Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Kristien J M Zaal"'
Autor:
Kristien J M Zaal, Ericka Reid, Kambiz Mousavi, Tan Zhang, Amisha Mehta, Elisabeth Bugnard, Vittorio Sartorelli, Evelyn Ralston
Publikováno v:
PLoS ONE, Vol 6, Iss 12, p e29057 (2011)
A wave of structural reorganization involving centrosomes, microtubules, Golgi complex and ER exit sites takes place early during skeletal muscle differentiation and completely remodels the secretory pathway. The mechanism of these changes and their
Externí odkaz:
https://doaj.org/article/7db8bde66d874ac5a42f5c01bfc7f9f2
Autor:
Natasha Silke, Manfred Boehm, Amanda K. Ombrello, Ivona Aksentijevich, Deborah L. Stone, Tina Romeo, Marco J Herold, Laurens Wachsmuth, Christine Biben, Beverly K. Barham, Lin Liu, Andrew J. Gross, Sergio D. Rosenzweig, Patrycja Hoffmann, Natalia Sampaio Moura, Gustavo Gutierrez-Cruz, Daniel L. Kastner, Steven E. Boyden, Kristien J. M. Zaal, Anne K. Voss, Holly Anderton, Anne Jones, Hongying Wang, Tobias Kratina, John Silke, Michael J. Lenardo, James C. Mullikin, Kate E. Lawlor, David B. Beck, Mark D. McKenzie, Amanda Light, Anthony K. Shum, Jae Jin Chae, Massimo Gadina, Qing Zhou, Diep Chau, Gineth Pinto-Patarroyo, Hirotsugu Oda, Geryl Wood, Mary Blake, Nima Etemadi, Kristy Shield-Artin, Edwin D. Hawkins, Monique Stoffels, Cathrine Hall, Dan Yang, Wanxia Li Tsai, Hye Sun Kuehn, Natalia I. Dmitrieva, Seth L. Masters, Lixin Zheng, Andrew J. Kueh, Manolis Pasparakis, Najoua Lalaoui
Publikováno v:
Nature
Nature, vol 577, iss 7788
Nature, vol 577, iss 7788
Receptor Interacting Protein Kinase 1 (RIPK1) is a key regulator of innate immune signalling pathways. To ensure an optimal inflammatory response, RIPK1 is post-translationally regulated by well characterised ubiquitylation and phosphorylation events
Autor:
Peter Schjerling, Thomas E. Jensen, Jonas R. Knudsen, Evelyn Ralston, Agnete B. Madsen, Lykke Sylow, Carlos Henríquez-Olguín, Yeliz Angin, Kristien J. M. Zaal
Publikováno v:
American Journal of Physiology-Endocrinology and Metabolism. 315:E110-E125
Studies in skeletal muscle cell cultures suggest that the cortical actin cytoskeleton is a major requirement for insulin-stimulated glucose transport, implicating the β-actin isoform, which in many cell types is the main actin isoform. However, it i
Autor:
Enrique J. deAndrés-Galiana, Brian S. Wolff, Leorey N. Saligan, Kristien J. M. Zaal, Li Rebekah Feng, Juan Luis Fernández-Martínez
Publikováno v:
Translational Psychiatry, Vol 8, Iss 1, Pp 1-11 (2018)
Scopus
RUO. Repositorio Institucional de la Universidad de Oviedo
instname
Translational Psychiatry
Scopus
RUO. Repositorio Institucional de la Universidad de Oviedo
instname
Translational Psychiatry
Cancer-related fatigue (CRF) is a common burden in cancer patients and little is known about its underlying mechanism. The primary aim of this study was to identify gene signatures predictive of post-radiotherapy fatigue in prostate cancer patients.
Autor:
Evelyn Ralston, Davide Randazzo, Aster Kenea, Bruno Alonso, Kristien J. M. Zaal, Sarah Oddoux
Publikováno v:
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology, Vol 7 (2019)
Frontiers in Cell and Developmental Biology, Vol 7 (2019)
Differentiated mammalian cells and tissues, such as skeletal muscle fibers, acquire an organization of Golgi complex and microtubules profoundly different from that in proliferating cells and still poorly understood. In adult rodent skeletal muscle,
Autor:
John T. Olthoff, Aster Kenea, Andrew L. Mammen, Umara Khalique, Davide Randazzo, Michelle D Tran, Katherine Pak, Dan L. Sackett, James M. Ervasti, Evelyn Ralston, Joseph J. Belanto, Dana M Talsness, Iago Pinal-Fernandez, Kristien J. M. Zaal
Publikováno v:
Human molecular genetics. 28(7)
In healthy adult skeletal muscle fibers microtubules form a three-dimensional grid-like network. In the mdx mouse, a model of Duchenne muscular dystrophy (DMD), microtubules are mostly disordered, without periodicity. These microtubule defects have b
Publikováno v:
Abstracts Accepted for Publication.
Background Neutrophils play a key role in the pathogenesis of autoimmune diseases through various mechanisms including the formation of neutrophil extracellular traps (NETs). NETosis, a recently described distinct form of program neutrophil cell deat
Autor:
Michael W. McBurney, Xiao Hong He, Kristien J. M. Zaal, Mona Dvir-Ginzberg, Christelle Sanchez, Viktoria Gagarina, Odile Gabay, Yingjie Song
Publikováno v:
Arthritis & Rheumatism. 65:159-166
Osteoarthritis (OA) is a multifactorial and complex degenerative disease of the cartilage. Different mechanisms are involved in cartilage degradation, including inflammation, apoptosis, and breakdown of major extracellular matrix (ECM) components, su
Autor:
Christelle Sanchez, Kristien J. M. Zaal, Mona Dvir-Ginzberg, H. Meir, Hanna Oppenhiemer, Odile Gabay
Publikováno v:
Annals of the Rheumatic Diseases. 71:613-616
Objective A growing body of evidence indicates that the protein deacetylase, SirT1, affects chondrocyte biology and survival. This report aims to evaluate in vivo attributes of SirT1 in cartilage biology of 129/J murine strains. Methods Heterozygous
Autor:
Ronald M. Laxer, Settara C. Chandrasekharappa, Yuan Zhang, Monique Stoffels, Xiaomin Yu, Annet Van Royen-Kerkof, Daniella M. Schwartz, Sarfaraz Hasni, Qing Zhou, Seza Ozen, Eric P. Hanson, Helen L. Leavis, Celeste Chen, Deborah L. Stone, Jonathan J. Lyons, Daniel L. Kastner, Ezgi Deniz Batu, Patrycja Hoffmann, Wanxia Li Tsai, Hongying Wang, Ingrid E. Wertz, Masaki Takeuchi, Joshua D. Milner, Zhen Yu, Anne Jones, Jae Jin Chae, Ahmet Gül, James C. Mullikin, Dan Yang, Manfred Boehm, David T. Chin, Erkan Demirkaya, Amanda K. Ombrello, Cailin H. Sibley, Ivona Aksentijevich, Kristien J. M. Zaal, Massimo Gadina, Richard M. Siegel, Yong Hwan Park, Beverly K. Barham, Claudia Ouyang
Publikováno v:
Paediatrics Publications
Nature genetics
Nature Genetics, 48(1), 67–73. Nature Publishing Group
Nature genetics
Nature Genetics, 48(1), 67–73. Nature Publishing Group
Systemic autoinflammatory diseases are driven by abnormal activation of innate immunity. Herein we describe a new disease caused by high-penetrance heterozygous germline mutations in TNFAIP3, which encodes the NF-κB regulatory protein A20, in six un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cabf0ac62097b01705876f580b78df12
https://ir.lib.uwo.ca/paedpub/1118
https://ir.lib.uwo.ca/paedpub/1118