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Literatura académica sobre el tema "461st"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 1 de febrero de 2022

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Artículos de revistas sobre el tema "461st"

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Wagner, Darcy E., Wellington V. Cardoso, Sarah E. Gilpin, Susan Majka, Harald Ott, Scott H. Randell, Bernard Thébaud, Thomas Waddell y Daniel J. Weiss. "An Official American Thoracic Society Workshop Report 2015. Stem Cells and Cell Therapies in Lung Biology and Diseases". Annals of the American Thoracic Society 13, n.º 8 (agosto de 2016): S259—S278. http://dx.doi.org/10.1513/annalsats.201606-466st.

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Lateef, Omar, James Wyatt y Rosalind Cartwright. "A CASE OF VIOLENT NON-REM PARASOMNIAS THAT RESOLVED WITH TREATMENT OF OBSTRUCTIVE SLEEP APNEA". Chest 128, n.º 4 (octubre de 2005): 461S. http://dx.doi.org/10.1378/chest.128.4_meetingabstracts.461s.

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Ward, Scott K., Cathy A. Stevens, Jennifer Keates-Baleeiro y Manoo Bhakta. "Therapeutic Benefit of Blood Transfusion in a Patient With Novel PGK1 Mutation (c.461T>C [p.L154P])". Journal of Pediatric Hematology/Oncology 42, n.º 4 (mayo de 2020): e228-e230. http://dx.doi.org/10.1097/mph.0000000000001463.

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Safni, Irda, Ilse Cleenwerck, Paul De Vos, Mark Fegan, Lindsay Sly y Ulrike Kappler. "Polyphasic taxonomic revision of the Ralstonia solanacearum species complex: proposal to emend the descriptions of Ralstonia solanacearum and Ralstonia syzygii and reclassify current R. syzygii strains as Ralstonia syzygii subsp. syzygii subsp. nov., R. solanacearum phylotype IV strains as Ralstonia syzygii subsp. indonesiensis subsp. nov., banana blood disease bacterium strains as Ralstonia syzygii subsp. celebesensis subsp. nov. and R. solanacearum phylotype I and III strains as Ralstonia pseudosolanacearum sp. nov." International Journal of Systematic and Evolutionary Microbiology 64, Pt_9 (1 de septiembre de 2014): 3087–103. http://dx.doi.org/10.1099/ijs.0.066712-0.

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The Ralstonia solanacearum species complex has long been recognized as a group of phenotypically diverse strains that can be subdivided into four phylotypes. Using a polyphasic taxonomic approach on an extensive set of strains, this study provides evidence for a taxonomic and nomenclatural revision of members of this complex. Data obtained from phylogenetic analysis of 16S-23S rRNA ITS gene sequences, 16S–23S rRNA intergenic spacer (ITS) region sequences and partial endoglucanase (egl) gene sequences and DNA–DNA hybridizations demonstrate that the R. solanacearum species complex comprises three genospecies. One of these includes the type strain of Ralstonia solanacearum and consists of strains of R. solanacearum phylotype II only. The second genospecies includes the type strain of Ralstonia syzygii and contains only phylotype IV strains. This genospecies is subdivided into three distinct groups, namely R. syzygii , the causal agent of Sumatra disease on clove trees in Indonesia, R. solanacearum phylotype IV strains isolated from different host plants mostly from Indonesia, and strains of the blood disease bacterium (BDB), the causal agent of the banana blood disease, a bacterial wilt disease in Indonesia that affects bananas and plantains. The last genospecies is composed of R. solanacearum strains that belong to phylotypes I and III. As these genospecies are also supported by phenotypic data that allow the differentiation of the three genospecies, the following taxonomic proposals are made: emendation of the descriptions of Ralstonia solanacearum and Ralstonia syzygii and descriptions of Ralstonia syzygii subsp. nov. (type strain R 001T = LMG 10661T = DSM 7385T) for the current R. syzygii strains, Ralstonia syzygii subsp. indonesiensis subsp. nov. (type strain UQRS 464T = LMG 27703T = DSM 27478T) for the current R. solanacearum phylotype IV strains, Ralstonia syzygii subsp. celebesensis subsp. nov. (type strain UQRS 627T = LMG 27706T = DSM 27477T) for the BDB strains and Ralstonia pseudosolanacearum sp. nov. (type strain UQRS 461T = LMG 9673T = NCPPB 1029T) for the strains of R. solanacearum phylotypes I and III.
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Johannson, Kerri A., Veronica S. Marcoux, Paul E. Ronksley y Christopher J. Ryerson. "Diagnostic Yield and Complications of Transbronchial Lung Cryobiopsy for Interstitial Lung Disease: A Systematic Review and Meta-analysis". Annals of the American Thoracic Society, 28 de julio de 2016. http://dx.doi.org/10.1513/annalsats.201606-461sr.

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Yan, Huan, Suan-Sin Foo, Weiqiang Chen, Ji-Seung Yoo, Woo-Jin Shin, Christine Wu y Jae U. Jung. "Efficient Inhibition of Human Papillomavirus Infection by L2 Minor Capsid-Derived Lipopeptide". mBio 10, n.º 4 (6 de agosto de 2019). http://dx.doi.org/10.1128/mbio.01834-19.

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ABSTRACT The amino (N)-terminal region of human papillomavirus (HPV) minor capsid protein (L2) is a highly conserved region which is essential for establishing viral infection. Despite its importance in viral infectivity, the role of the HPV N-terminal domain has yet to be fully characterized. Using fine mapping analysis, we identified a 36-amino-acid (aa) peptide sequence of the L2 N terminus, termed L2N, that is critical for HPV infection. Ectopic expression of L2N with the transmembrane sequence on the target cell surface conferred resistance to HPV infection. Additionally, L2N peptide with chemical or enzymatic lipidation at the carboxyl (C) terminus efficiently abrogated HPV infection in target cells. Among the synthetic L2N lipopeptides, a stearoylated lipopeptide spanning aa 13 to 46 (13-46st) exhibited the most potent anti-HPV activity, with a half-maximal inhibitory concentration (IC50) of ∼200 pM. Furthermore, we demonstrated that the 13-46st lipopeptide inhibited HPV entry by blocking trans-Golgi network retrograde trafficking of virion particles, leading to rapid degradation. Fundamentally, the inhibitory effect of L2N lipopeptides appeared to be evolutionarily conserved, as they showed cross-type inhibition among various papillomaviruses. In conclusion, our findings provide new insights into the critical role of the L2N sequence in the HPV entry mechanism and identify the therapeutic potential of L2N lipopeptide as an effective anti-HPV agent. IMPORTANCE HPV is a human oncogenic virus that causes a major public health problem worldwide, which is responsible for approximately 5% of total human cancers and almost all cases of cervical cancers. HPV capsid consists of two structure proteins, the major capsid L1 protein and the minor capsid L2 protein. While L2 plays critical roles during the viral life cycle, the molecular mechanism in viral entry remains elusive. Here, we performed fine mapping of the L2 N-terminal region and defined a short 36-amino-acid peptide, called L2N, which is critical for HPV infection. Specifically, L2N peptide with carboxyl-terminal lipidation acted as a potent and cross-type HPV inhibitor. Taken together, data from our study highlight the essential role of the L2N sequence at the early step of HPV entry and suggests the L2N lipopeptide as a new strategy to broadly prevent HPV infection.
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Libros sobre el tema "461st"

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46 Years Van Birthday Notebooks. I Miss Being Less Than 3 Feet Away from You Happy 46 Birthday : #QuarantineDiaries: 46 Years Old Birthday Journal Gift Lined Notebook for Man or Woman, Social Distancing 46st Birthday Gift, for Memories, Stories, Romantic Notebook for Lovers to Write In. Independently Published, 2020.

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