Mutations in HNF1A result in marked alterations of plasma glycan profile - Wikidata - awgldk - TriplyDB

Mutations in HNF1A result in marked alterations of plasma glycan profile

Mutations in HNF1A result in marked alterations of plasma glycan profile

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Undiagnosed MODY: Time for Action Hepatocyte Nuclear Factor 1A Is a Cell-Intrinsic Transcription Factor Required for B Cell Differentiation and Development in Mice Ubiquitous Importance of Protein Glycosylation.Transforming growth factor β signaling upregulates the expression of human GDP-fucose transporter by activating transcription factor Sp1.Urinary fetuin-A is a novel marker for diabetic nephropathy in type 2 diabetes identified by lectin microarray.High-Performance Mixed Models Based Genome-Wide Association Analysis with omicABEL software Circulating ghrelin level is higher in HNF1A-MODY and GCK-MODY than in polygenic forms of diabetes mellitus.Changes in total plasma and serum N-glycome composition and patient-controlled analgesia after major abdominal surgery.Classical galactosaemia: novel insights in IgG N-glycosylation and N-glycan biosynthesis.The challenge and promise of glycomics.The role of glycosylation in IBD.Clinical diagnostics and therapy monitoring in the congenital disorders of glycosylation When is it MODY? Challenges in the Interpretation of Sequence Variants in MODY Genes.Human aging in the post-GWAS era: further insights reveal potential regulatory variants.Recent Advances in the Analysis of Complex Glycoproteins.Identification of circulating microRNAs in HNF1A-MODY carriers.Glycosylation Changes in Brain Cancer.Functional Investigations of HNF1A Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population.Maturity onset diabetes of the young due to HNF1A variants in Croatia.Exploring the Genomic Roadmap and Molecular Phylogenetics Associated with MODY Cascades Using Computational Biology.Pregnancy Complicated by Maternal MODY 3 and Paternal MODY 2 Diabetes and Subsequent Rapidly Falling Insulin Requirement

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P2860

Mutations in HNF1A result in marked alterations of plasma glycan profile

http://www.wikidata.org/entity/Q36720490

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2012 nî lūn-bûn

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Mutations in HNF1A result in marked alterations of plasma glycan profile

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Mutations in HNF1A result in marked alterations of plasma glycan profile

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Mutations in HNF1A result in marked alterations of plasma glycan profile

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Mutations in HNF1A result in marked alterations of plasma glycan profile

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Mutations in HNF1A result in marked alterations of plasma glycan profile

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Mutations in HNF1A result in marked alterations of plasma glycan profile

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Mutations in HNF1A result in marked alterations of plasma glycan profile

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Abdelkader Essafi

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Alan F Wright

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Ana Muzinic

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Barbara Adamczyk

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Daniela Gasperikova

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Dragan Primorac

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Erling Tjora

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Gaya Thanabalasingham

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Harry Campbell

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Irma Redzic

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P2860

Three new mutations in the hepatocyte nuclear factor-1alpha gene in Japanese subjects with diabetes mellitus: clinical features and functional characterization

A map of human genome variation from population-scale sequencing

A method and server for predicting damaging missense mutations

Regulation of apolipoprotein M gene expression by MODY3 gene hepatocyte nuclear factor-1alpha: haploinsufficiency is associated with reduced serum apolipoprotein M levels

Genetic cause of hyperglycaemia and response to treatment in diabetes

On the frequency of protein glycosylation, as deduced from analysis of the SWISS-PROT database

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

Changes of serum glycans during sepsis and acute pancreatitis.

Evaluation of serum 1,5 anhydroglucitol levels as a clinical test to differentiate subtypes of diabetes

Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation.

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1329-1337

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10.2337/DB12-0880

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Caroline Hayward

Oluf Borbye Pedersen

Pål R Njølstad

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234011537

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