Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Linda Horner"'
Autor:
Tae-Yeon Eom, Seung Baek Han, Jieun Kim, Jay A. Blundon, Yong-Dong Wang, Jing Yu, Kara Anderson, Damian B. Kaminski, Sadie Miki Sakurada, Shondra M. Pruett-Miller, Linda Horner, Ben Wagner, Camenzind G. Robinson, Matthew Eicholtz, Derek C. Rose, Stanislav S. Zakharenko
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-17 (2020)
Schizophrenia is associated with brain ventricular enlargement. Here, the authors show in mice that 22q11 deletion, which is associated with schizophrenia, causes ventricular enlargement and motility abnormalities in cilia lining ventricle walls via
Externí odkaz:
https://doaj.org/article/015f5351a7344fa99035595c0123d9f5
Autor:
Yvan Campos, Xiaohui Qiu, Elida Gomero, Randall Wakefield, Linda Horner, Wojciech Brutkowski, Young-Goo Han, David Solecki, Sharon Frase, Antonella Bongiovanni, Alessandra d’Azzo
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-15 (2016)
Correct assembly of intercellular junctions is required to maintain epithelial polarity and barrier function. Here Campos et al. show that the scaffold protein Alix interacts with F-actin, the Par complex and ZO-1 to ensure the formation and maintena
Externí odkaz:
https://doaj.org/article/c1feeee6b4234f208945cf8f377982ec
Autor:
Viraj P. Ichhaporia, Jieun Kim, Kanisha Kavdia, Peter Vogel, Linda Horner, Sharon Frase, Linda M. Hendershot
Publikováno v:
Disease Models & Mechanisms, Vol 11, Iss 5 (2018)
Mutations in SIL1, a cofactor for the endoplasmic reticulum (ER)-localized Hsp70 chaperone, BiP, cause Marinesco-Sjögren syndrome (MSS), an autosomal recessive disorder. Using a mouse model, we characterized molecular aspects of the progressive myop
Externí odkaz:
https://doaj.org/article/f28ca7942d714c9ca1771367cfca05f3
Autor:
Tetsuji Yamashita, Pierre Hakizimana, Siva Wu, Ahmed Hassan, Stefan Jacob, Jamshid Temirov, Jie Fang, Marcia Mellado-Lagarde, Richard Gursky, Linda Horner, Barbara Leibiger, Sara Leijon, Victoria E Centonze, Per-Olof Berggren, Sharon Frase, Manfred Auer, William E Brownell, Anders Fridberger, Jian Zuo
Publikováno v:
PLoS Genetics, Vol 11, Iss 9, p e1005500 (2015)
Nature's fastest motors are the cochlear outer hair cells (OHCs). These sensory cells use a membrane protein, Slc26a5 (prestin), to generate mechanical force at high frequencies, which is essential for explaining the exquisite hearing sensitivity of
Externí odkaz:
https://doaj.org/article/ae9f8a167b014b09ac6113b4a1b70ee8
Autor:
Jieun Kim, Derek C. Rose, Seung Baek Han, Kara Anderson, Yong-Dong Wang, Jing Yu, Matthew Eicholtz, Camenzind G. Robinson, Sadie Miki Sakurada, Ben Wagner, Jay A. Blundon, Stanislav S. Zakharenko, Tae-Yeon Eom, Shondra M. Pruett-Miller, Linda Horner, Damian B. Kaminski
Publikováno v:
Nature Communications
Nature Communications, Vol 11, Iss 1, Pp 1-17 (2020)
Nature Communications, Vol 11, Iss 1, Pp 1-17 (2020)
Progressive ventricular enlargement, a key feature of several neurologic and psychiatric diseases, is mediated by unknown mechanisms. Here, using murine models of 22q11-deletion syndrome (22q11DS), which is associated with schizophrenia in humans, we
Autor:
Martin, Linda Horner
Publikováno v:
The British Journal of Social Work, 2018 Sep 01. 48(6), 1826-1828.
Externí odkaz:
https://www.jstor.org/stable/26613497
Autor:
Linda Horner Martin
Publikováno v:
The British Journal of Social Work. 48:1826-1828
Autor:
Linda Horner, Jieun Kim, Viraj P. Ichhaporia, Peter Vogel, Kanisha Kavdia, Linda M. Hendershot, Sharon Frase
Publikováno v:
Disease Models & Mechanisms.
Mutations in SIL1, a cofactor for the endoplasmic reticulum (ER)-localized Hsp70 chaperone, BiP, cause Marinesco-Sjogren syndrome (MSS), an autosomal recessive disorder. Using a mouse model, we characterized molecular aspects of the progressive myopa
Autor:
Mao Yang, Alfonso Lavado, Xinwei Cao, Bo Wang, Rekha Iyengar, Linda Horner, Joung Hyuck Joo, Xiujie Li-Harms, Douglas R. Green, Jun-Lin Guan, Sharon Frase, Christopher Wright, Mondira Kundu
Mammalian ULK1 (unc-51 like kinase 1) and ULK2, Caenorhabditis elegans UNC-51, and Drosophila melanogaster Atg1 are serine/threonine kinases that regulate flux through the autophagy pathway in response to various types of cellular stress. C. elegans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb0573e1342b5a68c18233ee27767b08
https://europepmc.org/articles/PMC6070005/
https://europepmc.org/articles/PMC6070005/
Autor:
Viraj P. Ichhaporia, Jieun Kim, Kanisha Kavdia, Peter Vogel, Linda Horner, Sharon Frase, Linda M. Hendershot
Publikováno v:
Disease Models & Mechanisms
Disease Models & Mechanisms, Vol 11, Iss 5 (2018)
Disease Models & Mechanisms, Vol 11, Iss 5 (2018)
Mutations in SIL1, a cofactor for the endoplasmic reticulum (ER)-localized Hsp70 chaperone, BiP, cause Marinesco-Sjögren syndrome (MSS), an autosomal recessive disorder. Using a mouse model, we characterized molecular aspects of the progressive myop