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ProteomicsSpatiotemporal proximity labeling tools to track GlcNAc-modified functional protein hubs during cellular signaling
A fundamental mechanism that all eukaryotic cells use to adapt to their environment is dynamic protein modification with monosaccharide sugars. In humans, O-linked N-acetylglucosamine (O-GlcNAc) is rapidly added and removed on diverse protein sites as a response to fluctuating nutrient levels, stres...
ORGANISM(S): Homo sapiens (Human) 
2022-10-15 | PXD033026 | Pride
Glycosylation Insulin signaling Proximity labeling Nucleocytoplasmic O-glcnac 
ProteomicsSpatiotemporal proximity labeling tools to track GlcNAc-modified functional protein hubs during cellular signaling
A fundamental mechanism that all eukaryotic cells use to adapt to their environment is dynamic protein modification with monosaccharide sugars. In humans, O-linked N-acetylglucosamine (O-GlcNAc) is rapidly added and removed on diverse protein sites as a response to fluctuating nutrient levels, stres...
ORGANISM(S): Homo sapiens (Human) 
2022-10-15 | PXD033043 | Pride
Glycosylation Insulin signaling Proximity labeling Nucleocytoplasmic O-glcnac 
ProteomicsSpatiotemporal proximity labeling tools to track GlcNAc-modified functional protein hubs during cellular signaling
A fundamental mechanism that all eukaryotic cells use to adapt to their environment is dynamic protein modification with monosaccharide sugars. In humans, O-linked N-acetylglucosamine (O-GlcNAc) is rapidly added and removed on diverse protein sites as a response to fluctuating nutrient levels, stres...
ORGANISM(S): Homo sapiens (Human) 
2022-10-15 | PXD033044 | Pride
Glycosylation Insulin signaling Proximity labeling Nucleocytoplasmic O-glcnac 
ProteomicsSpatiotemporal proximity labeling tools to track GlcNAc-modified functional protein hubs during cellular signaling
A fundamental mechanism that all eukaryotic cells use to adapt to their environment is dynamic protein modification with monosaccharide sugars. In humans, O-linked N-acetylglucosamine (O-GlcNAc) is rapidly added and removed on diverse protein sites as a response to fluctuating nutrient levels, stres...
ORGANISM(S): Homo sapiens (Human) 
2022-10-15 | PXD033066 | Pride
Glycosylation Insulin signaling Proximity labeling Nucleocytoplasmic O-glcnac 
ProteomicsSpatiotemporal proximity labeling tools to track GlcNAc-modified functional protein hubs during cellular signaling
A fundamental mechanism that all eukaryotic cells use to adapt to their environment is dynamic protein modification with monosaccharide sugars. In humans, O-linked N-acetylglucosamine (O-GlcNAc) is rapidly added and removed on diverse protein sites as a response to fluctuating nutrient levels, stres...
ORGANISM(S): Homo sapiens (Human) 
2022-10-15 | PXD033062 | Pride
Glycosylation Insulin signaling Proximity labeling Nucleocytoplasmic O-glcnac 
ProteomicsSpatiotemporal proximity labeling tools to track GlcNAc-modified functional protein hubs during cellular signaling
A fundamental mechanism that all eukaryotic cells use to adapt to their environment is dynamic protein modification with monosaccharide sugars. In humans, O-linked N-acetylglucosamine (O-GlcNAc) is rapidly added and removed on diverse protein sites as a response to fluctuating nutrient levels, stres...
ORGANISM(S): Homo sapiens (Human) 
2022-10-15 | PXD033063 | Pride
Glycosylation Insulin signaling Proximity labeling Nucleocytoplasmic O-glcnac 
TranscriptomicsTranscription profiling of E12.5 mouse whole embryo and E12.5 placenta total RNA pooled to create 25:75, 50:50, and 75:25 ratio mixtures to estimate transcript copy number
E12.5 mouse whole embryo and E12.5 placenta total RNA were pooled to create 25:75, 50:50, and 75:25 ratio mixtures, based on Bioanalyzer quantitation. These samples, along with the original unmixed RNAs, were used as templates for duplicate linear amplification labeling reactions. cRNA target mixtu...
ORGANISM(S): Mus musculus 
2005-01-01 | E-MNIA-67 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of E12.5 mouse whole embryo, E12.5 placenta, embryonic stem (ES) cells, and trophoblast stem (TS) cells on a novel microarray design to validate the system
E12.5 mouse whole embryo, E12.5 placenta, embryonic stem (ES) cells, and trophoblast stem (TS) cells were compared on a novel microarray design to validate the system. The in situ-synthesized 60-mer oligonucleotide microarray platform contains approximately 44,000 DNA features, and was designed to ...
ORGANISM(S): Mus musculus 
2005-01-01 | E-MNIA-66 | biostudies-arrayexpress
TranscriptomicsTranscript copy number estimation using a mouse whole-genome oligonucleotide microarray (22k Linearity)
E12.5 mouse whole embryo and E12.5 placenta total RNA were pooled to create 25:75, 50:50, and 75:25 ratio mixtures, based on Bioanalyzer quantitation. These samples, along with the original unmixed RNAs, were used as templates for duplicate linear amplification labeling reactions. cRNA target mixtu...
ORGANISM(S): Mus musculus 
2010-06-09 | E-GEOD-3508 | biostudies-arrayexpress
TranscriptomicsTranscript copy number estimation using a mouse whole-genome oligonucleotide microarray (WGA 2.1 Spike Test)
E12.5 mouse whole embryo, E12.5 placenta, embryonic stem (ES) cells, and trophoblast stem (TS) cells were compared on a novel microarray design to validate the system. The in situ-synthesized 60-mer oligonucleotide microarray platform contains approximately 44,000 DNA features, and was designed to ...
ORGANISM(S): Mus musculus 
2005-10-28 | E-GEOD-3509 | biostudies-arrayexpress
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