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1001por Kasaija, Paul D., Contreras, Marinela, Kirunda, Halid, Nanteza, Ann, Kabi, Fredrick, Mugerwa, Swidiq, de la Fuente, José“…Recent advances in various omics technologies and reverse vaccinology have enabled the identification of many candidate anti-tick antigens (ATAs), and are likely to usher in the next generation of vaccines, for which Africa should prepare to embrace. …”
Publicado 2022
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1002“…We also acknowledge that the evidence we usher in, while grounded in the research literature, is currently largely circumstantial, not direct. …”
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1003por Qiu, Yi, Kenana, Rosan, Beharry, Aruun, Wilhelm, Sarah D P, Hsu, Sung Yuan, Siu, Victoria M, Duennwald, Martin, Heinemann, Ilka U“…In histidyl-tRNA synthetase (HARS), autosomal dominant mutations V133F, V155G, Y330C and S356N in the HARS catalytic domain cause Charcot–Marie–Tooth disease type 2 W (CMT2W), while tRNA-binding domain mutation Y454S causes recessive Usher syndrome type IIIB. In a yeast model, all human HARS variants complemented a genomic deletion of the yeast ortholog HTS1 at high expression levels. …”
Publicado 2022
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1004por Tamadonfar, Kevin O., Di Venanzio, Gisela, Pinkner, Jerome S., Dodson, Karen W., Kalas, Vasilios, Zimmerman, Maxwell I., Bazan Villicana, Jesus, Bowman, Gregory R., Feldman, Mario F., Hultgren, Scott J.“…During such infections, like catheter-associated urinary tract infections (CAUTI), A. baumannii rely on adhesive, extracellular fibers, called chaperone-usher pathway (CUP) pili for critical binding interactions. …”
Publicado 2023
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1005por Tebbe, Lars, Mwoyosvi, Maggie L., Crane, Ryan, Makia, Mustafa S., Kakakhel, Mashal, Cosgrove, Dominic, Al-Ubaidi, Muayyad R., Naash, Muna I.“…Usher syndrome (USH) is the leading cause of combined deafness-blindness with type 2 A (USH2A) being the most common form. …”
Publicado 2023
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1006por Kelm, Jeremy M., Pandey, Deepti S., Malin, Evan, Kansou, Hussein, Arora, Sahil, Kumar, Raj, Gavande, Navnath S.“…The medicinal chemistry of PROTAC design has been a challenging area of active research, but the recent advances in the field will usher in an era of rational degrader design.…”
Publicado 2023
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1007por Bates, Steve, Dumoulin, Serge O., Folkers, Paul J. M., Formisano, Elia, Goebel, Rainer, Haghnejad, Aidin, Helmich, Rick C., Klomp, Dennis, van der Kolk, Anja G., Li, Yi, Nederveen, Aart, Norris, David G., Petridou, Natalia, Roell, Stefan, Scheenen, Tom W. J., Schoonheim, Menno M., Voogt, Ingmar, Webb, Andrew“…We anticipate that this initiative will usher in a new era of ultra-high-field MR.…”
Publicado 2023
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1008por Mathur, Pranav Dinesh, Zou, Junhuang, Neiswanger, Grace, Zhu, Daniel, Wang, Yong, Almishaal, Ali A., Vashist, Deepti, Hammond, H. Kirk, Park, Albert H., Yang, Jun“…In cochlear hair cells, AC6 distribution relies on an adhesion GPCR, ADGRV1, which is associated with Usher syndrome (USH), a condition of combined hearing and vision loss. …”
Publicado 2023
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1009por Tan, N. C., Yusoff, Y., Koot, D., Lau, Q. C., Lim, H., Hui, T. F., Cher, H. Y., Tan, P. Y. A., Koh, Y. L. E.“…A Healthcare-assistive Infection-control RObot (HIRO) is a healthcare-assistive robot that is deployed in an outpatient primary care clinic to sanitise the premises, monitor people in its proximity for their temperature and donning of masks, and usher them to service points. This study aimed to determine the acceptability, perceptions of safety, and concerns among the patients, visitors, and polyclinic healthcare workers (HCWs) regarding the HIRO. …”
Publicado 2023
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1010por Crane, Ryan, Tebbe, Lars, Mwoyosvi, Maggie L., Al-Ubaidi, Muayyad R., Naash, Muna I.“…Usher syndrome (USH) is the leading cause of combined deafness and blindness, with USH2A being the most prevalent form. …”
Publicado 2023
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1011“…BACKGROUND: Variants in the MYO7A gene commonly result in Usher syndrome, and in rare cases lead to autosomal dominant non-syndromic deafness (DFNA11). …”
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1012por Elsori, Deena, Rashid, Gowhar, Khan, Nihad Ashraf, Sachdeva, Punya, Jindal, Riya, Kayenat, Falak, Sachdeva, Bhuvi, Kamal, Mohammad Azhar, Babker, Asaad Ma, Fahmy, Sherif Ashraf“…The exploration of CNTs as a dual therapeutic arsenal for both brain tumors and Alzheimer’s disease holds great promise and may usher in a new era of effective treatment strategies for these challenging conditions.…”
Publicado 2023
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1013por Xie, Xiaodu, Hu, Jian, Liu, Lumiao, Lei, Pan, Zhang, Peng, Ran, Chongjun, Liang, Peihe“…The pathogenesis (especially at the genetic level) and treatment of hypogonadism such as Kallmann syndrome and Klinefelter syndrome have attracted increasing attention recently, which may usher in some breakthroughs in coming years.…”
Publicado 2023
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1014por Ebermann, Inga, Lopez, Irma, Bitner-Glindzicz, Maria, Brown, Carolyn, Karel Koenekoop, Robert, Jörn Bolz, Hanno“…BACKGROUND: Usher syndrome type 1 (USH1) is the leading cause of deafblindness. …”
Publicado 2007
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1015por Isosomppi, Juha, Västinsalo, Hanna, Geller, Scott F., Heon, Elise, Flannery, John G., Sankila, Eeva-Marja“…PURPOSE: Mutations of clarin 1 (CLRN1) cause Usher syndrome type 3 (USH3). To determine the effects of USH3 mutations on CLRN1 function, we examined the cellular distribution and stability of both normal and mutant CLRN1 in vitro. …”
Publicado 2009
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1016por Hurle, Belen, Marques-Bonet, Tomas, Antonacci, Francesca, Hughes, Inna, Ryan, Joseph F, Eichler, Evan E, Ornitz, David M, Green, Eric D“…We extend our evolutionary study to include the gene mutated in Usher syndrome (USH) subtype 1G (Ush1g), both because of the head-to-tail clustering of Ush1g with Otop2 and because Otop1 and Ush1g mutations result in inner ear phenotypes. …”
Publicado 2011
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1017por Kenney, M. Cristina, Chwa, Marilyn, Atilano, Shari R., Pavlis, Janelle M., Falatoonzadeh, Payam, Ramirez, Claudio, Malik, Deepika, Hsu, Tiffany, Woo, Grace, Soe, Kyaw, Nesburn, Anthony B., Boyer, David S., Kuppermann, Baruch D., Jazwinski, S. Michal, Miceli, Michael V., Wallace, Douglas C., Udar, Nitin“…Q-PCR analyses showed J cybrids had decreased expressions for CFH, C3, and EFEMP1 genes, high risk genes for AMD, and higher expression for MYO7A, a gene associated with retinal degeneration in Usher type IB syndrome. The H and J cybrids also have comparatively altered expression of nuclear genes involved in pathways for cell signaling, inflammation, and metabolism. …”
Publicado 2013
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1018por Corton, Marta, Nishiguchi, Koji M., Avila-Fernández, Almudena, Nikopoulos, Konstantinos, Riveiro-Alvarez, Rosa, Tatu, Sorina D., Ayuso, Carmen, Rivolta, Carlo“…Specifically, we detected pathogenic DNA variants (∼50% novel mutations) in the genes RP1, USH2A, CNGB3, NMNAT1, CHM, and ABCA4, responsible for retinitis pigmentosa, Usher syndrome, achromatopsia, Leber congenital amaurosis, choroideremia, or recessive Stargardt/cone-rod dystrophy cases. …”
Publicado 2013
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1019por Greene, Sarah E., Pinkner, Jerome S., Chorell, Erik, Dodson, Karen W., Shaffer, Carrie L., Conover, Matt S., Livny, Jonathan, Hadjifrangiskou, Maria, Almqvist, Fredrik, Hultgren, Scott J.“…Chaperone-usher pathway (CUP) pili are extracellular organelles produced by Gram-negative bacteria that mediate bacterial pathogenesis. …”
Publicado 2014
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1020por Ravanbakhsh, Siamak, Liu, Philip, Bjordahl, Trent C., Mandal, Rupasri, Grant, Jason R., Wilson, Michael, Eisner, Roman, Sinelnikov, Igor, Hu, Xiaoyu, Luchinat, Claudio, Greiner, Russell, Wishart, David S.“…We anticipate this tool will usher in high-throughput metabolomics and enable a wealth of new applications of NMR in clinical settings. …”
Publicado 2015
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