Developmental diseases caused by impaired nucleotide sugar transporters. - Wikidata - awgldk - TriplyDB

Developmental diseases caused by impaired nucleotide sugar transporters.

Developmental diseases caused by impaired nucleotide sugar transporters.

http://www.wikidata.org/entity/Q38004945

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Congenital disorder of fucosylation type 2c (LADII) presenting with short stature and developmental delay with minimal adhesion defect The Golgi localized bifunctional UDP-rhamnose/UDP-galactose transporter family of Arabidopsis.Transforming growth factor β signaling upregulates the expression of human GDP-fucose transporter by activating transcription factor Sp1.Inhibition of nucleotide sugar transport in Trypanosoma brucei alters surface glycosylation.The third dimension of reading the sugar code by lectins: design of glycoclusters with cyclic scaffolds as tools with the aim to define correlations between spatial presentation and activity.Harnessing Solute Carrier Transporters for Precision Oncology.Defective SLC35C1 causes congenital disorder of glycosylation 2C (CDG2C)Defective SLC35D1 causes Schneckenbecken dysplasia (SCHBCKD)Mutations in SLC35A3 cause autism spectrum disorder, epilepsy and arthrogryposis.Functional expression of a human GDP-L-fucose transporter in Escherichia coli.

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P2860

Developmental diseases caused by impaired nucleotide sugar transporters.

http://www.wikidata.org/entity/Q38004945

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Developmental diseases caused by impaired nucleotide sugar transporters.

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Developmental diseases caused by impaired nucleotide sugar transporters.

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Developmental diseases caused by impaired nucleotide sugar transporters.

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S10719-012-9375-4

P1433

Glycoconjugate Journal

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Developmental diseases caused by impaired nucleotide sugar transporters.

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Li Liu

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P2860

Nucleotide-sugar transporters: structure, function and roles in vivo

Nucleotide-sugar transporter SLC35D1 is critical to chondroitin sulfate synthesis in cartilage and skeletal development in mouse and human

Molecular characterization of human UDP-glucuronic acid/UDP-N-acetylgalactosamine transporter, a novel nucleotide sugar transporter with dual substrate specificity

Recurrent Severe Infections Caused by a Novel Leukocyte Adhesion Deficiency

The Leishmania GDP-mannose transporter is an autonomous, multi-specific, hexameric complex of LPG2 subunits.

Macrothrombocytopenia with abnormal demarcation membranes in megakaryocytes and neutropenia with a complete lack of sialyl-Lewis-X antigen in leukocytes--a new syndrome?

Leukocyte adhesion deficiency type II.

The Golgi GDPase of the fungal pathogen Candida albicans affects morphogenesis, glycosylation, and cell wall properties.

Impairment of the Golgi GDP-L-fucose transport and unresponsiveness to fucose replacement therapy in LAD II patients.

The role of nucleotide sugar transporters in development of eukaryotes.

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s10719-012-9375-4

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5-10

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scholarly article

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10.1007/S10719-012-9375-4

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1

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Carlos B Hirschberg

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2012-04-17T00:00:00Z

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1040679955

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