scholarly article | Q13442814 |
P50 | author | Cristiane Perácio Bastos | Q86865600 |
Cristina Guatimosim | Q89012336 | ||
Matheus P S Magalhães-Gomes | Q90024295 | ||
P2093 | author name string | Silvia Guatimosim | |
Marco A M Prado | |||
Gregorio Valdez | |||
Patrícia M Martinelli | |||
Vânia F Prado | |||
Candido C Coimbra | |||
Daisy Motta-Santos | |||
Grace S Pereira | |||
Jéssica N Andrade | |||
Sydney K Vaughan | |||
Diogo A S Guimarães | |||
Luana P L Schetino | |||
P2860 | cites work | Choline acetyltransferase mutations cause myasthenic syndrome associated with episodic apnea in humans | Q24612220 |
Cellular and molecular mechanisms of muscle atrophy | Q27012762 | ||
A new mathematical model for relative quantification in real-time RT-PCR | Q27860781 | ||
Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea | Q28115635 | ||
Transport mechanisms in acetylcholine and monoamine storage | Q28139005 | ||
Aberrant patterning of neuromuscular synapses in choline acetyltransferase-deficient mice | Q28505352 | ||
Roles of neurotransmitter in synapse formation: development of neuromuscular junctions lacking choline acetyltransferase | Q28508674 | ||
Modulation of ACh release by presynaptic muscarinic autoreceptors in the neuromuscular junction of the newborn and adult rat | Q28566042 | ||
Nerve activity-independent regulation of skeletal muscle atrophy: role of MyoD and myogenin in satellite cells and myonuclei | Q28576625 | ||
Distinct phenotypes of mutant mice lacking agrin, MuSK, or rapsyn | Q28584895 | ||
Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosis | Q28594483 | ||
Measuring energy metabolism in the mouse - theoretical, practical, and analytical considerations | Q28703778 | ||
The vesicular acetylcholine transporter is required for neuromuscular development and function | Q30436632 | ||
Dysautonomia due to reduced cholinergic neurotransmission causes cardiac remodeling and heart failure | Q33725534 | ||
Quantal release of acetylcholine in mice with reduced levels of the vesicular acetylcholine transporter | Q33836058 | ||
Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy | Q34146828 | ||
Retrograde influence of muscle fibers on their innervation revealed by a novel marker for slow motoneurons | Q34164858 | ||
Skeletal muscle atrophy and the E3 ubiquitin ligases MuRF1 and MAFbx/atrogin-1 | Q34200869 | ||
Shared resistance to aging and ALS in neuromuscular junctions of specific muscles | Q34224953 | ||
Rapid determination of myosin heavy chain expression in rat, mouse, and human skeletal muscle using multicolor immunofluorescence analysis | Q34243643 | ||
Analysis of neurotrophic factors in limb and extraocular muscles of mouse model of amyotrophic lateral sclerosis | Q34343728 | ||
Development of the neuromuscular junction: genetic analysis in mice | Q77468492 | ||
On the contraction of muscle, chiefly in relation to the presence of "receptive" substances: Part I | Q80321879 | ||
The proprioceptive and agonist roles of gastrocnemius, soleus and tibialis anterior muscles in maintaining human upright posture | Q83482138 | ||
An age-related type IIB to IIX myosin heavy chain switching in rat skeletal muscle | Q95816706 | ||
Mutant SNAP25B causes myasthenia, cortical hyperexcitability, ataxia, and intellectual disability | Q34777891 | ||
Reduced expression of the vesicular acetylcholine transporter and neurotransmitter content affects synaptic vesicle distribution and shape in mouse neuromuscular junction | Q35048052 | ||
Aging of skeletal muscle fibers | Q35554933 | ||
Graded Maximal Exercise Testing to Assess Mouse Cardio-Metabolic Phenotypes | Q35918375 | ||
A hitchhiker's guide to behavioral analysis in laboratory rodents. | Q36471789 | ||
Inherited disorders of the neuromuscular junction | Q36540407 | ||
Progressive Cl- channel defects reveal disrupted skeletal muscle maturation in R6/2 Huntington's mice | Q37565636 | ||
Presynaptic receptors in the neuromuscular junction | Q37601848 | ||
Understanding mitochondrial complex I assembly in health and disease | Q37933572 | ||
Fiber types in mammalian skeletal muscles | Q37947567 | ||
Regulation of cholinergic activity by the vesicular acetylcholine transporter | Q38081512 | ||
Mechanisms for fiber-type specificity of skeletal muscle atrophy | Q38089508 | ||
Neuromuscular synaptogenesis: coordinating partners with multiple functions | Q38286009 | ||
Modulation of neurotransmitter release by presynaptic autoreceptors | Q38357259 | ||
Control of transmitter release from the motor nerve by presynaptic nicotinic and muscarinic autoreceptors | Q38368518 | ||
Splicing regulation and dysregulation of cholinergic genes expressed at the neuromuscular junction. | Q39078041 | ||
Vesicular acetylcholine transporter defect underlies devastating congenital myasthenia syndrome | Q39201011 | ||
Cholinergic/glutamatergic co-transmission in striatal cholinergic interneurons: new mechanisms regulating striatal computation | Q39250067 | ||
Role of hippocampal signaling pathways in long-term memory formation of a nonassociative learning task in the rat | Q40416447 | ||
Effects of ageing on the motor unit. | Q40448741 | ||
Effects of age and training on skeletal muscle physiology and performance | Q40792792 | ||
Obesity, Inflammation, and Exercise Training: Relative Contribution of iNOS and eNOS in the Modulation of Vascular Function in the Mouse Aorta | Q41026978 | ||
Loss of MUNC13-1 function causes microcephaly, cortical hyperexcitability, and fatal myasthenia | Q41055450 | ||
Effects of oxotremorine demonstrate presynaptic muscarinic and dopaminergic receptors on motor nerve terminals | Q41644722 | ||
Prejunctional modulation of acetylcholine release from the skeletal neuromuscular junction: link between positive (nicotinic)- and negative (muscarinic)-feedback modulation | Q41868301 | ||
Novel synaptobrevin-1 mutation causes fatal congenital myasthenic syndrome | Q42060267 | ||
Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndrome. | Q42113919 | ||
Myogenin and Class II HDACs Control Neurogenic Muscle Atrophy by Inducing E3 Ubiquitin Ligases | Q42360652 | ||
Congenital myasthenic syndrome associated with episodic apnea and sudden infant death | Q44063736 | ||
Three myosin heavy chain isoforms in type 2 skeletal muscle fibres. | Q44241210 | ||
Skeletal muscle atrophy in old rats: differential changes in the three fiber types | Q44666713 | ||
IGF-I stimulates muscle growth by suppressing protein breakdown and expression of atrophy-related ubiquitin ligases, atrogin-1 and MuRF1. | Q44853225 | ||
Denervation effects on myonuclear domain size of rat diaphragm fibers | Q46892924 | ||
Mice deficient for the vesicular acetylcholine transporter are myasthenic and have deficits in object and social recognition | Q48430459 | ||
Vesicular acetylcholine transporter knock down-mice are more susceptible to inflammation, c-Fos expression and sickness behavior induced by lipopolysaccharide | Q48736335 | ||
A role for the endocannabinoid system in exercise-induced spatial memory enhancement in mice | Q48941763 | ||
Differential effects of age on motor performance in two mouse strains | Q49135939 | ||
Adaptations of diaphragm and medial gastrocnemius muscles to inactivity | Q51693058 | ||
Mutation of the IIB myosin heavy chain gene results in muscle fiber loss and compensatory hypertrophy. | Q52141003 | ||
Myosin heavy chain composition of muscle fibers in spinal muscular atrophy. | Q52248379 | ||
How chromosomal deletions can unmask recessive mutations? Deletions in 10q11.2 associated with CHAT or SLC18A3 mutations lead to congenital myasthenic syndrome. | Q52790594 | ||
Myostatin dysfunction is associated with reduction in overload induced hypertrophy of soleus muscle in mice. | Q52862926 | ||
Muscle fiber types: how many and what kind? | Q54171280 | ||
Thyroid hormone regulation of myosin heavy chain isoform composition in young and old rats, with special reference to IIX myosin | Q57973347 | ||
Satellite cells of the rat soleus muscle in the process of compensatory hypertrophy combined with denervation | Q66955672 | ||
THE DEVELOPMENT OF ACETYLCHOLINE SENSITIVITY IN NERVE-FREE SEGMENTS OF SKELETAL MUSCLE | Q76849791 | ||
P921 | main subject | vertical transmission | Q2834381 |
P304 | page(s) | 1-12 | |
P577 | publication date | 2018-07-09 | |
P1433 | published in | Neurochemistry International | Q7002160 |
P1476 | title | Fast and slow-twitching muscles are differentially affected by reduced cholinergic transmission in mice deficient for VAChT: A mouse model for congenital myasthenia | |
P478 | volume | 120 |
Q90732350 | Attenuating Cholinergic Transmission Increases the Number of Satellite Cells and Preserves Muscle Mass in Old Age | cites work | P2860 |
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