About: Maria Rita Passos-Bueno

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Maria Rita Passos-Bueno Goto Sponge NotDistinct Permalink

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

Brazilian geneticist, researcher and university professor

Attributes	Values
rdf:type	Item
description	Brazilian scientist (en-ca) Brazilian scientist (en-gb) científica brasilana (ast) wetenschapster uit Brazilië (nl) científica brasileña (es) عالمة برازيلية (ar) ബ്രസീലിയൻ ശാസ്ത്രജ്ഞ (ml) geneticista, pesquisadora e professora universitária brasileira (pt) geneticista, pesquisadora e professora universitária brasileira (pt-br) Brazilian geneticist, researcher and university professor (en)
rdfs:label	Maria Rita Passos-Bueno (ca) Maria Rita Passos-Bueno (en) Maria Rita Passos-Bueno (nl) Maria Rita Passos-Bueno (pt) Maria Rita Passos-Bueno (sl) Maria Rita Passos-Bueno (sq) Maria Rita Passos-Bueno (en-us) Maria Rita Passos-Bueno (pt-br) Maria Rita Passos-Bueno (ast)
skos:prefLabel	Maria Rita Passos-Bueno (ca) Maria Rita Passos-Bueno (en) Maria Rita Passos-Bueno (nl) Maria Rita Passos-Bueno (pt) Maria Rita Passos-Bueno (sl) Maria Rita Passos-Bueno (sq) Maria Rita Passos-Bueno (en-us) Maria Rita Passos-Bueno (pt-br) Maria Rita Passos-Bueno (ast)
name	Maria Rita Passos-Bueno (ca) Maria Rita Passos-Bueno (en) Maria Rita Passos-Bueno (nl) Maria Rita Passos-Bueno (pt) Maria Rita Passos-Bueno (sl) Maria Rita Passos-Bueno (sq) Maria Rita Passos-Bueno (en-us) Maria Rita Passos-Bueno (pt-br) Maria Rita Passos-Bueno (ast)
given name	wds:Q78114430-0128bfb3-475c-7346-9484-bd5d2d7c6abc
given name	Maria Rita
instance of	wds:Q78114430-6538D63D-85EB-4436-8FFF-159F5EFF4EDC
instance of	Homo sapiens
award received	wds:Q78114430-0a414834-466b-cc94-ba1c-510e8a89f657
award received	National Order of Scientific Merit
Google Knowledge Graph ID	wds:Q78114430-775F4661-DFAF-4E09-925D-35A6C4EE98BE
Google Knowledge Graph ID	http://g.co/kg/g/11fyx68yxy
Google Knowledge Graph ID	/g/11fyx68yxy
skos:altLabel	Maria Rita dos Santos e Passos Bueno (pt) Passos-Bueno, M. R. (en) Passos-Bueno, M. R. (pt) Passos-Bueno, M. R. (en-us) Passos-Bueno, M. R. (pt-br) Passos-Bueno, Maria Rita (en) Passos-Bueno, Maria Rita (pt) Passos-Bueno, Maria Rita (en-us) Passos-Bueno, Maria Rita (pt-br)
occupation	wds:Q78114430-04e48d14-4a11-e1ae-67eb-e77449b00ba1 wds:Q78114430-d0def04f-4347-6578-b267-daea15604af8
employer	wds:Q78114430-631bf7f9-4d03-3728-b934-2a1003735ac8 wds:Q78114430-E7762961-47F2-47F9-9E7F-E5763E1974FC
sex or gender	wds:Q78114430-31d60b4f-4586-8536-8524-4b0c01eb4534
country of citizenship	wds:Q78114430-d574ea16-49f0-7338-5be7-c26c0941fd90
member of	wds:Q78114430-de2a476f-41cc-7150-9417-3b335e9900f1
date of birth	wds:Q78114430-4217c07f-40d6-515c-b9d8-ebbd055ece39
educated at	wds:Q78114430-18d3e57b-4bd5-6092-c760-ba1afbf1a524
occupation	university teacher geneticist
employer	University of São Paulo Institute of Biosciences, University of São Paulo
sex or gender	female organism
country of citizenship	Brazil
member of	Brazilian Academy of Sciences
date of birth	1959-08-01 00:00:00Z (xsd:dateTime)
educated at	University of São Paulo
ORCID iD	wds:Q78114430-5e8e589a-4f3b-461b-e448-3e88c8de61d5
ORCID iD	https://orcid.org/0000-0002-9248-3008
ORCID iD	0000-0002-9248-3008
Lattes Platform number	wds:Q78114430-4fe8f883-43e7-c763-4e6d-7ea746f89ab9
Lattes Platform number	4063718580685742
ResearcherID	wds:Q78114430-E387EC46-0680-42D7-8A16-9E091D69A84C
ResearcherID	I-6796-2016
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q78114430 https://pt.wikipedia.org/wiki/Maria_Rita_Passos-Bueno
is author of	Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literature. Stem cell proliferation under low intensity laser irradiation: a preliminary study Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome) Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysis. A complex chromosomal rearrangement involving chromosomes 2, 5, and X in autism spectrum disorder. Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons RAB23 mutations in Carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesity Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin Caveolin-3 in muscular dystrophy Genetics of craniosynostosis: genes, syndromes, mutations and genotype-phenotype correlations Association of schizophrenia and Duchenne muscular dystrophy Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families. Immunofluorescence dystrophin study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal region of the protein A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12 Telethonin protein expression in neuromuscular disorders Reconstruction of large cranial defects in nonimmunosuppressed experimental design with human dental pulp stem cells

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 196 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software