248 related articles for article (PubMed ID: 21300852)
1. Modeling spinal muscular atrophy in Drosophila links Smn to FGF signaling.
Sen A; Yokokura T; Kankel MW; Dimlich DN; Manent J; Sanyal S; Artavanis-Tsakonas S
J Cell Biol; 2011 Feb; 192(3):481-95. PubMed ID: 21300852
[TBL] [Abstract][Full Text] [Related]
2. SMN is required for sensory-motor circuit function in Drosophila.
Imlach WL; Beck ES; Choi BJ; Lotti F; Pellizzoni L; McCabe BD
Cell; 2012 Oct; 151(2):427-39. PubMed ID: 23063130
[TBL] [Abstract][Full Text] [Related]
3. SMA-causing missense mutations in survival motor neuron (Smn) display a wide range of phenotypes when modeled in Drosophila.
Praveen K; Wen Y; Gray KM; Noto JJ; Patlolla AR; Van Duyne GD; Matera AG
PLoS Genet; 2014 Aug; 10(8):e1004489. PubMed ID: 25144193
[TBL] [Abstract][Full Text] [Related]
4. Developmental arrest of Drosophila survival motor neuron (Smn) mutants accounts for differences in expression of minor intron-containing genes.
Garcia EL; Lu Z; Meers MP; Praveen K; Matera AG
RNA; 2013 Nov; 19(11):1510-6. PubMed ID: 24006466
[TBL] [Abstract][Full Text] [Related]
5. Motor defects in a Drosophila model for spinal muscular atrophy result from SMN depletion during early neurogenesis.
Grice SJ; Liu JL
PLoS Genet; 2022 Jul; 18(7):e1010325. PubMed ID: 35877682
[TBL] [Abstract][Full Text] [Related]
6. Neuromuscular defects in a Drosophila survival motor neuron gene mutant.
Chan YB; Miguel-Aliaga I; Franks C; Thomas N; Trülzsch B; Sattelle DB; Davies KE; van den Heuvel M
Hum Mol Genet; 2003 Jun; 12(12):1367-76. PubMed ID: 12783845
[TBL] [Abstract][Full Text] [Related]
7. WDR79/TCAB1 plays a conserved role in the control of locomotion and ameliorates phenotypic defects in SMA models.
Di Giorgio ML; Esposito A; Maccallini P; Micheli E; Bavasso F; Gallotta I; Vernì F; Feiguin F; Cacchione S; McCabe BD; Di Schiavi E; Raffa GD
Neurobiol Dis; 2017 Sep; 105():42-50. PubMed ID: 28502804
[TBL] [Abstract][Full Text] [Related]
8. Modeling spinal muscular atrophy in Drosophila.
Chang HC; Dimlich DN; Yokokura T; Mukherjee A; Kankel MW; Sen A; Sridhar V; Fulga TA; Hart AC; Van Vactor D; Artavanis-Tsakonas S
PLoS One; 2008 Sep; 3(9):e3209. PubMed ID: 18791638
[TBL] [Abstract][Full Text] [Related]
9. A Drosophila melanogaster model of spinal muscular atrophy reveals a function for SMN in striated muscle.
Rajendra TK; Gonsalvez GB; Walker MP; Shpargel KB; Salz HK; Matera AG
J Cell Biol; 2007 Mar; 176(6):831-41. PubMed ID: 17353360
[TBL] [Abstract][Full Text] [Related]
10. Genetic Interactions between the Members of the SMN-Gemins Complex in Drosophila.
Borg RM; Bordonne R; Vassallo N; Cauchi RJ
PLoS One; 2015; 10(6):e0130974. PubMed ID: 26098872
[TBL] [Abstract][Full Text] [Related]
11. Reduced survival of motor neuron (SMN) protein in motor neuronal progenitors functions cell autonomously to cause spinal muscular atrophy in model mice expressing the human centromeric (SMN2) gene.
Park GH; Maeno-Hikichi Y; Awano T; Landmesser LT; Monani UR
J Neurosci; 2010 Sep; 30(36):12005-19. PubMed ID: 20826664
[TBL] [Abstract][Full Text] [Related]
12. Mechanisms of exercise-induced survival motor neuron expression in the skeletal muscle of spinal muscular atrophy-like mice.
Ng SY; Mikhail A; Ljubicic V
J Physiol; 2019 Sep; 597(18):4757-4778. PubMed ID: 31361024
[TBL] [Abstract][Full Text] [Related]
13. An SMN-dependent U12 splicing event essential for motor circuit function.
Lotti F; Imlach WL; Saieva L; Beck ES; Hao le T; Li DK; Jiao W; Mentis GZ; Beattie CE; McCabe BD; Pellizzoni L
Cell; 2012 Oct; 151(2):440-54. PubMed ID: 23063131
[TBL] [Abstract][Full Text] [Related]
14. Temperature-sensitive spinal muscular atrophy-causing point mutations lead to SMN instability, locomotor defects and premature lethality in
Raimer AC; Singh SS; Edula MR; Paris-Davila T; Vandadi V; Spring AM; Matera AG
Dis Model Mech; 2020 May; 13(5):. PubMed ID: 32501283
[TBL] [Abstract][Full Text] [Related]
15. Motor transmission defects with sex differences in a new mouse model of mild spinal muscular atrophy.
Deguise MO; De Repentigny Y; Tierney A; Beauvais A; Michaud J; Chehade L; Thabet M; Paul B; Reilly A; Gagnon S; Renaud JM; Kothary R
EBioMedicine; 2020 May; 55():102750. PubMed ID: 32339936
[TBL] [Abstract][Full Text] [Related]
16. Self-oligomerization regulates stability of survival motor neuron protein isoforms by sequestering an SCF
Gray KM; Kaifer KA; Baillat D; Wen Y; Bonacci TR; Ebert AD; Raimer AC; Spring AM; Have ST; Glascock JJ; Gupta K; Van Duyne GD; Emanuele MJ; Lamond AI; Wagner EJ; Lorson CL; Matera AG
Mol Biol Cell; 2018 Jan; 29(2):96-110. PubMed ID: 29167380
[TBL] [Abstract][Full Text] [Related]
17. 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.
Le TT; Pham LT; Butchbach ME; Zhang HL; Monani UR; Coovert DD; Gavrilina TO; Xing L; Bassell GJ; Burghes AH
Hum Mol Genet; 2005 Mar; 14(6):845-57. PubMed ID: 15703193
[TBL] [Abstract][Full Text] [Related]
18. Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy.
Kariya S; Park GH; Maeno-Hikichi Y; Leykekhman O; Lutz C; Arkovitz MS; Landmesser LT; Monani UR
Hum Mol Genet; 2008 Aug; 17(16):2552-69. PubMed ID: 18492800
[TBL] [Abstract][Full Text] [Related]
19. HuD interacts with survival motor neuron protein and can rescue spinal muscular atrophy-like neuronal defects.
Hubers L; Valderrama-Carvajal H; Laframboise J; Timbers J; Sanchez G; Côté J
Hum Mol Genet; 2011 Feb; 20(3):553-79. PubMed ID: 21088113
[TBL] [Abstract][Full Text] [Related]
20. Disruption of Survival Motor Neuron in Glia Impacts Survival but has no Effect on Neuromuscular Function in Drosophila.
Farrugia M; Vassallo N; Cauchi RJ
Neuroscience; 2022 May; 491():32-42. PubMed ID: 35314252
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]