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Search results 401 to 438 out of 438 for C9orf72

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0.028s

Type

Details

Score

Strain

MGI:6100945 | B6N.Cg-Tg(C9orf72*)19Lagi/J

Attribute String:

transgenic, mutant strain, congenic

•

Strain

MGI:5618294 | C57BL/6J-Tg(C9orf72_i2)8Lutzy/J

Attribute String:

coisogenic, mutant strain, transgenic

•

Genotype

Symbol:	Tg(C9orf72*)450BLagi/?
Background:	involves: C3H * C57BL/6
Zygosity:	ot
Has Mutant Allele:	true

•

Genotype

Symbol:	Tg(C9orf72_i3)112Lutzy/?
Background:	C57BL/6J-Tg(C9orf72_i3)112Lutzy/J
Zygosity:	ot
Has Mutant Allele:	true

•

Genotype

Symbol:	Tg(C9orf72_i2)8Lutzy/?
Background:	C57BL/6J-Tg(C9orf72_i2)8Lutzy/J
Zygosity:	ot
Has Mutant Allele:	true

•

Publication

23608112 | J:211734

First Author:	Herdewyn S
Year:	2013
Journal:	Neurobiol Aging
Title:	Progranulin does not affect motor neuron degeneration in mutant SOD1 mice and rats.
Volume:	34
Issue:	10
Pages:	2302-3

•

Strain

MGI:7564003 | FVB/NJ-Tg(C9orf72_i3)101Lutzy/J

Attribute String:

coisogenic, mutant strain, transgenic

•

Strain

MGI:6101186 | FVB/NJ-Tg(C9orf72)500Lpwr

Attribute String:

transgenic, mutant strain, coisogenic

•

Strain

MGI:5919953 | FVB/NJ-Tg(C9orf72)500Lpwr/J

Attribute String:

coisogenic, mutant strain, transgenic

•

Publication

29415125 | J:258732

First Author:	Bento-Abreu A
Year:	2018
Journal:	Hum Mol Genet
Title:	Elongator subunit 3 (ELP3) modifies ALS through tRNA modification.
Volume:	27
Issue:	7
Pages:	1276-1289

•

Publication

31061493 | J:281537

First Author:	Lu J
Year:	2019
Journal:	Nat Neurosci
Title:	L3MBTL1 regulates ALS/FTD-associated proteotoxicity and quality control.
Volume:	22
Issue:	6
Pages:	875-886

•

Publication

30310141 | J:268073

First Author:	Porta S
Year:	2018
Journal:	Nat Commun
Title:	Patient-derived frontotemporal lobar degeneration brain extracts induce formation and spreading of TDP-43 pathology in vivo.
Volume:	9
Issue:	1
Pages:	4220

•

Publication

27321923 | J:239629

First Author:	Lee S
Year:	2016
Journal:	Neuron
Title:	Activation of HIPK2 Promotes ER Stress-Mediated Neurodegeneration in Amyotrophic Lateral Sclerosis.
Volume:	91
Issue:	1
Pages:	41-55

•

Publication

35697676 | J:326744

First Author:	Gleixner AM
Year:	2022
Journal:	Nat Commun
Title:	NUP62 localizes to ALS/FTLD pathological assemblies and contributes to TDP-43 insolubility.
Volume:	13
Issue:	1
Pages:	3380

•

Publication

28093491 | J:241667

First Author:	Clayton EL
Year:	2017
Journal:	Hum Mol Genet
Title:	Early microgliosis precedes neuronal loss and behavioural impairment in mice with a frontotemporal dementia-causing CHMP2B mutation.
Volume:	26
Issue:	5
Pages:	873-887

•

Publication

28978466 | J:254206

First Author:	Coyne AN
Year:	2017
Journal:	Cell Rep
Title:	Post-transcriptional Inhibition of Hsc70-4/HSPA8 Expression Leads to Synaptic Vesicle Cycling Defects in Multiple Models of ALS.
Volume:	21
Issue:	1
Pages:	110-125

•

Publication

35379876 | J:338779

First Author:	Verdone BM
Year:	2022
Journal:	Sci Rep
Title:	A mouse model with widespread expression of the C9orf72-linked glycine-arginine dipeptide displays non-lethal ALS/FTD-like phenotypes.
Volume:	12
Issue:	1
Pages:	5644

•

Publication

27796305 | J:242632

First Author:	Tian F
Year:	2016
Journal:	Nat Commun
Title:	Monitoring peripheral nerve degeneration in ALS by label-free stimulated Raman scattering imaging.
Volume:	7

Pages:	13283

•

Allele

Tg(C9orf72*)30Rhbr | MGI:6101162

Name:	transgene insertion 30, Robert Brown Jr
Allele Type:	Transgenic
Attribute String:	Humanized sequence, Inserted expressed sequence

•

Strain

MGI:6101164 | B6J.Cg-Tg(C9orf72*)30Rhbr/J

Attribute String:

transgenic, mutant strain, congenic

•

Publication

30442666 | J:268243

First Author:	McAlpine W
Year:	2018
Journal:	Proc Natl Acad Sci U S A
Title:	Excessive endosomal TLR signaling causes inflammatory disease in mice with defective SMCR8-WDR41-C9ORF72 complex function.
Volume:	115
Issue:	49
Pages:	E11523-E11531

•

Publication

29458840 | J:262424

First Author:	Matamala JM
Year:	2018
Journal:	Neurobiol Aging
Title:	Genome-wide circulating microRNA expression profiling reveals potential biomarkers for amyotrophic lateral sclerosis.
Volume:	64

Pages:	123-138

•

Publication

32415281 | J:302747

First Author:	Gandelman M
Year:	2020
Journal:	Cell Death Differ
Title:	Staufen 1 amplifies proapoptotic activation of the unfolded protein response.
Volume:	27
Issue:	10
Pages:	2942-2951

•

Publication

31158439 | J:282904

First Author:	Van Acker ZP
Year:	2019
Journal:	Neuroscience
Title:	Non-Methylation-Linked Mechanism of REST-Induced Neuroglobin Expression Impacts Mitochondrial Phenotypes in a Mouse Model of Amyotrophic Lateral Sclerosis.
Volume:	412

Pages:	233-247

•

Publication

30496365 | J:303238

First Author:	Clayton EL
Year:	2018
Journal:	Brain
Title:	Frontotemporal dementia causative CHMP2B impairs neuronal endolysosomal traffic-rescue by TMEM106B knockdown.
Volume:	141
Issue:	12
Pages:	3428-3442

•

Publication

28344074 | J:244047

First Author:	Shang J
Year:	2017
Journal:	Neuroscience
Title:	Aberrant distributions of nuclear pore complex proteins in ALS mice and ALS patients.
Volume:	350

Pages:	158-168

•

Publication

24667415 | J:213426

First Author:	Bros-Facer V
Year:	2014
Journal:	Hum Mol Genet
Title:	Treatment with an antibody directed against Nogo-A delays disease progression in the SOD1G93A mouse model of Amyotrophic lateral sclerosis.
Volume:	23
Issue:	16
Pages:	4187-200

•

Publication

28539470 | J:252170

First Author:	Imamura K
Year:	2017
Journal:	Sci Transl Med
Title:	The Src/c-Abl pathway is a potential therapeutic target in amyotrophic lateral sclerosis.
Volume:	9
Issue:	391

•

Publication

27126638 | J:236991

First Author:	Busch JI
Year:	2016
Journal:	Hum Mol Genet
Title:	Increased expression of the frontotemporal dementia risk factor TMEM106B causes C9orf72-dependent alterations in lysosomes.
Volume:	25
Issue:	13
Pages:	2681-2697

•

Publication

25193032 | J:253702

First Author:	Ajroud-Driss S
Year:	2015
Journal:	Biochim Biophys Acta
Title:	Sporadic and hereditary amyotrophic lateral sclerosis (ALS).
Volume:	1852
Issue:	4
Pages:	679-84

•

Publication

32347002 | J:324634

First Author:	Jensen BK
Year:	2020
Journal:	EMBO Mol Med
Title:	Synaptic dysfunction induced by glycine-alanine dipeptides in C9orf72-ALS/FTD is rescued by SV2 replenishment.
Volume:	12
Issue:	5
Pages:	e10722

•

Publication

34118929 | J:314497

First Author:	Milani M
Year:	2021
Journal:	J Neuroinflammation
Title:	Targeting S100A4 with niclosamide attenuates inflammatory and profibrotic pathways in models of amyotrophic lateral sclerosis.
Volume:	18
Issue:	1
Pages:	132

•

Publication

33028409 | J:308483

First Author:	Huang M
Year:	2020
Journal:	Acta Neuropathol Commun
Title:	Network analysis of the progranulin-deficient mouse brain proteome reveals pathogenic mechanisms shared in human frontotemporal dementia caused by GRN mutations.
Volume:	8
Issue:	1
Pages:	163

•

Publication

29855382 | J:263969

First Author:	Nicholson AM
Year:	2018
Journal:	Acta Neuropathol Commun
Title:	Loss of Tmem106b is unable to ameliorate frontotemporal dementia-like phenotypes in an AAV mouse model of C9ORF72-repeat induced toxicity.
Volume:	6
Issue:	1
Pages:	42

•

Publication

35507432 | J:344849

First Author:	Wang SM
Year:	2023
Journal:	Autophagy
Title:	Nucleoporin POM121 signals TFEB-mediated autophagy via activation of SIGMAR1/sigma-1 receptor chaperone by pridopidine.
Volume:	19
Issue:	1
Pages:	126-151

•

Publication

35276083 | J:326153

First Author:	Arredondo C
Year:	2022
Journal:	Neuron
Title:	Excessive release of inorganic polyphosphate by ALS/FTD astrocytes causes non-cell-autonomous toxicity to motoneurons.
Volume:	110
Issue:	10
Pages:	1656-1670.e12

•

Publication

15489334 | -

First Author:	Gerhard DS
Year:	2004
Journal:	Genome Res
Title:	The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Volume:	14
Issue:	10B
Pages:	2121-7

•

Publication

19468303 | -

First Author:	Church DM
Year:	2009
Journal:	PLoS Biol
Title:	Lineage-specific biology revealed by a finished genome assembly of the mouse.
Volume:	7
Issue:	5
Pages:	e1000112

•

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