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Search results 1 to 100 out of 319 for Grm7

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Category: Publication
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Type Details Score
Publication
25921811 | J:310896
First Author: Xia W
Year: 2015
Journal: Stem Cell Reports
Title: GRM7 regulates embryonic neurogenesis via CREB and YAP.
Volume: 4
Issue: 5
Pages: 795-810
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Publication
33476302 | J:329223
 
First Author: Fisher NM
Year: 2021
Journal: JCI Insight
Title: A GRM7 mutation associated with developmental delay reduces mGlu7 expression and produces neurological phenotypes.
Volume: 6
Issue: 4
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Publication
32248644 | J:329632
First Author: Fisher NM
Year: 2020
Journal: Genes Brain Behav
Title: Phenotypic profiling of mGlu7 knockout mice reveals new implications for neurodevelopmental disorders.
Volume: 19
Issue: 7
Pages: e12654
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Publication
17936574 | J:130072
First Author: Vadasz C
Year: 2007
Journal: Genomics
Title: Glutamate receptor metabotropic 7 is cis-regulated in the mouse brain and modulates alcohol drinking.
Volume: 90
Issue: 6
Pages: 690-702
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Publication
32768991 | J:303025
 
First Author: Vadasz C
Year: 2020
Journal: Drug Alcohol Depend
Title: Cocaine-Induced Sensitization is Linked to Distal Chromosome 6 Region in Congenic Mouse Model.
Volume: 215
Pages: 108185
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Publication
21448595 | J:264963
First Author: Gyetvai B
Year: 2011
Journal: Neurochem Res
Title: mGluR7 genetics and alcohol: intersection yields clues for addiction.
Volume: 36
Issue: 6
Pages: 1087-100
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Publication
15313036 | J:96176
First Author: Hölscher C
Year: 2004
Journal: Behav Brain Res
Title: Lack of the metabotropic glutamate receptor subtype 7 selectively impairs short-term working memory but not long-term memory.
Volume: 154
Issue: 2
Pages: 473-81
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Publication
12814372 | J:89656
First Author: Cryan JF
Year: 2003
Journal: Eur J Neurosci
Title: Antidepressant and anxiolytic-like effects in mice lacking the group III metabotropic glutamate receptor mGluR7.
Volume: 17
Issue: 11
Pages: 2409-17
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Publication
32865662 | J:332705
First Author: Masugi-Tokita M
Year: 2020
Journal: Mol Neurobiol
Title: Metabotropic Glutamate Receptor Subtype 7 Is Essential for Ejaculation.
Volume: 57
Issue: 12
Pages: 5208-5218
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Publication
16204199 | J:114435
First Author: Hölscher C
Year: 2005
Journal: Learn Mem
Title: Lack of the metabotropic glutamate receptor subtype 7 selectively modulates Theta rhythm and working memory.
Volume: 12
Issue: 5
Pages: 450-5
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Publication
11698585 | J:72691
First Author: Sansig G
Year: 2001
Journal: J Neurosci
Title: Increased seizure susceptibility in mice lacking metabotropic glutamate receptor 7.
Volume: 21
Issue: 22
Pages: 8734-45
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Publication
36403690 | J:332147
 
First Author: Masugi-Tokita M
Year: 2022
Journal: Neuroscience
Title: Spinal Transection Switches the Effect of Metabotropic Glutamate Receptor Subtype 7 from the Facilitation to Inhibition of Ejaculation.
Volume: 509
Pages: 10-19
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Publication
16775145 | J:109594
First Author: Callaerts-Vegh Z
Year: 2006
Journal: J Neurosci
Title: Concomitant deficits in working memory and fear extinction are functionally dissociated from reduced anxiety in metabotropic glutamate receptor 7-deficient mice.
Volume: 26
Issue: 24
Pages: 6573-82
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Publication
18289889 | J:139605
First Author: Goddyn H
Year: 2008
Journal: Neurobiol Learn Mem
Title: Deficits in acquisition and extinction of conditioned responses in mGluR7 knockout mice.
Volume: 90
Issue: 1
Pages: 103-11
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Publication
17318264 | J:120738
First Author: Avila AM
Year: 2007
Journal: J Clin Invest
Title: Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophy.
Volume: 117
Issue: 3
Pages: 659-71
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Publication
29227625 | J:350352
First Author: Fisher NM
Year: 2018
Journal: ACS Chem Neurosci
Title: Genetic Reduction or Negative Modulation of mGlu(7) Does Not Impact Anxiety and Fear Learning Phenotypes in a Mouse Model of MECP2 Duplication Syndrome.
Volume: 9
Issue: 9
Pages: 2210-2217
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Publication
- | J:224658
     
First Author: SoRelle J
Year: 2015
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for shaky
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Publication
11706005 | J:73692
First Author: Perroy J
Year: 2002
Journal: J Biol Chem
Title: Permissive effect of voltage on mGlu 7 receptor subtype signaling in neurons.
Volume: 277
Issue: 2
Pages: 1223-8
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Publication
17650109 | J:127274
First Author: Martín R
Year: 2007
Journal: Eur J Neurosci
Title: mGluR7 inhibits glutamate release through a PKC-independent decrease in the activity of P/Q-type Ca2+ channels and by diminishing cAMP in hippocampal nerve terminals.
Volume: 26
Issue: 2
Pages: 312-22
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Publication
28193854 | J:241214
First Author: Woo CJ
Year: 2017
Journal: Proc Natl Acad Sci U S A
Title: Gene activation of SMN by selective disruption of lncRNA-mediated recruitment of PRC2 for the treatment of spinal muscular atrophy.
Volume: 114
Issue: 8
Pages: E1509-E1518
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Publication
31793148 | J:301908
First Author: Gryksa K
Year: 2020
Journal: Genes Brain Behav
Title: Metabotropic glutamate receptor subtype 7 controls maternal care, maternal motivation and maternal aggression in mice.
Volume: 19
Issue: 1
Pages: e12627
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Publication
23174341 | J:318126
 
First Author: Ferrero JJ
Year: 2013
Journal: Neuropharmacology
Title: Potentiation of mGlu7 receptor-mediated glutamate release at nerve terminals containing N and P/Q type Ca2+ channels.
Volume: 67
Pages: 213-22
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Publication
26748715 | J:353170
First Author: Rogoz K
Year: 2016
Journal: Cell Rep
Title: Identification of a Neuronal Receptor Controlling Anaphylaxis.
Volume: 14
Issue: 2
Pages: 370-9
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Publication
11584003 | J:73174
First Author: Perroy J
Year: 2001
Journal: J Biol Chem
Title: The C terminus of the metabotropic glutamate receptor subtypes 2 and 7 specifies the receptor signaling pathways.
Volume: 276
Issue: 49
Pages: 45800-5
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Publication
12065412 | J:114768
First Author: Perroy J
Year: 2002
Journal: EMBO J
Title: PICK1 is required for the control of synaptic transmission by the metabotropic glutamate receptor 7.
Volume: 21
Issue: 12
Pages: 2990-9
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Publication
27111068 | J:244184
First Author: Seo J
Year: 2016
Journal: PLoS One
Title: Oxidative Stress Triggers Body-Wide Skipping of Multiple Exons of the Spinal Muscular Atrophy Gene.
Volume: 11
Issue: 4
Pages: e0154390
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Publication
23220400 | J:318821
 
First Author: Mercier MS
Year: 2013
Journal: Neuropharmacology
Title: Characterisation of an mGlu8 receptor-selective agonist and antagonist in the lateral and medial perforant path inputs to the dentate gyrus.
Volume: 67
Pages: 294-303
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Publication
28814546 | J:245862
 
First Author: Gogliotti RG
Year: 2017
Journal: Sci Transl Med
Title: mGlu7 potentiation rescues cognitive, social, and respiratory phenotypes in a mouse model of Rett syndrome.
Volume: 9
Issue: 403
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Publication
23029491 | J:191961
First Author: Lee AJ
Year: 2012
Journal: PLoS One
Title: Limited phenotypic effects of selectively augmenting the SMN protein in the neurons of a mouse model of severe spinal muscular atrophy.
Volume: 7
Issue: 9
Pages: e46353
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Publication
25859009 | J:223348
First Author: Gombash SE
Year: 2015
Journal: Hum Mol Genet
Title: SMN deficiency disrupts gastrointestinal and enteric nervous system function in mice.
Volume: 24
Issue: 13
Pages: 3847-60
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Publication
21143597 | J:170420
First Author: Martín R
Year: 2011
Journal: J Neurochem
Title: Non-additive potentiation of glutamate release by phorbol esters and metabotropic mGlu7 receptor in cerebrocortical nerve terminals.
Volume: 116
Issue: 4
Pages: 476-85
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35551393 | J:348135
First Author: Comley LH
Year: 2022
Journal: Hum Mol Genet
Title: Motor unit recovery following Smn restoration in mouse models of spinal muscular atrophy.
Volume: 31
Issue: 18
Pages: 3107-3119
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Publication
24463453 | J:208442
First Author: Kariya S
Year: 2014
Journal: J Clin Invest
Title: Requirement of enhanced Survival Motoneuron protein imposed during neuromuscular junction maturation.
Volume: 124
Issue: 2
Pages: 785-800
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Publication
37957344 | J:348138
First Author: Valsecchi V
Year: 2023
Journal: Commun Biol
Title: SMN deficiency perturbs monoamine neurotransmitter metabolism in spinal muscular atrophy.
Volume: 6
Issue: 1
Pages: 1155
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Publication
26502195 | J:231487
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
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19332122 | J:150474
First Author: Turner BJ
Year: 2009
Journal: Neurobiol Dis
Title: Survival motor neuron deficiency enhances progression in an amyotrophic lateral sclerosis mouse model.
Volume: 34
Issue: 3
Pages: 511-7
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36757138 | J:341018
First Author: Ojala KS
Year: 2023
Journal: Hum Mol Genet
Title: Potentiation of neuromuscular transmission by a small molecule calcium channel gating modifier improves motor function in a severe spinal muscular atrophy mouse model.
Volume: 32
Issue: 11
Pages: 1901-1911
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Publication
19945425 | J:156779
First Author: Butchbach ME
Year: 2010
Journal: Biochem Biophys Res Commun
Title: Effect of diet on the survival and phenotype of a mouse model for spinal muscular atrophy.
Volume: 391
Issue: 1
Pages: 835-40
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Publication
19010792 | J:143540
First Author: Meyer K
Year: 2009
Journal: Hum Mol Genet
Title: Rescue of a severe mouse model for spinal muscular atrophy by U7 snRNA-mediated splicing modulation.
Volume: 18
Issue: 3
Pages: 546-55
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Publication
25104390 | J:216311
First Author: Naryshkin NA
Year: 2014
Journal: Science
Title: Motor neuron disease. SMN2 splicing modifiers improve motor function and longevity in mice with spinal muscular atrophy.
Volume: 345
Issue: 6197
Pages: 688-93
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Publication
33144430 | J:315666
First Author: Ando S
Year: 2020
Journal: In Vivo
Title: SMN Protein Contributes to Skeletal Muscle Cell Maturation Via Caspase-3 and Akt Activation.
Volume: 34
Issue: 6
Pages: 3247-3254
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Publication
23718187 | J:355102
First Author: Voigt T
Year: 2014
Journal: Neuropathol Appl Neurobiol
Title: The craniosacral progression of muscle development influences the emergence of neuromuscular junction alterations in a severe murine model for spinal muscular atrophy.
Volume: 40
Issue: 4
Pages: 416-34
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Publication
20693262 | J:164446
First Author: Heier CR
Year: 2010
Journal: Hum Mol Genet
Title: Arrhythmia and cardiac defects are a feature of spinal muscular atrophy model mice.
Volume: 19
Issue: 20
Pages: 3906-18
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20696672 | J:164444
First Author: Shababi M
Year: 2010
Journal: Hum Mol Genet
Title: Cardiac defects contribute to the pathology of spinal muscular atrophy models.
Volume: 19
Issue: 20
Pages: 4059-71
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Publication
31543414 | J:355101
First Author: Rashnonejad A
Year: 2019
Journal: Mol Ther
Title: Fetal Gene Therapy Using a Single Injection of Recombinant AAV9 Rescued SMA Phenotype in Mice.
Volume: 27
Issue: 12
Pages: 2123-2133
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Publication
38318851 | J:355109
   
First Author: Hann SH
Year: 2024
Journal: Elife
Title: Depletion of SMN protein in mesenchymal progenitors impairs the development of bone and neuromuscular junction in spinal muscular atrophy.
Volume: 12
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Publication
22306031 | J:181868
 
First Author: Fulceri F
Year: 2012
Journal: Brain Res
Title: Motor neuron pathology and behavioral alterations at late stages in a SMA mouse model.
Volume: 1442
Pages: 66-75
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Publication
26506088 | J:355106
First Author: Somers E
Year: 2016
Journal: Ann Neurol
Title: Vascular Defects and Spinal Cord Hypoxia in Spinal Muscular Atrophy.
Volume: 79
Issue: 2
Pages: 217-30
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Publication
20639395 | J:164456
First Author: Bevan AK
Year: 2010
Journal: Hum Mol Genet
Title: Early heart failure in the SMNDelta7 model of spinal muscular atrophy and correction by postnatal scAAV9-SMN delivery.
Volume: 19
Issue: 20
Pages: 3895-905
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Publication
35688133 | J:326049
First Author: Marasco LE
Year: 2022
Journal: Cell
Title: Counteracting chromatin effects of a splicing-correcting antisense oligonucleotide improves its therapeutic efficacy in spinal muscular atrophy.
Volume: 185
Issue: 12
Pages: 2057-2070.e15
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18455159 | J:137949
First Author: El-Khodor BF
Year: 2008
Journal: Exp Neurol
Title: Identification of a battery of tests for drug candidate evaluation in the SMNDelta7 neonate model of spinal muscular atrophy.
Volume: 212
Issue: 1
Pages: 29-43
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Publication
34734684 | J:355107
 
First Author: Boido M
Year: 2021
Journal: Eur J Histochem
Title: Organotypic spinal cord cultures: An in vitro 3D model to preliminary screen treatments for spinal muscular atrophy.
Volume: 65
Issue: s1
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24324819 | J:209739
First Author: d'Errico P
Year: 2013
Journal: PLoS One
Title: Selective vulnerability of spinal and cortical motor neuron subpopulations in delta7 SMA mice.
Volume: 8
Issue: 12
Pages: e82654
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Publication
19897588 | J:355114
First Author: Butchbach ME
Year: 2010
Journal: Hum Mol Genet
Title: Effects of 2,4-diaminoquinazoline derivatives on SMN expression and phenotype in a mouse model for spinal muscular atrophy.
Volume: 19
Issue: 3
Pages: 454-67
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Publication
36130491 | J:329300
First Author: Tisdale S
Year: 2022
Journal: Cell Rep
Title: SMN controls neuromuscular junction integrity through U7 snRNP.
Volume: 40
Issue: 12
Pages: 111393
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Publication
26911699 | J:231598
First Author: Zhou C
Year: 2016
Journal: J Neurosci
Title: Defects in Motoneuron-Astrocyte Interactions in Spinal Muscular Atrophy.
Volume: 36
Issue: 8
Pages: 2543-53
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30519476 | J:355115
First Author: Poirier A
Year: 2018
Journal: Pharmacol Res Perspect
Title: Risdiplam distributes and increases SMN protein in both the central nervous system and peripheral organs.
Volume: 6
Issue: 6
Pages: e00447
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20097677 | J:158347
First Author: Riessland M
Year: 2010
Journal: Hum Mol Genet
Title: SAHA ameliorates the SMA phenotype in two mouse models for spinal muscular atrophy.
Volume: 19
Issue: 8
Pages: 1492-506
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Publication
34368854 | J:325629
First Author: Zhao X
Year: 2021
Journal: Hum Mol Genet
Title: SMN protein is required throughout life to prevent spinal muscular atrophy disease progression.
Volume: 31
Issue: 1
Pages: 82-96
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24332368 | J:204134
First Author: Tisdale S
Year: 2013
Journal: Cell Rep
Title: SMN is essential for the biogenesis of U7 small nuclear ribonucleoprotein and 3'-end formation of histone mRNAs.
Volume: 5
Issue: 5
Pages: 1187-95
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Publication
26621405 | J:231139
 
First Author: Neve A
Year: 2016
Journal: Mol Cell Neurosci
Title: Central and peripheral defects in motor units of the diaphragm of spinal muscular atrophy mice.
Volume: 70
Pages: 30-41
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28172892 | J:238649
First Author: Eshraghi M
Year: 2016
Journal: Hum Mol Genet
Title: Effect of genetic background on the phenotype of the Smn2B/- mouse model of spinal muscular atrophy.
Volume: 25
Issue: 20
Pages: 4494-4506
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20832308 | J:231141
First Author: Voigt T
Year: 2010
Journal: Neuromuscul Disord
Title: Ultrastructural changes in diaphragm neuromuscular junctions in a severe mouse model for Spinal Muscular Atrophy and their prevention by bifunctional U7 snRNA correcting SMN2 splicing.
Volume: 20
Issue: 11
Pages: 744-52
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Publication
25692239 | J:231140
First Author: Huo Q
Year: 2014
Journal: RNA Biol
Title: Splicing changes in SMA mouse motoneurons and SMN-depleted neuroblastoma cells: evidence for involvement of splicing regulatory proteins.
Volume: 11
Issue: 11
Pages: 1430-46
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Publication
15703193 | J:97103
First Author: Le TT
Year: 2005
Journal: Hum Mol Genet
Title: SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN.
Volume: 14
Issue: 6
Pages: 845-57
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Publication
37218083 | J:355143
First Author: Cottam NC
Year: 2023
Journal: Brain Pathol
Title: Cerebellar structural, astrocytic, and neuronal abnormalities in the SMNΔ7 mouse model of spinal muscular atrophy.
Volume: 33
Issue: 5
Pages: e13162
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Publication
22669476 | J:355145
First Author: Murdocca M
Year: 2012
Journal: Mol Med
Title: IPLEX administration improves motor neuron survival and ameliorates motor functions in a severe mouse model of spinal muscular atrophy.
Volume: 18
Issue: 1
Pages: 1076-85
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Publication
32820007 | J:355144
First Author: Nichterwitz S
Year: 2020
Journal: Genome Res
Title: LCM-seq reveals unique transcriptional adaptation mechanisms of resistant neurons and identifies protective pathways in spinal muscular atrophy.
Volume: 30
Issue: 8
Pages: 1083-1096
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Publication
31272106 | J:355138
First Author: Pilato CM
Year: 2019
Journal: Hum Mol Genet
Title: Motor neuron loss in SMA is not associated with somal stress-activated JNK/c-Jun signaling.
Volume: 28
Issue: 19
Pages: 3282-3292
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Publication
21968514 | J:178856
First Author: Ling KK
Year: 2012
Journal: Hum Mol Genet
Title: Severe neuromuscular denervation of clinically relevant muscles in a mouse model of spinal muscular atrophy.
Volume: 21
Issue: 1
Pages: 185-95
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38561840 | J:355140
First Author: Virla F
Year: 2024
Journal: Stem Cell Res Ther
Title: Administration of adipose-derived stem cells extracellular vesicles in a murine model of spinal muscular atrophy: effects of a new potential therapeutic strategy.
Volume: 15
Issue: 1
Pages: 94
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Publication
30842449 | J:275605
First Author: Ohuchi K
Year: 2019
Journal: Sci Rep
Title: Notch Signaling Mediates Astrocyte Abnormality in Spinal Muscular Atrophy Model Systems.
Volume: 9
Issue: 1
Pages: 3701
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26582176 | J:355147
First Author: Cerveró C
Year: 2016
Journal: Neurotherapeutics
Title: Chronic Treatment with the AMPK Agonist AICAR Prevents Skeletal Muscle Pathology but Fails to Improve Clinical Outcome in a Mouse Model of Severe Spinal Muscular Atrophy.
Volume: 13
Issue: 1
Pages: 198-216
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Publication
38650097 | J:355146
First Author: Rhee J
Year: 2024
Journal: J Cachexia Sarcopenia Muscle
Title: Improved therapeutic approach for spinal muscular atrophy via ubiquitination-resistant survival motor neuron variant.
Volume: 15
Issue: 4
Pages: 1404-1417
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Publication
38413838 | J:347664
First Author: Xie Q
Year: 2024
Journal: EMBO Mol Med
Title: Improved gene therapy for spinal muscular atrophy in mice using codon-optimized hSMN1 transgene and hSMN1 gene-derived promotor.
Volume: 16
Issue: 4
Pages: 945-965
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24119341 | J:202752
First Author: Boyer JG
Year: 2013
Journal: Skelet Muscle
Title: Early onset muscle weakness and disruption of muscle proteins in mouse models of spinal muscular atrophy.
Volume: 3
Issue: 1
Pages: 24
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29982416 | J:265815
First Author: Iyer CC
Year: 2018
Journal: Hum Mol Genet
Title: Mild SMN missense alleles are only functional in the presence of SMN2 in mammals.
Volume: 27
Issue: 19
Pages: 3404-3416
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Publication
32339936 | J:304670
 
First Author: Deguise MO
Year: 2020
Journal: EBioMedicine
Title: Motor transmission defects with sex differences in a new mouse model of mild spinal muscular atrophy.
Volume: 55
Pages: 102750
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29259166 | J:355149
First Author: Piras A
Year: 2017
Journal: Cell Death Dis
Title: Inhibition of autophagy delays motoneuron degeneration and extends lifespan in a mouse model of spinal muscular atrophy.
Volume: 8
Issue: 12
Pages: 3223
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Publication
26892876 | J:355148
 
First Author: Butchbach MER
Year: 2016
Journal: Exp Neurol
Title: Protective effects of butyrate-based compounds on a mouse model for spinal muscular atrophy.
Volume: 279
Pages: 13-26
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Publication
35864358 | J:355194
First Author: Januel C
Year: 2022
Journal: Cell Mol Life Sci
Title: Moxifloxacin rescues SMA phenotypes in patient-derived cells and animal model.
Volume: 79
Issue: 8
Pages: 441
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Publication
34413305 | J:308940
First Author: Riboldi GM
Year: 2021
Journal: Nat Commun
Title: Sumoylation regulates the assembly and activity of the SMN complex.
Volume: 12
Issue: 1
Pages: 5040
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Publication
29767748 | J:355154
First Author: Cerveró C
Year: 2018
Journal: J Neuropathol Exp Neurol
Title: Glial Activation and Central Synapse Loss, but Not Motoneuron Degeneration, Are Prevented by the Sigma-1 Receptor Agonist PRE-084 in the Smn2B/- Mouse Model of Spinal Muscular Atrophy.
Volume: 77
Issue: 7
Pages: 577-597
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Publication
32075715 | J:355151
First Author: Valsecchi V
Year: 2020
Journal: Mol Ther
Title: miR-206 Reduces the Severity of Motor Neuron Degeneration in the Facial Nuclei of the Brainstem in a Mouse Model of SMA.
Volume: 28
Issue: 4
Pages: 1154-1166
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Publication
31563042 | J:355152
 
First Author: Baek J
Year: 2019
Journal: Phytomedicine
Title: Improvement of spinal muscular atrophy via correction of the SMN2 splicing defect by Brucea javanica (L.) Merr. extract and Bruceine D.
Volume: 65
Pages: 153089
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19150990 | J:355163
First Author: Heier CR
Year: 2009
Journal: Hum Mol Genet
Title: Translational readthrough by the aminoglycoside geneticin (G418) modulates SMN stability in vitro and improves motor function in SMA mice in vivo.
Volume: 18
Issue: 7
Pages: 1310-22
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Publication
22153987 | J:355162
First Author: Somers E
Year: 2012
Journal: Neuromuscul Disord
Title: Density, calibre and ramification of muscle capillaries are altered in a mouse model of severe spinal muscular atrophy.
Volume: 22
Issue: 5
Pages: 435-42
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Publication
22705478 | J:186551
First Author: Hayhurst M
Year: 2012
Journal: Dev Biol
Title: A cell-autonomous defect in skeletal muscle satellite cells expressing low levels of survival of motor neuron protein.
Volume: 368
Issue: 2
Pages: 323-34
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Publication
22750651 | J:355159
First Author: El-Khodor BF
Year: 2012
Journal: J Neurosci Methods
Title: Prediction of death in the SMNΔ7 mouse model of spinal muscular atrophy: insight into disease stage and progression.
Volume: 209
Issue: 2
Pages: 259-68
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Publication
24405637 | J:355161
 
First Author: Hadwen J
Year: 2014
Journal: Orphanet J Rare Dis
Title: VPAC2 receptor agonist BAY 55-9837 increases SMN protein levels and moderates disease phenotype in severe spinal muscular atrophy mouse models.
Volume: 9
Pages: 4
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Publication
19074460 | J:145746
First Author: Rose FF Jr
Year: 2009
Journal: Hum Mol Genet
Title: Delivery of recombinant follistatin lessens disease severity in a mouse model of spinal muscular atrophy.
Volume: 18
Issue: 6
Pages: 997-1005
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Publication
34808387 | J:355201
First Author: Bersani M
Year: 2022
Journal: Mol Ther
Title: Cell-penetrating peptide-conjugated Morpholino rescues SMA in a symptomatic preclinical model.
Volume: 30
Issue: 3
Pages: 1288-1299
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Publication
27456062 | J:355200
First Author: Odermatt P
Year: 2016
Journal: Mol Ther
Title: Somatic Therapy of a Mouse SMA Model with a U7 snRNA Gene Correcting SMN2 Splicing.
Volume: 24
Issue: 10
Pages: 1797-1805
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Publication
19884170 | J:155336
First Author: Murray LM
Year: 2010
Journal: Hum Mol Genet
Title: Pre-symptomatic development of lower motor neuron connectivity in a mouse model of severe spinal muscular atrophy.
Volume: 19
Issue: 3
Pages: 420-33
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Publication
20538619 | J:355206
First Author: Valori CF
Year: 2010
Journal: Sci Transl Med
Title: Systemic delivery of scAAV9 expressing SMN prolongs survival in a model of spinal muscular atrophy.
Volume: 2
Issue: 35
Pages: 35ra42
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Publication
26931466 | J:348120
First Author: Zhao X
Year: 2016
Journal: Hum Mol Genet
Title: Pharmacokinetics, pharmacodynamics, and efficacy of a small-molecule SMN2 splicing modifier in mouse models of spinal muscular atrophy.
Volume: 25
Issue: 10
Pages: 1885-1899
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Publication
33795885 | J:336198
First Author: Van Alstyne M
Year: 2021
Journal: Nat Neurosci
Title: Gain of toxic function by long-term AAV9-mediated SMN overexpression in the sensorimotor circuit.
Volume: 24
Issue: 7
Pages: 930-940
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Publication
27907033 | J:251397
First Author: Arnold WD
Year: 2016
Journal: PLoS One
Title: Normalization of Patient-Identified Plasma Biomarkers in SMNΔ7 Mice following Postnatal SMN Restoration.
Volume: 11
Issue: 12
Pages: e0167077
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Publication
14623865 | J:86712
First Author: Rossoll W
Year: 2003
Journal: J Cell Biol
Title: Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons.
Volume: 163
Issue: 4
Pages: 801-12
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Publication
18065780 | J:132467
First Author: Murray LM
Year: 2008
Journal: Hum Mol Genet
Title: Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy.
Volume: 17
Issue: 7
Pages: 949-62
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