Search details
1.
Functional rescue in a mouse model of congenital muscular dystrophy with megaconial myopathy.
Hum Mol Genet
; 28(16): 2635-2647, 2019 08 15.
Article
in English
| MEDLINE | ID: mdl-31216357
2.
Hanging on for the ride: adhesion to the extracellular matrix mediates cellular responses in skeletal muscle morphogenesis and disease.
Dev Biol
; 401(1): 75-91, 2015 May 01.
Article
in English
| MEDLINE | ID: mdl-25592225
3.
Choline kinase beta is required for normal endochondral bone formation.
Biochim Biophys Acta
; 1840(7): 2112-22, 2014 Jul.
Article
in English
| MEDLINE | ID: mdl-24637075
4.
A congenital muscular dystrophy with mitochondrial structural abnormalities caused by defective de novo phosphatidylcholine biosynthesis.
Am J Hum Genet
; 88(6): 845-851, 2011 Jun 10.
Article
in English
| MEDLINE | ID: mdl-21665002
5.
The SATB1-MIR22-GBA axis mediates glucocerebroside accumulation inducing a cellular senescence-like phenotype in dopaminergic neurons.
Aging Cell
; 23(4): e14077, 2024 Apr.
Article
in English
| MEDLINE | ID: mdl-38303548
6.
Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy.
Hum Mol Genet
; 20(19): 3841-51, 2011 Oct 01.
Article
in English
| MEDLINE | ID: mdl-21750112
7.
The SATB1-MIR22-GBA axis mediates glucocerebroside accumulation inducing a cellular senescence-like phenotype in dopaminergic neurons.
bioRxiv
; 2023 Jul 21.
Article
in English
| MEDLINE | ID: mdl-37503189
8.
Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease.
PLoS One
; 17(9): e0274615, 2022.
Article
in English
| MEDLINE | ID: mdl-36107978
9.
Differential expression of choline kinase isoforms in skeletal muscle explains the phenotypic variability in the rostrocaudal muscular dystrophy mouse.
Biochim Biophys Acta
; 1801(4): 446-54, 2010 Apr.
Article
in English
| MEDLINE | ID: mdl-20026284
10.
Effect of genetic background on phenotype variability in transgenic mouse models of amyotrophic lateral sclerosis: a window of opportunity in the search for genetic modifiers.
Amyotroph Lateral Scler
; 12(2): 79-86, 2011 Mar.
Article
in English
| MEDLINE | ID: mdl-21241159
11.
Understanding the muscular dystrophy caused by deletion of choline kinase beta in mice.
Biochim Biophys Acta
; 1791(5): 347-56, 2009 May.
Article
in English
| MEDLINE | ID: mdl-19236939
12.
Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease.
Nat Commun
; 11(1): 5022, 2020 Oct 01.
Article
in English
| MEDLINE | ID: mdl-33004807
13.
NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease.
Nat Commun
; 11(1): 4625, 2020 09 15.
Article
in English
| MEDLINE | ID: mdl-32934225
14.
The interaction of genetics and environmental toxicants in amyotrophic lateral sclerosis: results from animal models.
Neural Regen Res
; 12(6): 902-905, 2017 Jun.
Article
in English
| MEDLINE | ID: mdl-28761418
15.
Editor's Highlight: Embryonic Exposure to the Environmental Neurotoxin BMAA Negatively Impacts Early Neuronal Development and Progression of Neurodegeneration in the Sod1-G93R Zebrafish Model of Amyotrophic Lateral Sclerosis.
Toxicol Sci
; 157(1): 129-140, 2017 05 01.
Article
in English
| MEDLINE | ID: mdl-28123103
16.
Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron disease.
PLoS One
; 10(3): e0117848, 2015.
Article
in English
| MEDLINE | ID: mdl-25763819
17.
A major QTL on mouse chromosome 17 resulting in lifespan variability in SOD1-G93A transgenic mouse models of amyotrophic lateral sclerosis.
Amyotroph Lateral Scler Frontotemporal Degener
; 15(7-8): 588-600, 2014 Dec.
Article
in English
| MEDLINE | ID: mdl-25008789
18.
Rhabdomyosarcomas in aging A/J mice.
PLoS One
; 6(8): e23498, 2011.
Article
in English
| MEDLINE | ID: mdl-21853140
19.
A rostrocaudal muscular dystrophy caused by a defect in choline kinase beta, the first enzyme in phosphatidylcholine biosynthesis.
J Biol Chem
; 281(8): 4938-48, 2006 Feb 24.
Article
in English
| MEDLINE | ID: mdl-16371353
20.
Gait analysis detects early changes in transgenic SOD1(G93A) mice.
Muscle Nerve
; 32(1): 43-50, 2005 Jul.
Article
in English
| MEDLINE | ID: mdl-15880561