About: David A Stumpf

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	Forscher (de) forskare (sv) ikertzailea (eu) researcher (en) ricercatore (it) 研究者 (ja) investigador (es) chercheur (fr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) باحت (ary) изилдөөчү (ky) 研究者 (zh)
rdfs:label	David A Stumpf (en) Stumpf DA (es) Stumpf DA (nl) Stumpf DA (ast)
skos:prefLabel	David A Stumpf (en) Stumpf DA (es) Stumpf DA (nl) Stumpf DA (ast)
name	David A Stumpf (en) Stumpf DA (es) Stumpf DA (nl) Stumpf DA (ast)
given name	wds:Q67426880-3A81C812-DEC7-4F62-95DF-13078E2CF4A4
given name	David
instance of	wds:Q67426880-FCC8724D-B9A7-4143-A849-5B7F1B72D238
instance of	Homo sapiens
skos:altLabel	DA Stumpf (en) David Stumpf (en)
occupation	wds:Q67426880-779F38B6-8C21-4D3B-9276-B51D824FF8DA
employer	wds:Q67426880-A2133964-72D2-4117-875E-5E950592F7DB
sex or gender	wds:Q67426880-43AFBA23-3562-4356-AAA8-7CAB0D14406D
on focus list of Wikimedia project	wds:Q67426880-4d2745f6-4e17-fa24-5f09-a1023cc91469
educated at	wds:Q67426880-1228C925-1E66-4BCF-A78A-213195C9DF65 wds:Q67426880-36587F48-BA07-4416-8E61-BBA610817DCE wds:Q67426880-4E468FA6-62F5-4241-85B4-30861100BB6C wds:Q67426880-7F4370BD-F495-4200-A04F-FA696B726B76
family name	wds:Q67426880-24ED9C31-3A82-4D70-AF84-9638393FC53E
occupation	researcher
employer	Northwestern University
sex or gender	male
on focus list of Wikimedia project	WikiProject PCC Wikidata Pilot/Northwestern University Libraries
educated at	University of Colorado Boulder Oregon Health & Science University University of Colorado Denver Lewis & Clark College
family name	Stumpf
ORCID iD	wds:Q67426880-C01B43D9-339C-4877-B2B1-92DA45FDC2B8
ORCID iD	https://orcid.org/0000-0002-5101-0693
ORCID iD	0000-0002-5101-0693
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q67426880
is author of	Propionate inhibition of succinate:CoA ligase (GDP) and the citric acid cycle in mitochondria Adrenoleukodystrophy. Failure of immunosuppression to prevent neurological progression Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiency Isolated vitamin E deficiency in the absence of fat malabsorption--familial and sporadic cases: characterization and investigation of causes Friedreich's disease: V. Variant form with vitamin E deficiency and normal fat absorption Glutaric acidemia type II: clinical, biochemical, and morphologic considerations Inhibitory effects of sodium valproate on oxidative phosphorylation Carnitine deficiency, organic acidemias, and Reye's syndrome Lipoamide dehydrogenase deficiency with primary lactic acidosis: favorable response to treatment with oral lipoic acid Human mitochondrial electron transport chain: assay of succinate: cytochrome c reductase in leukocytes, platelets and cultured fibroblasts Studies in globoid (Krabbe) leukodystrophy (GLD). V. Controlled enzymic studies in ten human cases. B- and T-cell markers in opsoclonus-myoclonus syndrome: immunophenotyping of CSF lymphocytes. L-carnitine reduces brain injury after hypoxia-ischemia in newborn rats Effects of octanoate on rat brain and liver mitochondria. Metachromatic leukodystrophy (MLD). 8. MLD in adults; diagnosis and pathogenesis Metachromatic leukodystrophy (MLD). IX. Qualitative and quantitative differences in urinary arylsulfatase A in different forms of MLD Phenotypic heterogeneity in the syndromes of 3-methylglutaconic aciduria Organic Acid contents of soybean: age and source of nitrogen Subcellular distribution of two enzyme systems which degrade 3'-phosphoadenosine 5'-phosphosulfate ("active sulfate") A mechanism of toxicity of isovaleric acid in rat liver mitochondria Brain mitochondrial metabolism in experimental thiamine deficiency. A monospecific antibody to human sulfatase A. Preparation, characterization and significance Friedreich ataxia: III. Mitochondrial malic enzyme deficiency. Loosely coupled mitochondrial oxidative phosphorylation induced by protoporphyrin Propionate mitochondrial toxicity in liver and skeletal muscle: acyl CoA levels Friedreich's ataxia: I. Normal pyruvate dehydrogenase complex activity in platelets Werdnig Hoffman's disease (spinal muscular atrophy type I): A clinical study of 25 Saudi nationals in Al-Khobar Friedreich ataxia. II. Normal kinetics of lipoamide dehydrogenase Friedreich's disease: IV. Reduced mitochondrial malic enzyme activity in heterozygotes Biosynthesis of malonate in roots of soybean seedlings Carnitine deficiency with valproate therapy Ribulose 1,5-bisphosphate and activation of the carboxylase in the chloroplast Symptoms of B(12) deficiency can occur in women of childbearing age supplemented with folate. Aspartate kinase 2. A candidate gene of a quantitative trait locus influencing free amino acid content in maize endosperm Urea cycle regulation: I. Coupling of ornithine metabolism to mitochondrial oxidative phosphorylation Systemic lymphoma mimicking acute disseminated encephalomyelitis Acute ataxia Immunological studies of sulfatase A in normals and in metachromatic leukodystrophy The treatment of obesity The effect of malate on propionate mitochondrial toxicity. A micromethod for the purification and quantification of organic acids of the tricarboxylic acid cycle in plant tissues Radar systems Metachromatic leukodystrophy (MLD). X. Immunological studies of the abnormal sulfatase A Seizures, anticonvulsants, and pregnancy

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