About: Fiona Francis

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

researcher and zoologist

Attributes	Values
rdf:type	Item
description	Zoologin (de) zoöloog (nl) researcher and zoologist (en)
rdfs:label	Fiona Francis (ca) Fiona Francis (de) Fiona Francis (en) Fiona Francis (es) Fiona Francis (fr) Fiona Francis (it) Fiona Francis (nl) Fiona Francis (sl) Fiona Francis (sq) Fiona Francis (sv) Fiona Francis (ast)
skos:prefLabel	Fiona Francis (ca) Fiona Francis (de) Fiona Francis (en) Fiona Francis (es) Fiona Francis (fr) Fiona Francis (it) Fiona Francis (nl) Fiona Francis (sl) Fiona Francis (sq) Fiona Francis (sv) Fiona Francis (ast)
name	Fiona Francis (ca) Fiona Francis (de) Fiona Francis (en) Fiona Francis (es) Fiona Francis (fr) Fiona Francis (it) Fiona Francis (nl) Fiona Francis (sl) Fiona Francis (sq) Fiona Francis (sv) Fiona Francis (ast)
given name	wds:Q28468816-EF0C526D-73C4-4112-90AE-82388412340C
given name	Fiona
instance of	wds:Q28468816-2A76D4E5-BF91-4E95-A0E7-462E66DB240C
instance of	Homo sapiens
occupation	wds:Q28468816-F7563329-B859-4619-9BE1-1547E72272ED
sex or gender	wds:Q28468816-41531B9A-8200-4992-9BD1-A5DDA9D6A802
VIAF ID	wds:Q28468816-452bdd4e-e8a6-4cbc-bc35-febdf07a4a16
IdRef ID	wds:Q28468816-8DE70B35-FA0C-40A2-BEA0-131AA870737B
date of birth	wds:Q28468816-CADD39DF-32E7-432B-88FB-3E1B665FAB1C
family name	wds:Q28468816-690B6B1F-6A1E-44EC-A310-02C4408C3B5A
VIAF ID	http://viaf.org/viaf/198992879
IdRef ID	http://www.idref.fr/147934621/id
occupation	zoologist
sex or gender	female organism
VIAF ID	198992879
IdRef ID	147934621
date of birth	2000-01-01 00:00:00Z (xsd:dateTime)
family name	Francis
Springer Nature person ID	wds:Q28468816-04B1B9DF-5037-4A96-ABBF-50F4AEBBA025
ORCID iD	wds:Q28468816-13248F5F-2987-48C9-A2A5-0D1F18605CEB
Dimensions author ID	wds:Q28468816-4D66616D-8FCC-417C-AF06-7689DCA4EE2B
ORCID iD	https://orcid.org/0000-0001-8542-7537
Springer Nature person ID	01105723271.51
ORCID iD	0000-0001-8542-7537
Dimensions author ID	01105723271.51
is owl:sameAs of	Fiona Francis
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28468816
is author of	Cholinergic influences on cortical development and adult neurogenesis Spermine deficiency in Gy mice caused by deletion of the spermine synthase gene The genomic organization of NKG2C, E, F, and D receptor genes in the human natural killer gene complex Template-free 13-protofilament microtubule–MAP assembly visualized at 8 Å resolution Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1?22.2) BMX, a novel nonreceptor tyrosine kinase gene of the BTK/ITK/TEC/TXK family located in chromosome Xp22.2 Comparative aspects of cerebral cortical development Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy. Doublecortin, a stabilizer of microtubules A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia: evidence that the disorder is not a distinct entity from X-linked hypophosphatemic rickets. Non-random distribution of mutations in the PHEX gene and under-detected missense mutations at non-conserved residues Sequence analysis of an amphioxus cosmid containing a gene homologous to members of the aldo-keto reductase gene superfamily Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human Magnetic resonance imaging and histological studies of corpus callosal and hippocampal abnormalities linked to doublecortin deficiency. Human disorders of cortical development: from past to present Dampened hippocampal oscillations and enhanced spindle activity in an asymptomatic model of developmental cortical malformations ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation Doublecortin mutations cluster in evolutionarily conserved functional domains Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly Genetics and pathophysiology of mental retardation Neuroanatomical distribution of ARX in brain and its localisation in GABAergic neurons The DNA sequence of the human X chromosome Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout mice. The NKG2 natural killer cell receptor family: comparative analysis of promoter sequences. Linkage of the NKG2 and CD94 receptor genes to D12S77 in the human natural killer gene complex The DNA sequence of human chromosome 21 A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation. Structure of the human CD94 C-type lectin gene High resolution cosmid and P1 maps spanning the 14 Mb genome of the fission yeast S. pombe. Genomic organization of a 225-kb region in Xq28 containing the gene for X-linked myotubular myopathy (MTM1) and a related gene (MTMR1) Cloning of the region between HLA-DMB and LMP2 in the human major histocompatibility complex Characterization of the C3 YAC contig from proximal mouse chromosome 17 and analysis of allelic expression of genes flanking the imprinted Igf2r gene. Mechanism of microtubule stabilization by doublecortin Beta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdown So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutation Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons.

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