Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells.
about
Secreted sulfatases Sulf1 and Sulf2 have overlapping yet essential roles in mouse neonatal survivalThe knockout mouse projectStructures, enzymatic properties, and expression of novel human and mouse secretory phospholipase A(2)sCompensatory mechanism for homeostatic blood pressure regulation in Ephx2 gene-disrupted miceDynamic proteomics in individual human cells uncovers widespread cell-cycle dependence of nuclear proteinsMdm4 (Mdmx) regulates p53-induced growth arrest and neuronal cell death during early embryonic mouse development.A novel ubiquitin-binding protein ZNF216 functioning in muscle atrophyThe glomuvenous malformation protein Glomulin binds Rbx1 and regulates cullin RING ligase-mediated turnover of Fbw7The double-histone-acetyltransferase complex ATAC is essential for mammalian developmentProteinuria and perinatal lethality in mice lacking NEPH1, a novel protein with homology to NEPHRINDwarfism and impaired gut development in insulin-like growth factor II mRNA-binding protein 1-deficient micePhenotype microarrays for high-throughput phenotypic testing and assay of gene functionLong noncoding RNAs in mouse embryonic stem cell pluripotency and differentiationAbnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6)Insulin-degrading enzyme regulates the levels of insulin, amyloid beta-protein, and the beta-amyloid precursor protein intracellular domain in vivoGene trap mutagenesis of hnRNP A2/B1: a cryptic 3' splice site in the neomycin resistance gene allows continued expression of the disrupted cellular geneGenerating and manipulating transgenic animals using transposable elementsDiscovery of mammalian genes that participate in virus infectionGene trap and gene inversion methods for conditional gene inactivation in the mouseSuppression of nonsense-mediated mRNA decay permits unbiased gene trapping in mouse embryonic stem cellsGene trapping identifies transiently induced survival genes during programmed cell deathLoss of the cytoskeletal protein Pdlim7 predisposes mice to heart defects and hemostatic dysfunctionDab2IP GTPase activating protein regulates dendrite development and synapse number in cerebellumLoss of the putative catalytic domain of HDAC4 leads to reduced thermal nociception and seizures while allowing normal bone developmentRhoE deficiency produces postnatal lethality, profound motor deficits and neurodevelopmental delay in miceMonoamine metabolism and behavioral responses to ethanol in mitochondrial aldehyde dehydrogenase knockout mice.Creation of genome-wide protein expression libraries using random activation of gene expressionLipid-lowering effects of anti-angiopoietin-like 4 antibody recapitulate the lipid phenotype found in angiopoietin-like 4 knockout miceInsertional mutagenesis in mice: new perspectives and toolsCharacterization of PTPRG in knockdown and phosphatase-inactive mutant mice and substrate trapping analysis of PTPRG in mammalian cellsKeratinocyte migration in the developing eyelid requires LIMK2Loss of ASP but not ROPN1 reduces mammalian ciliary motilityMurine UDP-GlcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase lacking the gamma-subunit retains substantial activity toward acid hydrolasesMitoNEET is an iron-containing outer mitochondrial membrane protein that regulates oxidative capacityA stabilizing factor for mitochondrial respiratory supercomplex assembly regulates energy metabolism in muscleTissue-dependent loss of phosphofructokinase-M in mice with interrupted activity of the distal promoter: impairment in insulin secretionAblation of mouse phosphomannose isomerase (Mpi) causes mannose 6-phosphate accumulation, toxicity, and embryonic lethalityCa2+ Activation kinetics of the two aspartate-glutamate mitochondrial carriers, aralar and citrin: role in the heart malate-aspartate NADH shuttleDisruption of forkhead transcription factor (FOXO) family members in mice reveals their functional diversificationADP-ribosylation factor-like 3 is involved in kidney and photoreceptor development
P2860
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P2860
Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells.
description
1998 nî lūn-bûn
@nan
1998 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells.
@ast
Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells.
@en
type
label
Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells.
@ast
Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells.
@en
prefLabel
Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells.
@ast
Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells.
@en
P2093
P356
P1433
P1476
Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells.
@en
P2093
Friedrich GA
Lilleberg SL
Zambrowicz BP
P2888
P304
P356
10.1038/33423
P407
P577
1998-04-01T00:00:00Z
P6179
1005145915