About: A new mouse model for infantile neuroaxonal dystrophy, inad mouse, maps to mouse chromosome 1

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scientific article published on 01 February 2005

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2005 (fr) наукова стаття, опублікована в лютому 2005 (uk) artículu científicu espublizáu en febreru de 2005 (ast) artikull shkencor i botuar më 01 shkurt 2005 (sq) scientific article published on 01 February 2005 (en)
publication date	wds:Q81696532-D64803B1-F8FE-4CC5-BDC3-35B779DA50E8
publication date	2005-02-01 00:00:00Z (xsd:dateTime)
exact match	wds:Q81696532-0152FCF8-BEB6-470B-8009-1E5765ABD7A9
exact match	https://scigraph.springernature.com/pub.10.1007/s00335-004-3017-5
cites work	wds:Q81696532-1718985E-B687-4108-ABB0-5D7F7897952A wds:Q81696532-3350C451-2B3E-4009-9582-501BB1523D5F wds:Q81696532-343F1BB5-443B-4E84-A44F-8D2830EEA77A wds:Q81696532-5C303C52-97D6-4240-B03B-E1640FABF4FF wds:Q81696532-65DACCD4-15D5-4610-A3E9-A4039328F507 wds:Q81696532-7E0EAF05-D6CE-4FDD-BD89-F4048EB3E835 wds:Q81696532-D1FDA4B5-32A0-43A8-8AEE-661FFC407B3F wds:Q81696532-E62B521A-A101-4793-B9AD-180542834287 wds:Q81696532-F61BE6AC-EF41-4170-A9E7-CD61D931FC64
cites work	Infantile neuroaxonal dystrophy (Seitelberger's disease). Cloning of a major heparan sulfate proteoglycan from brain and identification as the rat form of glypican Map Manager QTX, cross-platform software for genetic mapping Infantile neuroaxonal dystrophy Immunocytochemical and in situ hybridization studies of the heparan sulfate proteoglycan, glypican, in nervous tissue. Gracile axonal dystrophy (GAD), a new neurological mutant in the mouse Infantile neuroaxonal dystrophy Structure and splice products of the human gene encoding sds22, a putative mitotic regulator of protein phosphatase-1 Dying back type axonal degeneration of sensory nerve terminals in muscle spindles of the gracile axonal dystrophy (GAD) mutant mouse
author name string	wds:Q81696532-1A26FF3A-F7C7-4196-AD16-92524BF1A8A4 wds:Q81696532-616F2358-B01C-4BE3-9BA1-F2EFA55895DB wds:Q81696532-620BD7C3-50A6-4C39-A890-89C384DF7BFC wds:Q81696532-73C958B1-AAE9-4A3D-A37D-9CB154E28E73 wds:Q81696532-8B3E464B-1EC1-4FF5-A247-F8FE78228A18 wds:Q81696532-94A2B209-D6FB-4F28-B01E-DFC24C5222DA wds:Q81696532-D1B584EA-4449-412B-AD4B-071B3D8F93A5
author name string	Nobutsune Ichihara Akira Ishikawa Hisae Kikuchi Tateki Kikuchi Yasushi Ishijima Yoshibumi Matsushima Masayoshi Tachibana
rdfs:label	A new mouse model for infantile neuroaxonal dystrophy, inad mouse, maps to mouse chromosome 1 (en) A new mouse model for infantile neuroaxonal dystrophy, inad mouse, maps to mouse chromosome 1 (nl) A new mouse model for infantile neuroaxonal dystrophy, inad mouse, maps to mouse chromosome 1 (sq)
skos:prefLabel	A new mouse model for infantile neuroaxonal dystrophy, inad mouse, maps to mouse chromosome 1 (en) A new mouse model for infantile neuroaxonal dystrophy, inad mouse, maps to mouse chromosome 1 (nl) A new mouse model for infantile neuroaxonal dystrophy, inad mouse, maps to mouse chromosome 1 (sq)
name	A new mouse model for infantile neuroaxonal dystrophy, inad mouse, maps to mouse chromosome 1 (en) A new mouse model for infantile neuroaxonal dystrophy, inad mouse, maps to mouse chromosome 1 (nl) A new mouse model for infantile neuroaxonal dystrophy, inad mouse, maps to mouse chromosome 1 (sq)
title	wds:Q81696532-876648F3-DBD1-44EF-ABCA-31ADEC560114
title	A new mouse model for infantile neuroaxonal dystrophy, inad mouse, maps to mouse chromosome 1 (en)
page(s)	wds:Q81696532-42A496C8-6716-4276-B258-672B5150B11F
page(s)	73-78
instance of	wds:Q81696532-2501E3D3-68BF-4D27-9A5E-633D30EDA179
instance of	scholarly article
main subject	wds:Q81696532-917F33FB-BAF3-4876-8D1E-6C34F4030EF1
main subject	Infantile neuroaxonal dystrophy
PubMed ID	wds:Q81696532-DE1AC881-B737-41C0-9321-5D96A889B1E7
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/15859351
PubMed ID	15859351
published in	wds:Q81696532-99B4D294-F3DC-41CB-9E3A-A1E86A61641A
published in	Mammalian Genome
issue	wds:Q81696532-3DE11E57-C131-4A55-922C-4D657F3EB03B
volume	wds:Q81696532-D7FB1075-2B7A-4B0D-ACC4-56614C9D1224
issue	2
volume	16
number of pages	wds:Q81696532-73425CC3-DF12-4FEB-863F-EFCBCF51FE5D
number of pages	6 (xsd:decimal)
DOI	wds:Q81696532-C70A9475-A3A1-459E-9AF2-4AE7F1D02390
DOI	http://dx.doi.org/10.1007/S00335-004-3017-5
DOI	10.1007/S00335-004-3017-5
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q81696532
is cites work of	Disrupted membrane homeostasis and accumulation of ubiquitinated proteins in a mouse model of infantile neuroaxonal dystrophy caused by PLA2G6 mutations Spontaneous murine neuroaxonal dystrophy: a model of infantile neuroaxonal dystrophy Identification of the PLA2G6 c.1579G>A Missense Mutation in Papillon Dog Neuroaxonal Dystrophy Using Whole Exome Sequencing Analysis.
is cites work of	wds:Q36559669-90F45865-400C-4089-92B0-5DE8CBD7FE70 wds:Q37596252-48F0E70A-EA61-4DDF-B1EA-283EC107E9B3 wds:Q36177182-A5680E26-2428-4EA8-8C7D-5B00C60A654E

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