(Q36742428)

English

Identification of O-linked N-acetylglucosamine (O-GlcNAc)-modified osteoblast proteins by electron transfer dissociation tandem mass spectrometry reveals proteins critical for bone formation

scientific article published on 26 February 2013

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scholarly article

1 reference

Europe PubMed Central

16 August 2017

Identification of O-linked N-acetylglucosamine (O-GlcNAc)-modified osteoblast proteins by electron transfer dissociation tandem mass spectrometry reveals proteins critical for bone formation (English)

1 reference

Europe PubMed Central

16 August 2017

0 references

5

object named as

Lauren E Ball

1 reference

Europe PubMed Central

16 August 2017

author name string

Alexis K Nagel

1

1 reference

Europe PubMed Central

16 August 2017

Michael Schilling

2

1 reference

Europe PubMed Central

16 August 2017

Susana Comte-Walters

3

1 reference

Europe PubMed Central

16 August 2017

Mary N Berkaw

4

1 reference

Europe PubMed Central

16 August 2017

publication date

26 February 2013

1 reference

Europe PubMed Central

16 August 2017

Molecular & Cellular Proteomics

1 reference

Europe PubMed Central

16 August 2017

12

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Europe PubMed Central

16 August 2017

4

1 reference

Europe PubMed Central

16 August 2017

945-955

1 reference

Europe PubMed Central

16 August 2017

The increase in O-linked N-acetylglucosamine protein modification stimulates chondrogenic differentiation both in vitro and in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

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Global identification and characterization of both O-GlcNAcylation and phosphorylation at the murine synapse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

29 September 2017

O-GlcNAcylation of kinases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

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Tandem mass spectrometry identifies many mouse brain O-GlcNAcylated proteins including EGF domain-specific O-GlcNAc transferase targets

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

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Modification site localization scoring: strategies and performance

1 reference

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Dynamic O-GlcNAc modification regulates CREB-mediated gene expression and memory formation

1 reference

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O-GlcNAc modification of PPARγ reduces its transcriptional activity

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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The Ccr4--not complex

1 reference

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1 reference

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Polycomb repressive complex 2 is necessary for the normal site-specific O-GlcNAc distribution in mouse embryonic stem cells

1 reference

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1 reference

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29 September 2017

Cross talk between O-GlcNAcylation and phosphorylation: roles in signaling, transcription, and chronic disease

1 reference

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CREB and the CRTC co-activators: sensors for hormonal and metabolic signals

1 reference

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1 reference

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A tissue-specific atlas of mouse protein phosphorylation and expression

1 reference

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Intracellular protein glycosylation modulates insulin mediated lifespan in C.elegans

1 reference

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Conserved regulatory motifs in osteogenic gene promoters integrate cooperative effects of canonical Wnt and BMP pathways.

1 reference

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Human OGA binds substrates in a conserved peptide recognition groove

1 reference

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1 reference

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Insulin signaling in osteoblasts integrates bone remodeling and energy metabolism

1 reference

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LIM-domain proteins TRIP6 and LPP associate with shelterin to mediate telomere protection

1 reference

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29 September 2017

The p38 MAPK pathway is essential for skeletogenesis and bone homeostasis in mice

1 reference

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29 September 2017

Improving software performance for peptide electron transfer dissociation data analysis by implementation of charge state- and sequence-dependent scoring

1 reference

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O-GlcNAc cycling: emerging roles in development and epigenetics

1 reference

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29 September 2017

Dynamic O-GlcNAc cycling at promoters of Caenorhabditis elegans genes regulating longevity, stress, and immunity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

29 September 2017

Modulation of transcription factor function by O-GlcNAc modification

1 reference

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1 reference

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FoxO1 expression in osteoblasts regulates glucose homeostasis through regulation of osteocalcin in mice

1 reference

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29 September 2017

The transcription factor ATF4 regulates glucose metabolism in mice through its expression in osteoblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

29 September 2017

Enrichment and site mapping of O-linked N-acetylglucosamine by a combination of chemical/enzymatic tagging, photochemical cleavage, and electron transfer dissociation mass spectrometry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

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Control of alpha-herpesvirus IE gene expression by HCF-1 coupled chromatin modification activities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

29 September 2017

O-linked N-acetylglucosamine modification of insulin receptor substrate-1 occurs in close proximity to multiple SH2 domain binding motifs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

29 September 2017

Drosophila O-GlcNAc transferase (OGT) is encoded by the Polycomb group (PcG) gene, super sex combs (sxc).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

29 September 2017

Bone as an endocrine organ.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

29 September 2017

O-linked N-acetylglucosamine modification on CCAAT enhancer-binding protein beta: role during adipocyte differentiation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

29 September 2017

Identification of protein O-GlcNAcylation sites using electron transfer dissociation mass spectrometry on native peptides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

29 September 2017

O-GlcNAc modifications regulate cell survival and epiboly during zebrafish development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

29 September 2017

Elevation of Global O-GlcNAc Levels in 3T3-L1 Adipocytes by Selective Inhibition of O-GlcNAcase Does Not Induce Insulin Resistance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

29 September 2017

O-linked beta-N-acetylglucosaminyltransferase substrate specificity is regulated by myosin phosphatase targeting and other interacting proteins.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

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A potent mechanism-inspired O-GlcNAcase inhibitor that blocks phosphorylation of tau in vivo

1 reference

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29 September 2017

Phosphoinositide signalling links O-GlcNAc transferase to insulin resistance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

29 September 2017

Endocrine regulation of energy metabolism by the skeleton

1 reference

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The utility of ETD mass spectrometry in proteomic analysis

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Caenorhabditis elegans ortholog of a diabetes susceptibility locus: oga-1 (O-GlcNAcase) knockout impacts O-GlcNAc cycling, metabolism, and dauer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

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1 reference

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O-GlcNAc a sensor of cellular state: the role of nucleocytoplasmic glycosylation in modulating cellular function in response to nutrition and stress

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3617341

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Peptide and protein sequence analysis by electron transfer dissociation mass spectrometry

1 reference

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Ogt-dependent X-chromosome-linked protein glycosylation is a requisite modification in somatic cell function and embryo viability

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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29 September 2017

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1 reference

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1 reference

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1 reference

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1 reference

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28 June 2018

Essential role of the glycosyltransferase sxc/Ogt in polycomb repression.

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5 September 2018

Parallel identification of O-GlcNAc-modified proteins from cell lysates

1 reference

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5 September 2018

Using optimized collision energies and high resolution, high accuracy fragment ion selection to improve glycopeptide detection by precursor ion scanning

1 reference

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1 reference

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Characterization of a mouse monoclonal antibody specific for O-linked N-acetylglucosamine

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strawberry notch encodes a conserved nuclear protein that functions downstream of Notch and regulates gene expression along the developing wing margin of Drosophila

1 reference

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5 September 2018

Purification and Identification ofO-GlcNAc-Modified Peptides Using Phosphate-Based Alkyne CLICK Chemistry in Combination with Titanium Dioxide Chromatography and Mass Spectrometry

1 reference

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21 January 2018

Topography and polypeptide distribution of terminal N-acetylglucosamine residues on the surfaces of intact lymphocytes. Evidence for O-linked GlcNAc

1 reference

https://pubmed.ncbi.nlm.nih.gov/23443134

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1074/MCP.M112.026633

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

16 August 2017

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