About: Nenad Blau

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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	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) باحت (ary) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq)
rdfs:label	Nenad Blau (en) Nenad Blau (es) Nenad Blau (it) Nenad Blau (nl) Nenad Blau (sl) Nenad Blau (ast)
skos:prefLabel	Nenad Blau (en) Nenad Blau (es) Nenad Blau (it) Nenad Blau (nl) Nenad Blau (sl) Nenad Blau (ast)
name	Nenad Blau (en) Nenad Blau (es) Nenad Blau (it) Nenad Blau (nl) Nenad Blau (sl) Nenad Blau (ast)
given name	wds:Q42323607-54B7153A-DD75-47B1-BB4A-33607F2B6E30
given name	Nenad
instance of	wds:Q42323607-076275D9-4435-405F-96F6-5E6D2AD15917
instance of	Homo sapiens
Nationale Thesaurus voor Auteursnamen ID	wds:Q42323607-956c6c6d-2d15-4ba4-9c9b-64bb1e1f63b2
occupation	wds:Q42323607-181EA84E-23E1-4889-94F1-024FF359E13B
NUKAT ID	wds:Q42323607-D72F43EB-C192-4263-8CCC-6C0BDB86D3D2
sex or gender	wds:Q42323607-D0647DC6-2BEC-4480-8D28-48A216238A80
ISNI	wds:Q42323607-7F6B70E9-C4FB-448A-9C53-94AF5F96E839
VIAF ID	wds:Q42323607-978BE52B-5255-4381-9C2F-82A0B00F33B9
GND ID	wds:Q42323607-ae95d592-f7e1-41ef-a817-9b12c3ac101e
Library of Congress authority ID	wds:Q42323607-90A874AB-C60B-45AA-852C-60CA8B7D7FF3
IdRef ID	wds:Q42323607-9B969A82-44C1-49C4-B2FC-5DDA5246581A
SBN author ID	wds:Q42323607-A6ED6666-7041-4104-8A40-634709D77935
date of birth	wds:Q42323607-4597A4EA-BFE2-49D1-BAED-9013AD11299B
family name	wds:Q42323607-22F99658-6F02-47FC-9259-3F4DCCFBE38E
WorldCat Identities ID (superseded)	wds:Q42323607-AE33D278-9A09-4BFF-92CD-382DDC3911EC
Nationale Thesaurus voor Auteursnamen ID	http://data.bibliotheken.nl/id/thes/p341433705
VIAF ID	http://viaf.org/viaf/112959702
GND ID	https://d-nb.info/gnd/11474632X
Library of Congress authority ID	http://id.loc.gov/authorities/names/n87864896
IdRef ID	http://www.idref.fr/031774008/id
Nationale Thesaurus voor Auteursnamen ID	341433705
occupation	researcher
NUKAT ID	n2009701430
sex or gender	male
ISNI	0000000109368854
VIAF ID	112959702
GND ID	11474632X
Library of Congress authority ID	n87864896
IdRef ID	031774008
SBN author ID	CAGV622204
date of birth	2000-01-01 00:00:00Z (xsd:dateTime)
family name	Blau
WorldCat Identities ID (superseded)	lccn-n87864896
ORCID iD	wds:Q42323607-3776C6E4-4615-4E96-9D5C-E0F89542509C
ORCID iD	https://orcid.org/0000-0003-4347-3230
ORCID iD	0000-0003-4347-3230
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42323607
is author of	Reduced folate transport to the CNS in female Rett patients Nuclear localization of tetrahydrobiopterin biosynthetic enzymes 7-substituted pterins in humans with suspected pterin-4a-carbinolamine dehydratase deficiency. Mechanism of formation via non-enzymatic transformation from 6-substituted pterins Efficacy of oral citrate administration in primary hyperoxaluria Tetrahydrobiopterin is a secretory product of murine vascular endothelial cells. Phenylalanine hydroxylase-stimulating protein/pterin-4 alpha-carbinolamine dehydratase from rat and human liver. Purification, characterization, and complete amino acid sequence Expression and characterization of recombinant human and rat liver 6-pyruvoyl tetrahydropterin synthase. Modified cysteine residues inhibit the enzyme activity Pyridoxal phosphate-responsive seizures in a patient with cerebral folate deficiency (CFD) and congenital deafness with labyrinthine aplasia, microtia and microdontia (LAMM). GTP cyclohydrolase I deficiency, a new enzyme defect causing hyperphenylalaninemia with neopterin, biopterin, dopamine, and serotonin deficiencies and muscular hypotonia. Increase of GTP cyclohydrolase I activity in mononuclear blood cells by stimulation: detection of heterozygotes of GTP cyclohydrolase I deficiency Hyperphenylalaninaemia presumably due to carbinolamine dehydratase deficiency: loading tests with pterin derivatives Suspected pterin-4a-carbinolamine dehydratase deficiency: hyperphenylalaninaemia due to inhibition of phenylalanine hydroxylase by tetrahydro-7-biopterin Diagnosis of dopa-responsive dystonia and other tetrahydrobiopterin disorders by the study of biopterin metabolism in fibroblasts. Gene expression profiling of inflamed human endothelial cells and influence of activated protein C. Pathogenesis of cognitive dysfunction in phenylketonuria: review of hypotheses. Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene Tetrahydrobiopterin biosynthesis, regeneration and functions Critical role of interleukin-1beta for transcriptional regulation of endothelial 6-pyruvoyltetrahydropterin synthase Regulation of the L-arginine-dependent and tetrahydrobiopterin-dependent biosynthesis of nitric oxide in murine macrophages Mitochondrial complex I encephalomyopathy and cerebral 5-methyltetrahydrofolate deficiency Cerebral folate deficiency with developmental delay, autism, and response to folinic acid Mitochondrial diseases associated with cerebral folate deficiency. Purification and characterization of 6-pyruvoyl tetrahydropterin synthase from human pituitary gland. 6-pyruvoyl tetrahydropterin synthase from salmon liver: amino acid sequence analysis by tandem mass spectrometry

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