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1

Billiotte-Thieblemont, Nathalie. "(5 5)." L'en-je lacanien 33, no. 2 (2019): 193. http://dx.doi.org/10.3917/enje.033.0193.

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2

Choudhry, Ajai. "The Diophantine Equation $ax^5+by^5+cz^5=au^5+bv^5+cw^5$." Rocky Mountain Journal of Mathematics 29, no. 2 (June 1999): 459–62. http://dx.doi.org/10.1216/rmjm/1181071645.

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3

Ten Hoeve, W., H. Wynberg, E. E. Havinga, and E. W. Meijer. "Substituted 2,2':5',2'':5'',2''':5''',2'''':5'''',2''''': 5''''',2'''''':5'''''',2''''''':5''''''',2'''''''':5'''''''',2''''''''':5''''''''',2''''''''''-undecithiophenes, the longest characterized oligothiophenes." Journal of the American Chemical Society 113, no. 15 (July 1991): 5887–89. http://dx.doi.org/10.1021/ja00015a067.

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4

Patel, Bhisma Kumar, and Fritz Eckstein. "5′-Deoxy-5′-thioribonucleoside-5′-triphosphates." Tetrahedron Letters 38, no. 6 (February 1997): 1021–24. http://dx.doi.org/10.1016/s0040-4039(97)00084-1.

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5

Hegde, Vishnumurthy R., Katherine L. Seley, Stewart W. Schneller, and Thomas J. J. Elder. "5‘-Amino-5‘-deoxy-5‘-noraristeromycin." Journal of Organic Chemistry 63, no. 20 (October 1998): 7092–94. http://dx.doi.org/10.1021/jo972078c.

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6

TEN HOEVE, W., H. WYNBERG, E. E. HAVINGA, and E. W. MEIJER. "ChemInform Abstract: Substituted 2,2′:5′,2′′:5′′,2′′′:5′′′,2′′′′:5′′′′,2′′′′′:5′′′′′,2′′′′′′ :5′′′′′′,2′′′′′′′:5′′′′′′′,2′′′′′′′′:5′′′′′′′′,2′′′′′′′′′: 5′′′′′′′′′, 2′′′′′′′′′′-Undecithiophenes: The Longest Characterized Oligothiophenes." ChemInform 22, no. 42 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199142165.

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7

Roy, Atanu, and Stewart W. Schneller. "Enantiospecific synthesis of 5′,5′,5′-trifluoro-5′-deoxyneplanocin A." Tetrahedron Letters 46, no. 51 (December 2005): 8913–15. http://dx.doi.org/10.1016/j.tetlet.2005.10.064.

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8

Das, Subha R., and Stewart W. Schneller. "The 5′-Nor Aristeromycin Analogues of 5′-Deoxy-5′-Methylthioadenosine and 5′-Deoxy-5′-Thiophenyladenosine." Nucleosides, Nucleotides and Nucleic Acids 33, no. 10 (September 15, 2014): 668–77. http://dx.doi.org/10.1080/15257770.2014.917671.

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9

Turnbull, Douglas, Paul Hazendonk, Stacey D. Wetmore, and Michael Gerken. "Stabilisation of [WF 5 ] + and WF 5 by Pyridine: Facile Access to [WF 5 (NC 5 H 5 ) 3 ] + and WF 5 (NC 5 H 5 ) 2." Chemistry – A European Journal 26, no. 30 (May 7, 2020): 6879–86. http://dx.doi.org/10.1002/chem.202000424.

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10

TAKATSU, Kiyoshi. "Interleukin-5, IL-5." Journal of Japan Atherosclerosis Society 23, no. 10 (1996): 599–603. http://dx.doi.org/10.5551/jat1973.23.10_599.

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11

Harrisville, Roy A. "Romans 5:1–5." Interpretation: A Journal of Bible and Theology 45, no. 2 (April 1991): 181–85. http://dx.doi.org/10.1177/002096430004500208.

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12

Guloksuz, Sinan, and Jim van Os. "Renaming schizophrenia: 5 × 5." Epidemiology and Psychiatric Sciences 28, no. 03 (October 18, 2018): 254–57. http://dx.doi.org/10.1017/s2045796018000586.

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AbstractThere had been a long way to go before we felt comfortable about even discussing the issues revolving around the concept of ‘schizophrenia’, let alone reckoning on mere semantic revision. In this editorial, we aim to extend our discussion on the reasons behind the slow death of the concept of ‘schizophrenia’ and the benefits of changing the name and embracing a spectrum approach with an umbrella psychosis spectrum disorder (PSD) category (similar to autism spectrum disorder) that goes further than a mere semantic revision. We attempted to cover the topic of the renaming by providing five most pertinent points categorised under five domains: reasons, signals, challenges, promises and steps for the change. Admittedly, even a modest revision, such as classifying all psychotic disorder categories under an umbrella category of PSD, and abolishing the term schizophrenia requires careful deliberation and some effort in the beginning, but the revision is well worth the effort considering the benefits in the long run. Renaming a particular form of mental suffering should be accompanied by a broader debate of the entire diagnosis-evidence-based-practice (EBP)-symptom-reduction model as the normative factor driving the content and organisation of mental health services that may be detached from patients’ needs and reality, overlooks the trans-syndromal structure of mental difficulties, appraises the significance of the technical features over the relational and ritual components of care, and underestimates the lack of EBP group-to-individual generalisability. Individuals may make great strides in attaining well-being by accommodating to living with mental vulnerabilities through building resilience in the social and existential domains. Changing the name and the concept of ‘schizophrenia’, which goes beyond a mere semantic revision, may become the first step that allows catalysation of the process of modernising psychiatric science and services worldwide.
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13

Touzet, Patrick. "5/5 Michel Foucault." Soins Psychiatrie 36, no. 301 (November 2015): 45–46. http://dx.doi.org/10.1016/j.spsy.2015.09.008.

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14

Alyea, E. C., G. Ferguson, J. Malito, and B. L. Ruhl. "5-Phenyldibenzophosphole 5-selenide." Acta Crystallographica Section C Crystal Structure Communications 42, no. 7 (July 1, 1986): 882–84. http://dx.doi.org/10.1107/s0108270186094192.

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15

Li, Weikuan, Xueqiang Yin, and Stewart W. Schneller. "5′-Fluoro-5′-deoxyaristeromycin." Bioorganic & Medicinal Chemistry Letters 18, no. 1 (January 2008): 220–22. http://dx.doi.org/10.1016/j.bmcl.2007.10.095.

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16

G. Micetich, Ronald, Chia C. Shaw, Tse W. Hall, Paul Spevak, Robert A. Fortier, Peter Wolfert, Brian C. Foster, and Buljit K. Bains. "The 5-Alkoxymethyl-, 5-Alkylthiomethyl-, and 5-Dialkylaminomethylisoxazoles." HETEROCYCLES 23, no. 3 (1985): 571. http://dx.doi.org/10.3987/r-1985-03-0571.

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17

HEGDE, V. R., K. L. SELEY, S. W. SCHNELLER, and T. J. J. ELDER. "ChemInform Abstract: 5′-Amino-5′-deoxy-5′-noraristeromycin." ChemInform 30, no. 7 (June 17, 2010): no. http://dx.doi.org/10.1002/chin.199907253.

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18

Mori, Akira, Ryoji Mori, Manabu Takemoto, Shin-ichi Yamamoto, Daiki Kuribayashi, Katsuyuki Uno, Kanji Kubo, and Seiji Ujiie. "Troponoid metallomesogens with 5-alkoxy, 5-alkoxycarbonyl, 5-alkanoyloxy, 5-alkyl, 5-alkoxy-2-amino, and 5-alkoxy-2-alkylamino substituents." Journal of Materials Chemistry 15, no. 29 (2005): 3005. http://dx.doi.org/10.1039/b501974e.

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19

Sufrin, Janice R., Arthur J. Spiess, Debora L. Kramer, Paul R. Libby, John T. Miller, Ralph J. Bernacki, Younha Lee, Ronald T. Borchardt, and Carl W. Porter. "Targeting 5'-deoxy-5'-(methylthio)adenosine phosphorylase by 5'-haloalkyl analogs of 5'-deoxy-5'-(methylthio)adenosine." Journal of Medicinal Chemistry 34, no. 8 (August 1991): 2600–2606. http://dx.doi.org/10.1021/jm00112a039.

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20

Zhang, Qinghong. "The maximal angle between 5×5 positive semidefinite and 5×5 nonnegative matrices." Electronic Journal of Linear Algebra 37 (November 19, 2021): 698–708. http://dx.doi.org/10.13001/ela.2021.6647.

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The paper is devoted to the study of the maximal angle between the $5\times 5$ semidefinite matrix cone and $5\times 5$ nonnegative matrix cone. A signomial geometric programming problem is formulated in the process to find the maximal angle. Instead of using an optimization problem solver to solve the problem numerically, the method of Lagrange Multipliers is used to solve the signomial geometric program, and therefore, to find the maximal angle between these two cones.
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21

Hiebl, Johann, Erich Zbiral, Jan Balzarini, and Erik De Clercq. "Synthesis and antiretrovirus properties of 5'-isocyano-5'-deoxythymidine,5'-isocyano-2',5'-dideoxyuridine,3'-azido-5'-isocyano-3',5'-dideoxythymidine, and 3'-azido-5'-isocyano-2',3',5'-trideoxyuridine." Journal of Medicinal Chemistry 34, no. 4 (April 1991): 1426–30. http://dx.doi.org/10.1021/jm00108a028.

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22

Kennedy, Anne. "Researching children researching the world: 5×5×5=creativity." Early Years 30, no. 1 (March 2010): 95–96. http://dx.doi.org/10.1080/09575140903358133.

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23

Zhang, Cong, Christian Ludin, Marcel K. Eberle, Helen Stoeckli-Evans, and Reinhart Keese. "Asymmetric Synthesis of (S)-5,5,5,5?,5?,5?,5?-Hexafluoroleucine." Helvetica Chimica Acta 81, no. 1 (January 12, 1998): 174–81. http://dx.doi.org/10.1002/hlca.19980810116.

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24

Chang, Shengmei, and Nan Zhu. "5:20:20:5 EFFICIENCY." PUPIL: International Journal of Teaching, Education and Learning 2, no. 2 (July 14, 2018): 12–19. http://dx.doi.org/10.20319/pijtel.2018.22.1219.

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25

Eichberger, G�nter, Walter Hayden, Wolfgang Schwarz, and Herfried Griengl. "5-Ethylthiomethyl- und 5-Ethylsulfonylmethylpyrimidine." Monatshefte f�r Chemie Chemical Monthly 117, no. 3 (March 1986): 385–92. http://dx.doi.org/10.1007/bf00816533.

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26

Berman, Abraham, and Changqing Xu. "5×5 Completely positive matrices." Linear Algebra and its Applications 393 (December 2004): 55–71. http://dx.doi.org/10.1016/j.laa.2004.08.004.

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27

Walker, James K. "5-2-5 matrix system." Journal of the Acoustical Society of America 105, no. 2 (1999): 582. http://dx.doi.org/10.1121/1.426980.

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28

Schaible, H. G., J. W. Bats, and J. W. Engels. "5'-Azido-2',5'-dideoxythymidine." Acta Crystallographica Section C Crystal Structure Communications 51, no. 11 (November 15, 1995): 2410–12. http://dx.doi.org/10.1107/s0108270195009310.

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29

Rivallan, Armel. "5/5 Ernest-Charles Lasègue." Soins Psychiatrie 38, no. 313 (November 2017): 45–46. http://dx.doi.org/10.1016/j.spsy.2017.09.010.

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30

Eknoian, M. W., T. R. Webb, S. D. Worley, A. Braswell, and J. Hadley. "5-(4-Pyridyl)-5-phenylhydantoin." Acta Crystallographica Section C Crystal Structure Communications 55, no. 3 (March 15, 1999): 405–7. http://dx.doi.org/10.1107/s0108270198014528.

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31

Staff, EID Editorial. "Erratum Vol. 5, No. 5." Emerging Infectious Diseases 6, no. 3 (June 2000): 317. http://dx.doi.org/10.3201/eid0603.000318.

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32

Hegde, Vishnumurthy R., Katherine L. Seley, and Stewart W. Schneller. "Carbocyclic 5′-norcytidine (5′-norcarbodine)." Journal of Heterocyclic Chemistry 37, no. 5 (September 2000): 1361–62. http://dx.doi.org/10.1002/jhet.5570370558.

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33

Greif, Dieter. "5. Fachtagung Iminiumsalze (ImSaT 5)." Nachrichten aus der Chemie 50, no. 3 (March 2002): 387. http://dx.doi.org/10.1002/nadc.20020500328.

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34

Kubo, Kanji, Emi Yamamoto, and Akira Mori. "5-Cyanotropolone and 5-nitrotropolone." Acta Crystallographica Section C Crystal Structure Communications 57, no. 5 (May 15, 2001): 611–13. http://dx.doi.org/10.1107/s0108270101002463.

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35

Villeneuve, Michael, and Don Wildfong. "Canada’s Top 5 in 5." Healthcare Quarterly 16, no. 3 (July 23, 2013): 14–16. http://dx.doi.org/10.12927/hcq.2013.23505.

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36

Podgurskii, A. I., S. G. Zlotin, and O. A. Luk'yanov. "5-?-Nitroalkyl- and 5-?,?-dinitroalkyltetrazoles." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 35, no. 1 (January 1986): 215–16. http://dx.doi.org/10.1007/bf00952883.

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37

Catapan, Edilson Antonio. "Editorial – v. 5, n. 5." Brazilian Applied Science Review 5, no. 5 (September 1, 2021): 1970. http://dx.doi.org/10.34115/basr.v5i5.35319.

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38

Catapan, Edilson Antonio. "Editorial – v. 5, n. 5." Brazilian Applied Science Review 5, no. 5 (September 1, 2021): 1970. http://dx.doi.org/10.34115/basr.v5i5.35319.

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39

García Moro, María, Matías Astroza Rodríguez, Enrique García Merino, Enrique García Sánchez, and Jose Elías García Sánchez. "5 películas para 5 pandemias." Revista de Medicina y Cine 16, e (January 29, 2021): 511–20. http://dx.doi.org/10.14201/rmc202016e511520.

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A lo largo de la historia diferentes pandemias han asolado a la humanidad. De todas ellas, salvo de la Covid-19, pues aún no ha habido tiempo de llevarla a la gran pantalla, ha habido numerosas representaciones en el cine comercial, algunas muy relevantes desde el punto de vista de la calidad cinematográfica y de la calidad científica con la que están documentados los guiones. Sería inalcanzable enumerar todas y cada una de ellas. Por tanto, en este artículo se plantea ofrecer a los lectores un ejemplo de cada una de estas pandemias (Peste, Viruela, Cólera, Gripe y VIH) que pueden ser útiles para la docencia y para la educación sanitaria de la población.
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40

Mascia, Laura, and Piero Luigi Ipata. "Activation pathways of 5-fluorouracil in rat organs and in PC12 cells11Abbreviations: PRPP, 5-phosphoribosyl 1-pyrophosphate; 5-FU, 5-fluorouracil; FUrd, 5-fluorouridine; 5-FUMP, 5-FUDP, and 5-FUTP, 5-fluorouridine 5′-mono-, -di-, and -triphosphate, 5-Fdeoxyuridine, 5-fluoro-2′-deoxyuridine; 5-FdeoxyUMP, 5-FdeoxyUDP, and 5-FdeoxyUTP, 5-fluoro-2′-deoxyuridine 5′-mono-, -di-, and triphosphate; Rib1-P, ribose 1-phosphate; and deoxyRib1-P, 2′-deoxyribose 1-phosphate." Biochemical Pharmacology 62, no. 2 (July 2001): 213–18. http://dx.doi.org/10.1016/s0006-2952(01)00650-5.

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41

Roth, B. "5-Hydroxytryptamine2-Family Receptors (5-Hydroxytryptamine2A, 5-Hydroxytryptamine2B, 5-Hydroxytryptamine2C) Where Structure Meets Function." Pharmacology & Therapeutics 79, no. 3 (October 1998): 231–57. http://dx.doi.org/10.1016/s0163-7258(98)00019-9.

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42

Crooks, Peter A., Trevor Deeks, and Francesco Desimone. "Synthesis of 5-benzoyl-5-phenyl- and 5-phenylhydroxymethyl-5-phenylhydantoins as potential anticonvulsants." Journal of Heterocyclic Chemistry 26, no. 4 (July 1989): 1113–17. http://dx.doi.org/10.1002/jhet.5570260439.

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43

Schlüter, H., I. Grobeta, J. Bachmann, R. Kaufmann, M. van der Giet, M. Tepel, J. R. Nofer, et al. "Adenosine(5') oligophospho-(5') guanosines and guanosine(5') oligophospho-(5') guanosines in human platelets." Journal of Clinical Investigation 101, no. 3 (February 1, 1998): 682–88. http://dx.doi.org/10.1172/jci119882.

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44

Kvasyuk, Evgeny I., Igor A. Mikhailopulo, Robert J. Suhadolnik, Earl E. Henderson, Nicholas F. Muto, Kathryn T. Iacono, Joseph Homon, and Wolfgang Pfleiderer. "Synthesis and Biological Activity of 2′,5′-Oligoadenylate Trimers Containing 5′-Terminal 5′-Amino-5′-deoxy- and 5′-Amino-3′,5′-dideoxyadenosine Derivatives." Nucleosides and Nucleotides 18, no. 6-7 (June 1999): 1483–84. http://dx.doi.org/10.1080/07328319908044760.

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45

HIEBL, J., E. ZBIRAL, J. BALZARINI, and E. DE CLERCQ. "ChemInform Abstract: Synthesis and Antiretrovirus Properties of 5′-Isocyano-5′- deoxythymidine, 5′-Isocyano-2′,5′-dideoxyuridine, 3′-Azido-5′-isocyano- 3′,5′-dideoxythymidine, and 3′-Azido-5′-isocyano-2′,3′,5′- trideoxyuridine." ChemInform 22, no. 44 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199144294.

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46

Creuven, Isabelle, Bernadette Norberg, Anne Olivier, Christine Evrard, Guy Evrard, Piet Wigerinck, Piet Herdewijn, and François Durant. "5-(thien-2-yl) uracil analogs: 5-(5-methylthien-2-yl)-2′-deoxyuridine, 5-(5-thien-2-yl)-2′-deoxyuridine, and 5-(5-bromothien-2-yl)-2′-deoxyuridine." Journal of Chemical Crystallography 26, no. 11 (November 1996): 777–89. http://dx.doi.org/10.1007/bf01664656.

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47

Font, J., A. Gracia, and P. de March. "Synthesis of 5-alkyl-4-bromo-5-hydroxy-2(5)-furanones and 5-alkylidene-4-bromo-2(5)-furanones." Tetrahedron Letters 31, no. 38 (January 1990): 5517–20. http://dx.doi.org/10.1016/s0040-4039(00)97887-0.

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48

SUFRIN, J. R., A. J. SPIESS, D. L. KRAMER, P. R. LIBBY, J. T. MILLER, R. J. BERNACKI, Y. LEE, R. T. BORCHARDT, and C. W. PORTER. "ChemInform Abstract: Targeting 5′-Epoxy-5′-(methylthio)adenosine Phosphorylase by 5′-Haloalkyl Analogues of 5′-Deoxy-5′-(methylthio)adenosine." ChemInform 23, no. 2 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199202319.

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49

G. Micetich, Ronald, Chia C. Shaw. Tse W. Hall, Paul Spevak, and Buljit K. Bains. "Lithiation Reactions of 5-Alkoxymethyl-, 5-Alkylthiomethyl-, and 5-Dialkylaminomethylisoxazoles." HETEROCYCLES 23, no. 3 (1985): 585. http://dx.doi.org/10.3987/r-1985-03-0585.

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50

Yang, Minmin, and Stewart W. Schneller. "Amino substituted derivatives of 5′-amino-5′-deoxy-5′-noraristeromycin." Bioorganic & Medicinal Chemistry 13, no. 3 (February 2005): 877–82. http://dx.doi.org/10.1016/j.bmc.2004.10.031.

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