Muscular Dystrophy and Neuronal Migration Disorder Caused by Mutations in a Glycosyltransferase, POMGnT1

Developmental cell, 2001-11, Vol.1 (5), p.717-724

2001

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C.P.3.08 Biochemical approach for α-dystroglycanopathies: Identification of consensus sequence for protein O -mannosylation

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.872-872

2007

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Disentangling the Separate and Intersecting Pathways of Carbon and Nitrogen Response to Overlapping Drivers

Ruckhaus, Manya H

2022

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Mutations of the POMT1 gene found in patients with Walker–Warburg syndrome lead to a defect of protein O-mannosylation

Biochemical and biophysical research communications, 2004-12, Vol.325 (1), p.75-79

2004

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C.P.3.12 POMGnT1-null myoblasts poorly proliferate in vitro

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.873-873

2007

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Étude ethnobotanique, biologique et chimique de plantes réputées anticariogènes à Lubumbashi – RD Congo

Phytothérapie (Paris, France), 2017-02, Vol.15 (1), p.2-9

2017

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S.O.5 - Identification of a post-translational modification with ribitol-phosphate and its defect in muscular dystrophy

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S90-S90

2016

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The Twisted Abdomen Phenotype of Drosophila POMT1 and POMT2 Mutants Coincides with Their Heterophilic Protein O-Mannosyltransferase Activity

The Journal of biological chemistry, 2004-10, Vol.279 (41), p.42638-42647

2004

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C.P.3.03 Novel POMT2 mutations associated with a marked reduction of POMT activity causing congenital muscular dystrophy with mental retardation and microcephaly

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.870-870

2007

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Comparative Study of the Asparagine-Linked Sugar Chains of Human Lipocalin-Type Prostaglandin D Synthase Purified from Urine and Amniotic Fluid, and Recombinantly Expressed in Chinese Hamster Ovary Cells

Journal of biochemistry (Tokyo), 2000-06, Vol.127 (6), p.1001-1011

2000

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Loss-of-function of an N-acetylglucosaminyltransferase, POMGnT1, in muscle–eye–brain disease

Biochemical and biophysical research communications, 2003-06, Vol.306 (1), p.93-97

2003

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Deficiency of α-Dystroglycan in Muscle–Eye–Brain Disease

Biochemical and biophysical research communications, 2002-03, Vol.291 (5), p.1283-1286

2002

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Structure-function analysis of human protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase 1, POMGnT1

Biochemical and biophysical research communications, 2004-07, Vol.320 (1), p.39-44

2004

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Worldwide distribution and broader clinical spectrum of muscle–eye–brain disease

Human molecular genetics, 2003-03, Vol.12 (5), p.527-534

2003

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Galectin-1 induces astrocyte differentiation, which leads to production of brain-derived neurotrophic factor

Glycobiology (Oxford), 2004-04, Vol.14 (4), p.357-363

2004

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Potential Climate and Human Water-Use Effects on Water-Quality Trends in a Semiarid, Western U.S. Watershed: Fountain Creek, Colorado, USA

Function and Change with Aging of α-Klotho in the Kidney

Structural and biochemical characterization of O-mannose-linked human natural killer-1 glycan expressed on phosphacan in developing mouse brains

Protein O-mannosylation is necessary for normal embryonic development in zebrafish

Identification of a post-translational modification with ribitol-phosphate and its defect in muscular dystrophy

Hepatitis C virus among blood donors in Lubumbashi, DRC: Seroprevalence and molecular characterisation

G.P.11 Fukutin-related protein (FKRP) is involved in the post-phosphoryl modification of α -dystroglycan

Protective effect of N-glycan bisecting GlcNAc residues on -amyloid production in Alzheimer's disease

FP.37 CDP-ribitol prodrug treatment ameliorates ISPD-deficient muscular dystrophy mouse model

Demonstration of Mammalian Protein O-Mannosyltransferase Activity: Coexpression of POMT1 and POMT2 Required for Enzymatic Activity

Muscular Dystrophy and Neuronal Migration Disorder Caused by Mutations in a Glycosyltransferase, POMGnT1

C.P.3.08 Biochemical approach for α-dystroglycanopathies: Identification of consensus sequence for protein O -mannosylation

Disentangling the Separate and Intersecting Pathways of Carbon and Nitrogen Response to Overlapping Drivers

Mutations of the POMT1 gene found in patients with Walker–Warburg syndrome lead to a defect of protein O-mannosylation

C.P.3.12 POMGnT1-null myoblasts poorly proliferate in vitro

Étude ethnobotanique, biologique et chimique de plantes réputées anticariogènes à Lubumbashi – RD Congo

S.O.5 - Identification of a post-translational modification with ribitol-phosphate and its defect in muscular dystrophy

The Twisted Abdomen Phenotype of Drosophila POMT1 and POMT2 Mutants Coincides with Their Heterophilic Protein O-Mannosyltransferase Activity

C.P.3.03 Novel POMT2 mutations associated with a marked reduction of POMT activity causing congenital muscular dystrophy with mental retardation and microcephaly

Comparative Study of the Asparagine-Linked Sugar Chains of Human Lipocalin-Type Prostaglandin D Synthase Purified from Urine and Amniotic Fluid, and Recombinantly Expressed in Chinese Hamster Ovary Cells

Loss-of-function of an N-acetylglucosaminyltransferase, POMGnT1, in muscle–eye–brain disease

Deficiency of α-Dystroglycan in Muscle–Eye–Brain Disease

Structure-function analysis of human protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase 1, POMGnT1

Worldwide distribution and broader clinical spectrum of muscle–eye–brain disease

Galectin-1 induces astrocyte differentiation, which leads to production of brain-derived neurotrophic factor

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