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Search results 3001 to 3100 out of 3140 for Sod1

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Type Details Score
Publication  
First Author: King AE
Year: 2012
Journal: Brain Res
Title: Degeneration of axons in spinal white matter in G93A mSOD1 mouse characterized by NFL and α-internexin immunoreactivity.
Volume: 1465
Pages: 90-100
Publication  
First Author: Malacarne C
Year: 2021
Journal: Int J Mol Sci
Title: Dysregulation of Muscle-Specific MicroRNAs as Common Pathogenic Feature Associated with Muscle Atrophy in ALS, SMA and SBMA: Evidence from Animal Models and Human Patients.
Volume: 22
Issue: 11
Publication
First Author: Deguise MO
Year: 2019
Journal: Ann Clin Transl Neurol
Title: Abnormal fatty acid metabolism is a core component of spinal muscular atrophy.
Volume: 6
Issue: 8
Pages: 1519-1532
Publication
First Author: Keren-Shaul H
Year: 2017
Journal: Cell
Title: A Unique Microglia Type Associated with Restricting Development of Alzheimer's Disease.
Volume: 169
Issue: 7
Pages: 1276-1290.e17
Publication
First Author: Setter DO
Year: 2018
Journal: Restor Neurol Neurosci
Title: Identification of a resilient mouse facial motoneuron population following target disconnection by injury or disease.
Volume: 36
Issue: 3
Pages: 417-422
Publication
First Author: Deng B
Year: 2018
Journal: J Cell Biochem
Title: FGF9 modulates Schwann cell myelination in developing nerves and induces a pro-inflammatory environment during injury.
Volume: 119
Issue: 10
Pages: 8643-8658
Publication
First Author: Zhang Y
Year: 2003
Journal: J Neurochem
Title: Depletion of wild-type huntingtin in mouse models of neurologic diseases.
Volume: 87
Issue: 1
Pages: 101-6
Publication
First Author: Ozdinler PH
Year: 2011
Journal: J Neurosci
Title: Corticospinal motor neurons and related subcerebral projection neurons undergo early and specific neurodegeneration in hSOD1G⁹³A transgenic ALS mice.
Volume: 31
Issue: 11
Pages: 4166-77
Publication
First Author: Tung YT
Year: 2019
Journal: Cell Stem Cell
Title: Mir-17∼92 Confers Motor Neuron Subtype Differential Resistance to ALS-Associated Degeneration.
Volume: 25
Issue: 2
Pages: 193-209.e7
Publication
First Author: Comley LH
Year: 2016
Journal: J Comp Neurol
Title: Cross-disease comparison of amyotrophic lateral sclerosis and spinal muscular atrophy reveals conservation of selective vulnerability but differential neuromuscular junction pathology.
Volume: 524
Issue: 7
Pages: 1424-42
Publication
First Author: Mejia Maza A
Year: 2021
Journal: Sci Rep
Title: NMJ-Analyser identifies subtle early changes in mouse models of neuromuscular disease.
Volume: 11
Issue: 1
Pages: 12251
Publication
First Author: Montañana-Rosell R
Year: 2024
Journal: Sci Adv
Title: Spinal inhibitory neurons degenerate before motor neurons and excitatory neurons in a mouse model of ALS.
Volume: 10
Issue: 22
Pages: eadk3229
Publication
First Author: Apolloni S
Year: 2013
Journal: Hum Mol Genet
Title: Ablation of P2X7 receptor exacerbates gliosis and motoneuron death in the SOD1-G93A mouse model of amyotrophic lateral sclerosis.
Volume: 22
Issue: 20
Pages: 4102-16
Publication
First Author: Lewis CA
Year: 2009
Journal: Glia
Title: Bone marrow-derived cells in the central nervous system of a mouse model of amyotrophic lateral sclerosis are associated with blood vessels and express CX(3)CR1.
Volume: 57
Issue: 13
Pages: 1410-9
Publication
First Author: Bowerman M
Year: 2015
Journal: Hum Mol Genet
Title: Tweak regulates astrogliosis, microgliosis and skeletal muscle atrophy in a mouse model of amyotrophic lateral sclerosis.
Volume: 24
Issue: 12
Pages: 3440-56
Publication
First Author: Nascimento F
Year: 2024
Journal: Cell Rep
Title: Spinal microcircuits go through multiphasic homeostatic compensations in a mouse model of motoneuron degeneration.
Volume: 43
Issue: 12
Pages: 115046
Publication
First Author: Yasvoina MV
Year: 2013
Journal: J Neurosci
Title: eGFP expression under UCHL1 promoter genetically labels corticospinal motor neurons and a subpopulation of degeneration-resistant spinal motor neurons in an ALS mouse model.
Volume: 33
Issue: 18
Pages: 7890-904
Publication
First Author: Eschbach J
Year: 2013
Journal: Hum Mol Genet
Title: PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis.
Volume: 22
Issue: 17
Pages: 3477-84
Publication
First Author: Pérez-Cabello JA
Year: 2023
Journal: Proc Natl Acad Sci U S A
Title: MAPK/MAK/MRK overlapping kinase (MOK) controls microglial inflammatory/type-I IFN responses via Brd4 and is involved in ALS.
Volume: 120
Issue: 28
Pages: e2302143120
Publication    
First Author: Castro R
Year: 2020
Journal: Elife
Title: Specific labeling of synaptic schwann cells reveals unique cellular and molecular features.
Volume: 9
Publication
First Author: Shapiro D
Year: 2022
Journal: Sci Rep
Title: Argonaute 2 is lost from neuromuscular junctions affected with amyotrophic lateral sclerosis in SOD1G93A mice.
Volume: 12
Issue: 1
Pages: 4630
Publication  
First Author: Sleigh JN
Year: 2020
Journal: Front Cell Neurosci
Title: Altered Sensory Neuron Development in CMT2D Mice Is Site-Specific and Linked to Increased GlyRS Levels.
Volume: 14
Pages: 232
Publication
First Author: Vaknin I
Year: 2011
Journal: PLoS One
Title: Excess circulating alternatively activated myeloid (M2) cells accelerate ALS progression while inhibiting experimental autoimmune encephalomyelitis.
Volume: 6
Issue: 11
Pages: e26921
Publication
First Author: Deng HX
Year: 2007
Journal: Hum Mol Genet
Title: Distal axonopathy in an alsin-deficient mouse model.
Volume: 16
Issue: 23
Pages: 2911-20
Publication  
First Author: Milanese M
Year: 2014
Journal: Neurobiol Dis
Title: Knocking down metabotropic glutamate receptor 1 improves survival and disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
Volume: 64
Pages: 48-59
Publication  
First Author: Ling KK
Year: 2018
Journal: Neurobiol Dis
Title: Antisense-mediated reduction of EphA4 in the adult CNS does not improve the function of mice with amyotrophic lateral sclerosis.
Volume: 114
Pages: 174-183
Publication  
First Author: Mavlyutov TA
Year: 2013
Journal: Neuroscience
Title: Lack of sigma-1 receptor exacerbates ALS progression in mice.
Volume: 240
Pages: 129-34
Publication
First Author: Komiya H
Year: 2020
Journal: Mol Brain
Title: CCR2 is localized in microglia and neurons, as well as infiltrating monocytes, in the lumbar spinal cord of ALS mice.
Volume: 13
Issue: 1
Pages: 64
Publication  
First Author: Garofalo S
Year: 2022
Journal: Brain Behav Immun
Title: Blocking immune cell infiltration of the central nervous system to tame Neuroinflammation in Amyotrophic lateral sclerosis.
Volume: 105
Pages: 1-14
Publication
First Author: Cho E
Year: 2023
Journal: Nat Commun
Title: Ratiometric measurement of MAM Ca(2+) dynamics using a modified CalfluxVTN.
Volume: 14
Issue: 1
Pages: 3586
Publication
First Author: Soulard C
Year: 2020
Journal: Cell Rep
Title: Spinal Motoneuron TMEM16F Acts at C-boutons to Modulate Motor Resistance and Contributes to ALS Pathogenesis.
Volume: 30
Issue: 8
Pages: 2581-2593.e7
Publication
First Author: Harris-Cerruti C
Year: 2004
Journal: Eur J Neurosci
Title: Functional and morphological alterations in compound transgenic mice overexpressing Cu/Zn superoxide dismutase and amyloid precursor protein [correction].
Volume: 19
Issue: 5
Pages: 1174-90
Publication  
First Author: Wang F
Year: 2017
Journal: Nat Commun
Title: Protein kinase C-alpha suppresses autophagy and induces neural tube defects via miR-129-2 in diabetic pregnancy.
Volume: 8
Pages: 15182
Publication
First Author: Starbuck JM
Year: 2014
Journal: Am J Med Genet A
Title: Overlapping trisomies for human chromosome 21 orthologs produce similar effects on skull and brain morphology of Dp(16)1Yey and Ts65Dn mice.
Volume: 164A
Issue: 8
Pages: 1981-1990
Publication
First Author: Jiang Y
Year: 2019
Journal: J Neurosci
Title: Lysosomal Dysfunction in Down Syndrome Is APP-Dependent and Mediated by APP-βCTF (C99).
Volume: 39
Issue: 27
Pages: 5255-5268
Publication
First Author: Colas D
Year: 2008
Journal: Neurobiol Dis
Title: Sleep and EEG features in genetic models of Down syndrome.
Volume: 30
Issue: 1
Pages: 1-7
Publication
First Author: Duchon A
Year: 2011
Journal: Mamm Genome
Title: Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling Down syndrome.
Volume: 22
Issue: 11-12
Pages: 674-84
Publication
First Author: Villar AJ
Year: 2005
Journal: Mamm Genome
Title: Identification and characterization of a new Down syndrome model, Ts[Rb(12.1716)]2Cje, resulting from a spontaneous Robertsonian fusion between T(171)65Dn and mouse chromosome 12.
Volume: 16
Issue: 2
Pages: 79-90
Publication
First Author: Belichenko PV
Year: 2007
Journal: J Comp Neurol
Title: Synaptic and cognitive abnormalities in mouse models of Down syndrome: exploring genotype-phenotype relationships.
Volume: 504
Issue: 4
Pages: 329-45
Publication
First Author: Herault Y
Year: 2017
Journal: Dis Model Mech
Title: Rodent models in Down syndrome research: impact and future opportunities.
Volume: 10
Issue: 10
Pages: 1165-1186
Publication
First Author: Salehi A
Year: 2009
Journal: Sci Transl Med
Title: Restoration of norepinephrine-modulated contextual memory in a mouse model of Down syndrome.
Volume: 1
Issue: 7
Pages: 7ra17
Publication
First Author: Richtsmeier JT
Year: 2002
Journal: Am J Med Genet
Title: Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome.
Volume: 107
Issue: 4
Pages: 317-24
Publication
First Author: Xu JC
Year: 2013
Journal: EMBO J
Title: Usp16: key controller of stem cells in Down syndrome.
Volume: 32
Issue: 21
Pages: 2788-9
Publication
First Author: Siddiqui A
Year: 2008
Journal: Genes Brain Behav
Title: Molecular responses of the Ts65Dn and Ts1Cje mouse models of Down syndrome to MK-801.
Volume: 7
Issue: 7
Pages: 810-20
Publication
First Author: Olson LE
Year: 2004
Journal: Dev Dyn
Title: Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes.
Volume: 230
Issue: 3
Pages: 581-9
Publication
First Author: Klusmann JH
Year: 2010
Journal: Genes Dev
Title: Developmental stage-specific interplay of GATA1 and IGF signaling in fetal megakaryopoiesis and leukemogenesis.
Volume: 24
Issue: 15
Pages: 1659-72
Publication
First Author: Hayashi H
Year: 2020
Journal: PLoS One
Title: Monitoring the autophagy-endolysosomal system using monomeric Keima-fused MAP1LC3B.
Volume: 15
Issue: 6
Pages: e0234180
Genotype
Symbol: Als2/Als2 Tg(SOD1*G93A)1Gur/?
Background: involves: 129/Sv * C57BL/6 * SJL
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Tg(Gria2*586N)238.2Rsp/? Tg(SOD1*G93A)1Gur/?
Background: involves: C57BL/6Ico
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Cx3cr1/Cx3cr1 Tg(SOD1*G93A)1Gur/?
Background: involves: 129P2/OlaHsd * C57BL/6 * SJL
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> Tg(Pgk1-cre)1Lni/? Tg(SOD1*G93A)1Gur/?
Background: B6J.Cg-Tg(Pgk1-cre)1Lni Gt(ROSA)26Sor Tg(SOD1*G93A)1Gur
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Gt(ROSA)26Sor/Gt(ROSA)26Sor Tg(Pgk1-cre)1Lni/? Tg(SOD1*G93A)1Gur/?
Background: B6J.Cg-Tg(Pgk1-cre)1Lni Gt(ROSA)26Sor Tg(SOD1*G93A)1Gur
Zygosity: cn
Has Mutant Allele: true
Genotype
Symbol: Fgfbp1/Fgfbp1 Tg(SOD1*G93A)1Gur/? Tg(Thy1-YFP)16Jrs/?
Background: involves: 129S5/SvEvBrd * C57BL/6J * CBA * SJL
Zygosity: cx
Has Mutant Allele: true
Publication
First Author: Adorno M
Year: 2013
Journal: Nature
Title: Usp16 contributes to somatic stem-cell defects in Down's syndrome.
Volume: 501
Issue: 7467
Pages: 380-4
Publication
First Author: Montagna C
Year: 2019
Journal: Cell Death Dis
Title: nNOS/GSNOR interaction contributes to skeletal muscle differentiation and homeostasis.
Volume: 10
Issue: 5
Pages: 354
Publication
First Author: Bien-Ly N
Year: 2015
Journal: Neuron
Title: Lack of Widespread BBB Disruption in Alzheimer's Disease Models: Focus on Therapeutic Antibodies.
Volume: 88
Issue: 2
Pages: 289-97
Publication  
First Author: Choudhury TZ
Year: 2024
Journal: JCI Insight
Title: Impact of genetic factors on antioxidant rescue of maternal diabetes-associated congenital heart disease.
Volume: 9
Issue: 23
Publication  
First Author: Murano T
Year: 2019
Journal: Commun Biol
Title: Transcriptomic immaturity inducible by neural hyperexcitation is shared by multiple neuropsychiatric disorders.
Volume: 2
Pages: 32
Publication
First Author: Yang P
Year: 2013
Journal: Sci Signal
Title: Maternal hyperglycemia activates an ASK1-FoxO3a-caspase 8 pathway that leads to embryonic neural tube defects.
Volume: 6
Issue: 290
Pages: ra74
Publication
First Author: Guttenplan KA
Year: 2020
Journal: Nat Commun
Title: Knockout of reactive astrocyte activating factors slows disease progression in an ALS mouse model.
Volume: 11
Issue: 1
Pages: 3753
Publication
First Author: Woodruff TM
Year: 2014
Journal: Proc Natl Acad Sci U S A
Title: Role for terminal complement activation in amyotrophic lateral sclerosis disease progression.
Volume: 111
Issue: 1
Pages: E3-4
Publication
First Author: Madaro L
Year: 2018
Journal: Nat Cell Biol
Title: Denervation-activated STAT3-IL-6 signalling in fibro-adipogenic progenitors promotes myofibres atrophy and fibrosis.
Volume: 20
Issue: 8
Pages: 917-927
Publication
First Author: Kaplan A
Year: 2014
Journal: Neuron
Title: Neuronal matrix metalloproteinase-9 is a determinant of selective neurodegeneration.
Volume: 81
Issue: 2
Pages: 333-48
Publication
First Author: Sobue A
Year: 2021
Journal: Acta Neuropathol Commun
Title: Microglial gene signature reveals loss of homeostatic microglia associated with neurodegeneration of Alzheimer's disease.
Volume: 9
Issue: 1
Pages: 1
Publication
First Author: Graffmo KS
Year: 2013
Journal: Hum Mol Genet
Title: Expression of wild-type human superoxide dismutase-1 in mice causes amyotrophic lateral sclerosis.
Volume: 22
Issue: 1
Pages: 51-60
Publication
First Author: Crotti A
Year: 2014
Journal: Nat Neurosci
Title: Mutant Huntingtin promotes autonomous microglia activation via myeloid lineage-determining factors.
Volume: 17
Issue: 4
Pages: 513-21
Publication
First Author: Kim JK
Year: 2023
Journal: Neuron
Title: A spinal muscular atrophy modifier implicates the SMN protein in SNARE complex assembly at neuromuscular synapses.
Volume: 111
Issue: 9
Pages: 1423-1439.e4
Publication  
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
First Author: Cheroni C
Year: 2009
Journal: Hum Mol Genet
Title: Functional alterations of the ubiquitin-proteasome system in motor neurons of a mouse model of familial amyotrophic lateral sclerosis.
Volume: 18
Issue: 1
Pages: 82-96
Publication
First Author: Maday S
Year: 2012
Journal: J Cell Biol
Title: Autophagosomes initiate distally and mature during transport toward the cell soma in primary neurons.
Volume: 196
Issue: 4
Pages: 407-17
Publication
First Author: Lin MY
Year: 2017
Journal: Neuron
Title: Releasing Syntaphilin Removes Stressed Mitochondria from Axons Independent of Mitophagy under Pathophysiological Conditions.
Volume: 94
Issue: 3
Pages: 595-610.e6
Publication
First Author: Philips T
Year: 2013
Journal: Brain
Title: Oligodendrocyte dysfunction in the pathogenesis of amyotrophic lateral sclerosis.
Volume: 136
Issue: Pt 2
Pages: 471-82
Publication
First Author: Yusuf IO
Year: 2022
Journal: Acta Neuropathol Commun
Title: Protein citrullination marks myelin protein aggregation and disease progression in mouse ALS models.
Volume: 10
Issue: 1
Pages: 135
Publication  
First Author: Gautam M
Year: 2019
Journal: Front Cell Neurosci
Title: Mitoautophagy: A Unique Self-Destructive Path Mitochondria of Upper Motor Neurons With TDP-43 Pathology Take, Very Early in ALS.
Volume: 13
Pages: 489
Publication  
First Author: Buck E
Year: 2017
Journal: Front Mol Neurosci
Title: Comparison of Sirtuin 3 Levels in ALS and Huntington's Disease-Differential Effects in Human Tissue Samples vs. Transgenic Mouse Models.
Volume: 10
Pages: 156
Publication
First Author: Sun W
Year: 2017
Journal: J Neurosci
Title: SOX9 Is an Astrocyte-Specific Nuclear Marker in the Adult Brain Outside the Neurogenic Regions.
Volume: 37
Issue: 17
Pages: 4493-4507
Publication
First Author: Klinman E
Year: 2015
Journal: Cell Rep
Title: Stress-Induced CDK5 Activation Disrupts Axonal Transport via Lis1/Ndel1/Dynein.
Volume: 12
Issue: 3
Pages: 462-73
Publication
First Author: Maniatis S
Year: 2019
Journal: Science
Title: Spatiotemporal dynamics of molecular pathology in amyotrophic lateral sclerosis.
Volume: 364
Issue: 6435
Pages: 89-93
Publication    
First Author: Maimon R
Year: 2021
Journal: EMBO J
Title: A CRMP4-dependent retrograde axon-to-soma death signal in amyotrophic lateral sclerosis.
Pages: e107586
Publication  
First Author: Eykens C
Year: 2018
Journal: Neurobiol Aging
Title: Conditional deletion of Id2 or Notch1 in oligodendrocyte progenitor cells does not ameliorate disease outcome in SOD1G93A mice.
Volume: 68
Pages: 1-4
Publication    
First Author: Commisso B
Year: 2018
Journal: Elife
Title: Stage-dependent remodeling of projections to motor cortex in ALS mouse model revealed by a new variant retrograde-AAV9.
Volume: 7
Publication
First Author: Chandra S
Year: 2005
Journal: Cell
Title: Alpha-synuclein cooperates with CSPalpha in preventing neurodegeneration.
Volume: 123
Issue: 3
Pages: 383-96
Publication
First Author: Bilsland LG
Year: 2010
Journal: Proc Natl Acad Sci U S A
Title: Deficits in axonal transport precede ALS symptoms in vivo.
Volume: 107
Issue: 47
Pages: 20523-8
Publication
First Author: Kiryu-Seo S
Year: 2022
Journal: EMBO J
Title: Impaired disassembly of the axon initial segment restricts mitochondrial entry into damaged axons.
Volume: 41
Issue: 20
Pages: e110486
Publication
First Author: Tian F
Year: 2011
Journal: Autophagy
Title: In vivo optical imaging of motor neuron autophagy in a mouse model of amyotrophic lateral sclerosis.
Volume: 7
Issue: 9
Pages: 985-92
Publication
First Author: Li H
Year: 2016
Journal: Genetics
Title: Penetrance of Congenital Heart Disease in a Mouse Model of Down Syndrome Depends on a Trisomic Potentiator of a Disomic Modifier.
Volume: 203
Issue: 2
Pages: 763-70
Publication
First Author: Rachidi M
Year: 2007
Journal: Neurosci Res
Title: Mental retardation in Down syndrome: from gene dosage imbalance to molecular and cellular mechanisms.
Volume: 59
Issue: 4
Pages: 349-69
Publication
First Author: Wiseman FK
Year: 2009
Journal: Hum Mol Genet
Title: Down syndrome--recent progress and future prospects.
Volume: 18
Issue: R1
Pages: R75-83
Publication
First Author: Davisson M
Year: 2007
Journal: Hum Reprod
Title: Impact of trisomy on fertility and meiosis in male mice.
Volume: 22
Issue: 2
Pages: 468-76
Publication
First Author: Forejt J
Year: 2003
Journal: Comp Funct Genomics
Title: Segmental trisomy of mouse chromosome 17: introducing an alternative model of Down's syndrome.
Volume: 4
Issue: 6
Pages: 647-52
Publication  
First Author: Molnar-Kasza A
Year: 2021
Journal: Front Mol Neurosci
Title: Evaluation of Neuropathological Features in the SOD1-G93A Low Copy Number Transgenic Mouse Model of Amyotrophic Lateral Sclerosis.
Volume: 14
Pages: 681868
Publication
First Author: Alexander GM
Year: 2022
Journal: PLoS One
Title: Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease.
Volume: 17
Issue: 9
Pages: e0274615
Publication
First Author: Staecker H
Year: 2001
Journal: Acta Otolaryngol
Title: Oxidative stress in aging in the C57B16/J mouse cochlea.
Volume: 121
Issue: 6
Pages: 666-72
Publication
First Author: Zhou Q
Year: 2020
Journal: Int J Biol Sci
Title: Nicotinamide Riboside Enhances Mitochondrial Proteostasis and Adult Neurogenesis through Activation of Mitochondrial Unfolded Protein Response Signaling in the Brain of ALS SOD1G93A Mice.
Volume: 16
Issue: 2
Pages: 284-297
Publication
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
First Author: Krasemann S
Year: 2017
Journal: Immunity
Title: The TREM2-APOE Pathway Drives the Transcriptional Phenotype of Dysfunctional Microglia in Neurodegenerative Diseases.
Volume: 47
Issue: 3
Pages: 566-581.e9
Publication
First Author: Hoye ML
Year: 2017
Journal: J Neurosci
Title: MicroRNA Profiling Reveals Marker of Motor Neuron Disease in ALS Models.
Volume: 37
Issue: 22
Pages: 5574-5586
Publication
First Author: Jiang LL
Year: 2019
Journal: J Clin Invest
Title: Membralin deficiency dysregulates astrocytic glutamate homeostasis leading to ALS-like impairment.
Volume: 129
Issue: 8
Pages: 3103-3120
Publication
First Author: Yim AKY
Year: 2022
Journal: Nat Neurosci
Title: Disentangling glial diversity in peripheral nerves at single-nuclei resolution.
Volume: 25
Issue: 2
Pages: 238-251
Publication
First Author: Marinkovic P
Year: 2012
Journal: Proc Natl Acad Sci U S A
Title: Axonal transport deficits and degeneration can evolve independently in mouse models of amyotrophic lateral sclerosis.
Volume: 109
Issue: 11
Pages: 4296-301