Výsledky vyhledávání - "Azahara Civera-Tregón"

Akademický článek

Mitochondria and calcium defects correlate with axonal dysfunction in GDAP1-related Charcot-Marie-Tooth mouse model

Autor: Azahara Civera-Tregón, Laura Domínguez, Paula Martínez-Valero, Clàudia Serrano, Alex Vallmitjana, Raúl Benítez, Janet Hoenicka, Jorgina Satrústegui, Francesc Palau

Publikováno v: Neurobiology of Disease, Vol 152, Iss , Pp 105300- (2021)

Ganglioside-induced differentiation associated protein 1 (GDAP1) gene encodes a protein of the mitochondrial outer membrane and of the mitochondrial membrane contacts with the endoplasmic reticulum (MAMs) and lysosomes. Since mutations in GDAP1 cause

Externí odkaz: https://doaj.org/article/514e4792cc8848fbaf12d9db9ad223b4

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Akademický článek

Lack of GDAP1 induces neuronal calcium and mitochondrial defects in a knockout mouse model of charcot-marie-tooth neuropathy.

Autor: Manuela Barneo-Muñoz, Paula Juárez, Azahara Civera-Tregón, Laura Yndriago, David Pla-Martin, Jennifer Zenker, Carmen Cuevas-Martín, Anna Estela, María Sánchez-Aragó, Jerónimo Forteza-Vila, José M Cuezva, Roman Chrast, Francesc Palau

Publikováno v: PLoS Genetics, Vol 11, Iss 4, p e1005115 (2015)

Mutations in GDAP1, which encodes protein located in the mitochondrial outer membrane, cause axonal recessive (AR-CMT2), axonal dominant (CMT2K) and demyelinating recessive (CMT4A) forms of Charcot-Marie-Tooth (CMT) neuropathy. Loss of function reces

Externí odkaz: https://doaj.org/article/20f2961b9f7842e68e92dce769828c76

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Mitochondria–lysosome membrane contacts are defective in GDAP1-related Charcot–Marie–Tooth disease

Autor: Francesc Palau, Elena Juárez-Escoto, María Rodríguez-Sanz, Azahara Civera-Tregón, Janet Hoenicka, Monica Roldan, Lara Cantarero, Raul Benitez

Publikováno v: UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
Human Molecular Genetics

Mutations in the GDAP1 gene cause Charcot–Marie–Tooth (CMT) neuropathy. GDAP1 is an atypical glutathione S-transferase (GST) of the outer mitochondrial membrane and the mitochondrial membrane contacts with the endoplasmic reticulum (MAMs). Here,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce3cf618872517a35eba977dc55a0c68
https://doi.org/10.1093/hmg/ddaa243

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Mitochondria and calcium defects correlate with axonal dysfunction in GDAP1-related Charcot-Marie-Tooth mouse model

Autor: Jorgina Satrústegui, Laura Domínguez, Clàudia Serrano, Paula Martínez-Valero, Alexander Vallmitjana, Francesc Palau, Azahara Civera-Tregón, Raul Benitez, Janet Hoenicka

Publikováno v: Digital.CSIC. Repositorio Institucional del CSIC
instname
Neurobiology of Disease, Vol 152, Iss, Pp 105300-(2021)
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68c656367631587cef1bd010b3f277b7
https://pubmed.ncbi.nlm.nih.gov/33582224

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Neuroinflammation in the pathogenesis of axonal Charcot-Marie-Tooth disease caused by lack of GDAP1

Autor: Isabel Herrer, Lara Cantarero, Paula Juárez, Francesc Palau, Azahara Civera-Tregón, Sara Fernandez-Lizarbe, Janet Hoenicka

Publikováno v: EXPERIMENTAL NEUROLOGY
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu

Mutations in the GDAP1 mitochondrial outer membrane gene cause Charcot-Marie-Tooth (CMT) neuropathy. Reduction or absence of GDAP1 has been associated with abnormal changes in the mitochondrial morphology and dynamics, oxidative stress and changes in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a08db91313aaa0c679e0e865d013cfb8
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=16407

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Motion estimation of subcellular structures from fluorescence microscopy images

Autor: Azahara Civera-Tregón, Janet Hoenicka, Francesc Palau, Raul Benitez, Alexander Vallmitjana

Publikováno v: EMBC

We present an automatic image processing framework to study moving intracellular structures from live cell fluorescence microscopy. The system includes the identification of static and dynamic structures from time-lapse images using data clustering a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cf455c17f2cc616389d8630a0ea2637
https://doi.org/10.1109/embc.2017.8037836

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Lack of GDAP1 induces neuronal calcium and mitochondrial defects in a knockout mouse model of Charcot-Marie-tooth neuropathy

Autor: Azahara Civera-Tregón, Jerónimo Forteza-Vila, Carmen Cuevas-Martín, Manuela Barneo-Muñoz, David Pla-Martín, Paula Juárez, Jennifer Zenker, Roman Chrast, María Sánchez-Aragó, Francesc Palau, Anna Estela, Laura Yndriago, José M. Cuezva

Publikováno v: Biblos-e Archivo. Repositorio Institucional de la UAM
instname
PLoS Genetics
r-CIPF: Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)
Plos Genetics, vol. 11, no. 4, pp. e1005115
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
PLoS Genetics, Vol 11, Iss 4, p e1005115 (2015)
Digital.CSIC. Repositorio Institucional del CSIC
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)

27 páginas, 9 figuras.
Mutations in GDAP1, which encodes protein located in the mitochondrial outer membrane, cause axonal recessive (AR-CMT2), axonal dominant (CMT2K) and demyelinating recessive (CMT4A) forms of Charcot-Marie-Tooth (CMT) neuro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1883c7648c733c6908d3c233e83a3583
https://doi.org/10.1371/journal.pgen.1005115

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