Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse. - Wikidata - awgldk - TriplyDB

Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse.

Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse.

http://www.wikidata.org/entity/Q43758997

about

Mitochondrial 2,4-dienoyl-CoA reductase deficiency in mice results in severe hypoglycemia with stress intolerance and unimpaired ketogenesis Fetal fatty acid oxidation disorders, their effect on maternal health and neonatal outcome: impact of expanded newborn screening on their diagnosis and management A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency Medium-chain acyl-CoA dehydrogenase deficiency in gene-targeted mice A general introduction to the biochemistry of mitochondrial fatty acid β-oxidation Mitochondrial dysfunction in fatty acid oxidation disorders: insights from human and animal studies Mitochondrial long chain fatty acid beta-oxidation in man and mouse Mitochondrial dysfunction due to long-chain Acyl-CoA dehydrogenase deficiency causes hepatic steatosis and hepatic insulin resistance Cardiac hypertrophy in mice with long-chain acyl-CoA dehydrogenase or very long-chain acyl-CoA dehydrogenase deficiency SIRT3 regulates mitochondrial fatty-acid oxidation by reversible enzyme deacetylation Carnitine supplementation attenuates myocardial lipid accumulation in long-chain acyl-CoA dehydrogenase knockout mice Mitochondrial protein acetylation is driven by acetyl-CoA from fatty acid oxidation Long-chain acyl-CoA dehydrogenase deficiency as a cause of pulmonary surfactant dysfunction Carnitine content and expression of mitochondrial beta-oxidation enzymes in placentas of wild-type (OCTN2(+/+)) and OCTN2 Null (OCTN2(-/-)) Mice Human acyl-CoA dehydrogenase-9 plays a novel role in the mitochondrial beta-oxidation of unsaturated fatty acids.Dynamic simulations on the mitochondrial fatty acid beta-oxidation network.Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.CARNITINE HOMEOSTASIS, MITOCHONDRIAL FUNCTION, AND CARDIOVASCULAR DISEASE.Mitochondrial fatty acid oxidation disorders: pathophysiological studies in mouse models Mouse models for disorders of mitochondrial fatty acid beta-oxidation.Plasma fatty acids as diagnostic markers in autistic patients from Saudi Arabia.Recombinant adeno-associated virus-mediated gene delivery of long chain acyl coenzyme A dehydrogenase (LCAD) into LCAD-deficient mice Dietary fat impacts fetal growth and metabolism: uptake of chylomicron remnant core lipids by the placenta.Prolonged QT interval and lipid alterations beyond β-oxidation in very long-chain acyl-CoA dehydrogenase null mouse hearts.Mitochondrial beta-oxidation.Acadl-SNP based genotyping assay for long-chain acyl-CoA dehydrogenase deficient mice Aortic wall proteomic analysis in spontaneously hypertensive rats with a blood pressure decrease induced by 6-week load-free swimming.Cell and gene therapy for genetic diseases: inherited disorders affecting the lung and those mimicking sudden infant death syndrome Anaplerotic treatment of long-chain fat oxidation disorders with triheptanoin: Review of 15 years Experience Homozygous carnitine palmitoyltransferase 1b (muscle isoform) deficiency is lethal in the mouse Genetic interactions among Idd3, Idd5.1, Idd5.2, and Idd5.3 protective loci in the nonobese diabetic mouse model of type 1 diabetes.Increased expression of fatty acid synthase and acetyl-CoA carboxylase in the prefrontal cortex and cerebellum in the valproic acid model of autism Sensitivity of lipid metabolism and insulin signaling to genetic alterations in hepatic peroxisome proliferator-activated receptor-gamma coactivator-1alpha expression Metabolism as a complex genetic trait, a systems biology approach: implications for inborn errors of metabolism and clinical diseases Hepatic triacylglycerol accumulation and insulin resistance.Brain-specific carnitine palmitoyl-transferase-1c: role in CNS fatty acid metabolism, food intake, and body weight Low expression of long-chain acyl-CoA dehydrogenase in human skeletal muscle Fatty acid oxidation and meiotic resumption in mouse oocytes Very long-chain acyl-CoA dehydrogenase (VLCAD-) deficiency-studies on treatment effects and long-term outcomes in mouse models.Biochemical correction of very long-chain acyl-CoA dehydrogenase deficiency following adeno-associated virus gene therapy.

P2860

Q21563343-99E3A3E2-3293-4E07-9988-49D325F1E795 Q24616340-2A84EC1C-6B49-4774-817A-981E0FD4BA5D Q24676560-6F0055FB-5F23-4D7D-A611-11654274796D Q24814997-D0694A25-FCEB-4BD5-B67E-1F9FC8F3DE32 Q26699142-C69C2126-8DF6-482A-9958-7518C1F28DDA Q28085600-23C25B17-3A37-442D-8B84-F50934693647 Q28246062-16347B64-3DD6-49B0-BD52-2019121BF96C Q28253498-3F70AB10-9C10-4240-83B3-1290DA8E0076 Q28257772-E00AB982-BED9-467A-B66E-7B5942050C41 Q28275010-4D38B3C3-E114-4E1C-A0D2-2B8848C44B1C Q28288565-226A1B72-327D-4386-8E0A-C2B05F3CFCA1 Q28307555-2A72A76A-A1AE-42F4-93F0-A028594DA734 Q28308215-7AA3F26E-9B1E-4609-BA95-A17BFF7B40EF Q28507159-FA978FBA-9842-4EFD-AB6B-8A3950A55A1C Q33219567-65B4B8EB-37E9-4AB7-B67C-7172DDFAE044 Q33397846-DE56578B-028D-44EE-A45E-DD4BD8F33D08 Q33617698-4C51BBB0-0B04-4308-8A37-3086ADCFD91A Q34002504-030EC70D-E3A5-4ABC-B14B-E6EA998DCF42 Q34163820-78A5FE54-0026-4121-BFDA-05CF55CFE521 Q34578754-2EA45B88-3012-489F-B5D6-86D31027C9D9 Q35023635-9AF2A7A7-FDF5-43B5-A52E-14239FAA6CD0 Q35055915-6AE7630D-9E85-4F97-9620-7F3AC6C3BF97 Q35159373-0DDB4E60-6C73-4A66-BA9F-106161618084 Q35315061-30DBE6C3-5E40-405F-8BEF-3FC1824C462C Q35631612-341FD269-72B4-4D8D-9CD2-B2971FBDFBDE Q35911338-0986A88E-0C66-4CC7-BA5E-59F7465005E1 Q35948057-3346775C-C77D-4CF8-9EA8-7C4A06B66CCB Q36084447-4ACBF711-A70B-4ECA-8B54-22C138466B5B Q36461753-B07DAB02-9614-4FDB-B43F-45C92D89809A Q36501934-13086302-979E-4E68-A17E-6B73A81D961A Q36718178-CE6B98EE-AD61-4341-8CAD-722649A887A9 Q37204659-99E8EF52-64B4-4099-9AD5-91FBAD214DE3 Q37236343-336F7E23-50BB-47D3-A20C-C267671B2ACC Q37287373-3503E80A-873A-477A-9098-598BFF2983A9 Q37321860-742052D3-A0B7-433E-87B2-760F575AC3FB Q37465084-CCC0E52D-DA50-4BC2-9425-ED2E102FA34C Q37682615-3E6A2BA9-1486-4156-A7EE-3D4A2C1F7103 Q37716335-A405812F-4FAB-4839-B035-F18B48DBB0B7 Q39155672-EB27087C-DD9B-4E45-A082-0148C983CB93 Q39504973-A75D3FF9-6AC1-4BE8-8AAE-4B42176E7405

P2860

Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse.

http://www.wikidata.org/entity/Q43758997

description

2001 nî lūn-bûn

@nan

2001年の論文

@ja

2001年学术文章

@wuu

2001年学术文章

@zh-cn

2001年学术文章

@zh-hans

2001年学术文章

@zh-my

2001年学术文章

@zh-sg

2001年學術文章

@yue

2001年學術文章

@zh

2001年學術文章

@zh-hant

name

Gestational, pathologic and bi ...... enase deficiency in the mouse.

@en

Gestational, pathologic and bi ...... enase deficiency in the mouse.

@nl

type

label

Gestational, pathologic and bi ...... enase deficiency in the mouse.

@en

Gestational, pathologic and bi ...... enase deficiency in the mouse.

@nl

prefLabel

Gestational, pathologic and bi ...... enase deficiency in the mouse.

@en

Gestational, pathologic and bi ...... enase deficiency in the mouse.

@nl

P1433

Q43758997-55333352-9781-49E7-845D-CAD0E2747834

P1476

Q43758997-C4F6891C-E49C-4E6D-BC38-7489CABB8421

P2093

Q43758997-1EA73F4A-BDFE-4029-B9CF-481D11971A68

Q43758997-341031F8-BDF8-4EB8-BDB2-46C4B49EF342

Q43758997-3D47BB64-E101-4F46-AFF5-1E7FB9DAE93B

Q43758997-4BECF773-50EC-44D0-B039-AB2281178A25

Q43758997-5D845022-F46F-44B9-9745-909181CF70D7

Q43758997-959C94DB-AD62-41DA-8510-7A631AFFCC32

Q43758997-98300ECA-4BA4-4D29-AA84-E664F986A98B

Q43758997-D81D0C88-9449-4AE8-BF0F-D10BA9323BE4

Q43758997-E3988EA5-531B-4F8C-83E5-89E2F09B43B4

Q43758997-E5DC662F-F9CC-4F23-A853-FF469176A0DA

P304

Q43758997-0A7A527A-E607-4341-A186-B578958D93CA

P31

Q43758997-34512F8D-290B-43B3-9DCD-E860238F3E25

P356

Q43758997-7AF6AE66-E7ED-4E58-B22D-AADD49428BF9

P433

Q43758997-946A4BF4-19FE-4A5C-AF24-42D38ACBAE0E

P478

Q43758997-AF0A351B-5F31-48F8-B267-2B1D72A6267C

P577

Q43758997-50B65541-F7D6-4C81-BE82-EEBFA9A8EAA1

P698

Q43758997-61274061-B7A3-4286-99C2-1C19A317DD19

P921

Q43758997-FBCC5A67-4C30-4861-936B-798D1F2AC924

P356

P1433

Human Molecular Genetics

P1476

Gestational, pathologic and bi ...... enase deficiency in the mouse.

@en

P2093

Cox KB

http://www.w3.org/2001/XMLSchema#string

Hamm DA

http://www.w3.org/2001/XMLSchema#string

Lindsey JR

http://www.w3.org/2001/XMLSchema#string

Matern D

http://www.w3.org/2001/XMLSchema#string

Millington DS

http://www.w3.org/2001/XMLSchema#string

Pinkert CA

http://www.w3.org/2001/XMLSchema#string

Rhead WJ

http://www.w3.org/2001/XMLSchema#string

Rinaldo P

http://www.w3.org/2001/XMLSchema#string

Vockley J

http://www.w3.org/2001/XMLSchema#string

Wood PA

http://www.w3.org/2001/XMLSchema#string

P304

2069-2077

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1093/HMG/10.19.2069

http://www.w3.org/2001/XMLSchema#string

P433

19

http://www.w3.org/2001/XMLSchema#string

P478

10

http://www.w3.org/2001/XMLSchema#string

P577

2001-09-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

11590124

http://www.w3.org/2001/XMLSchema#string

P921

very long chain acyl-CoA dehydrogenase deficiency