About: Stefania Corti

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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) গবেষক (bn) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідниця (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtuese (sq) ricercatrice (it)
rdfs:label	Stefania Corti (en) Stefania Corti (es) Stefania Corti (it) Stefania Corti (nl) Stefania Corti (sl) Stefania Corti (ast)
skos:prefLabel	Stefania Corti (en) Stefania Corti (es) Stefania Corti (it) Stefania Corti (nl) Stefania Corti (sl) Stefania Corti (ast)
name	Stefania Corti (en) Stefania Corti (es) Stefania Corti (it) Stefania Corti (nl) Stefania Corti (sl) Stefania Corti (ast)
Scopus author ID	wds:Q42624238-54EB9F17-A5AF-4D2D-A8A5-44D826BE6545
Scopus author ID	7003759380
given name	wds:Q42624238-392098D2-C233-461B-AA20-977034D94C50
given name	Stefania
instance of	wds:Q42624238-9600BA19-470F-44A0-A740-AEFF67E36A5C
instance of	Homo sapiens
occupation	wds:Q42624238-98DA43C1-E754-476D-AE01-E5DC2AE2929F
employer	wds:Q42624238-2CB27B08-3F88-4A1B-A28F-41CA9354B6CA wds:Q42624238-4086CE05-1B64-4A2B-B3AE-E076589BB935 wds:Q42624238-82E69169-8371-433E-A107-14BAD75A33D7 wds:Q42624238-8FF8F15E-09B6-47B4-9F10-BE48E61E63A8
place of birth	wds:Q42624238-dc3d974d-413f-6f88-626c-e6574f9c7327
sex or gender	wds:Q42624238-38997141-D5E2-40A8-B0CB-0FD04812370D
VIAF ID	wds:Q42624238-51C5E2CB-110C-4FE5-85D8-AF7E62719600
SBN author ID	wds:Q42624238-B28247A4-B2FE-4764-8AAD-767C6B0C82E2
date of birth	wds:Q42624238-5D324900-1F7F-49F4-B765-2613BE839BDC
educated at	wds:Q42624238-3EDDE96C-91B5-4EA5-A6DD-E7BA6F19DC38 wds:Q42624238-6538FC17-2545-4492-87C2-19344AD1642A wds:Q42624238-7ECA7A46-C4AA-4C21-B4A2-0B61EBB65B24
family name	wds:Q42624238-0A94C033-B316-4B5C-A2E2-85858D0CF340
WorldCat Identities ID (superseded)	wds:Q42624238-D8FB4D9D-FA67-4796-A6C0-B9F0698D0E66
VIAF ID	http://viaf.org/viaf/307337310
occupation	researcher
employer	Department of Mathematics "Federigo Enriques" Ospedale Maggiore Policlinico
place of birth	Milan
sex or gender	female organism
VIAF ID	307337310
SBN author ID	CFIV253833
date of birth	1972-06-15 00:00:00Z (xsd:dateTime)
educated at	Department of Mathematics "Federigo Enriques"
family name	Corti
WorldCat Identities ID (superseded)	viaf-307337310
ORCID iD	wds:Q42624238-E00FC226-3F53-41AB-9C4F-904B95F074F9
ORCID iD	https://orcid.org/0000-0001-5425-969X
ORCID iD	0000-0001-5425-969X
PubliCatt author ID	wds:Q42624238-C532009F-1210-4DCE-A519-94FFA85A059D
PubliCatt author ID	18902
ResearcherID	wds:Q42624238-9A6707B6-BCE1-4594-B3E7-9FC51C4B8E83
Publons author ID	wds:Q42624238-59d725ca-5f45-4679-a50a-d64944e0a5d8
ResearcherID	K-6034-2016
Publons author ID	2239625
Aisberg author ID	wds:Q42624238-68196D19-5533-4496-9A2B-B1EF33535BC5
Aisberg author ID	01273
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42624238
is author of	Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophy Embryonic stem cell-derived neural stem cells improve spinal muscular atrophy phenotype in mice. Motoneuron Transplantation Rescues the Phenotype of SMARD1 (Spinal Muscular Atrophy with Respiratory Distress Type 1) Antisense oligonucleotide therapy for the treatment of C9ORF72 ALS/FTD diseases. The wide spectrum of clinical phenotypes of spinal muscular atrophy with respiratory distress type 1: a systematic review Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study Mutational analysis of COQ2 in patients with MSA in Italy A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations. Transplanted ALDHhiSSClo neural stem cells generate motor neurons and delay disease progression of nmd mice, an animal model of SMARD1. Fas small interfering RNA reduces motoneuron death in amyotrophic lateral sclerosis mice. Genetic correction of human induced pluripotent stem cells from patients with spinal muscular atrophy A subpopulation of murine bone marrow cells fully differentiates along the myogenic pathway and participates in muscle repair in the mdx dystrophic mouse Skeletal muscle differentiation potential of human adult bone marrow cells Stem cell therapy in stroke. The mitochondrial disulfide relay system protein GFER is mutated in autosomal-recessive myopathy with cataract and combined respiratory-chain deficiency Direct reprogramming of human astrocytes into neural stem cells and neurons. Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients Neural stem cells LewisX+ CXCR4+ modify disease progression in an amyotrophic lateral sclerosis model. Isolation and characterization of murine neural stem/progenitor cells based on Prominin-1 expression. Identification of a primitive brain-derived neural stem cell population based on aldehyde dehydrogenase activity.

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