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Akademický článek

Serum dosage of CPK-MB in dogs with ST deviation by chemiluminescence

Autor: André L.F. Santos, Guilherme G. Pereira, Mário M. Santos, Vanda C.R. Gutierrez, Priscila C. Calyjur, Maria Helena M.A. Larsson

Publikováno v: Pesquisa Veterinária Brasileira, Vol 34, Iss suppl 1, Pp 74-78 (2014)

Abstract: Although frequently in humans, hypoxic and ischemic heart diseases are poorly documented in dogs, with only few reports of acute myocardial infarction (AMI) in this species. Some electrocardiographic findings might suggest myocardium hypoxi

Externí odkaz: https://doaj.org/article/0b1abae98d044b8ca8031bd42e0d5ad2

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Association of Three Different Mutations in the CLCN1 Gene Modulating the Phenotype in a Consanguineous Family with Myotonia Congenita

Autor: Lucas Santos Souza, P. Calyjur, Mariz Vainzof, Juliana Gurgel-Giannetti, Antonio Fernando Ribeiro, Mayana Zatz, Rita de Cássia M. Pavanello

Publikováno v: Journal of Molecular Neuroscience. 71:2275-2280

Myotonia congenita is a genetic disease caused by mutations in the CLCN1 gene, which encodes for the major chloride skeletal channel ClC-1, involved in the normal repolarization of muscle action potentials and consequent relaxation of the muscle afte

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::18780cd7cfd866e1f4dfc5b81e52a457
https://doi.org/10.1007/s12031-020-01785-4

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Akademický článek

The mdx Mutation in the 129/Sv Background Results in a Milder Phenotype: Transcriptome Comparative Analysis Searching for the Protective Factors.

Autor: Priscila Clara Calyjur, Camila de Freitas Almeida, Danielle Ayub-Guerrieri, Antonio Fernando Ribeiro, Stephanie de Alcântara Fernandes, Renata Ishiba, Andre Luis Fernandes Dos Santos, Paula Onofre-Oliveira, Mariz Vainzof

Publikováno v: PLoS ONE, Vol 11, Iss 3, p e0150748 (2016)

The mdx mouse is a good genetic and molecular murine model for Duchenne Muscular Dystrophy (DMD), a progressive and devastating muscle disease. However, this model is inappropriate for testing new therapies due to its mild phenotype. Here, we transfe

Externí odkaz: https://doaj.org/article/f023a65be0e541b8981778303abd58d7

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Akademický článek

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Serum dosage of CPK-MB in dogs with ST deviation by chemiluminescence

Autor: P. Calyjur, G. G Pereira, Maria Helena Matiko Akao Larsson, A.L.F. Santos, Vanda C.R. Gutierrez, Mário Marcondes Santos

Publikováno v: Pesquisa Veterinária Brasileira, Vol 34, Iss suppl 1, Pp 74-78 (2014)
Pesquisa Veterinária Brasileira v.34 suppl.1 2014
Pesquisa Veterinária Brasileira
Colégio Brasileiro de Patologia Animal (CBPA)
instacron:EMBRAPA

Although frequently in humans, hypoxic and ischemic heart diseases are poorly documented in dogs, with only few reports of acute myocardial infarction (AMI) in this species. Some electrocardiographic findings might suggest myocardium hypoxia/ischemia

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e308c491702054a91272ecd47fa8c4c1
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2014001300074&lng=en&tlng=en

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The mdx Mutation in the 129/Sv Background Results in a Milder Phenotype: Transcriptome Comparative Analysis Searching for the Protective Factors

Autor: Antonio Fernando Ribeiro, Camila F. Almeida, D. Ayub-Guerrieri, P.C.G. Onofre-Oliveira, A.L.F. Santos, Stephanie A. Fernandes, Mariz Vainzof, Renata Ishiba, P. Calyjur

Publikováno v: PLoS ONE, Vol 11, Iss 3, p e0150748 (2016)
PLoS ONE

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d0669fb9319d6e781784ccdfd8ed572
http://europepmc.org/articles/PMC4783004?pdf=render

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Akademický článek

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Akademický článek

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P.4.5 Muscle NMR imaging in the rare E650K mutation in the DNM2 gene in a centronuclear myopathy patient

Autor: Juliana Gurgel-Giannetti, P. Calyjur, R.Y. Carlier, M.C.G. Otaduy, Pierre G. Carlier, A.B. Martins-Bach, Camila F. Almeida, Mariz Vainzof, Edson Amaro

Publikováno v: Neuromuscular Disorders. 23:761

Autosomal dominant centronuclear myopathy (CNM) is characterized by slowly progressive muscular weakness and wasting, and high frequency of centrally located nuclei in muscle fibers. The disorder involves mainly limb girdle, trunk and neck muscles bu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::092e47cbac9db6050f5118e795fa3b26
https://doi.org/10.1016/j.nmd.2013.06.443

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