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Articles de revues sur le sujet « Max »

Auteur : Grafiati

Publié le 4 juin 2021

Mis à jour le 25 juillet 2025

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1

Perkinson, Robert. "Mad Max." Punishment & Society 8, no. 1 (2006): 125–30. http://dx.doi.org/10.1177/1462474506059146.

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2

Malec, Bogusz. "Utopian Thinking in "Mad Max: Fury Road"." Annales Universitatis Mariae Curie-Sklodowska, sectio FF, Philologia 34, no. 2 (2017): 137. http://dx.doi.org/10.17951/ff.2016.34.137.

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Malec, Bogusz. "Utopian Thinking in "Mad Max: Fury Road"." Annales Universitatis Mariae Curie-Sklodowska, sectio FF, Philologia 34, no. 2 (2017): 137. http://dx.doi.org/10.17951/ff.2016.34.2.137.

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4

Andelman, David A. "Mad Max Redux." World Policy Journal 26, no. 1 (2009): 105–12. http://dx.doi.org/10.1162/wopj.2009.26.1.105.

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5

Lee, Haram. "Anthropocene Time in Max Frisch’s Man in the Holocene." Journal of English Studies in Korea 42 (June 15, 2022): 5–43. http://dx.doi.org/10.46562/jesk.42.1.

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6

Sharrett, Christopher. ": Mad Max beyond Thunderdome ." Film Quarterly 40, no. 3 (1987): 59. http://dx.doi.org/10.1525/fq.1987.40.3.04a00190.

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7

Sharrett, Christopher. "Mad Max beyond Thunderdome." Film Quarterly 40, no. 3 (1987): 59. http://dx.doi.org/10.2307/1212474.

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8

Hay, John. "The American Mad Max." Science Fiction Film & Television 10, no. 3 (2017): 307–27. http://dx.doi.org/10.3828/sfftv.2017.22.

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9

Baydar, Gökçe. "Potential of Feminist Action Film: On Mad Max Fury Road." Moment Journal 2, no. 2 (2015): 104–34. http://dx.doi.org/10.17572/mj2015.2.104134.

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10

Kvyetnyy, R. N., S. G. Krivogubchenko, and Yu Yu Ivanov. "HARDWARE IMPLEMENTATION AND EXPERIMENTAL RESEARCHES OF MAX-LOG-MAP TURBO-DECODER." Information Technology And Computer Engineering 43, no. 3 (2018): 48–53. http://dx.doi.org/10.31649/1999-9941-2018-43-3-48-53.

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11

Nair, Satish K., and Stephen K. Burley. "X-Ray Structures of Myc-Max and Mad-Max Recognizing DNA." Cell 112, no. 2 (2003): 193–205. http://dx.doi.org/10.1016/s0092-8674(02)01284-9.

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12

Loo, K. K., K. Salman, T. Alukaidey, and S. A. Jimaa. "Parallelised max-Log-Map model." Electronics Letters 38, no. 17 (2002): 971. http://dx.doi.org/10.1049/el:20020663.

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13

Baudino, Troy A., and John L. Cleveland. "The Max Network Gone Mad." Molecular and Cellular Biology 21, no. 3 (2001): 691–702. http://dx.doi.org/10.1128/mcb.21.3.691-702.2001.

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14

Urry, John. "Medieval worlds and Mad Max." postmedieval: a journal of medieval cultural studies 4, no. 2 (2013): 233–37. http://dx.doi.org/10.1057/pmed.2013.6.

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15

Faiola, Francesco, Yi-Ting Wu, Songqin Pan, Kangling Zhang, Anthony Farina, and Ernest Martinez. "Max is acetylated by p300 at several nuclear localization residues." Biochemical Journal 403, no. 3 (2007): 397–407. http://dx.doi.org/10.1042/bj20061593.

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Max is a ubiquitous transcription factor with a bHLHZip [basic HLH (helix–loop–helix) leucine zipper] DNA-binding/dimerization domain and the central component of the Myc/Max/Mad transcription factor network that controls cell growth, proliferation, differentiation and apoptotic cell death in metazoans. Max is the obligatory DNA-binding and dimerization partner for all the bHLHZip regulators of the Myc/Max/Mad network, including the Myc family of oncoproteins and the Mad family of Myc antagonists, which recognize E-box DNA elements in the regulatory regions of target genes. Max lacks a transcr

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16

KRIPPNER-HEIDENREICH, Anja, Robert V. TALANIAN, Renate SEKUL, et al. "Targeting of the transcription factor Max during apoptosis: phosphorylation-regulated cleavage by caspase-5 at an unusual glutamic acid residue in position P1." Biochemical Journal 358, no. 3 (2001): 705–15. http://dx.doi.org/10.1042/bj3580705.

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Max is the central component of the Myc/Max/Mad network of transcription factors that regulate growth, differentiation and apoptosis. Whereas the Myc and Mad genes and proteins are highly regulated, Max expression is constitutive and no post-translational regulation is known. We have found that Max is targeted during Fas-induced apoptosis. Max is first dephosphorylated and subsequently cleaved by caspases. Two specific cleavage sites for caspases in Max were identified, one at IEVE10↓S and one at SAFD135↓G near the C-terminus, which are cleaved in vitro by caspase-5 and caspase-7 respectively.

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17

Grinberg, Asya V., Chang-Deng Hu, and Tom K. Kerppola. "Visualization of Myc/Max/Mad Family Dimers and the Competition for Dimerization in Living Cells." Molecular and Cellular Biology 24, no. 10 (2004): 4294–308. http://dx.doi.org/10.1128/mcb.24.10.4294-4308.2004.

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ABSTRACT Myc and Mad family proteins play opposing roles in the control of cell growth and proliferation. We have visualized the subcellular locations of complexes formed by Myc/Max/Mad family proteins using bimolecular fluorescence complementation (BiFC) analysis. Max was recruited to different subnuclear locations by interactions with Myc versus Mad family members. Complexes formed by Max with Mxi1, Mad3, or Mad4 were enriched in nuclear foci, whereas complexes formed with Myc were more uniformly distributed in the nucleoplasm. Mad4 was localized to the cytoplasm when it was expressed separa

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18

Scaff, Lawrence A. "Max Weber's Legacy." Annual review of sociology 2015, no. 28 (2015): 18–27. http://dx.doi.org/10.5690/kantoh.2015.18.

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19

Xiang, Yueming. "MAX-INJECTIVE, MAX-FLAT MODULES AND MAX-COHERENT RINGS." Bulletin of the Korean Mathematical Society 47, no. 3 (2010): 611–22. http://dx.doi.org/10.4134/bkms.2010.47.3.611.

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20

KRAUSE, Stefan W., Michael REHLI, Sven HEINZ, Reinhard EBNER, and Reinhard ANDREESEN. "Characterization of MAX.3 antigen, a glycoprotein expressed on mature macrophages, dendritic cells and blood platelets: identity with CD84." Biochemical Journal 346, no. 3 (2000): 729–36. http://dx.doi.org/10.1042/bj3460729.

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MAX.3 is a monoclonal antibody that preferentially reacts with mature macrophages (MAC), monocyte-derived dendritic cells, megakaryocytes and platelets. In this study, we describe the characterization, purification and identification of the MAX.3 antigen. Immunoprecipitation and SDS/PAGE revealed different molecular masses of MAX.3 antigen in MAC (60-90 kDa) and platelets (58-64 kDa), whereas a similar size (45 kDa) was observed in both cell types after digestion with N-glycosidase F. Lectin affinity and sequential treatment with different glycosidases suggests complex type glycosylation of MA

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21

El Ghina, Miftah Fathi, Widawati Widawati, and Rizki Rahmawati Lestari. "Asupan Energi, Protein, Status Gizi, dan VO2 Max Atlet Futsal MAN 1 Pekanbaru." Jurnal Ilmu Gizi dan Dietetik 2, no. 3 (2023): 175–81. http://dx.doi.org/10.25182/jigd.2023.2.3.175-181.

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Tujuan penelitian adalah menganalisis hubungan asupan gizi dan VO2 max atlet futsal MAN 1 Pekanbaru. Jenis penelitian ini adalah kuantitatif pendekatan analitik dengan desain penelitian cross sectional. Penelitian ini dilakukan di MAN 1 Pekanbaru pada 8-12 Maret 2023 dengan jumlah subjek 40 atlet diperoleh dengan teknik total sampling. Data asupan gizi diperoleh melalui wawancara food recall 2x24 jam, data status gizi diperoleh melalui pengukuran tinggi dan berat badan, data VO2 max diperoleh menggunakan metode Multystage Fitness Test (MFT). Analisa yang digunakan adalah univariat dan bivariat

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22

Loužek, Marek. "Max Weber - an economist." Politická ekonomie 55, no. 1 (2007): 91–105. http://dx.doi.org/10.18267/j.polek.592.

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23

Sarikakis, Katharine, and Francisco Seoane Pérez. "Media theory for Mad Max times." International Journal of Media & Cultural Politics 10, no. 2 (2014): 125–28. http://dx.doi.org/10.1386/macp.10.2.125_2.

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24

Gordya, Andressa. "Mad Max e a feminilidade ativa." Ciência e Cultura 69, no. 1 (2017): 60–62. http://dx.doi.org/10.21800/2317-66602017000100020.

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25

Cohen, Charles Lloyd. "Mad Max (Weber) in New England." Reviews in American History 25, no. 1 (1997): 19–24. http://dx.doi.org/10.1353/rah.1997.0008.

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26

Hassler-Forest, Dan. "Mad Max: between apocalypse and utopia." Science Fiction Film & Television 10, no. 3 (2017): 301–6. http://dx.doi.org/10.3828/sfftv.2017.21.

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27

Sanders, Jennifer A., and Philip A. Gruppuso. "Coordinated regulation of c-Myc and Max in rat liver development." American Journal of Physiology-Gastrointestinal and Liver Physiology 290, no. 1 (2006): G145—G155. http://dx.doi.org/10.1152/ajpgi.00545.2004.

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The processes of liver development and regeneration involve regulation of a key network of transcription factors, the c -myc/ max/ mad network. This network regulates the expression of genes involved in hepatocyte proliferation, growth, metabolism, and differentiation. In previous studies on the expression and localization of c-Myc in the fetal and adult liver, we made the unexpected observation that c-Myc content was similar in the two. However, c-Myc was localized predominantly to the nucleolus in the adult liver. On the basis of this finding, we went on to characterize the expression patter

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28

Herman, Herman, and Muhammad Akbar Syafruddin. "Perbandingan Pengaruh Latihan Fartlek Dengan Latihan Sirkuit Training Terhadap Kapasitas Kerja Maksimal VO2 Max Pada Siswa MAN 1 Makassar." Jendela Olahraga 6, no. 1 (2021): 139–49. http://dx.doi.org/10.26877/jo.v6i1.6933.

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This research is a descriptive study to determine (1) the effect of fartlek training on maximal working capacity of VO2 Max in MAN 1 Makassar (2) to determine the circuit training exercise on maximal working capacity of VO2 Max in MAN 1 Makassar (3) to determine differences in the effect of fartlek training with circuit training exercise on maximal working capacity of VO2 Max in MAN 2 Makassar. Population in this study were all students of MAN 1 Makassar while the sample in this study 40 students of class XI were taken by random sampling. The results of this study were (1) the data maximal wor

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29

Cultraro, C. M., T. Bino, and S. Segal. "Function of the c-Myc antagonist Mad1 during a molecular switch from proliferation to differentiation." Molecular and Cellular Biology 17, no. 5 (1997): 2353–59. http://dx.doi.org/10.1128/mcb.17.5.2353.

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Mad-Max heterodimers have been shown to antagonize Myc transforming activity by a mechanism requiring multiple protein-protein and protein-DNA interactions. However, the mechanism by which Mad functions in differentiation is unknown. Here, we present evidence that Mad functions by an active repression mechanism to antagonize the growth-promoting function(s) of Myc and bring about a transition from cellular proliferation to differentiation. We demonstrate that exogenously expressed c-Myc blocks inducer-mediated differentiation of murine erythroleukemia cells without disrupting the induction of

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30

Ichinokawa, Yasutaka. "Max Weber in Japan." Annual review of sociology 2015, no. 28 (2015): 28–34. http://dx.doi.org/10.5690/kantoh.2015.28.

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31

Zhang, Qiqiang, Yanchun Zhou, Xingyuan San, et al. "Zr2SeB and Hf2SeB: Two new MAB phase compounds with the Cr2AlC-type MAX phase (211 phase) crystal structures." Journal of Advanced Ceramics 11, no. 11 (2022): 1764–76. http://dx.doi.org/10.1007/s40145-022-0646-7.

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AbstractThe ternary or quaternary layered compounds called MAB phases are frequently mentioned recently together with the well-known MAX phases. However, MAB phases are generally referred to layered transition metal borides, while MAX phases are layered transition metal carbides and nitrides with different types of crystal structure although they share the common nano-laminated structure characteristics. In order to prove that MAB phases can share the same type of crystal structure with MAX phases and extend the composition window of MAX phases from carbides and nitrides to borides, two new MA

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32

Ockert, Jason. "Max." Iowa Review 41, no. 1 (2011): 140–56. http://dx.doi.org/10.17077/0021-065x.7003.

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33

Capdvila, Max. "Max." Periferica, no. 20 (2019): 8–9. http://dx.doi.org/10.25267/periferica.2019.i20.02.

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34

Hunter, Wendy L. M., Victor C. Strasburger, David M. Snyder, and Martin T. Stein. "Max." Journal of Developmental & Behavioral Pediatrics 27, no. 6 (2006): 488–92. http://dx.doi.org/10.1097/00004703-200612000-00007.

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35

Kuokka, Daniel R. "MAX." ACM SIGART Bulletin 2, no. 4 (1991): 93–97. http://dx.doi.org/10.1145/122344.122363.

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36

Yap, Kok-KIONG, Vikram Srinivasan, and Mehul Motani. "MAX." ACM Transactions on Sensor Networks 4, no. 4 (2008): 1–34. http://dx.doi.org/10.1145/1387663.1387672.

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37

Litwin, Mark S. "Max." JAMA: The Journal of the American Medical Association 257, no. 16 (1987): 2210. http://dx.doi.org/10.1001/jama.1987.03390160096036.

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38

King, Roy D., and Sandra L. Resodihardjo. "To max or not to max." Punishment & Society 12, no. 1 (2009): 65–84. http://dx.doi.org/10.1177/1462474509349010.

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39

Farhangi, Hadi, Dincer Konur, and Cihan H. Dagli. "Combining Max-min and Max-max Approaches for Robust SoS Architecting." Procedia Computer Science 95 (2016): 103–10. http://dx.doi.org/10.1016/j.procs.2016.09.299.

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40

Hopewell, R., and E. B. Ziff. "The nerve growth factor-responsive PC12 cell line does not express the Myc dimerization partner Max." Molecular and Cellular Biology 15, no. 7 (1995): 3470–78. http://dx.doi.org/10.1128/mcb.15.7.3470.

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Heterodimerization of Max with the nuclear oncoprotein Myc and the differentiation-associated proteins Mad and Mxi1 enables these factors to bind E-box sites in DNA and control genes implicated in cell proliferation and differentiation. We show that in the PC12 pheochromocytoma tumor cell line, functional Max protein is not expressed because of the synthesis of a mutant max transcript. This transcript encodes a protein incapable of homo- or heterodimerization. Furthermore, the mutant Max protein, unlike wild-type Max, is incapable of repressing transcription from an E-box element. Synthesis of

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41

Zada, A. Peer, J. Pulikkan, D. Bararia, et al. "Proteomic Discovery of Max as a Novel Interacting Partner of C/EBPa: A Myc/Max/Mad Link." Blood 108, no. 11 (2006): 1175. http://dx.doi.org/10.1182/blood.v108.11.1175.1175.

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Abstract In the present study, we sought to identify novel C/EBPa interacting proteins in vivo through immunoprecipitation using mass spectrometry-based proteomic techniques. We identified Max, a heterodimeric partner of Myc, as one of the interacting proteins of C/EBPa in our screen. We confirmed the in vivo interaction of C/EBPa with Max and showed that this interaction involves the basic region of C/EBPa. Endogenous C/EBPa and Max, but not Myc and Max co-localize in intranuclear structures during granulocytic differentiation of myeloid U937 cells. Max enhanced the transactivation capacity o

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42

Peters, M. A., K. G. Sollenberger, T. L. Kao, and E. J. Taparowsky. "A minimal regulatory region maintains constitutive expression of the max gene." Molecular and Cellular Biology 17, no. 3 (1997): 1037–48. http://dx.doi.org/10.1128/mcb.17.3.1037.

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Max is a basic helix-loop-helix/leucine zipper protein that forms heterodimers with the Myc family of proteins to promote cell growth and with the Mad/Mxi1 family of proteins to inhibit cell growth. The role of Max as the obligate binding partner for these two protein families necessitates the observed constitutive expression and relatively long half-life of the max mRNA under a variety of growth conditions. In this study, we have used the chicken max gene to map DNA elements maintaining max gene expression in vertebrate cells. We have identified a minimal regulatory region (MRR) that resides

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43

Horne, G. "Max Yergan: Race Man, Internationalist, Cold Warrior." Journal of American History 93, no. 3 (2006): 925–26. http://dx.doi.org/10.2307/4486530.

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44

Tranter, Kieran. "Mad Max: The Car and Australian Governance." National Identities 5, no. 1 (2003): 67–81. http://dx.doi.org/10.1080/14608940307120.

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45

Stebbing, Nicolas. "Max Yergan: Race Man, Internationalist, Cold Warrior." Journal of Religion in Africa 38, no. 1 (2008): 81–82. http://dx.doi.org/10.1163/157006608x262764.

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46

Graef, Nils, Joachim Hammerschmidt, and Carl-Erik Sundberg. "A low-complexity max-log-MAP detector." IEEE Transactions on Communications 57, no. 8 (2009): 2251–54. http://dx.doi.org/10.1109/tcomm.2009.08.070126.

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47

Vogt, J., and A. Finger. "Improving the max-log-MAP turbo decoder." Electronics Letters 36, no. 23 (2000): 1937. http://dx.doi.org/10.1049/el:20001357.

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48

Andreesen, R., KJ Bross, J. Osterholz, and F. Emmrich. "Human macrophage maturation and heterogeneity: analysis with a newly generated set of monoclonal antibodies to differentiation antigens." Blood 67, no. 5 (1986): 1257–64. http://dx.doi.org/10.1182/blood.v67.5.1257.1257.

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Abstract We have analyzed the expression of late differentiation antigens during terminal in vitro maturation of human macrophages (M phi) from blood monocytes (MO) in comparison to their distribution among mature M phi residing in various tissue sites. By immunizing mice with M phi derived from blood MO by culture on hydrophobic Teflon foils, monoclonal antibodies (mAbs) were developed (MAX.1, MAX.2, MAX.3, MAX.11) that reacted with lineage-restricted differentiation antigens. These antigens were expressed exclusively on M phi or were markedly increased after in vitro differentiation. The onl

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49

Andreesen, R., KJ Bross, J. Osterholz, and F. Emmrich. "Human macrophage maturation and heterogeneity: analysis with a newly generated set of monoclonal antibodies to differentiation antigens." Blood 67, no. 5 (1986): 1257–64. http://dx.doi.org/10.1182/blood.v67.5.1257.bloodjournal6751257.

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We have analyzed the expression of late differentiation antigens during terminal in vitro maturation of human macrophages (M phi) from blood monocytes (MO) in comparison to their distribution among mature M phi residing in various tissue sites. By immunizing mice with M phi derived from blood MO by culture on hydrophobic Teflon foils, monoclonal antibodies (mAbs) were developed (MAX.1, MAX.2, MAX.3, MAX.11) that reacted with lineage-restricted differentiation antigens. These antigens were expressed exclusively on M phi or were markedly increased after in vitro differentiation. The only overlap

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50

Reglińska-Jemioł, Anna. "Victim-Warriors and Restorers—Heroines in the Post-Apocalyptic World of Mad Max: Fury Road." Text Matters: A Journal of Literature, Theory and Culture, no. 11 (November 22, 2021): 106–18. http://dx.doi.org/10.18778/2083-2931.11.08.

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The article discusses the evolving image of female characters in the Mad Max saga directed by George Miller, focusing on Furiosa’s rebellion in the last film—Mad Max: Fury Road. Interestingly, studying Miller’s post-apocalyptic action films, we can observe the evolution of this post-apocalyptic vision from the male-dominated world with civilization collapsing into chaotic violence visualized in the previous series to a more hopeful future created by women in the last part of the saga: Mad Max: Fury Road (2015). We observe female heroes: the vengeful Furiosa, the protector of oppressed girls an

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