Zobrazeno 1 - 10
of 54
pro vyhledávání: '"James M Holaska"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-15 (2024)
Abstract During metastasis, cancer cells traverse the vasculature by squeezing through very small gaps in the endothelium. Thus, nuclei in metastatic cancer cells must become more malleable to move through these gaps. Our lab showed invasive breast c
Externí odkaz:
https://doaj.org/article/8fd52e3b1a9048d4b6daa6ed984a17e7
Autor:
Adam J Koch, James M Holaska
Publikováno v:
PLoS ONE, Vol 7, Iss 5, p e37262 (2012)
Emerin is an integral membrane protein of the inner nuclear membrane. Mutations in emerin cause X-linked Emery-Dreifuss muscular dystrophy (EDMD), a disease characterized by skeletal muscle wasting and dilated cardiomyopathy. Current evidence suggest
Externí odkaz:
https://doaj.org/article/20c2b1b98cfd4adebae6d412adbd330c
Publikováno v:
PLoS Biology, Vol 2, Iss 9, p E231 (2004)
X-linked Emery-Dreifuss muscular dystrophy is caused by loss of emerin, a LEM-domain protein of the nuclear inner membrane. To better understand emerin function, we used affinity chromatography to purify emerin-binding proteins from nuclear extracts
Externí odkaz:
https://doaj.org/article/f3d37424c6eb493ab31991629bc0f791
Autor:
Nicholas Marano, James M. Holaska
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
X-Linked Emery-Dreifuss muscular dystrophy is caused by mutations in the gene encoding emerin. Emerin is an inner nuclear membrane protein important for repressive chromatin organization at the nuclear periphery. Myogenic differentiation is a tightly
Externí odkaz:
https://doaj.org/article/f4b65b35a2604bada541343d89285a05
Autor:
Emily Hansen, James M. Holaska
Publikováno v:
Oncotarget. 14:317-320
Autor:
James M. Holaska, Isabelle Mercier, Mallory C. Campbell, Chelsea A. McNamara, Alexandra G. Liddane
S1. Emerin-null myogenic progenitor nuclei are smaller than wild-type myogenic progenitor nuclei. S2. GFP-emerin increases nuclear area in MDA-157 cells. S3. GFP-emerin and GFP-emerin mutants do not affect cell cycle progression or apoptosis. S4. GFP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00db1fdbe71f8aa7a58026673fa88e19
https://doi.org/10.1158/1541-7786.22526567.v1
https://doi.org/10.1158/1541-7786.22526567.v1
Autor:
James M. Holaska, Isabelle Mercier, Mallory C. Campbell, Chelsea A. McNamara, Alexandra G. Liddane
Nuclear envelope proteins play an important role in regulating nuclear size and structure in cancer. Altered expression of nuclear lamins are found in many cancers and its expression is correlated with better clinical outcomes. The nucleus is the lar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3eb11bf0b46131006990c5d24812a54
https://doi.org/10.1158/1541-7786.c.6545135.v1
https://doi.org/10.1158/1541-7786.c.6545135.v1
Publikováno v:
Muscle Nerve
Introduction Emery-Dreifuss muscular dystrophy (EDMD) is a disease characterized by skeletal muscle wasting, major tendon contractures, and cardiac conduction defects. Mutations in the gene encoding emerin cause EDMD1. Our previous studies suggested
Autor:
Wendy Lilián Gómez-Monsivais, James M. Holaska, Jesús Mauricio Ernesto Hernández-Méndez, Jhon Rivera-Monroy, Paulina Margarita Azuara-Medina, Jonathan J. Magaña, Raúl Argüello-García, Steve J. Winder, Bulmaro Cisneros, Feliciano Monterrubio-Ledezma, Ivette Martínez-Vieyra, Efraín Garrido, Alma Alamillo-Iniesta, Jazmin Huerta-Cantillo, Ricardo Mondragon-Gonzalez, Ian García-Aguirre, Fernando Navarro-Garcia, Andrea Brancaccio
Publikováno v:
International Journal of Molecular Sciences
International journal of molecular sciences (Online) 21 (2020): 1–20. doi:10.3390/ijms21175944
info:cnr-pdr/source/autori:Gomez-Monsivais W.L.; Monterrubio-Ledezma F.; Huerta-Cantillo J.; Mondragon-Gonzalez R.; Alamillo-Iniesta A.; Garcia-Aguirre I.; Azuara-Medina P.M.; Arguello-Garcia R.; Rivera-Monroy J.E.; Holaska J.M.; Hernandez-Mendez J.M.E.; Garrido E.; Magana J.J.; Winder S.J.; Brancaccio A.; Martinez-Vieyra I.; Navarro-Garcia F.; Cisneros B./titolo:The molecular basis and biologic significance of the ?-dystroglycan-emerin interaction/doi:10.3390%2Fijms21175944/rivista:International journal of molecular sciences (Online)/anno:2020/pagina_da:1/pagina_a:20/intervallo_pagine:1–20/volume:21
International Journal of Molecular Sciences, Vol 21, Iss 5944, p 5944 (2020)
Volume 21
Issue 17
Gómez-Monsiváis, W L, Monterrubio-Ledezma, F, Huerta-Cantillo, J, Mondragon-Gonzalez, R, Alamillo-Iniesta, A, García-Aguirre, I, Azuara-Medina, P M, Arguello-García, R, Rivera-Monroy, J E, Holaska, A M, Hernández-Méndez, J M E, Garrido, E, Javier Magaña, J, Winder, S, Brancaccio, A, Martínez-Vieyra, I, Navarro-Garcia, F & Cisneros, B 2020, ' The molecular basis and biological significance of the β-dystroglycan-emerin interaction ', International Journal of Molecular Sciences, vol. 21, no. 17, 5944 . https://doi.org/10.3390/ijms21175944
International journal of molecular sciences (Online) 21 (2020): 1–20. doi:10.3390/ijms21175944
info:cnr-pdr/source/autori:Gomez-Monsivais W.L.; Monterrubio-Ledezma F.; Huerta-Cantillo J.; Mondragon-Gonzalez R.; Alamillo-Iniesta A.; Garcia-Aguirre I.; Azuara-Medina P.M.; Arguello-Garcia R.; Rivera-Monroy J.E.; Holaska J.M.; Hernandez-Mendez J.M.E.; Garrido E.; Magana J.J.; Winder S.J.; Brancaccio A.; Martinez-Vieyra I.; Navarro-Garcia F.; Cisneros B./titolo:The molecular basis and biologic significance of the ?-dystroglycan-emerin interaction/doi:10.3390%2Fijms21175944/rivista:International journal of molecular sciences (Online)/anno:2020/pagina_da:1/pagina_a:20/intervallo_pagine:1–20/volume:21
International Journal of Molecular Sciences, Vol 21, Iss 5944, p 5944 (2020)
Volume 21
Issue 17
Gómez-Monsiváis, W L, Monterrubio-Ledezma, F, Huerta-Cantillo, J, Mondragon-Gonzalez, R, Alamillo-Iniesta, A, García-Aguirre, I, Azuara-Medina, P M, Arguello-García, R, Rivera-Monroy, J E, Holaska, A M, Hernández-Méndez, J M E, Garrido, E, Javier Magaña, J, Winder, S, Brancaccio, A, Martínez-Vieyra, I, Navarro-Garcia, F & Cisneros, B 2020, ' The molecular basis and biological significance of the β-dystroglycan-emerin interaction ', International Journal of Molecular Sciences, vol. 21, no. 17, 5944 . https://doi.org/10.3390/ijms21175944
&beta
dystroglycan (&beta
DG) assembles with lamins A/C and B1 and emerin at the nuclear envelope (NE) to maintain proper nuclear architecture and function. To provide insight into the nuclear function of &beta
DG, we characterized the
dystroglycan (&beta
DG) assembles with lamins A/C and B1 and emerin at the nuclear envelope (NE) to maintain proper nuclear architecture and function. To provide insight into the nuclear function of &beta
DG, we characterized the
Autor:
Ashvin Iyer, James M. Holaska
Publikováno v:
Cells
Cells, Vol 9, Iss 1463, p 1463 (2020)
Volume 9
Issue 6
Cells, Vol 9, Iss 1463, p 1463 (2020)
Volume 9
Issue 6
Mutations in the gene encoding emerin (EMD) cause Emery&ndash
Dreifuss muscular dystrophy (EDMD1), an inherited disorder characterized by progressive skeletal muscle wasting, irregular heart rhythms and contractures of major tendons. The skeleta
Dreifuss muscular dystrophy (EDMD1), an inherited disorder characterized by progressive skeletal muscle wasting, irregular heart rhythms and contractures of major tendons. The skeleta