Jessica N. Andrade

Belo Horizonte, MG, Brazil

Last Updated: 09/26/2026

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Found 9 publications

Increased Cholinergic Tone Causes Pre-synaptic Neuromuscular Degeneration and is Associated with Impaired Diaphragm Function.

Increased Cholinergic Tone Causes Pre-synaptic Neuromuscular Degeneration and is Associated with Impaired Diaphragm Function.

Journal: Neuroscience

Published: April 02, 2020

Abnormalities in the Motor Unit of a Fast-Twitch Lower Limb Skeletal Muscle in Huntington's Disease.

Abnormalities in the Motor Unit of a Fast-Twitch Lower Limb Skeletal Muscle in Huntington's Disease.

Journal: ASN neuro

Published: December 11, 2019

Evaluation of the neuromuscular junction in a middle-aged mouse model of congenital myasthenic syndrome.

Evaluation of the neuromuscular junction in a middle-aged mouse model of congenital myasthenic syndrome.

Journal: Muscle & nerve

Published: June 07, 2019

Increased oxidative stress and CaMKII activity contribute to electro-mechanical defects in cardiomyocytes from a murine model of Huntington's disease.

Increased oxidative stress and CaMKII activity contribute to electro-mechanical defects in cardiomyocytes from a murine model of Huntington's disease.

Journal: The FEBS journal

Published: August 29, 2018

Corrigendum to "Neuromuscular synapse degeneration without muscle function loss in the diaphragm of a murine model for Huntington's Disease" [Neurochem. Int. 116 (2018) 30-42].

Corrigendum to "Neuromuscular synapse degeneration without muscle function loss in the diaphragm of a murine model for Huntington's Disease" [Neurochem. Int. 116 (2018) 30-42].

Journal: Neurochemistry international

Published: May 28, 2018

Fast and slow-twitching muscles are differentially affected by reduced cholinergic transmission in mice deficient for VAChT: A mouse model for congenital myasthenia.

Fast and slow-twitching muscles are differentially affected by reduced cholinergic transmission in mice deficient for VAChT: A mouse model for congenital myasthenia.

Journal: Neurochemistry international

Published: February 13, 2018

Neuromuscular synapse degeneration without muscle function loss in the diaphragm of a murine model for Huntington's Disease.

Neuromuscular synapse degeneration without muscle function loss in the diaphragm of a murine model for Huntington's Disease.

Journal: Neurochemistry international

Published: October 20, 2017

Muscle atrophy is associated with cervical spinal motoneuron loss in BACHD mouse model for Huntington's disease.

Muscle atrophy is associated with cervical spinal motoneuron loss in BACHD mouse model for Huntington's disease.

Journal: The European journal of neuroscience

Published: April 18, 2016

The mGluR5 positive allosteric modulator, CDPPB, ameliorates pathology and phenotypic signs of a mouse model of Huntington's disease.

The mGluR5 positive allosteric modulator, CDPPB, ameliorates pathology and phenotypic signs of a mouse model of Huntington's disease.

Journal: Neurobiology of disease

Published: May 09, 2014

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Last Updated: 09/26/2026