Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Pamela Barraza-Flores"'
Autor:
Casie Genetti, Pamela Barraza-Flores, Wanqing Shao, Sundos Al-Husayni, Courtney French, Shira Rockowitz, Alan Beggs
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101551- (2024)
Externí odkaz:
https://doaj.org/article/10fc7decbd4643fb81d53455f96ec20b
Autor:
Enrico Bugiardini, Andreia M. Nunes, Ariany Oliveira‐Santos, Marisela Dagda, Tatiana M. Fontelonga, Pamela Barraza‐Flores, Alan M. Pittman, Jasper M. Morrow, Matthew Parton, Henry Houlden, Perry M. Elliott, Petros Syrris, Roderick P. Maas, Mohammed M. Akhtar, Benno Küsters, Joost Raaphorst, Meyke Schouten, Erik‐Jan Kamsteeg, Baziel van Engelen, Michael G. Hanna, Rahul Phadke, Luis R. Lopes, Emma Matthews, Dean J. Burkin
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 11, Iss 23 (2022)
Background Integrin α7β1 is a major laminin receptor in skeletal and cardiac muscle. In skeletal muscle, integrin α7β1 plays an important role during muscle development and has been described as an important modifier of skeletal muscle diseases.
Externí odkaz:
https://doaj.org/article/350a26baecc8491eac3c63f5cd504fe7
Autor:
Pamela Barraza-Flores, Hailey J. Hermann, Christina R. Bates, Tyler G. Allen, Timothy T. Grunert, Dean J. Burkin
Publikováno v:
Skeletal Muscle, Vol 10, Iss 1, Pp 1-12 (2020)
Abstract Background Laminin-α2-related congenital muscular dystrophy (LAMA2-CMD) is a devastating genetic disease caused by mutations in the LAMA2 gene. These mutations result in progressive muscle wasting and inflammation leading to delayed milesto
Externí odkaz:
https://doaj.org/article/83246edb7b9c4aa8b12fab77ad92d44e
Autor:
Takako I. Jones, Guo-Liang Chew, Pamela Barraza-Flores, Spencer Schreier, Monique Ramirez, Ryan D. Wuebbles, Dean J. Burkin, Robert K. Bradley, Peter L. Jones
Publikováno v:
Skeletal Muscle, Vol 10, Iss 1, Pp 1-28 (2020)
Abstract Background All types of facioscapulohumeral muscular dystrophy (FSHD) are caused by the aberrant activation of the somatically silent DUX4 gene, the expression of which initiates a cascade of cellular events ultimately leading to FSHD pathop
Externí odkaz:
https://doaj.org/article/812ce4b6ddbc49389bddf06254db2254
Autor:
Ryan D. Wuebbles, Vivian Cruz, Pam Van Ry, Pamela Barraza-Flores, Paul D. Brewer, Peter Jones, Dean J. Burkin
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 13, Iss , Pp 145-153 (2019)
Duchenne muscular dystrophy (DMD) is a devastating disease caused by mutations in the dystrophin gene that result in the complete absence of dystrophin protein. We have shown previously that recombinant mouse Galectin-1 treatment improves physiologic
Externí odkaz:
https://doaj.org/article/7cb9207feebe46a59941dbb479c9bbe1
Autor:
Adrian J Luna, Rosa T Sterk, Anastacia M Griego-Fisher, Joon-Yong Chung, Kiersten L Berggren, Virginie Bondu, Pamela Barraza-Flores, Andrew T Cowan, Gregory N Gan, Emrullah Yilmaz, Hanbyoul Cho, Jae-Hoon Kim, Stephen M Hewitt, Julie E Bauman, Michelle A Ozbun
Publikováno v:
PLoS Pathogens, Vol 17, Iss 1, p e1009216 (2021)
Intracellular pathogens have evolved to utilize normal cellular processes to complete their replicative cycles. Pathogens that interface with proliferative cell signaling pathways risk infections that can lead to cancers, but the factors that influen
Externí odkaz:
https://doaj.org/article/b67497d0ad704213af20b825b4d9d246
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 13 (2020)
Laminin-α2-related congenital muscular dystrophy (LAMA2-CMD) is a devastating neuromuscular disease caused by mutations in the LAMA2 gene. These mutations result in the complete absence or truncated expression of the laminin-α2 chain. The α2-chain
Externí odkaz:
https://doaj.org/article/7123fb1512804142b1393b64f4d36749
Autor:
Ariany Oliveira-Santos, Brandon W Conner, Dean J. Burkin, Pamela Barraza-Flores, Katherine E. Bukovec, Robert W. Grange, Marisela Dagda
Publikováno v:
Hum Mol Genet
Laminin-α2 related congenital muscular dystrophy (LAMA2-CMD) is a fatal muscle disease caused by mutations in the LAMA2 gene. Laminin-α2 is critical for the formation of laminin-211 and -221 heterotrimers in the muscle basal lamina. LAMA2-CMD patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::350230639b02da55a7ebe67343db6ec5
https://doi.org/10.1093/hmg/ddaa104
https://doi.org/10.1093/hmg/ddaa104
Autor:
Pam Van Ry, Ryan D. Wuebbles, Pamela Barraza-Flores, Peter L. Jones, Vivian Cruz, Dean J. Burkin, Paul Duffield Brewer
Publikováno v:
Molecular Therapy. Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 13, Iss, Pp 145-153 (2019)
Molecular Therapy: Methods & Clinical Development, Vol 13, Iss, Pp 145-153 (2019)
Duchenne muscular dystrophy (DMD) is a devastating disease caused by mutations in the dystrophin gene that result in the complete absence of dystrophin protein. We have shown previously that recombinant mouse Galectin-1 treatment improves physiologic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16c091173d1192e19c88b532c935251e
http://europepmc.org/articles/PMC6369265
http://europepmc.org/articles/PMC6369265
Autor:
Virginie Bondu, Julie E. Bauman, A. Cowan, Pamela Barraza-Flores, Anastacia M Griego-Fisher, Rosa T. Sterk, Gregory N Gan, Michelle A. Ozbun, Hanbyoul Cho, Stephen M. Hewitt, Jae Hoon Kim, Joon-Yong Chung, Adrian J Luna, Kiersten L. Berggren, Emrullah Yilmaz
Publikováno v:
PLoS Pathogens, Vol 17, Iss 1, p e1009216 (2021)
PLoS Pathogens
PLoS Pathogens
Intracellular pathogens have evolved to utilize normal cellular processes to complete their replicative cycles. Pathogens that interface with proliferative cell signaling pathways risk infections that can lead to cancers, but the factors that influen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db5f49387935eb8b1f7bb4ffe1844b2f
https://doaj.org/article/b67497d0ad704213af20b825b4d9d246
https://doaj.org/article/b67497d0ad704213af20b825b4d9d246