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Journal articles on the topic '3 Expression'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

PEYTON JONES, SIMON. "3 Expressions." Journal of Functional Programming 13, no. 1 (2003): 17–38. http://dx.doi.org/10.1017/s0956796803000510.

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3.1 Errors 193.2 Variables, Constructors, Operators, and Literals 203.3 Curried Applications and Lambda Abstractions 213.4 Operator Applications 213.5 Sections 223.6 Conditionals 233.7 Lists 233.8 Tuples 243.9 Unit Expressions and Parenthesized Expessions 253.10 Arithmetic Sequences 253.11 List Comprehensions 253.12 Let Expressions 273.13 Case Expressions 273.14 Do Expressions 293.15 Datatypes with Field Labels 293.16 Expression Type Signatures 323.17 Pattern Matching 32

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2

Vargas, Thiago, Lidia Pulz, and Ricardo Strefezzi. "Immunohistochemical expression of Galectin-3 in canine tumors." Brazilian Journal of Veterinary Pathology 11, no. 1 (2018): 01–06. http://dx.doi.org/10.24070/bjvp.1983-0246.v11i1p01-06.

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Vargas, Thiago, Lidia Pulz, and Ricardo Strefezzi. "Immunohistochemical expression of Galectin-3 in canine tumors." Brazilian Journal of Veterinary Pathology 11, no. 1 (2018): 1–6. http://dx.doi.org/10.24070/bjvp.1983-0246.v11i1p1-6.

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4

Gao, Xiang. "PRL-3 Expression in Cancer." Biomedicine & Pharmacotherapy 62, no. 7 (2008): 423. http://dx.doi.org/10.1016/j.biopha.2008.06.010.

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Greenfield, Peter. "Bagof/3 to ZF expression." ACM SIGPLAN Notices 25, no. 7 (1990): 59–62. http://dx.doi.org/10.1145/382076.382645.

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6

Huang, Yuan-Li, Yueh-Chien Lin, Chu-Cheng Lin, Wei-Min Chen, Benjamin P. C. Chen, and Hsinyu Lee. "High Glucose Induces VEGF-C Expression via the LPA1/3-Akt-ROS-LEDGF Signaling Axis in Human Prostate Cancer PC-3 Cells." Cellular Physiology and Biochemistry 50, no. 2 (2018): 597–611. http://dx.doi.org/10.1159/000494177.

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Background/Aims: Hyperglycemia has been shown to increase the incidence and metastasis in various types of cancers. However, the correlation between hyperglycemia and lymphatic metastasis in prostate cancer (PCa) remains unclear. Our previous study demonstrated that lysophosphatidic acid (LPA) enhances vascular endothelial growth factor-C (VEGF-C) expression, a lymphangiogenic factor, through activating it receptors LPA1/3 in prostate cancer (PCa) cells. Moreover, hyperglycemia up-regulates autotaxin (ATX) expression, a LPA-generating enzyme. Therefore, we propose that high glucose promotes VE

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7

Thewes, M., G. Pohlmann, M. Atkinson, J. Mueller, B. Pütz, and H. Höfler. "Stromelysin-3 (ST-3) mRNA Expression in Colorectal Carcinomas." Diagnostic Molecular Pathology 5, no. 4 (1996): 284–90. http://dx.doi.org/10.1097/00019606-199612000-00010.

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8

Jones, David H. A., Harry Martin, Joel Madrazo, et al. "Expression and Structural Analysis of 14-3-3 Proteins." Journal of Molecular Biology 245, no. 4 (1995): 375–84. http://dx.doi.org/10.1006/jmbi.1994.0031.

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9

Shen, Yi, Valerie Barbier, Ingrid G. Winkler, Jean Hendy, and Jean-Pierre Levesque. "The Role of Tissue Inhibitor of Metalloproteinase-3 (TIMP-3) in Hematopoiesis." Blood 112, no. 11 (2008): 1362. http://dx.doi.org/10.1182/blood.v112.11.1362.1362.

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Abstract Matrix metalloproteinase (MMP) activity is regulated by tissue inhibitor of metalloproteinases (TIMPs). We found that while TIMP-1 and -2 expressions were unaffected, and TIMP-4 was not expressed, TIMP-3 mRNA expression decreased 10-fold within the bone marrow (BM) during G-CSF induced mobilization. In addition, through reverse zymography, the level of biologically active TIMP-3 protein was also shown to decrease during mobilization. Down-regulation of TIMP-3 may contribute to the accumulation of active MMPs within the BM, allowing for the release of hematopoieticstem/progenitor cells

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10

Keshav, Aris, and Lal Zimman. "“That 3-word-ultimatum”." Journal of Language and Sexuality 14, no. 1 (2025): 1–30. https://doi.org/10.1075/jls.22008.kes.

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Abstract I love you is among the most meaningful utterances in English speakers’ organization of intimacy, yet remains understudied by scholars of language. This article investigates metapragmatic discourse about the first exchange of I love you between romantic partners using data from the social media platform Reddit. The discourse reveals a normative model in which I love you functions not only as an expression of emotion but a speech act that is ideologically constructed as committing the speaker and inviting the listener onto a relationship path that includes monogamy, long-term commitmen

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Zaky, EmanA, AlaaH Maraeea, and HalaS El-Rebey. "Caspase-3 expression in lichen planus." Menoufia Medical Journal 29, no. 2 (2016): 396. http://dx.doi.org/10.4103/1110-2098.192428.

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12

Burugu, Samantha, Dongxia Gao, Samuel Leung, Stephen K. Chia, and Torsten O. Nielsen. "TIM-3 expression in breast cancer." OncoImmunology 7, no. 11 (2018): e1502128. http://dx.doi.org/10.1080/2162402x.2018.1502128.

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13

Holmes, David. "SOCS-3 expression detrimental in AKI." Nature Reviews Nephrology 10, no. 3 (2014): 124. http://dx.doi.org/10.1038/nrneph.2014.11.

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14

Banet, Natalie, Allen M. Gown, Ie-Ming Shih, et al. "GATA-3 Expression in Trophoblastic Tissues." American Journal of Surgical Pathology 39, no. 1 (2015): 101–8. http://dx.doi.org/10.1097/pas.0000000000000315.

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15

Siderova, Mira, Kiril Hristozov, Ivan Krasnaliev, Radoslav Radev, and Rumen Nenkov. "Galectin-3 expression in thyroid tumors." Scripta Scientifica Medica 48, no. 3 (2016): 58. http://dx.doi.org/10.14748/ssm.v48i3.1739.

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16

Sabatier, Laetitia, Nicolai Miosge, Dirk Hubmacher, Guoqing Lin, Elaine C. Davis, and Dieter P. Reinhardt. "Fibrillin-3 expression in human development." Matrix Biology 30, no. 1 (2011): 43–52. http://dx.doi.org/10.1016/j.matbio.2010.10.003.

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17

Stahl, U., J. Wenk, F. Wagener, et al. "Phosphoinositid-3-Kinase- (PI3-K) Expression." Der Pathologe 25, no. 1 (2004): 31–37. http://dx.doi.org/10.1007/s00292-003-0673-2.

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18

SKACEL, PATRICIA O., та WINIFRED M. WATKINS. "α-3-Fucosyltransferase expression in leukaemia". Biochemical Society Transactions 16, № 6 (1988): 1034–35. http://dx.doi.org/10.1042/bst0161034.

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19

SIMON, ZOLTÁN BOLDIZSÁR. "3. THE EXPRESSION OF HISTORICAL EXPERIENCE." History and Theory 54, no. 2 (2015): 178–94. http://dx.doi.org/10.1111/hith.10752.

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20

Danilova, N. V., K. A. Anikina, N. A. Oleynikova, D. V. Vychuzhanin, and P. G. Malkov. "Claudin-3 expression in gastric cancer." Arkhiv patologii 82, no. 2 (2020): 5. http://dx.doi.org/10.17116/patol2020820215.

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21

Yu, Limin, Haodong Xu, Matthew J. Wasco, Patricia A. Bourne, and Linglei Ma. "IMP-3 expression in melanocytic lesions." Journal of Cutaneous Pathology 37, no. 3 (2010): 316–22. http://dx.doi.org/10.1111/j.1600-0560.2009.01428.x.

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22

Korepanov, Igor. "Multiplicative Expression for the Coefficient in Fermionic 3–3 Relation." Mathematics 4, no. 1 (2016): 3. http://dx.doi.org/10.3390/math4010003.

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23

Spooner, Heather, Maartje F. Westhoff, Husna Ibrahimkhail, Aleena Yarovaya, Eamonn J. Dickson, and Rose E. Dixon. "14-3-3 regulates cardiac CaV1.2 clustering, expression, and trafficking." Biophysical Journal 122, no. 3 (2023): 378a. http://dx.doi.org/10.1016/j.bpj.2022.11.2077.

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24

Bajpai, U., R. Sharma, T. Kausar, S. Dattagupta, T. K. Chattopadhayay, and R. Ralhan. "Clinical Significance of 14-3-3 Zeta in Human Esophageal Cancer." International Journal of Biological Markers 23, no. 4 (2008): 231–37. http://dx.doi.org/10.1177/172460080802300406.

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We recently found 14-3-3 zeta to be overexpressed in esophageal squamous cell carcinomas (ESCCs) by differential display. In the present study we determined the clinical significance of 14-3-3 zeta in esophageal tumorigenesis. Immunohistochemical analysis was carried out in 61 ESCCs, 33 dysplasia samples, 14 hyperplasia samples and 7 matched histologically normal esophageal tissues and correlated with clinicopathological parameters. Cytoplasmic expression of 14-3-3 zeta protein was observed in 95% of ESCCs; 63% of tumors also showed nuclear localization. All hyperplastic and dysplastic tissues

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25

Orimo, Hideo. "3. Gene Delivery and Expression Series Gene Delivery and Expression (1)." Nihon Ika Daigaku Igakkai Zasshi 7, no. 2 (2011): 92–96. http://dx.doi.org/10.1272/manms.7.92.

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26

Wang, Moyu, Hongmei Li, Xiyu Sun та ін. "J Subgroup Avian Leukosis Virus Strain Promotes Cell Proliferation by Negatively Regulating 14-3-3σ Expressions in Chicken Fibroblast Cells". Viruses 15, № 2 (2023): 404. http://dx.doi.org/10.3390/v15020404.

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This study focuses on clarifying the regulation of chicken 14-3-3σ protein on the fibrous histiocyte proliferation caused by ALV-J-SD1005 strain infection. DF-1 cells were inoculated with 102 TCID50 of ALV-J-SD1005 strain; the cell proliferation viability was dramatically increased and 14-3-3σ expressions were dramatically decreased within 48 hours after inoculation. Chicken 14-3-3σ over-expression could significantly decrease the cell proliferation and the ratio of S-phase cells, but increase the ratio of G2/M-phase cells in ALV-J-infected DF-1 cells; by contrast, chicken 14-3-3σ knockdown ex

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27

Hustinx, Steven R., Noriyoshi Fukushima, Marianna L. Zahurak, et al. "Expression and prognostic significance of 14-3-3 sigma and ERM family protein expression in periampullary neoplasms." Cancer Biology & Therapy 4, no. 5 (2005): 596–601. http://dx.doi.org/10.4161/cbt.4.5.1748.

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28

MARTINEZ-GONZALEZ, Jose, Carlos BUESA, Maria-Dolos PIULACHS, Xavier BELLES, and Fausto G. HEGARDT. "3-Hydroxy-3-methylglutaryl-coenzyme-A synthase from Blattella germanica. Cloning, expression, developmental pattern and tissue expression." European Journal of Biochemistry 217, no. 2 (1993): 691–99. http://dx.doi.org/10.1111/j.1432-1033.1993.tb18295.x.

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29

Wei, Wei, Liefeng Ji, Wanli Duan, and Jiang Zhu. "Klotho protects chondrocyte viability via FOXO1/3 in osteoarthritis." Tropical Journal of Pharmaceutical Research 20, no. 9 (2021): 1961–68. http://dx.doi.org/10.4314/tjpr.v20i9.24.

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Purpose: To investigate the effect of Klotho and FOXO1/3 on the CH viability in OA.Methods: The survival rate of CHs, Klotho and FOXO1/3 protein expression, and ROS production were measured in the OA cartilages of different degenerative phases. H2O2 was also used to injure CHs, and the cell viability, Klotho and FOXO1/3 expressions, as well as ROS levels were investigated to clarify the effect of exogenic Klotho on the injured CHs. Additionally, in order to verify the role of FOXO1/3 in Klotho-treated CHs, SOD2, GPX1, inflammatory factors, collagen I/II, SOX9, and Runx-2 levels were analyzed b

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30

Wen, Min, Zi-Zheng Zou, Tiao Luo, et al. "ZLM-7 Blocks Breast Cancer Progression by Inhibiting MDM2 via Upregulation of 14-3-3 Sigma." Pharmaceuticals 15, no. 7 (2022): 874. http://dx.doi.org/10.3390/ph15070874.

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Breast cancer is one of the most prevalent malignancies with poor prognosis. Inhibition of angiogenesis is becoming a valid and evident therapeutic strategy to treat cancer. Recent studies uncovered the antiangiogenic activity of ZLM-7 (a combretastain A-4 derivative), but the regulatory mechanism is unclear. ZLM-7 treatment was applied in estrogen receptor-positive cell MCF-7, triple-negative breast cancer cell MDA-MB-231 and xenograft models. Transfections were conducted to overexpress or knockdown targeted genes. The gene and protein expressions were measured by qPCR and Western blotting as

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31

Shi, Xiao, Cui-Wei Li, Li-Cheng Tan, et al. "Immune Co-inhibitory Receptors PD-1, CTLA-4, TIM-3, LAG-3, and TIGIT in Medullary Thyroid Cancers: A Large Cohort Study." Journal of Clinical Endocrinology & Metabolism 106, no. 1 (2020): 120–32. http://dx.doi.org/10.1210/clinem/dgaa701.

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Abstract Context Programmed cell death protein-1 (PD-1), cytotoxic T-lymphocyte antigen 4 (CTLA-4), T-cell immunoglobulin and mucin-domain containing-3 (TIM-3), lymphocyte activation gene-3 (LAG-3), and T-cell immunoglobulin and ITIM domain (TIGIT) are considered major immune co-inhibitory receptors (CIRs) and the most promising immunotherapeutic targets in cancer treatment, but they are largely unexplored in medullary thyroid carcinoma (MTC). Objective We aimed to provide the first evidence regarding the expression profiles and clinical significance of CIRs in a large cohort of MTC patients.

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32

Zhu, Wei, Wenxue Li, Guangyu Yang, Quanxin Zhang, Ming Li, and Xingfen Yang. "Indole-3-Carbinol Inhibits Nasopharyngeal Carcinoma." International Journal of Toxicology 29, no. 2 (2010): 185–92. http://dx.doi.org/10.1177/1091581809356481.

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This study explored the effects of indole-3-carbinol on the proliferation of human nasopharyngeal carcinoma, both in vitro and in vivo, and the underlying mechanisms in inducing apoptosis of CNE1 cells. Proliferation, apoptosis, malondialdehyde, superoxide dismutase, glutathione peroxidase, expressions of caspase-9, and caspase-3 in human nasopharyngeal carcinoma cells CNE1 were examined. Indole-3-carbinol suppressed proliferation, induced apoptosis, decreased malondialdehyde level, increased the activity of superoxide dismutase and glutathione peroxidase, and up-regulated the expression of ac

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33

Amlal, Hassane, Charles E. Burnham, and Manoocher Soleimani. "Characterization of Na+/ HCO 3 − cotransporter isoform NBC-3." American Journal of Physiology-Renal Physiology 276, no. 6 (1999): F903—F913. http://dx.doi.org/10.1152/ajprenal.1999.276.6.f903.

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Na+-[Formula: see text]cotransporters mediate the transport of[Formula: see text] into or out of the cell. Two Na+-[Formula: see text]cotransporters (NBC) have been identified previously, which are referred to as NBC-1 and NBC-2. A cDNA library from uninduced human NT-2 cells was screened with an NBC-2 cDNA probe. Several clones were identified and isolated. Sequence analysis of these clones identified a partial coding region (2 kb) of a novel NBC (called here NBC-3), which showed 53% and 72% identity with NBC-1 and NBC-2, respectively. Northern blot analysis revealed that NBC-3 encodes a 4.4-

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34

Leal, Mariana Ferreira. "Clinical implication of 14-3-3 epsilon expression in gastric cancer." World Journal of Gastroenterology 18, no. 13 (2012): 1531. http://dx.doi.org/10.3748/wjg.v18.i13.1531.

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35

Thorrez, Lieven, Leon-Charles Tranchevent, Hui Ju Chang, Yves Moreau, and Frans Schuit. "Detection of novel 3' untranslated region extensions with 3' expression microarrays." BMC Genomics 11, no. 1 (2010): 205. http://dx.doi.org/10.1186/1471-2164-11-205.

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36

Fernández-Orth, Juncal, Petra Ehling, Tobias Ruck, et al. "14-3-3 Proteins regulate K2P5.1 surface expression on T lymphocytes." Traffic 18, no. 1 (2016): 29–43. http://dx.doi.org/10.1111/tra.12455.

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37

MacKay, Rachel K., Natalie J. Colson, Peter R. Dodd, and Joanne M. Lewohl. "Differential Expression of 14-3-3 Isoforms in Human Alcoholic Brain." Alcoholism: Clinical and Experimental Research 35, no. 6 (2011): 1041–49. http://dx.doi.org/10.1111/j.1530-0277.2011.01436.x.

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38

Namikawa, Kazuhiko, Qingning Su, Sumiko Kiryu-Seo, and Hiroshi Kiyama. "Enhanced expression of 14-3-3 family members in injured motoneurons." Molecular Brain Research 55, no. 2 (1998): 315–20. http://dx.doi.org/10.1016/s0169-328x(98)00012-6.

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39

LUSKEY, KENNETH L. "Structure and Expression of 3-Hydroxy-3-methylglutaryl Coenzyme A Reductase." Annals of the New York Academy of Sciences 478, no. 1 Metabolic Reg (1986): 249–54. http://dx.doi.org/10.1111/j.1749-6632.1986.tb15535.x.

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40

Yang, Xiaoliang, Weidong Cao, Hong Lin, et al. "Isoform-specific expression of 14-3-3 proteins in human astrocytoma." Journal of the Neurological Sciences 276, no. 1-2 (2009): 54–59. http://dx.doi.org/10.1016/j.jns.2008.08.040.

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41

Liu, Yang, Rui-feng Tian, Yun-ming Li, et al. "The expression of seven 14-3-3 isoforms in human meningioma." Brain Research 1336 (June 2010): 98–102. http://dx.doi.org/10.1016/j.brainres.2010.04.009.

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KÖDITZ, BARBARA, ANDREAS STOG, HEIKE GÖBEL, et al. "Vimentin 3 Expression in Prostate Cancer Cells." Anticancer Research 41, no. 1 (2021): 169–74. http://dx.doi.org/10.21873/anticanres.14762.

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43

Lefebvre, O., C. Regnier, M. P. Chenard, et al. "Developmental expression of mouse stromelysin-3 mRNA." Development 121, no. 4 (1995): 947–55. http://dx.doi.org/10.1242/dev.121.4.947.

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We have used northern blot analysis and in situ hybridization to study the spatial distribution of stromelysin-3 (ST3) expression during mouse embryogenesis. ST3 mRNA was observed in trophoblastic cells at the site of embryonic implantation (7.5-8.5 days) and in a variety of developing embryonic tissues. In these tissues, the highest ST3 expression levels were observed during the development of the external features of limb, tail and snout, and during bone and spinal cord morphogenesis. In limb, tail and snout, ST3 expression was specifically detected in mesenchymal cells lining the basement m

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44

Umezaki, Taizo, Takashi Hirano, and Yukio Sato. "Automatic Synthesis of 3-D Facial Expression." IEEJ Transactions on Electronics, Information and Systems 121, no. 2 (2001): 417–22. http://dx.doi.org/10.1541/ieejeiss1987.121.2_417.

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KÖDITZ, BARBARA, ANDREAS STOG, HEIKE GÖBEL, et al. "Vimentin 3 Expression in Prostate Cancer Cells." Anticancer Research 41, no. 1 (2021): 169–74. http://dx.doi.org/10.21873/anticanres.14762.

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Lee, Hee Jae, Chong Woo Chu, Moo Jun Baek, et al. "PRL-3 Expression in Primary Colorectal Cancer." Journal of the Korean Society of Coloproctology 23, no. 6 (2007): 497. http://dx.doi.org/10.3393/jksc.2007.23.6.497.

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47

Stewart, Colin J. R., and Maxine L. Crook. "Galectin-3 Expression in Uterine Endometrioid Adenocarcinoma." International Journal of Gynecological Pathology 29, no. 6 (2010): 555–61. http://dx.doi.org/10.1097/pgp.0b013e3181e4ee4ea.

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48

GIMM, O., U. KRAUSE, M. BRAUCKHOFF, C. HOANG-VU, and H. DRALLE. "Distinct Expression of Galectin-3 in Pheochromocytomas." Annals of the New York Academy of Sciences 1073, no. 1 (2006): 571–77. http://dx.doi.org/10.1196/annals.1353.028.

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Charbonneau, Alexander A., Elizabeth J. Reicks, John F. Cambria, et al. "CUREs for high-level Galectin-3 expression." Protein Expression and Purification 221 (September 2024): 106516. http://dx.doi.org/10.1016/j.pep.2024.106516.

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Pulaski, Lukasz, Izabela Jatczak-Pawlik, Marta Sobalska-Kwapis, Dominik Strapagiel, Grzegorz Bartosz, and Izabela Sadowska-Bartosz. "3-Bromopyruvate induces expression of antioxidant genes." Free Radical Research 53, no. 2 (2019): 170–78. http://dx.doi.org/10.1080/10715762.2018.1541176.

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