About: Mild inborn errors of metabolism in commonly used inbred mouse strains

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scientific article published on 24 January 2019

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rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2019 (fr) artículu científicu espublizáu en xineru de 2019 (ast) im April 2019 veröffentlichter wissenschaftlicher Artikel (de) наукова стаття, опублікована у квітні 2019 (uk) scientific article published on 24 January 2019 (en)
publication date	wds:Q64117220-29026E97-2354-454C-A119-592086242781
publication date	2019-01-24 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q64117220-8013A6D0-9A60-463F-9E23-DC96BA154587
language of work or name	English
cites work	wds:Q64117220-1750D9C1-1C10-4516-AE75-CCEBF2339DCE wds:Q64117220-1A7B3549-C1D6-4716-9930-721FFA456EB6 wds:Q64117220-1AE551D1-3DD0-4A91-B8FE-9DE1DCAD7D93 wds:Q64117220-270695D9-131D-48B9-B206-BB99AC4FB91A wds:Q64117220-29C03DEC-2BC4-481D-BEED-9189C1A6B1A9 wds:Q64117220-2C3A8D92-643B-4E71-B6D9-44024E94A850 wds:Q64117220-2D80A07B-B790-4FA9-8BE9-1294CC8F1509 wds:Q64117220-38124E9E-E3B4-46C0-A544-C097E47A79AF wds:Q64117220-3DF160B5-AEB4-416F-82B4-C06CCF3246C8 wds:Q64117220-411BDC13-1B0A-45E6-9197-C1F5433A767C wds:Q64117220-47E1F2E2-F85E-4279-A0CB-7BF348199B59 wds:Q64117220-530954EC-8077-4D99-A408-0ABA984D0753 wds:Q64117220-5A5F83E6-CF0C-4F3C-A535-AB6B24354B91 wds:Q64117220-6089FCE0-CCD3-4D2A-B59C-235C49B04F94 wds:Q64117220-6110B579-C109-47A3-8F04-1DADD281348E wds:Q64117220-61AA41DE-1BE2-42CA-A390-2F588A05C4F3 wds:Q64117220-6984F094-1B59-418A-A95A-628CD6EDE70A wds:Q64117220-6BE430AD-E8C2-4C8E-895D-ADDA7FDFC8F9 wds:Q64117220-71E5A5C2-43DC-45F8-8F83-430929657065 wds:Q64117220-78DC7031-E44C-429B-8929-7C95BBA37793 wds:Q64117220-7B1C460F-B23F-4633-AED5-B9A95F6660A7 wds:Q64117220-7DE1D9A1-AB9F-4B06-99BC-7FA00BE33E18 wds:Q64117220-8229BD92-AF29-40B6-AE04-8B6BB20D4733 wds:Q64117220-93893E08-F61D-4173-91D1-7F41C2EC1A5C wds:Q64117220-9427FC34-AB3F-40D5-9E15-1D0C21707BF9 wds:Q64117220-94AC109B-D1A0-4B02-AE98-3EB9BBDB2AE0 wds:Q64117220-952A0359-7A5E-4003-879C-F819F1FB09B2 wds:Q64117220-A8FB7807-B9B6-4F47-B8CE-9472077A44DC wds:Q64117220-B4509D57-A81A-4279-93F0-E9974E0EF2EC wds:Q64117220-C4857569-50E9-49AC-8AA3-CFE991355CCC wds:Q64117220-CB08D669-9B50-4D33-BEAF-65BF5455A34D wds:Q64117220-D10BD74F-C5D9-4AF3-B66D-38B0D0E990B7 wds:Q64117220-D6253628-3DB0-4C1C-8D0A-5F29537B3D10 wds:Q64117220-DF932F9E-3DD8-4DF7-A0D0-1A0FDF1619FF wds:Q64117220-E30780F5-5B45-4415-BE7A-49B7616A4345 wds:Q64117220-E5A32154-611D-4B87-B85D-D6C58E4CC0E8 wds:Q64117220-E7ECE3D9-9BEA-4D11-9C12-4732A76EAFED wds:Q64117220-EADCED29-5DA0-45DC-A3A3-7A5A33758D61 wds:Q64117220-EE0A8408-315F-4826-BA18-B93074559FC5 wds:Q64117220-F61BAD11-080D-4790-84B3-BBCFAAB2993A wds:Q64117220-F9706ED9-4E1C-45C1-A5AD-E1911A656C2C wds:Q64117220-FD1EBD38-22F8-44C5-A08F-83A83D5BA8F8
cites work	Mouse genomic variation and its effect on phenotypes and gene regulation Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome The genomic landscape shaped by selection on transposable elements across 18 mouse strains Positional cloning of the mouse obese gene and its human homologue Obese, a new mutation in the house mouse Sequence-based characterization of structural variation in the mouse genome Molecular heterogeneity of variant isovaleryl-CoA dehydrogenase from cultured isovaleric acidemia fibroblasts Retroviral elements and their hosts: insertional mutagenesis in the mouse germ line Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter Mobile elements: drivers of genome evolution The Convergence of Systems and Reductionist Approaches in Complex Trait Analysis Systems genetics of metabolism: the use of the BXD murine reference panel for multiscalar integration of traits Multilayered genetic and omics dissection of mitochondrial activity in a mouse reference population DHTKD1 mutations cause 2-aminoadipic and 2-oxoadipic aciduria Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice Integrative genomics viewer Regulation of Mouse Retroelement MuERV-L/MERVL Expression by REX1 and Epigenetic Control of Stem Cell Potency Murine endogenous retroviruses Null allele at Bcd-1 locus in BALB/cByJ mice is due to a deletion in the short-chain acyl-CoA dehydrogenase gene and results in missplicing of mRNA STAR: ultrafast universal RNA-seq aligner Conserved cysteine to serine mutation in tyrosinase is responsible for the classical albino mutation in laboratory mice Supercomplex assembly determines electron flux in the mitochondrial electron transport chain Isovaleric acidemia: new aspects of genetic and phenotypic heterogeneity Systems proteomics of liver mitochondria function A rapid, sensitive method for quantitative analysis of underivatized amino acids by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Genetic modifiers of the phenotype of mice deficient in mitochondrial superoxide dismutase. Mouse phenogenomics: the fast track to "systems metabolism". Untargeted Metabolome Quantitative Trait Locus Mapping Associates Variation in Urine Glycerate to Mutant Glycerate Kinase Defining the consequences of genetic variation on a proteome-wide scale. Variant maple syrup urine disease (MSUD)--the entire spectrum. Phylogenetic and DNA methylation analysis reveal novel regions of variable methylation in the mouse IAP class of transposons Simultaneous detection of lysine metabolites by a single LC-MS/MS method: monitoring lysine degradation in mouse plasma. Mouse lysine catabolism to aminoadipate occurs primarily through the saccharopine pathway; implications for pyridoxine dependent epilepsy (PDE). Metabolomic analysis of normal (C57BL/6J, 129S1/SvImJ) mice by gas chromatography-mass spectrometry: detection of strain and gender differences. Genetic basis of alpha-aminoadipic and alpha-ketoadipic aciduria New Cases of DHTKD1 Mutations in Patients with 2-Ketoadipic Aciduria Elevated glutaric acid levels in Dhtkd1-/Gcdh- double knockout mice challenge our current understanding of lysine metabolism Diet, Genetics, and the Gut Microbiome Drive Dynamic Changes in Plasma Metabolites. Identification and characterization of Eci3, a murine kidney-specific Δ3,Δ2-enoyl-CoA isomerase Mind your mouse strain Bioinformatic analysis of TE-spliced new exons within human, mouse and zebrafish genomes
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