JP2015500297A5 - - Google Patents

Download PDF

Info

Publication number
JP2015500297A5
JP2015500297A5 JP2014546242A JP2014546242A JP2015500297A5 JP 2015500297 A5 JP2015500297 A5 JP 2015500297A5 JP 2014546242 A JP2014546242 A JP 2014546242A JP 2014546242 A JP2014546242 A JP 2014546242A JP 2015500297 A5 JP2015500297 A5 JP 2015500297A5
Authority
JP
Japan
Prior art keywords
stem cells
use according
condition
nrp2
mice
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2014546242A
Other languages
English (en)
Japanese (ja)
Other versions
JP2015500297A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/AU2012/001530 external-priority patent/WO2013086574A1/en
Publication of JP2015500297A publication Critical patent/JP2015500297A/ja
Publication of JP2015500297A5 publication Critical patent/JP2015500297A5/ja
Pending legal-status Critical Current

Links

JP2014546242A 2011-12-13 2012-12-13 治療方法 Pending JP2015500297A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
AU2011905180A AU2011905180A0 (en) 2011-12-13 Method of treatment
AU2011905180 2011-12-13
PCT/AU2012/001530 WO2013086574A1 (en) 2011-12-13 2012-12-13 Method of treatment

Publications (2)

Publication Number Publication Date
JP2015500297A JP2015500297A (ja) 2015-01-05
JP2015500297A5 true JP2015500297A5 (https=) 2016-02-04

Family

ID=48611719

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014546242A Pending JP2015500297A (ja) 2011-12-13 2012-12-13 治療方法

Country Status (9)

Country Link
US (1) US20140348793A1 (https=)
EP (1) EP2791324B1 (https=)
JP (1) JP2015500297A (https=)
KR (1) KR20140116103A (https=)
CN (1) CN104540938A (https=)
AU (1) AU2012350357A1 (https=)
CA (1) CA2859213A1 (https=)
IN (1) IN2014DN05769A (https=)
WO (1) WO2013086574A1 (https=)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20230218213A1 (en) * 2020-07-02 2023-07-13 The Johns Hopkins University Fmri-hippocampus acoustic battery (fhab)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030003572A1 (en) * 1999-03-05 2003-01-02 David J. Anderson Isolation and enrichment of neural stem cells from uncultured tissue based on cell-surface marker expression
ITNA20060017A1 (it) * 2006-02-20 2007-08-21 Aquino Riccardo D Tecnica di prelievo e selezione di un una popolazione di cellule staminali di tipo embrionale da tessuti follicolari peridentari di uomo adulto.
US8815581B2 (en) * 2010-02-03 2014-08-26 Samsung Life Public Welfare Foundation Method for proliferating stem cells by activating c-MET/HGF signaling and notch signaling
WO2013040650A1 (en) * 2011-09-22 2013-03-28 Central Adelaide Local Health Network Incorporated Screening method

Similar Documents

Publication Publication Date Title
Corbo et al. Doublecortin is required in mice for lamination of the hippocampus but not the neocortex
Lee et al. APP family regulates neuronal excitability and synaptic plasticity but not neuronal survival
Haigh et al. Cortical and retinal defects caused by dosage-dependent reductions in VEGF-A paracrine signaling
McCarty et al. Selective ablation of αv integrins in the central nervous system leads to cerebral hemorrhage, seizures, axonal degeneration and premature death
Pujadas et al. Reelin regulates postnatal neurogenesis and enhances spine hypertrophy and long-term potentiation
Shen et al. Schizophrenia-related neural and behavioral phenotypes in transgenic mice expressing truncated Disc1
Menzies et al. Mena and vasodilator-stimulated phosphoprotein are required for multiple actin-dependent processes that shape the vertebrate nervous system
Sanchez-Ortiz et al. TrkA gene ablation in basal forebrain results in dysfunction of the cholinergic circuitry
Furuyama et al. Abnormal angiogenesis in Foxo1 (Fkhr)-deficient mice
Gu et al. Impaired conditioned fear and enhanced long-term potentiation inFmr2 knock-out mice
Hirata et al. Zinc finger gene fez‐like functions in the formation of subplate neurons and thalamocortical axons
Marmorstein et al. Formation and progression of sub-retinal pigment epithelium deposits in Efemp1 mutation knock-in mice: a model for the early pathogenic course of macular degeneration
Zimmermann et al. Neural stem cell lineage-specific cannabinoid type-1 receptor regulates neurogenesis and plasticity in the adult mouse hippocampus
AU747691B2 (en) Apolipoprotein E transgenic animals and assay methods
Carlisle et al. Deletion of densin-180 results in abnormal behaviors associated with mental illness and reduces mGluR5 and DISC1 in the postsynaptic density fraction
Kappeler et al. Magnetic resonance imaging and histological studies of corpus callosal and hippocampal abnormalities linked to doublecortin deficiency
Oaks et al. Cc2d1a loss of function disrupts functional and morphological development in forebrain neurons leading to cognitive and social deficits
Gutilla et al. Long-term consequences of conditional genetic deletion of PTEN in the sensorimotor cortex of neonatal mice
Sultana et al. Deletion of olfactomedin 2 induces changes in the AMPA receptor complex and impairs visual, olfactory, and motor functions in mice
Licht et al. Age-dependent remarkable regenerative potential of the dentate gyrus provided by intrinsic stem cells
Lamballe et al. Pool-specific regulation of motor neuron survival by neurotrophic support
Ezan et al. Neuron-specific deletion of Scrib in mice leads to neuroanatomical and locomotor deficits
Wen et al. Selective expression of presenilin 1 in neural progenitor cells rescues the cerebral hemorrhages and cortical lamination defects in presenilin 1-null mutant mice
Mohn et al. Phenotypic analysis of mice lacking the highly abundant Purkinje cell-and bipolar neuron-specific PCP2 protein
JP2015500297A5 (https=)