About: Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death

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About: Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death Goto Sponge NotDistinct Permalink

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scientific journal article

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rdf:type	Item
description	artículu científicu espublizáu en 2001 (ast) vědecký článek publikovaný v roce 2001 (cs) 2001 թվականի հունիսին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована в червні 2001 (uk) 2001 թուականի Յունիսին հրատարակուած գիտական յօդուած (hyw) مقالة علمية (نشرت في يونيو 2001) (ar) vedecký článok (publikovaný 2001/06/01) (sk) wetenschappelijk artikel (gepubliceerd op 2001/06/01) (nl) im Juni 2001 veröffentlichter wissenschaftlicher Artikel (de) scientific journal article (en)
publication date	wds:Q28505245-D87531EB-6063-4A16-809A-76719FD7CF4C
publication date	2001-06-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28505245-D1C2F3DD-008A-450D-A039-9F1C4FFD9BF9
language of work or name	English
cites work	wds:Q28505245-0B47012A-8435-4506-9F25-AE516472527E wds:Q28505245-20257C9F-8A2A-46CA-BFB6-B8336CF1CA8D wds:Q28505245-20808EE6-49D7-4F8D-B26C-603666D1B0F4 wds:Q28505245-2E5E39ED-FDA5-4EE5-8279-557EDD0F7830 wds:Q28505245-34E96E67-8F9B-4778-A245-EBBA2C1457DC wds:Q28505245-3DE8916C-590F-4047-8ACE-F30CA003E85B wds:Q28505245-43071449-F0F7-4739-BC5D-458CF6553B22 wds:Q28505245-4BC33498-2871-4555-8C49-5A02D98C84B8 wds:Q28505245-4FF90923-58C8-4AB6-8762-C35F4DE91FD6 wds:Q28505245-580EAFAD-1DFE-49E7-9985-90EDEE8826A8 wds:Q28505245-5EAA0657-488C-4EB8-A077-2C5862A87F3B wds:Q28505245-5EACACBE-CFDE-4B08-8E2C-EA7FE50952A9 wds:Q28505245-64512A08-0D0D-47A9-866B-23C87736AD1C wds:Q28505245-AA4A6044-EBC6-4111-B6B4-67966AA90500 wds:Q28505245-B05CB6C6-E2FA-4DC3-BAF0-07351DC79885 wds:Q28505245-B7F34BD1-CDA5-4372-9A84-96903E1512FD wds:Q28505245-C37213EB-4448-44C5-8903-434922EB4021 wds:Q28505245-DAB5E1CB-4F00-4525-9200-830C64E596F1 wds:Q28505245-DC996F21-0385-4CDA-807C-307C636486C4 wds:Q28505245-E40CB85D-E364-4B1E-9725-74853398926A wds:Q28505245-E6E0E197-1C9E-4283-A366-C31058D09E7F wds:Q28505245-F0F0D547-BBAC-4599-9674-B21080AA0BC8 wds:Q28505245-F82D5F54-6E0F-4BF4-A543-0772627BE050 wds:Q28505245-FD24DF53-E061-4B9B-9A0E-B738E134E9B5
cites work	The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy Disorders of mitochondrial fatty acyl-CoA beta-oxidation Two alpha subunit donor splice site mutations cause human trifunctional protein deficiency Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women Combined enzyme defect of mitochondrial fatty acid oxidation Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenase Pregnancy and fetal long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Novel fatty acid beta-oxidation enzymes in rat liver mitochondria. II. Purification and properties of enoyl-coenzyme A (CoA) hydratase/3-hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase trifunctional protein Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction wd:Q28287645 Recognition and management of fatty acid oxidation defects: a series of 107 patients. Mild trifunctional protein deficiency is associated with progressive neuropathy and myopathy and suggests a novel genotype-phenotype correlation Mitochondrial trifunctional protein deficiency. Catalytic heterogeneity of the mutant enzyme in two patients Molecular characterization of mitochondrial trifunctional protein deficiency: formation of the enzyme complex is important for stabilization of both alpha- and beta-subunits Human trifunctional protein deficiency: A new disorder of mitochondrial fatty acid β-oridation Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children Liver disease in pregnancy and fetal fatty acid oxidation defects Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: variable expressivity of maternal illness during pregnancy and unusual presentation with infantile cholestasis and hypocalcaemia. Clinical and biochemical presentation of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency Biochemical diagnosis of fatty acid oxidation disorders by metabolite analysis of postmortem liver. Structural analysis of cDNAs for subunits of human mitochondrial fatty acid beta-oxidation trifunctional protein
author name string	wds:Q28505245-0200CD03-6CCD-405D-8B31-0DFCF456AD7B wds:Q28505245-5ED4F7C4-013C-45C1-A3A3-78285E8681AA wds:Q28505245-7EB4345F-2C78-449B-8471-4B4287396CD8 wds:Q28505245-99C7CF67-AE7F-4584-81CD-ADBE63E93B8C wds:Q28505245-A2498AB1-076E-4467-A30A-254F5F103630 wds:Q28505245-AA912710-D7C3-4026-937B-AE2F16BECC35 wds:Q28505245-B878766D-F271-4B29-8B7E-C7E6B4866FD5 wds:Q28505245-D7B67703-65A4-464E-9B64-0CDD41F9C76C wds:Q28505245-E4D1CBFA-79F8-47CC-BA85-C15C427AB569 wds:Q28505245-E9819E5B-F741-4DF3-8CC0-C3B91C47252E
OpenCitations bibliographic resource ID	wds:Q28505245-8A96D634-B6DE-45F3-80B3-E59D02A34115
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/962173
author name string	Y. Zhao M. J. Bennett A. W. Strauss H. Paul M. Cline P. Rinaldo D. Matern J. A. Ibdah K. Salleng S. Binford
OpenCitations bibliographic resource ID	962173
rdfs:label	Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death (en) Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death (nl) Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death (ast)
skos:prefLabel	Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death (en) Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death (nl) Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death (ast)
name	Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death (en) Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death (nl) Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death (ast)
title	wds:Q28505245-46919381-FAFE-42D3-B07B-954372A2E878
title	Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death (en)
page(s)	wds:Q28505245-D7C4D110-65C1-413F-8EE2-40FE26D86C3A
page(s)	1403–1409
instance of	wds:Q28505245-CD0EB266-2B2B-475F-8887-C7BA8C52346E

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