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1“…KlcA shows anti-methylation only during transformation. …”
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2por Kargar- Dastjerdy, Pegah, Tavalaee, Marziyeh, Salehi, Mansoor, Falahati, Mojtaba, Izadi, Tayebeh, Nasr Esfahani, Mohammad Hossein“…BACKGROUND: KLC3 protein as a member of the kinesin light-chain protein family plays an important role in spermatogenesis, during formation of mitochondrial sheath in the mid piece of the sperm tail. …”
Publicado 2016
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3por Xing, Jianxiao, Wang, Ying, Zhao, Xincheng, Li, Junqin, Hou, Ruixia, Niu, Xuping, Yin, Guohua, Li, Xinhua, Zhang, Kaiming“…Among the 13 genes, the variant frequencies of protein kinase C epsilon (PRKCE) (c.240T>C, 35.9% vs 47.7%, P < 0.05) and kinesin light chain 1 (KLC1) (c.216A>G, 2.9% vs 98.1%, P< 0.01) were significantly lower in psoriasis than in normal Asian individuals. …”
Publicado 2022
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4por Liang, Wei, Xie, Yingzhou, Xiong, Wei, Tang, Yu, Li, Gang, Jiang, Xiaofei, Lu, Yuan“…These findings suggest that the anti-restriction protein, KlcA(HS), represents a novel mechanism that facilitates the increased transfer of bla(KPC-2) and KlcA(HS)-carrying plasmids among K. pneumoniae strains.…”
Publicado 2017
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5“…Further analysis confirmed the expression of the endogenous KLC2 in the testes, which was not detected in the previous RNA sequencing data. …”
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6por Keyhanvar, Neda, Zarghami, Nosratollah, Seifalian, Alexander, Keyhanvar, Peyman, Sarvari, Rana, Salehi, Roya, Rahbarghazi, Reza, Ranjkesh, Mohammadreza, Akbarzadeh, Molood, Mahdipour, Mahdi, Nouri, Mohammad“…The culture of AT-MSCs induced typical keratinocyte morphology and up-regulatedthe expression of cytokeratin-14, Involucrin, and P63 compared to AT-MSCs cultured on theplastic surface (P < 0.05). Besides, KLC sheets were generated once slight changes occur in theenvironment temperature. …”
Publicado 2022
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7por Haynes, Elizabeth M, Burnett, Korri H, He, Jiaye, Jean-Pierre, Marcel W, Jarzyna, Martin, Eliceiri, Kevin W, Huisken, Jan, Halloran, Mary C“…Using live imaging approaches in klc4 mutant zebrafish, we show that KLC4 is required for stabilization of nascent axon branches, proper microtubule (MT) dynamics, and endosomal transport. …”
Publicado 2022
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8por Gümüşderelioğlu, Selin, Resch, Lauren, Brock, Trisha, Luxton, G. W. Gant, Cope, Heidi, Tan, Queenie K.-G., Hopkins, Christopher, Starr, Daniel A.“…We created a humanized Caenorhabditis elegans model in which klc-2 was replaced by human KLC4 (referred to as hKLC4) and assessed the extent to which hKLC4 retained function in the worm. …”
Publicado 2023
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9por Jiang, Mei, Esteve-Rudd, Julian, Lopes, Vanda S., Diemer, Tanja, Lillo, Concepción, Rump, Agrani, Williams, David S.“…Lack of KLC1 did not inhibit phagosome speed, but run length was decreased, and phagosome localization and degradation were impaired. …”
Publicado 2015
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10por Cockburn, Joseph J.B., Hesketh, Sophie J., Mulhair, Peter, Thomsen, Maren, O'Connell, Mary J., Way, Michael“…The kinesin-1 light chain (KLC) mediates cargo binding and regulates kinesin-1 motility. …”
Publicado 2018
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11por Fukuda, Yusuke, Pazyra-Murphy, Maria F., Silagi, Elizabeth S., Tasdemir-Yilmaz, Ozge E., Li, Yihang, Rose, Lillian, Yeoh, Zoe C., Vangos, Nicholas E., Geffken, Ezekiel A., Seo, Hyuk-Soo, Adelmant, Guillaume, Bird, Gregory H., Walensky, Loren D., Marto, Jarrod A., Dhe-Paganon, Sirano, Segal, Rosalind A.“…Here, we demonstrate that a complex containing RNA and the RNA-binding protein (RBP) SFPQ interacts selectively with a tetrameric kinesin containing the adaptor KLC1 and the motor KIF5A. We show that the binding of SFPQ to the KIF5A/KLC1 motor complex is required for axon survival and is impacted by KIF5A mutations that cause Charcot-Marie Tooth (CMT) disease. …”
Publicado 2020
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12por Chiba, Kyoko, Chien, Ko-yi, Sobu, Yuriko, Hata, Saori, Kato, Shun, Nakaya, Tadashi, Okada, Yasushi, Nairn, Angus C., Kinjo, Masataka, Taru, Hidenori, Wang, Rong, Suzuki, Toshiharu“…Previously, we showed that EFV requires conventional interaction between the JIP1b C-terminal region and the kinesin light chain 1 (KLC1) tetratricopeptide repeat, whereas EHF requires a novel interaction between the central region of JIP1b and the coiled-coil domain of KLC1. …”
Publicado 2017
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13por Dietz, Steffen, Christopoulos, Petros, Gu, Lisa, Volckmar, Anna-Lena, Endris, Volker, Yuan, Zhao, Ogrodnik, Simon J., Zemojtel, Tomasz, Heussel, Claus-Peter, Schneider, Marc A., Meister, Michael, Muley, Thomas, Reck, Martin, Schlesner, Matthias, Thomas, Michael, Stenzinger, Albrecht, Sültmann, Holger“…Here, we report the case of a KLC1–ALK-rearranged NSCLC patient responding to crizotinib treatment and demonstrate how analysis of plasma and serum biomarkers can be used to identify the ALK fusion partner and monitor therapy over time. …”
Publicado 2019
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14por Gümüşderelioğlu, Selin, Resch, Lauren, Brock, Trisha, Luxton, G.W. Gant, Tan, Queenie K-G, Hopkins, Christopher, Starr, Daniel A.“…We created a humanized C. elegans model where klc-2 was replaced with human KLC4 and assessed the extent to which hKLC4 retained function in the worm. …”
Publicado 2023
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15por Moamer, Alaa, Hachim, Ibrahim Y., Binothman, Najat, Wang, Ni, Lebrun, Jean-Jacques, Ali, Suhad“…In contrast, the epithelial differentiation factor and EMT suppressor prolactin (PRL) was found to repress KIF5B gene expression and KIF5B-Snail1 nuclear accumulation, but enhanced KLC1 gene expression and KIF5B-KLC1 interaction. …”
Publicado 2019
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16por Togashi, Yuki, Soda, Manabu, Sakata, Seiji, Sugawara, Emiko, Hatano, Satoko, Asaka, Reimi, Nakajima, Takashi, Mano, Hiroyuki, Takeuchi, Kengo“…To the best of our knowledge, KLC1-ALK is the first novel oncogenic fusion identified using only FFPE tissues. …”
Publicado 2012
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17por de Farias, Allysson Allan, Nunes, Kelly, Lemes, Renan Barbosa, Moura, Ronald, Fernandes, Gustavo Ribeiro, Melo, Uirá Souto, Zatz, Mayana, Kok, Fernando, Santos, Silvana“…Here, we calculated inbreeding levels using a runs of homozygosity approach, mutation age and local ancestry to infer the origin of each chromosomal segments containing disorder-causing mutations in KLC2, IMPA1, MED25 and WNT7A. Genotyped data were generated from 18 patients affected by AR diseases and combined to the 1000 genome project (1KGP) and Simons genome diversity project (SGDP) databases to infer local ancestry. …”
Publicado 2018
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18por Bahramian, Aghil, Khoshnood, Saeed, Shariati, Aref, Doustdar, Farahnoosh, Chirani, Alireza Salimi, Heidary, Mohsen“…The aim of this study was to show the frequency of the pilS2 gene, and its association with P. aeruginosa plasmid pKLC102 and PAPI-1 pathogenicity island among P. aeruginosa strains. …”
Publicado 2019
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19por Serfiotis-Mitsa, Dimitra, Herbert, Andrew P., Roberts, Gareth A., Soares, Dinesh C., White, John H., Blakely, Garry W., Uhrín, Dušan, Dryden, David T. F.“…In this article, we characterize ArdB anti-restriction proteins and their close homologues, the KlcA proteins from a range of mobile genetic elements; including an ArdB encoded on a pathogenicity island from uropathogenic Escherichia coli and a KlcA from an IncP-1b plasmid, pBP136 isolated from Bordetella pertussis. …”
Publicado 2010
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20“…CONCLUSION: These data point to significant reductions in KLC1 in AD and AD-DS. In so doing, they raise the possibility of compromised KLC1-mediated axonal transport in these conditions, a posit that can now be pursued in model systems in which KLC1 expression is reduced. …”
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