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Journal articles on the topic 'None of these'

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Published: 10 March 2023

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1

Wallace, Paul. "eGEMs: An Opportunity for Better Science." eGEMs (Generating Evidence & Methods to improve patient outcomes) 1, no. 1 (January 17, 2013): 6. http://dx.doi.org/10.13063/none.

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2

Chapman, Peter M. "Selenium: When a Good Nutrient Goes Bad." Integrated Environmental Assessment and Management 5, no. 3 (2009): 363. http://dx.doi.org/10.1897/none.1.

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3

Kotorova, E. G. "None." Tomsk Journal of Linguistics and Anthropology, no. 3 (2019): 152–56. http://dx.doi.org/10.23951/2307-6119-2019-3-25-152-156.

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4

Дамбуев, Игорь Александрович. "None." Tomsk Journal of Linguistics and Anthropology, no. 2(28) (September 18, 2020): 106–17. http://dx.doi.org/10.23951/2307-6119-2020-2-106-117.

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Статья посвящена исследованию употребления бурятского цветообозначения сагаан ‘белый’ в топонимии. Актуальность исследования обусловлена необходимостью более глубокого осмысления национально-культурного своеобразия бурятской топонимии, способного выявить особенности ментальности монгольских народов и более адекватно представлять бурятскую топонимическую лексику в лексикографических изданиях. Новизна исследования заключается в том, что впервые в качестве объекта исследования выступает употребление бурятского цветообозначения в топонимии этнической Бурятии. В работе рассматривается на материале лексикографических источников и предшествующих исследований концептуальное содержание цветообозначения сагаан в бурятском языке и культуре. Особое внимание уделяется изучению бурятских топонимовсловосочетаний с цветообозначением сагаан и определяемым компонентом, выраженным именем существительным. Показано, что с цветообозначением сагаан употребляется широкий перечень компонентов, обозначающих орографические и гидрографические объекты, особенности грунта, растительного и животного мира. Приведены количественные данные по частотности употребления компонентов. Автор выдвигает предположение, что в большинстве случаев цветообозначение сагаан употребляется в топонимии в своем основном цветовом значении, указывая на белизну глауберовой соли, известняка, мрамора, мела и т.д. Показаны возможные случаи нецветового употребления цветообозначения, связанные с реализацией переносного значения ‘открытости’, ‘ровности’ при номинации островов и степных пространств, а также ‘проходимости’ обозначаемого объекта при характеристике перевалов. Автор также проводит сравнение употребления бурятского цветообозначения сагаан и русского цветообозначения белый в топонимии. Установлены как сходства, так и различия в употреблении, которые можно объяснить различиями на концептуальном уровне.
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5

Harrison, Gerald K., and Julia Tanner. "None." Philosophers' Magazine, no. 75 (2016): 72–77. http://dx.doi.org/10.5840/tpm201675133.

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6

Im SeongSoon. "None." Seoul Tax Law Review 23, no. 1 (April 2017): 415–48. http://dx.doi.org/10.16974/stlr.2017.23.1.010.

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Chang Hee Lee. "none." Seoul Tax Law Review 23, no. 1 (April 2017): 449–542. http://dx.doi.org/10.16974/stlr.2017.23.1.011.

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8

Ahn Kyeong-Bong. "none." Seoul Tax Law Review 23, no. 1 (April 2017): 543–47. http://dx.doi.org/10.16974/stlr.2017.23.1.012.

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Beom June Kim. "none." Seoul Tax Law Review 23, no. 1 (April 2017): 549–50. http://dx.doi.org/10.16974/stlr.2017.23.1.013.

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황남석. "none." Seoul Tax Law Review 23, no. 1 (April 2017): 551–52. http://dx.doi.org/10.16974/stlr.2017.23.1.014.

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11

A, Dr Suchetha. "None." RGUHS Journal of Dental Sciences 11, no. 1 (2019): 1. http://dx.doi.org/10.26715/rjds.11_1_1.

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12

Verwey, Sonja. "none." Communicare: Journal for Communication Studies in Africa 16, no. 2 (November 3, 2022): 1. http://dx.doi.org/10.36615/jcsa.v16i2.1886.

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13

Melissa, Plesac. "See None, Do None, Teach None? The Idiosyncratic Nature of Graduate Medical Education." Journal of Hospital Medicine 14, no. 4 (2019): 255. http://dx.doi.org/10.12788/jhm.3185.

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14

Casson, Christopher, and Christopher Fitz-Simon. "Division None." Books Ireland, no. 176 (1994): 79. http://dx.doi.org/10.2307/20626860.

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15

Reed, Randall. "A Book for None? Teaching Biblical Studies to Millennial Nones." Teaching Theology & Religion 19, no. 2 (April 2016): 154–74. http://dx.doi.org/10.1111/teth.12329.

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16

Redaktion, TATuP. "Veranstaltungen." TATuP - Zeitschrift für Technikfolgenabschätzung in Theorie und Praxis 16, no. 1 (April 1, 2007): none. http://dx.doi.org/10.14512/tatup.16.1.none.

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17

Redaktion, TATuP. "Veranstaltungen." TATuP - Zeitschrift für Technikfolgenabschätzung in Theorie und Praxis 17, no. 3 (November 1, 2008): none. http://dx.doi.org/10.14512/tatup.17.3.none.

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Redaktion, TATuP. "Veranstaltungen." TATuP - Zeitschrift für Technikfolgenabschätzung in Theorie und Praxis 18, no. 1 (April 1, 2009): none. http://dx.doi.org/10.14512/tatup.18.1.none.

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19

Redaktion, TATuP. "Veranstaltungen." TATuP - Zeitschrift für Technikfolgenabschätzung in Theorie und Praxis 18, no. 2 (August 1, 2009): none. http://dx.doi.org/10.14512/tatup.18.2.none.

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Redaktion, TATuP. "Veranstaltungen." TATuP - Zeitschrift für Technikfolgenabschätzung in Theorie und Praxis 18, no. 3 (November 1, 2009): none. http://dx.doi.org/10.14512/tatup.18.3.none.

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21

Blamey, R. "The BASO II trial of adjuvant radiotherapy. V. None and tamoxifen. V. None in small, node negative, grade I tumours." European Journal of Cancer 38, no. 11 (March 2002): S149. http://dx.doi.org/10.1016/s0959-8049(02)80499-3.

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22

Blamey, R. W., U. Chetty, and A. Mitchell. "The BASO II trial of adjuvant radiotherapy. V. None and tamoxifen. V. None in small, node negative, grade I tumours." European Journal of Cancer 37 (September 2001): 2. http://dx.doi.org/10.1016/s0959-8049(01)80037-x.

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23

Biermann, David. "None Should Sleep." Musical Times 132, no. 1784 (October 1991): 491. http://dx.doi.org/10.2307/966566.

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24

Senior, Tim. "Exclusion criteria: none." British Journal of General Practice 70, no. 691 (January 30, 2020): 83. http://dx.doi.org/10.3399/bjgp20x708005.

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25

Bates, Jane. "None too clever." Nursing Standard 27, no. 36 (May 8, 2013): 24–25. http://dx.doi.org/10.7748/ns2013.05.27.36.24.s30.

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26

Phillips, Peter, Stanley Sadie, John Tyrell, and Laura Macy. "Better Than None." Musical Times 143, no. 1879 (2002): 74. http://dx.doi.org/10.2307/1004606.

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27

Ball, Philip. "None more black." Nature Materials 15, no. 5 (April 26, 2016): 500. http://dx.doi.org/10.1038/nmat4633.

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28

Wake, Martyn C. "None so blind." BMJ 335, no. 7621 (September 27, 2007): 628.1–628. http://dx.doi.org/10.1136/bmj.39346.513808.3a.

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29

Shermer, Michael. "None So Blind." Scientific American 290, no. 3 (March 2004): 42. http://dx.doi.org/10.1038/scientificamerican0304-42.

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30

Kerwin, Ann. "None Too Solid." Knowledge 15, no. 2 (December 1993): 166–85. http://dx.doi.org/10.1177/107554709301500204.

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31

Moore, A. M. "Master of none?" Physics World 4, no. 6 (June 1991): 22. http://dx.doi.org/10.1088/2058-7058/4/6/18.

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32

BAUM, RUDY M. "None Too Bright." Chemical & Engineering News Archive 89, no. 23 (June 6, 2011): 5. http://dx.doi.org/10.1021/cen-v089n023.p005.

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33

Miller, Mark D. "ALL or None?" Clinics in Sports Medicine 37, no. 1 (January 2018): xv. http://dx.doi.org/10.1016/j.csm.2017.10.002.

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34

Jenkins, Simon. "Accountable to none." Public Money & Management 16, no. 2 (April 1996): 3–4. http://dx.doi.org/10.1080/09540969609387913.

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35

Morgan, F. "None so blind." BMJ 330, no. 7482 (January 6, 2005): 78. http://dx.doi.org/10.1136/bmj.330.7482.78.

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36

Bennett, Ronan. "None So Blind." Index on Censorship 31, no. 2 (April 2002): 132–40. http://dx.doi.org/10.1080/03064220208537056.

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37

Mirsky, Steve. "None So Blind." Scientific American 316, no. 2 (January 17, 2017): 74. http://dx.doi.org/10.1038/scientificamerican0217-74.

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38

Rajkumar, S. Vincent. "Second to none." Blood 120, no. 8 (August 23, 2012): 1537–39. http://dx.doi.org/10.1182/blood-2012-07-439158.

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39

Nathan, Laurie. "‘None But Ourselves’." RUSI Journal 152, no. 4 (August 2007): 46–50. http://dx.doi.org/10.1080/03071840701574706.

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40

Paul-Choudhury, Sumit. "None more black." New Scientist 225, no. 3006 (January 2015): 45. http://dx.doi.org/10.1016/s0262-4079(15)60219-6.

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41

Palmer, Bob. "None so blind." European Eating Disorders Review 5, no. 3 (September 1997): 218. http://dx.doi.org/10.1002/(sici)1099-0968(199709)5:3<218::aid-erv207>3.0.co;2-s.

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42

Dennett, Daniel C., and Marcel Kinsbourne. "Counting consciousnesses: None, one, two, or none of the above?" Behavioral and Brain Sciences 17, no. 1 (March 1994): 178–80. http://dx.doi.org/10.1017/s0140525x0003394x.

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43

Montoya, Melissa, and Beverly A. Gray. "See None, Do None, Teach None: How Dismantling Roe Impacts Medical Education and Physician Training." American Journal of Bioethics 22, no. 8 (August 2, 2022): 52–54. http://dx.doi.org/10.1080/15265161.2022.2089282.

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44

Anang, D., T. H. Ramwadhdoebe, J. Hahnlein, B. van Kuijk, S. Noortje, K. P. van Lienden, M. Maas, et al. "OP0099 INCREASED FREQUENCY OF CD4+ AND CD8+ FOLLICULAR HELPER T CELLS IN HUMAN LYMPH NODE BIOPSIES DURING THE EARLIEST STAGES OF RHEUMATOID ARTHRITIS." Annals of the Rheumatic Diseases 81, Suppl 1 (May 23, 2022): 65.2–66. http://dx.doi.org/10.1136/annrheumdis-2022-eular.289.

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BackgroundFollicular T helper (Tfh) cells provide key help for B cell differentiation into plasma and memory B cells and are essential in germinal center formation and (auto) antibody generation (1).ObjectivesTo gain more insights into the role of Tfh cells in RA development, we assessed whether Tfh cells have an altered frequency, phenotype and cytokine profile in peripheral blood, lymphoid and synovial tissues during the earliest stages of RA development.MethodsUsing flow cytometry, we analyzed the phenotpe, frequencies and cytokine profile of Tfh cells and B cells in peripheral blood and lymph node biopsies of healthy controls (HCs), autoantibody positive individuals at risk for developing RA (RA-risk individuals), and early RA patients. Using immunofluorescene we confirmed the presence of Tfh in B cell follicles of lymph nodes and synovial tissue biopsies of RA patients.ResultsIn blood, the frequency of Tfh cells did not differ between study groups. In lymphoid and synovial tissue, Tfh cells were localized in B-cell areas, and their frequencies correlated strongly with the frequency of CD19+ B cells. Compared to lymphoid tissue of healthy controls, that of RA patients and RA-risk individuals, showed more CD19+ B cells and more CD4+CXCR5+ and CD8+CXCR5+ follicular T cells. Of note, compared to healthy controls, specifically lymph node Tfh cells of RA-risk and early RA patients produced less IL-21 upon ex-vivo stimulation.ConclusionTfh cells are localised in B-cell rich areas in lymphoid and synovial tissues of early RA patients. The analysis of lymph node tissue in early RA patients showed increased frequencies of Tfh cells, where they clearly associate with B cells. Interestingly, IL-21 production is already aberrant in the very early at risk phase of the disease. Our data suggest that Tfh cells may present a novel rationale for therapeutic targeting during the preclinical stage of RA to prevent further disease progression.References[1]Ise W, Fujii K, Shiroguchi K, Ito A, Kometani K, Takeda K, et al. T Follicular Helper Cell-Germinal Center B Cell Interaction Strength Regulates Entry into Plasma Cell or Recycling Germinal Center Cell Fate. Immunity. 2018;48(4):702-15.e4.AcknowledgementsWe thank the participants in the study, the radiology department at the Academic Medical Center (AMC) for lymph node sampling; the flow cytometry facility at the Hematology department at AMC, especially J.A. Dobber; and the core facility Cellular Imaging of the Amsterdam UMC, location AMC.Disclosure of InterestsDornatien Anang: None declared, Tamara H.Ramwadhdoebe: None declared, Janine Hahnlein: None declared, Bo van Kuijk: None declared, Smits Noortje: None declared, Krijn P. van Lienden: None declared, Mario Maas: None declared, Danielle Gerlag Employee of: Employee of UCB Pharma. UCB pharma was not involved in this study, Paul-Peter Tak Employee of: Employee of Candel therapeutics. Candel therapeutics was not involved in the study, Niek de Vries: None declared, Lisa van Baarsen: None declared.
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45

Elkasem, Hossam Abd Ellatif Abo, and Ahmed Abdel Kahaar Aldardeer. "Axillary dissection versus non dissection in negative sentinel node biopsy patients." International Surgery Journal 6, no. 9 (August 28, 2019): 3083. http://dx.doi.org/10.18203/2349-2902.isj20194038.

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Background: The goal of this series was to compare performing axillary clearance versus none performing in patients with node biopsy negative.Methods: This study included 114 patients had breast cancer , presented with breast mass no enlarged axillary node either clinically or radiologically and all patients had negative sentinel lymph node intraoperatively those patients presented to Sohag Cancer Center and General Surgery Department Sohag, Egypt during the period of May 2018 to May 2019. Analysis of the clinical presentation, grade of breast cancer and radiological findings was done. All patients with above mentioned criteria were fitted for the study.Results: A total of 114 patients, all of them had sentinel lymph node negative, axillary dissection done in 55 patients of them while 59 patients had no dissection. We divided the patients in our series into group A (with axillary dissection) and group B with non-dissection; in group A 27 (49.1%) patients had lymphoedema on post-operative follow up while in group B none of patients complained from lymphoedema. Numbness was found in 11 (20%) patients among group A patients, while in group B none of patients complained from numbness. On follow up of seroma we discovered that in group A all the patients had seroma while in group B only 9 (15.3%) patients had seroma. None of our 114 patients either with or without dissection had recurrence on follow up period.Conclusions: Clearance of the axilla in sentinel node negative patients has no significant difference in overall survival but also increased rates of lymphoedema, seroma and haematoma.
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46

Möller, K., M. Lennartz, R. Abu-Hashem, NC Blessin, T. Mandelkow, E. Bady, C. Hube-Magg, et al. "P03.06 Pattern of Ki67+expanding CD8+cytotoxic T cells in healthy tissues, inflammation and the cancer microenvironment." Journal for ImmunoTherapy of Cancer 8, Suppl 2 (October 2020): A24.2—A25. http://dx.doi.org/10.1136/jitc-2020-itoc7.46.

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BackgroundExpansion of CD8+ cytotoxic T lymphocytes is a prerequisite for anti-cancer immune activity. In the era of immune checkpoint therapy, profound knowledge of the dynamics of CD8+ has regained considerable interest. However, systematically acquired data on CD8+ proliferation in large sets of normal and diseased tissues are sparse.Materials and MethodsHere, we applied multiplex fluorescence immunohistochemistry to conventional large sections and tissue microarrays in order to quantitate Ki67+CD8+ cells in >20 different compartments of normal lymphoid tissues, 7 types of inflammatory diseases and 785 cancers.ResultsIn most normal lymphoid tissues (tonsil, lymph node, thymus, Peyer’s patches, spleen, colon, appendix) the percentage of Ki67+CD8+ cells typically did not exceed 3%. The percentage of Ki67+CD8+ cells was markedly higher (45%) in the immune-active cortex of the thymus, however. In inflammatory conditions (including Hashimoto thyroiditis, Lichen sclerosus of the penis, sarcoidosis, sialadenitis, IgG4 pancreatitis, Crohn’s disease and eczema), the percentage of Ki67+CD8+ cells was much more variable and often sharply higher than in normal tissues. It ranged from 0.5% in one patient with sialadenitis to 19% in the intraepithelial compartment of Crohn’s disease. In 765 colorectal cancers, the fraction of Ki67 positive CD8+ cytotoxic T cells ranged from 0 to 100% (mean: 20.6%). A high fraction of Ki67+CD8+ cells was significantly associated with microsatellite instability (p<0.0001), low pT stage (p<0.0001) and absence of nodal metastases (p=0.0005).ConclusionsIn summary, our data show a variable increase of the fraction of proliferating CD8+ T cells in cancers and in inflammatory diseases as compared to healthy secondary lymphoid organs. The striking link with microsatellite instability and unfavorable tumor features suggest a potential clinical utility of assessing Ki67+CD8+ in colorectal cancer.Disclosure InformationK. Möller: None. M. Lennartz: None. R. Abu-Hashem: None. N.C. Blessin: None. T. Mandelkow: None. E. Bady: None. C. Hube-Magg: None. R. Simon: None. G. Sauter: None. C. Fraune: None. T.S. Clauditz: None. F. Büscheck: None. A.M. Luebke: None.
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47

Anthony, Glenda J., and Margaret A. Walshaw. "Zero: A None Number?" Teaching Children Mathematics 11, no. 1 (August 2004): 38–42. http://dx.doi.org/10.5951/tcm.11.1.0038.

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In his book The Mathematical Brain, Brian Butterworth (1999) claims that one of the most important abilities modern man possesses is the ability to use numbers. Butterworth argues that this ability has “raised us from cave-dwellers using stone tools to creators of great cities and modern science” (p. 1). In the history of the development of our decimal number system, the introduction of zero was the most significant achievement—an achievement that enabled calculation with greater numbers to become commonplace. Although we use the symbol 0 constantly, many misconceptions abound, and the placement of zero in school curricula mirrors the somewhat meandering pathway of its development.
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48

Jones, Gary. "None of your business." Nursing Standard 26, no. 38 (May 23, 2012): 26–27. http://dx.doi.org/10.7748/ns.26.38.26.s30.

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49

Jones, Gary J. "None of your business." Nursing Standard 26, no. 38 (May 23, 2012): 26–27. http://dx.doi.org/10.7748/ns2012.05.26.38.26.p8410.

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50

Opiela, Nancy. "One Size Fits None." CFA Institute Magazine 24, no. 2 (March 2013): 30–32. http://dx.doi.org/10.2469/cfm.v24.n2.19.

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