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Search results 201 to 300 out of 434 for Grm7

0.036s
Type Details Score
GXD Expression    
Probe: MGI:5001974
Assay Type: RNA in situ
Annotation Date: 2014-02-07
Strength: Absent
Sex: Female
Emaps: EMAPS:1796223
Stage: TS23
Assay Id: MGI:5542528
Age: embryonic day 15.5
Image: GUDMAP:8471
Specimen Label: GUDMAP:8471
Detected: false
Specimen Num: 1
GXD Expression        
Assay Type: In situ reporter (knock in)
Annotation Date: 2006-07-27
Strength: Absent
Sex: Male
Emaps: EMAPS:1868228
Stage: TS28
Assay Id: MGI:3639195
Age: postnatal day 53
Specimen Label: Mouse 101621
Detected: false
Specimen Num: 27
Publication
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
Publication
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
Publication
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
Publication
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
Publication
First Author: McGovern VL
Year: 2021
Journal: Hum Mol Genet
Title: Intragenic complementation of amino and carboxy terminal SMN missense mutations can rescue Smn null mice.
Volume: 29
Issue: 21
Pages: 3493-3503
Publication  
First Author: Chen TH
Year: 2023
Journal: Mol Ther Nucleic Acids
Title: MiR34 contributes to spinal muscular atrophy and AAV9-mediated delivery of MiR34a ameliorates the motor deficits in SMA mice.
Volume: 32
Pages: 144-160
Publication
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
Publication
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
Publication
First Author: Monani UR
Year: 2003
Journal: J Cell Biol
Title: A transgene carrying an A2G missense mutation in the SMN gene modulates phenotypic severity in mice with severe (type I) spinal muscular atrophy.
Volume: 160
Issue: 1
Pages: 41-52
Publication  
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
Publication
First Author: Gavrilina TO
Year: 2008
Journal: Hum Mol Genet
Title: Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effect.
Volume: 17
Issue: 8
Pages: 1063-75
Publication
First Author: Workman E
Year: 2009
Journal: Hum Mol Genet
Title: A SMN missense mutation complements SMN2 restoring snRNPs and rescuing SMA mice.
Volume: 18
Issue: 12
Pages: 2215-29
Publication
First Author: Bertaso F
Year: 2008
Journal: Nat Neurosci
Title: PICK1 uncoupling from mGluR7a causes absence-like seizures.
Volume: 11
Issue: 8
Pages: 940-8
Publication
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
Publication
First Author: Hunter G
Year: 2014
Journal: Hum Mol Genet
Title: SMN-dependent intrinsic defects in Schwann cells in mouse models of spinal muscular atrophy.
Volume: 23
Issue: 9
Pages: 2235-50
Publication
First Author: Sleigh JN
Year: 2011
Journal: Dis Model Mech
Title: The contribution of mouse models to understanding the pathogenesis of spinal muscular atrophy.
Volume: 4
Issue: 4
Pages: 457-67
Publication    
First Author: O'Hern PJ
Year: 2017
Journal: Elife
Title: Decreased microRNA levels lead to deleterious increases in neuronal M2 muscarinic receptors in Spinal Muscular Atrophy models.
Volume: 6
Publication
First Author: Mutsaers CA
Year: 2011
Journal: Hum Mol Genet
Title: Reversible molecular pathology of skeletal muscle in spinal muscular atrophy.
Volume: 20
Issue: 22
Pages: 4334-44
Publication
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
Publication
First Author: Gogliotti RG
Year: 2011
Journal: Neurobiol Dis
Title: Characterization of a commonly used mouse model of SMA reveals increased seizure susceptibility and heightened fear response in FVB/N mice.
Volume: 43
Issue: 1
Pages: 142-51
Publication
First Author: Ling KK
Year: 2010
Journal: PLoS One
Title: Synaptic defects in the spinal and neuromuscular circuitry in a mouse model of spinal muscular atrophy.
Volume: 5
Issue: 11
Pages: e15457
Publication
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
Publication
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
Publication  
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
Publication
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
Publication
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
Publication
First Author: Miller N
Year: 2016
Journal: Hum Mol Genet
Title: Motor neuron mitochondrial dysfunction in spinal muscular atrophy.
Volume: 25
Issue: 16
Pages: 3395-3406
Publication
First Author: McGovern VL
Year: 2008
Journal: Hum Mol Genet
Title: Embryonic motor axon development in the severe SMA mouse.
Volume: 17
Issue: 18
Pages: 2900-9
Publication
First Author: Ruggiu M
Year: 2012
Journal: Mol Cell Biol
Title: A role for SMN exon 7 splicing in the selective vulnerability of motor neurons in spinal muscular atrophy.
Volume: 32
Issue: 1
Pages: 126-38
Publication
First Author: Rodriguez-Muela N
Year: 2017
Journal: Cell Rep
Title: Single-Cell Analysis of SMN Reveals Its Broader Role in Neuromuscular Disease.
Volume: 18
Issue: 6
Pages: 1484-1498
Publication
First Author: Cobb MS
Year: 2013
Journal: Hum Mol Genet
Title: Development and characterization of an SMN2-based intermediate mouse model of Spinal Muscular Atrophy.
Volume: 22
Issue: 9
Pages: 1843-55
Publication
First Author: Osman EY
Year: 2014
Journal: Hum Mol Genet
Title: Morpholino antisense oligonucleotides targeting intronic repressor Element1 improve phenotype in SMA mouse models.
Volume: 23
Issue: 18
Pages: 4832-45
Publication
First Author: Lee YI
Year: 2011
Journal: Dev Biol
Title: Muscles in a mouse model of spinal muscular atrophy show profound defects in neuromuscular development even in the absence of failure in neuromuscular transmission or loss of motor neurons.
Volume: 356
Issue: 2
Pages: 432-44
Publication
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
Publication
First Author: Luchetti A
Year: 2015
Journal: Int J Mol Sci
Title: A Perturbed MicroRNA Expression Pattern Characterizes Embryonic Neural Stem Cells Derived from a Severe Mouse Model of Spinal Muscular Atrophy (SMA).
Volume: 16
Issue: 8
Pages: 18312-27
Publication
First Author: Arbab M
Year: 2023
Journal: Science
Title: Base editing rescue of spinal muscular atrophy in cells and in mice.
Volume: 380
Issue: 6642
Pages: eadg6518
Publication  
First Author: Boido M
Year: 2018
Journal: Front Cell Neurosci
Title: Increasing Agrin Function Antagonizes Muscle Atrophy and Motor Impairment in Spinal Muscular Atrophy.
Volume: 12
Pages: 17
Publication
First Author: Carlini MJ
Year: 2022
Journal: PLoS One
Title: Neuromuscular denervation and deafferentation but not motor neuron death are disease features in the Smn2B/- mouse model of SMA.
Volume: 17
Issue: 8
Pages: e0267990
Publication
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
Publication
First Author: Rimer M
Year: 2019
Journal: Sci Rep
Title: Nerve sprouting capacity in a pharmacologically induced mouse model of spinal muscular atrophy.
Volume: 9
Issue: 1
Pages: 7799
Publication
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
Publication
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
Publication
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
Publication
First Author: Kye MJ
Year: 2014
Journal: Hum Mol Genet
Title: SMN regulates axonal local translation via miR-183/mTOR pathway.
Volume: 23
Issue: 23
Pages: 6318-31
Publication  
First Author: Tapia O
Year: 2017
Journal: Neurobiol Dis
Title: Cellular bases of the RNA metabolism dysfunction in motor neurons of a murine model of spinal muscular atrophy: Role of Cajal bodies and the nucleolus.
Volume: 108
Pages: 83-99
Publication
First Author: Valsecchi V
Year: 2015
Journal: PLoS One
Title: Expression of Muscle-Specific MiRNA 206 in the Progression of Disease in a Murine SMA Model.
Volume: 10
Issue: 6
Pages: e0128560
Publication
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
Publication
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
Publication
First Author: Bebee TW
Year: 2012
Journal: Hum Mol Genet
Title: Hypoxia is a modifier of SMN2 splicing and disease severity in a severe SMA mouse model.
Volume: 21
Issue: 19
Pages: 4301-13
Publication
First Author: Dominguez E
Year: 2011
Journal: Hum Mol Genet
Title: Intravenous scAAV9 delivery of a codon-optimized SMN1 sequence rescues SMA mice.
Volume: 20
Issue: 4
Pages: 681-93
Publication
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
Publication
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
Publication
First Author: Ruiz R
Year: 2010
Journal: J Neurosci
Title: Altered intracellular Ca2+ homeostasis in nerve terminals of severe spinal muscular atrophy mice.
Volume: 30
Issue: 3
Pages: 849-57
Publication
First Author: Farooq F
Year: 2013
Journal: Hum Mol Genet
Title: Celecoxib increases SMN and survival in a severe spinal muscular atrophy mouse model via p38 pathway activation.
Volume: 22
Issue: 17
Pages: 3415-24
Publication  
First Author: Rietz A
Year: 2021
Journal: Life Sci Alliance
Title: Short-duration splice promoting compound enables a tunable mouse model of spinal muscular atrophy.
Volume: 4
Issue: 1
Publication
First Author: Robbins KL
Year: 2014
Journal: Hum Mol Genet
Title: Defining the therapeutic window in a severe animal model of spinal muscular atrophy.
Volume: 23
Issue: 17
Pages: 4559-68
Publication  
First Author: Sun J
Year: 2019
Journal: Front Cell Neurosci
Title: The Alteration of Intrinsic Excitability and Synaptic Transmission in Lumbar Spinal Motor Neurons and Interneurons of Severe Spinal Muscular Atrophy Mice.
Volume: 13
Pages: 15
Publication  
First Author: Arnold W
Year: 2016
Journal: Neurobiol Dis
Title: The neuromuscular impact of symptomatic SMN restoration in a mouse model of spinal muscular atrophy.
Volume: 87
Pages: 116-23
Publication
First Author: Zhang Z
Year: 2013
Journal: Proc Natl Acad Sci U S A
Title: Dysregulation of synaptogenesis genes antecedes motor neuron pathology in spinal muscular atrophy.
Volume: 110
Issue: 48
Pages: 19348-53
Publication
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
Publication
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
Publication
First Author: Osman EY
Year: 2019
Journal: Sci Rep
Title: Functional characterization of SMN evolution in mouse models of SMA.
Volume: 9
Issue: 1
Pages: 9472
Publication  
First Author: Miralles MP
Year: 2022
Journal: Front Cell Neurosci
Title: Survival motor neuron protein and neurite degeneration are regulated by Gemin3 in spinal muscular atrophy motoneurons.
Volume: 16
Pages: 1054270
Publication
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
Publication  
First Author: Ikenaka A
Year: 2023
Journal: Life Sci Alliance
Title: SMN promotes mitochondrial metabolic maturation during myogenesis by regulating the MYOD-miRNA axis.
Volume: 6
Issue: 3
Publication
First Author: Simon CM
Year: 2021
Journal: J Neurosci
Title: Chronic Pharmacological Increase of Neuronal Activity Improves Sensory-Motor Dysfunction in Spinal Muscular Atrophy Mice.
Volume: 41
Issue: 2
Pages: 376-389
Publication  
First Author: Tharaneetharan A
Year: 2021
Journal: Neuroscience
Title: Functional Abnormalities of Cerebellum and Motor Cortex in Spinal Muscular Atrophy Mice.
Volume: 452
Pages: 78-97
Publication
First Author: Butchbach ME
Year: 2007
Journal: Neurobiol Dis
Title: Abnormal motor phenotype in the SMNDelta7 mouse model of spinal muscular atrophy.
Volume: 27
Issue: 2
Pages: 207-19
Publication
First Author: Feng Z
Year: 2016
Journal: Hum Mol Genet
Title: Pharmacologically induced mouse model of adult spinal muscular atrophy to evaluate effectiveness of therapeutics after disease onset.
Volume: 25
Issue: 5
Pages: 964-75
Publication
First Author: McGivern JV
Year: 2013
Journal: Glia
Title: Spinal muscular atrophy astrocytes exhibit abnormal calcium regulation and reduced growth factor production.
Volume: 61
Issue: 9
Pages: 1418-1428
Publication
First Author: Boyer JG
Year: 2014
Journal: Hum Mol Genet
Title: Myogenic program dysregulation is contributory to disease pathogenesis in spinal muscular atrophy.
Volume: 23
Issue: 16
Pages: 4249-59
Publication
First Author: Long KK
Year: 2019
Journal: Hum Mol Genet
Title: Specific inhibition of myostatin activation is beneficial in mouse models of SMA therapy.
Volume: 28
Issue: 7
Pages: 1076-1089
Publication
First Author: Khairallah MT
Year: 2017
Journal: Hum Mol Genet
Title: SMN deficiency negatively impacts red pulp macrophages and spleen development in mouse models of spinal muscular atrophy.
Volume: 26
Issue: 5
Pages: 932-941
Publication
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
Publication
First Author: Porensky PN
Year: 2012
Journal: Hum Mol Genet
Title: A single administration of morpholino antisense oligomer rescues spinal muscular atrophy in mouse.
Volume: 21
Issue: 7
Pages: 1625-38
Publication
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
Publication
First Author: Sison SL
Year: 2017
Journal: Hum Mol Genet
Title: Astrocyte-produced miR-146a as a mediator of motor neuron loss in spinal muscular atrophy.
Volume: 26
Issue: 17
Pages: 3409-3420
Publication  
First Author: Dachs E
Year: 2013
Journal: Neuroscience
Title: Chronic treatment with lithium does not improve neuromuscular phenotype in a mouse model of severe spinal muscular atrophy.
Volume: 250
Pages: 417-33
Publication
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
Publication
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
Publication
First Author: Kong L
Year: 2009
Journal: J Neurosci
Title: Impaired synaptic vesicle release and immaturity of neuromuscular junctions in spinal muscular atrophy mice.
Volume: 29
Issue: 3
Pages: 842-51
Publication
First Author: Tisdale S
Year: 2022
Journal: Cell Rep
Title: SMN controls neuromuscular junction integrity through U7 snRNP.
Volume: 40
Issue: 12
Pages: 111393
Publication
First Author: Dale JM
Year: 2011
Journal: Acta Neuropathol
Title: The spinal muscular atrophy mouse model, SMAΔ7, displays altered axonal transport without global neurofilament alterations.
Volume: 122
Issue: 3
Pages: 331-41
Publication
First Author: Torres-Benito L
Year: 2011
Journal: PLoS One
Title: SMN requirement for synaptic vesicle, active zone and microtubule postnatal organization in motor nerve terminals.
Volume: 6
Issue: 10
Pages: e26164
Publication
First Author: Stachniak TJ
Year: 2019
Journal: J Neurosci
Title: Elfn1-Induced Constitutive Activation of mGluR7 Determines Frequency-Dependent Recruitment of Somatostatin Interneurons.
Volume: 39
Issue: 23
Pages: 4461-4474
Publication
First Author: Zhang CS
Year: 2008
Journal: J Neurosci
Title: Knock-in mice lacking the PDZ-ligand motif of mGluR7a show impaired PKC-dependent autoinhibition of glutamate release, spatial working memory deficits, and increased susceptibility to pentylenetetrazol.
Volume: 28
Issue: 34
Pages: 8604-14
Publication
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
Publication  
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
Publication
First Author: Monani UR
Year: 2000
Journal: Hum Mol Genet
Title: The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy.
Volume: 9
Issue: 3
Pages: 333-9
Publication
First Author: See K
Year: 2014
Journal: Hum Mol Genet
Title: SMN deficiency alters Nrxn2 expression and splicing in zebrafish and mouse models of spinal muscular atrophy.
Volume: 23
Issue: 7
Pages: 1754-70
Publication
First Author: Walker MP
Year: 2008
Journal: Hum Mol Genet
Title: SMN complex localizes to the sarcomeric Z-disc and is a proteolytic target of calpain.
Volume: 17
Issue: 21
Pages: 3399-410
Publication
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
Publication
First Author: Thomson SR
Year: 2012
Journal: PLoS One
Title: Morphological characteristics of motor neurons do not determine their relative susceptibility to degeneration in a mouse model of severe spinal muscular atrophy.
Volume: 7
Issue: 12
Pages: e52605
Publication
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
Publication
First Author: Sansa A
Year: 2021
Journal: Acta Neuropathol Commun
Title: Spinal Muscular Atrophy autophagy profile is tissue-dependent: differential regulation between muscle and motoneurons.
Volume: 9
Issue: 1
Pages: 122
Publication
First Author: Novoyatleva T
Year: 2008
Journal: Hum Mol Genet
Title: Protein phosphatase 1 binds to the RNA recognition motif of several splicing factors and regulates alternative pre-mRNA processing.
Volume: 17
Issue: 1
Pages: 52-70
Publication
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
Publication
First Author: Zhang H
Year: 2010
Journal: PLoS One
Title: Electrophysiological properties of motor neurons in a mouse model of severe spinal muscular atrophy: in vitro versus in vivo development.
Volume: 5
Issue: 7
Pages: e11696