Detalhe da pesquisa
1.
Conditional deletion of SMN in cell culture identifies functional SMN alleles.
Hum Mol Genet
; 29(21): 3477-3492, 2020 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33075805
2.
Intragenic complementation of amino and carboxy terminal SMN missense mutations can rescue Smn null mice.
Hum Mol Genet
; 29(21): 3493-3503, 2020 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33084884
3.
Mild SMN missense alleles are only functional in the presence of SMN2 in mammals.
Hum Mol Genet
; 27(19): 3404-3416, 2018 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29982416
4.
Muscle contractility dysfunction precedes loss of motor unit connectivity in SOD1(G93A) mice.
Muscle Nerve
; 59(2): 254-262, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30370671
5.
HuD and the Survival Motor Neuron Protein Interact in Motoneurons and Are Essential for Motoneuron Development, Function, and mRNA Regulation.
J Neurosci
; 37(48): 11559-11571, 2017 11 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-29061699
6.
SMN expression is required in motor neurons to rescue electrophysiological deficits in the SMNΔ7 mouse model of SMA.
Hum Mol Genet
; 24(19): 5524-41, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26206889
7.
Low levels of Survival Motor Neuron protein are sufficient for normal muscle function in the SMNΔ7 mouse model of SMA.
Hum Mol Genet
; 24(21): 6160-73, 2015 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26276812
8.
SMN deficiency disrupts gastrointestinal and enteric nervous system function in mice.
Hum Mol Genet
; 24(13): 3847-60, 2015 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25859009
9.
SMN deficiency disrupts gastrointestinal and enteric nervous system function in mice.
Hum Mol Genet
; 24(19): 5665, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26223459
10.
The m6A methyltransferase METTL3 regulates muscle maintenance and growth in mice.
Nat Commun
; 13(1): 168, 2022 01 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35013323
11.
Voluntary wheel running with and without follistatin overexpression improves NMJ transmission but not motor unit loss in late life of C57BL/6J mice.
Neurobiol Aging
; 101: 285-296, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33678425
12.
Follistatin-induced muscle hypertrophy in aged mice improves neuromuscular junction innervation and function.
Neurobiol Aging
; 104: 32-41, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33964607
13.
Neuromuscular junction transmission failure is a late phenotype in aging mice.
Neurobiol Aging
; 86: 182-190, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31866157
14.
Early-onset aging and mitochondrial defects associated with loss of histone acetyltransferase 1 (Hat1).
Aging Cell
; 18(5): e12992, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31290578
15.
Muscle strength and size are associated with motor unit connectivity in aged mice.
Neurobiol Aging
; 67: 128-136, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29656012
16.
Normalization of Patient-Identified Plasma Biomarkers in SMNΔ7 Mice following Postnatal SMN Restoration.
PLoS One
; 11(12): e0167077, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27907033
17.
Deletion of atrophy enhancing genes fails to ameliorate the phenotype in a mouse model of spinal muscular atrophy.
Neuromuscul Disord
; 24(5): 436-44, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24656734
18.
Electrophysiological Biomarkers in Spinal Muscular Atrophy: Preclinical Proof of Concept.
Ann Clin Transl Neurol
; 1(1): 34-44, 2014 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24511555