About: Han-Xiang Deng

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

About: Han-Xiang Deng Goto Sponge NotDistinct Permalink

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	ikertzailea (eu) researcher (en) 연구원 (ko) 研究者 (ja) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) onderzoeker (nl)
rdfs:label	Han-Xiang Deng (en) Han-Xiang Deng (es) Han-Xiang Deng (nl) Han-Xiang Deng (sl)
skos:prefLabel	Han-Xiang Deng (en) Han-Xiang Deng (es) Han-Xiang Deng (nl) Han-Xiang Deng (sl)
name	Han-Xiang Deng (en) Han-Xiang Deng (es) Han-Xiang Deng (nl) Han-Xiang Deng (sl)
Scopus author ID	wds:Q55692589-9A1FD8BE-466D-47F0-AD57-AB113369B6A6
Scopus author ID	7401775578
instance of	wds:Q55692589-9FC88948-2CAE-48A9-8C51-4B5C1CA5588B
instance of	Homo sapiens
Semantic Scholar author ID	wds:Q55692589-40A912F7-46A7-4E95-A419-C38EE68F7DC2
Semantic Scholar author ID	46959499
skos:altLabel	H X Deng (en) H-X Deng (en) H. X. Deng (en) H.-X. Deng (en)
occupation	wds:Q55692589-1ADDAAF2-0D57-4CE0-AC5A-0D738AEB8E6D
employer	wds:Q55692589-1D1A7469-164A-4512-B558-4A52F03AF5C6
sex or gender	wds:Q55692589-8f3ec4f1-4979-4f04-b019-58a72497a878
on focus list of Wikimedia project	wds:Q55692589-C5EB6DAA-FC0B-4630-9B4C-435EAF766171
educated at	wds:Q55692589-0A7B4B75-381F-412A-8548-BBC2445DAD70
occupation	researcher
employer	Northwestern University
sex or gender	male
on focus list of Wikimedia project	WikiProject PCC Wikidata Pilot/Northwestern University Libraries
educated at	Nagasaki University
ORCID iD	wds:Q55692589-BBDA43E0-1EB1-49B2-ABD7-CFDE99A59F1B
ORCID iD	https://orcid.org/0000-0002-0030-8465
ORCID iD	0000-0002-0030-8465
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55692589
is author of	The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis Iron accumulation in deep cortical layers accounts for MRI signal abnormalities in ALS: correlating 7 tesla MRI and pathology. Differential involvement of optineurin in amyotrophic lateral sclerosis with or without SOD1 mutations Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia Dendritic spinopathy in transgenic mice expressing ALS/dementia-linked mutant UBQLN2. Wild-type SOD1 overexpression accelerates disease onset of a G85R SOD1 mouse. Intense superoxide dismutase-1 immunoreactivity in intracytoplasmic hyaline inclusions of familial amyotrophic lateral sclerosis with posterior column involvement. Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase Disulfide cross-linked protein represents a significant fraction of ALS-associated Cu, Zn-superoxide dismutase aggregates in spinal cords of model mice Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondria Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis Alzheimer disease and amyotrophic lateral sclerosis: an etiopathogenic connection Hyperactive intracellular calcium signaling associated with localized mitochondrial defects in skeletal muscle of an animal model of amyotrophic lateral sclerosis Marked accumulation of 27-hydroxycholesterol in SPG5 patients with hereditary spastic paresis TDP-43 pathology in primary progressive aphasia and frontotemporal dementia with pathologic Alzheimer disease Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4. FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia Chromosome-band-specific painting: chromosome in situ suppression hybridization using PCR products from a microdissected chromosome band as a probe pool. Microdissection of human chromosomal regions 8q23.3–q24.11 and 2q33-qter: Construction of DNA libraries and isolation of their clones Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosis Penta X syndrome: a case report with review of the literature. Transgenic mouse models and human neurodegenerative disorders. A Simple and Efficient Amplification Method of DNA with Unknown Sequences and Its Application to Microdissection/Microcloning1 Distal axonopathy in an alsin-deficient mouse model Molecular dissection of ALS-associated toxicity of SOD1 in transgenic mice using an exon-fusion approach. Multiple transcripts of the human Cu,Zn superoxide dismutase gene. Clinicopathologic report of ocular involvement in ALS patients with C9orf72 mutation Parental origin and mechanism of formation of polysomy X: an XXXXX case and four XXXXY cases determined with RFLPs Mutant TRPV4-mediated toxicity is linked to increased constitutive function in axonal neuropathies. Parental origin and mechanism of formation of X chromosome structural abnormalities: Four cases determined with RFLPs Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid. Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly Mutation analysis of hereditary multiple exostoses in the Chinese Possible mapping of the gene for transient myeloproliferative syndrome at 21q11.2 A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset, incomplete penetrance and a sensory neuropathy Recent advances in the genetics of hereditary axonal sensory-motor neuropathies type 2. TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies. Lack of association of VEGF promoter polymorphisms with sporadic ALS A novel locus (DSAP2) for disseminated superficial actinic porokeratosis maps to chromosome 15q25.1-26.1 Identification of TMEM230 mutations in familial Parkinson's disease Restricted expression of mutant SOD1 in spinal motor neurons and interneurons induces motor neuron pathology Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy. The D90A mutation results in a polymorphism of Cu, Zn superoxide dismutase that is prevalent in northern Sweden and Finland A novel ALS-associated variant in UBQLN4 regulates motor axon morphogenesis Early Impairment of Synaptic and Intrinsic Excitability in Mice Expressing ALS/Dementia-Linked Mutant UBQLN2 Confirmation and refinement of a genetic locus for disseminated superficial actinic porokeratosis (DSAP1) at 12q23.2-24.1 Human Genetic Diseases The Parkinson's disease-linked protein TMEM230 is required for Rab8a-mediated secretory vesicle trafficking and retromer trafficking. Assignment of mitotic arrest deficient protein 2 (MAD2L1) to human chromosome band 5q23.3 by in situ hybridization Sirt3 protects dopaminergic neurons from mitochondrial oxidative stress.

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, 180 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software