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1

Bryant, Julie E. "Retracted article: In-cell protein dynamics." Molecular BioSystems 2, no. 9 (2006): 406. http://dx.doi.org/10.1039/b604684c.

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2

Spinu, Marina, Pall Emoke, Niculae Mihaela, et al. "Original article Interdependence of productive effort and in vitro vegetal extract treatment on specific cell-mediated immunity in horses." Annals of Phytomedicine: An International Journal 7, no. 2 (2018): 55–60. http://dx.doi.org/10.21276/ap.2018.7.2.7.

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3

Ionut, Mates C., Spinu Marina, Pall Emoke, et al. "Original article Target cell type dependent immune activity of plant extracts in bovine raised under different technologies." Annals of Phytomedicine: An International Journal 7, no. 2 (2018): 81–84. http://dx.doi.org/10.21276/ap.2018.7.2.12.

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4

Ionut, Mates C., Spinu Marina, Pall Emoke, et al. "Original article Target cell type dependent immune activity of plant extracts in bovine raised under different technologies." Annals of Phytomedicine: An International Journal 7, no. 2 (2018): 85–87. http://dx.doi.org/10.21276/ap.2018.7.2.13.

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5

Constantin, Vasiu, Niculae Mihaela, Popescu Silvana, et al. "Original article In vitro changes in adaptive cell-mediated immunity under medicinal plant extract treatment in resting horses from different workout backgrounds." Annals of Phytomedicine: An International Journal 7, no. 2 (2018): 61–63. http://dx.doi.org/10.21276/ap.2018.7.2.8.

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6

Awitor, Komla Oscar, Laurent Bernard, Olivier Bonnin, Bernard Coupat, Jean Paul Fournier, and Philippe Verdier. "Article." Canadian Journal of Chemistry 77, no. 2 (1999): 243–48. http://dx.doi.org/10.1139/v98-237.

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Mercurous chloride (Hg2Cl2), or calomel, was prepared by direct synthesis from commercial mercury and mercuric chloride. The mercuric chloride mass fraction in the synthesized material is particularly small. The mercurous chloride vapor pressure was measured between 353 and 453 K by the Knudsen cell method. In order to obtain the mercurous chloride vapor pressure, we took into account the dissociation in the vapor phase into mercury and mercuric chloride. Our results are compared with those in the literature.Key words: mercurous chloride, calomel, vapor pressure, mass spectrometry, Knudsen cell.
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7

Myland, Jan C., Keith B. Oldham, Jörg Schiewe, and Alicia L. Taylor. "Article." Canadian Journal of Chemistry 76, no. 11 (1998): 1688–94. http://dx.doi.org/10.1139/v98-129.

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Three methods are discussed by which the internal geometry of a porous insulator may be investigated electrochemically. By adopting a simple model, the pore geometry is characterized by two parameters: the tortuosity and the porosity. In each method, a cylindrical sample of the porous medium is soaked with an aqueous electrolyte solution and its lower face is brought into contact with a mercury pool electrode. The other electrode is also a mercury pool, but in the first technique it is remote, whereas in the second and third methods it floods the upper surface of the cylindrical sample. The first technique employs a d.c. potential step, whereby the concentration of a probe ion is depleted at the lower electrode. The attempt of diffusion to replenish this surface concentration leads to a faradaic current whose time dependence is analyzed to provide estimates of the tortuosity and porosity parameters. The second method measures the frequency-dependent cell impedance. The pore structure parameters are estimated from the equivalent circuit of the cell. No faradaic process is involved in the third method, which measures the frequency-dependent conductance of the cell as a means of characterizing the pore structure. These methods are applied successfully to sandstone and fritted glass samples.Key words: porous media, Fourier-transform methods, impedance.
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8

Galstyan, T. V., and V. Drnoyan. "Article." Canadian Journal of Physics 76, no. 2 (1998): 163–67. http://dx.doi.org/10.1139/p98-007.

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Light-induced molecular orientation switching and large intrinsichysteresis in a homeotropic cell of nematic liquid crystals areobtained. Both the switching threshold and the hysteresis width areeffectively controlled by the elliptical symmetry of a noncoherentoptical field. We confirmed the predicted doubling of the switchingthreshold in the case of the light with circular symmetry and vanishingangular momentum.PACS No. 78.47
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9

Pramanik, Soma, Pinkey Rawal, and Ramesh C. "Evaluation of Methanol Extract of Tephrosia villosa For in vitro Anticancer and Antioxidant Potentials Against Cancer Cell Lines (Research Article)." International Journal of Pharmacy and Biological Sciences 11, no. 1 (2021): 194–203. http://dx.doi.org/10.21276/ijpbs.2021.11.1.26.

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10

Al Farii, Humaid, Sarah Zhou, and Anthony Albers. "Management of Osteomyelitis in Sickle Cell Disease: Review Article." JAAOS: Global Research and Reviews 4, no. 9 (2020): e20.00002-10. http://dx.doi.org/10.5435/jaaosglobal-d-20-00002.

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11

Borlongan, Cesar V., Guolong Yu, Noriyuki Matsukawa, Takao Yasuhara, Koichi Hara, and Lin Xu. "Article Commentary: Cell Transplantation: Stem Cells in the Spotlight." Cell Transplantation 14, no. 8 (2005): 519–26. http://dx.doi.org/10.3727/000000005783982774.

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12

Heng, Julian Ik-Tsen, Gustave Moonen, and Laurent Nguyen. "REVIEW ARTICLE: Neurotransmitters regulate cell migration in the telencephalon." European Journal of Neuroscience 26, no. 3 (2007): 537–46. http://dx.doi.org/10.1111/j.1460-9568.2007.05694.x.

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13

Wolf, Marc Alain. "Article." Canadian Journal of Psychiatry 32, no. 2 (1987): 105–11. http://dx.doi.org/10.1177/070674378703200205.

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This article aims to clarify and organize the recent advances in research on the central action mechanism of lithium. It begins by tackling the process of cellular transport of the cation, then it moves on to describe the effects of lithium on ionic distribution and on membranous functioning in general. Neurotransmission in this article is the object of a more detailed study. The metabolism of neurotransmitters (and their disturbances) is first discussed. The emphasis is placed on certain current domains, the gabaergic system in particular. Neurotransmitters, by themselves, do not satisfy any longer the curiosity of biologists. Technological progress has given these scientists access to the intimate functioning of receptors and to their natural support system, the membrane. The stabilizing effect of lithium is mentioned often. Initially seen at a superficial level, it leads to a study of the mechanisms of the transference of information from the receptor to the cell. The membranous phospholipids and the enzymatic systems controlling the metabolism of the second messengers (cyclic nucleotides but also calcium) will provide as many potential targets to the action of lithium.
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14

Li, Chi. "Article Commentary: Increased Mitochondrial Activity in Anthrax-Induced Cell Death." Journal of Cell Death 2 (January 2009): 117967070900200. http://dx.doi.org/10.1177/117967070900200001.

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Pathogenesis of anthrax lethal toxin (LT) is attributed to its ability to cause death of infected cells. New work has demonstrated that increase of mitochondrial F1F0 ATPase activity and subsequent depletion of cellular ATP level are critical early events during LT-induced cell death.
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15

Zong, Guijuan, Zhiwei Xu, Shusen Zhang, et al. "RETRACTED ARTICLE: CD109 Mediates Cell Survival in Hepatocellular Carcinoma Cells." Digestive Diseases and Sciences 61, no. 8 (2016): 2303–14. http://dx.doi.org/10.1007/s10620-016-4149-7.

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16

Borecka-Bednarz, Bozena, Alan V. Bree, Brian O. Patrick, John R. Scheffer, and James Trotter. "Article." Canadian Journal of Chemistry 76, no. 11 (1998): 1616–32. http://dx.doi.org/10.1139/v98-135.

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Second-harmonic generation in the solid state is restricted to materials that crystallize in non-centrosymmetric space groups. Unfortunately, the vast majority of solids crystallize in centrosymmetric space groups and are therefore SHG-inactive. The requirement for solid-state asymmetry is addressed in a new series of organic salts. The acid p-nitrophenylglycine, SHG-inactive due to its centrosymmetric (P1) packing, was coupled to six optically pure amines to form salts and (or) complexes that, by virtue of their chiral counterion, crystallized in non-centrosymmetric space groups. The 1064 nm output from a Nd:YAG laser produced 532 nm second-harmonic generation from each of the six salts, with three of the salts producing second-harmonic intensities at least an order of magnitude greater than that of our standard, urea. X-ray crystallographic analysis was carried out on five of the six salts, and an attempt was made to rationalize the second-harmonic intensity of each of these five salts based on the orientation of its molecular charge-transfer axis in the unit cell and on its chromophore density.Key words: second-harmonic generation, nonlinear optics, chiral organic salts, crystal structures.
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17

Abou-Elhamd, Kamal-Eldin Ahmed. "Article Commentary: Fas and Cancer." Clinical medicine. Ear, nose and throat 3 (January 2010): CMENT.S3147. http://dx.doi.org/10.4137/cment.s3147.

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Apoptosis is an active process of programmed cell death. Fas is a cell-surface protein which is expressed on activated lymphocytes and known as CD95, TNFRSF6 or APO-1. Fas-L is ligand of Fas and known as CD95 LG or TNFSF6. Apoptosis or cell death is a result of binding of Fas-L to Fas which is expressed on the surfaces of these cells. Cancer cells escape this binding by overexpression of Fas-L or down expression of Fas. Fas and Fas-L exist in membrane bound and soluble forms. The serum level of sFas and sFas-L can be evaluated by immunostaining, immunohistochemical methods, immunofluorescence, flow cytometry and Western blotting. Head and neck squamous cell carcinoma diagnosis, staging and prognosis can be evaluated early and accurately by sFas and sFas-L expression levels detection.
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18

Eve, David J., and Paul R. Sanberg. "Article Commentary: Stem Cell Research in Cell Transplantation: An Analysis of Geopolitical Influence by Publications." Cell Transplantation 16, no. 8 (2007): 867–73. http://dx.doi.org/10.3727/000000007783465190.

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One of the fastest growing fields in researching treatments for neurodegenerative and other disorders is the use of stem cells. These cells are naturally occurring and can be obtained from three different stages of an organism's life: embryonic, fetal, and adult. In the US, political doctrine has restricted use of federal funds for stem cells, enhancing research towards an adult source. In order to determine how this legislation may be represented by the stem cell field, a retrospective analysis of stem cell articles published in the journal Cell Transplantation over a 2-year period was performed. Cell Transplantation is considered a translational journal from preclinical to clinical, so it was of interest to determine the publication outcome of stem cell articles 6 years after the US regulations. The distribution of the source of stem cells was found to be biased towards the adult stage, but relatively similar over the embryonic and fetal stages. The fetal stem cell reports were primarily neural in origin, whereas the adult stem cell ones were predominantly mesenchymal and used mainly in neural studies. The majority of stem cell studies published in Cell Transplantation were found to fall under the umbrella of neuroscience research. American scientists published the most articles using stem cells with a bias towards adult stem cells, supporting the effect of the legislation, whereas Europe was the leading continent with a bias towards embryonic and fetal stem cells, where research is “controlled” but not restricted. Japan was also a major player in the use of stem cells. Allogeneic transplants (where donor and recipient are the same species) were the most common transplants recorded, although the transplantation of human-derived stem cells into rodents was the most common specific transplantation performed. This demonstrates that the use of stem cells is an increasingly important field (with a doubling of papers between 2005 and 2006), which is likely to develop into a major therapeutic area over the next few decades and that funding restrictions can affect the type of research being performed.
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19

Stathopoulos, G. P., and T. Boulikas. "Lipoplatin Formulation Review Article." Journal of Drug Delivery 2012 (August 29, 2012): 1–10. http://dx.doi.org/10.1155/2012/581363.

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Patented platform technologies have been used for the liposomal encapsulation of cisplatin (Lipoplatin) into tumor-targeted 110 nm (in diameter) nanoparticles. The molecular mechanisms, preclinical and clinical data concerning lipoplatin, are reviewed here. Lipoplatin has been successfully administered in three randomized Phase II and III clinical trials. The clinical data mainly include non-small-cell lung cancer but also pancreatic, breast, and head and neck cancers. It is anticipated that lipoplatin will replace cisplatin as well as increase its potential applications. For the first time, a platinum drug has shown superiority to cisplatin, at least in non-squamous non-small-cell lung cancer as reported in a Phase III study which documented a simultaneous lowering of all of the side effects of cisplatin.
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20

HENDRY, KAY A. K., AMANDA J. MacCALLUM, CHRISTOPHER H. KNIGHT, and COLIN J. WILDE. "REVIEW ARTICLE Laminitis in the dairy cow: a cell biological approach." Journal of Dairy Research 64, no. 3 (1997): 475–86. http://dx.doi.org/10.1017/s002202999700229x.

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Lameness is a major welfare concern in dairy cattle. Estimates of the annual incidence of lameness range from 4 to 30%, and even in well managed herds as many as 15% of animals can be affected (Esselmont, 1990). In addition to the cost in animal suffering, lameness is accompanied by loss of production on a scale comparable, in temperate countries, with that caused by mastitis. Lost production, veterinary charges and milk discard costs coupled with reduced fertility or premature culling in turn make lameness a major economic factor in dairy farming. In the UK alone, the estimated cost in lost production is £44–£90 million per annum, equivalent to £10–20 per cow (Booth, 1989; Esselmont, 1990).
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21

DABELSTEEN, ERIK. "REVIEW ARTICLE. CELL SURFACE CARBOHYDRATES AS PROGNOSTIC MARKERS IN HUMAN CARCINOMAS." Journal of Pathology 179, no. 4 (1996): 358–69. http://dx.doi.org/10.1002/(sici)1096-9896(199608)179:4<358::aid-path564>3.0.co;2-t.

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22

Groer, Maureen, Nagwa El-Badri, Julie Djeu, Monalisa Harrington, and Jeanne Van Eepoel. "ORIGINAL ARTICLE: Suppression of Natural Killer Cell Cytotoxicity in Postpartum Women." American Journal of Reproductive Immunology 63, no. 3 (2010): 209–13. http://dx.doi.org/10.1111/j.1600-0897.2009.00788.x.

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23

Sujesh, M., V. Rangarajan, C. Ravi Kumar, and G. Sunil Kumar. "RETRACTED ARTICLE: Stem Cell Mediated Tooth Regeneration: New Vistas in Dentistry." Journal of Indian Prosthodontic Society 12, no. 1 (2011): 1–7. http://dx.doi.org/10.1007/s13191-011-0110-9.

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24

Pitra, Tomas, Kristyna Pivovarcikova, Reza Alaghehbandan, and Ondrej Hes. "Chromosomal numerical aberration pattern in papillary renal cell carcinoma: Review article." Annals of Diagnostic Pathology 40 (June 2019): 189–99. http://dx.doi.org/10.1016/j.anndiagpath.2017.11.004.

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25

Czaja, Albert J. "Review article: targeting the B cell activation system in autoimmune hepatitis." Alimentary Pharmacology & Therapeutics 54, no. 7 (2021): 902–22. http://dx.doi.org/10.1111/apt.16574.

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26

Meinel, Jörn, Khaled Radad, Wolf-Dieter Rausch, Heinz Reichmann, and Gabriele Gille. "Original article Cabergoline protects dopaminergic neurons against rotenone-induced cell death in primary mesencephalic cell culture." Folia Neuropathologica 1 (2015): 29–40. http://dx.doi.org/10.5114/fn.2015.49972.

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27

Sengupta, Soumish, Supriya Basu, and Kadambari Ghosh. "Recent advances in the systemic management of non-clear cell renal cell carcinoma: a review article." International Journal of Advances in Medicine 7, no. 9 (2020): 1446. http://dx.doi.org/10.18203/2349-3933.ijam20203613.

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Non-clear cell renal cell carcinoma (nccRCC) is not as common as clear cell renal cell carcinoma (ccRcc). But then it is not uncommon in regular urological practice. It usually carries a grave prognosis. Authors need to converse ourselves with National comprehensive cancer network (NCCN) categories for evidence and we need to converse as well with NCCN categories for preferences. ‘Preferred intervention’ is based on superior efficacy, safety and evidence and when appropriate, affordability. ‘Other recommended interventions’ are somewhat less efficacious, more toxic, or based on less mature data or significantly less affordable for similar outcomes. ‘Useful in certain circumstances’ are interventions that may be used for a selected patient population. Clinical trials for targeted agents are mainly directed at ccRCC because of its high prevalence. According to the NCCN panel, enrolment in clinical trials is the preferred strategy for nccRCC. Outcomes of patients with nccRCC have improved with the introduction of targeted therapy. Precise pathological diagnosis of the types of nccRCC by immunohistochemical analysis is mandatory. This enables specific treatments for individual nccRCC. Currently TKIs are the drug of choice (both first and second line) for metastatic papillary RCC. Both TKIs and mTOR inhibitors are effective against chromophobe RCC. Platinum based chemotherapy should be used for metastatic CDC. Further evidence is required for management of nccRCC.
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28

Shindler, Kenneth S. "Article Commentary: Retinal Ganglion Cell Loss in Diabetes Associated with Elevated Homocysteine." Ophthalmology and Eye Diseases 1 (January 2009): OED.S3417. http://dx.doi.org/10.4137/oed.s3417.

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A number of studies have suggested that homocysteine may be a contributing factor to development of retinopathy in diabetic patients based on observed correlations between elevated homocysteine levels and the presence of retinopathy. The significance of such a correlation remains to be determined, and potential mechanisms by which homocysteine might induce retinopathy have not been well characterized. Ganapathy and colleagues 1 used mutant mice that have endogenously elevated homocysteine levels due to heterozygous deletion of the cystathionine-β-synthase gene to examine changes in retinal pathology following induction of diabetes. Their finding that elevated homocysteine levels hastens loss of cells in the retinal ganglion cell layer suggests that toxicity to ganglion cells may warrant further investigation as a potential mechanism of homocysteine enhanced susceptibility to diabetic retinopathy.
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29

Tao, Sifeng, Haifei He, and Qiang Chen. "RETRACTED ARTICLE: ChIP-seq analysis of androgen receptor in LNCaP cell line." Molecular Biology Reports 41, no. 9 (2014): 6291–96. http://dx.doi.org/10.1007/s11033-014-3511-0.

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30

BURG, GÜNTER, DOROTHEA VON DER HELM, PETER KAUDEWITZ, KRISTINA KLEPZIG, and OTTO BRAUN-FALCO. "ARTICLE: Antihuman T-Cell Leukemia/Lymphoma Virus Antibodies in Three Patients with Primary Cutaneous B-Cell Lymphoma." Journal of Dermatologic Surgery and Oncology 14, no. 6 (1988): 653–56. http://dx.doi.org/10.1111/j.1524-4725.1988.tb03395.x.

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31

Wang, Luping, Junyu Wang, Hong Zhao, et al. "RETRACTED ARTICLE: Soyasapogenol B exhibits anti-growth and anti-metastatic activities in clear cell renal cell carcinoma." Naunyn-Schmiedeberg's Archives of Pharmacology 392, no. 5 (2019): 551–63. http://dx.doi.org/10.1007/s00210-018-01607-w.

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32

Muliani, Nurlina, and Hotimah Masdan Salim. "REVIEW ARTICLE: AMEBIASIS MOLECULAR PATHOGENESIS DEVELOPMENT." Medical and Health Science Journal 3, no. 2 (2019): 6. http://dx.doi.org/10.33086/mhsj.v3i2.1195.

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Amebiasis is one of the gastrointestinal tract infection disease caused by Entamoeba histolytica ,a parasitic protozoan. Amebiasis is the second disease, caused by parasite, that leading cause of death after malaria. Infection occurs through faecal-oral route and after ingestion a contaminated food and beverages by human faeces. The pathogenesis of E. histolytica can be classified into 3 processes, i.e: death of host cell, inflammation, and parasitic invasion. The recent years, a molecularly amebiasis pathogenesis has been developed, i.e: adherence, phagocytosis, tropogocytosis of host cell and how the parasites can survive and attack host cells so it can cause an infection in humans. Molecular development is an important thing to be considered in the selection of amebiasis therapy.
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33

Schwan, Jonas, and Stuart G. Campbell. "Article Commentary: Prospects for In Vitro Myofilament Maturation in Stem Cell-Derived Cardiac Myocytes." Biomarker Insights 10s1 (January 2015): BMI.S23912. http://dx.doi.org/10.4137/bmi.s23912.

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Cardiomyocytes derived from human stem cells are quickly becoming mainstays of cardiac regenerative medicine, in vitro disease modeling, and drug screening. Their suitability for such roles may seem obvious, but assessments of their contractile behavior suggest that they have not achieved a completely mature cardiac muscle phenotype. This could be explained in part by an incomplete transition from fetal to adult myofilament protein isoform expression. In this commentary, we review evidence that supports this hypothesis and discuss prospects for ultimately generating engineered heart tissue specimens that behave similarly to adult human myocardium. We suggest approaches to better characterize myofilament maturation level in these in vitro systems, and illustrate how new computational models could be used to better understand complex relationships between muscle contraction, myofilament protein isoform expression, and maturation.
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34

Fahmy, Amal, and Magda Abd El-Atty. "Evaluation of the Current Situation of Cell Phone Waste in Egypt: Review Article." Journal of High Institute of Public Health 42, no. 2 (2012): 208–23. http://dx.doi.org/10.21608/jhiph.2012.20133.

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35

Lee, Chyi Chia R., and Shoji Fukushima. "Review article Alterations in cyclin D1, p53, and the cell cycle related elements." Urologic Oncology: Seminars and Original Investigations 4, no. 3 (1998): 58–72. http://dx.doi.org/10.1016/s1078-1439(98)00033-7.

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36

Taishikhina, I. O., M. E. Lokhmatova та L. N. Shelikhova. "Hematopoietic stem cell transplantation in patients with transfusion-dependent β-thalassemia. Review article". Pediatric Hematology/Oncology and Immunopathology 19, № 2 (2020): 178–83. http://dx.doi.org/10.24287/1726-1708-2020-19-2-178-183.

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Thalassemia is the most common form of hereditary anemia from the hemoglobinopathy group. The genetic disorder underlying thalassemia leads to impaired erythrocyte maturation, hemolysis, and the development of ineffective erythropoiesis with erythroid gland hyperplasia in the bone marrow and extramedullary. Regular blood transfusions and chelator therapy are standard therapy for patients with b-thalassemia. This method increases life expectancy, but does not improve its quality and does not cure the disease. Currently, allogeneic hematopoietic stem cell transplantation remains the only radical treatment for thalassemia. The paper discusses the historical aspects of the development of allogeneic hematopoietic stem cell transplantation in the context of transfusion-dependent form of b-thalassemia treatment.
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37

SAWYERR, A. M., A. J. WAKEFIELD, M. HUDSON, A. P. DHILLON, and R. E. POUNDER. "Review article: the pharmacological implications of leucocyte-endothelial cell interactions in Crohn's disease." Alimentary Pharmacology & Therapeutics 5, no. 1 (2007): 1–14. http://dx.doi.org/10.1111/j.1365-2036.1991.tb00001.x.

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38

Barjaktarevic, Igor, and Stanislav Vukmanovic. "ORIGINAL ARTICLE: Paternal Cell Immunization Raises Autoantibodies and Improves Pregnancy Success in Mice." American Journal of Reproductive Immunology 60, no. 6 (2008): 497–500. http://dx.doi.org/10.1111/j.1600-0897.2008.00646.x.

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39

Sanchez-Ramos, J., S. Song, M. Dailey, et al. "Article Commentary: The X-gal Caution in Neural Transplantation Studies." Cell Transplantation 9, no. 5 (2000): 657–67. http://dx.doi.org/10.1177/096368970000900510.

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Cell transplantation into host brain requires a reliable cell marker to trace lineage and location of grafted cells in host tissue. The lacZ gene encodes the bacterial (E. coli) enzyme β-galactosidase (β-gal) and is commonly visualized as a blue intracellular precipitate following its incubation with a substrate, “X-gal,” in an oxidation reaction. LacZ is the “reporter gene” most commonly employed to follow gene expression in neural tissue or to track the fate of transplanted exogenous cells. If the reaction is not performed carefully—with adequate optimization and individualization of various parameters (e.g., pH, concentration of reagents, addition of chelators, composition of fixatives) and the establishment of various controls—then misleading nonspecific background X-gal positivity can result, leading to the misidentification of cells. Some of this background results from endogenous nonbacterial β-gal activity in discrete populations of neurons in the mammalian brain; some results from an excessive oxidation reaction. Surprisingly, few articles have emphasized how to recognize and to eliminate these potential confounding artifacts in order to maximize the utility and credibility of this histochemical technique as a cell marker. We briefly review the phenomenon in general, discuss a specific case that illustrates how an insufficiently scrutinized X-gal positivity can be a pitfall in cell transplantation studies, and then provide recommendations for optimizing the specificity and reliability of this histochemical reaction for discerning E. coli β-gal activity.
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40

Chong, Elise A., and David L. Porter. "Immunotherapy with cells (article not eligible for CME credit)." Hematology 2020, no. 1 (2020): 590–97. http://dx.doi.org/10.1182/hematology.2020000174.

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Abstract Both older and newer cell therapies have demonstrated impressive responses in otherwise poor-prognosis lymphomas. Consequently, cellular therapy now plays a major role in the management of many non-Hodgkin lymphomas. In this article, we examine the role of chimeric antigen receptor (CAR) T cells, allogeneic stem cell transplantation, and virus-directed T cells for treatment of lymphomas. We review the current indications for CAR T cells and discuss our clinical approach to selecting and treating patients with aggressive B-cell lymphomas to receive CD19-directed CAR T cells. In addition, we highlight newer cell therapies and provide an overview of promising future approaches that have the potential to transform immunotherapy with cells to treat lymphomas.
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41

Engelhardt, V. A. "About circular chemical processes in the cell." Kazan medical journal 32, no. 1 (2021): 7–14. http://dx.doi.org/10.17816/kazmj80261.

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In No. 11-12 of the Kazan medical journal for 1931, in the editorial article that opens the issue, a rather significant place is devoted to an assessment of two of my works that appeared in the same journal (1,2). Completely and completely in solidarity with the guidelines of the Editors developed at the beginning of the article, which, as the very title of the article indicates, takes as the basis of all its work the practical implementation of the instructions of Comrade Stalin on the fight against alien theories and on vigilance on the ideological front, I cannot agree with the assessment of my works given in the article, as allegedly imbued with theories alien to dialectical materialism, and revealing mechanistic attitudes.
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42

Nasadyuk, C. "Cell therapy in gastroenterology." Cell and Organ Transplantology 3, no. 1 (2015): 78–81. http://dx.doi.org/10.22494/cot.v3i1.25.

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The article highlights the up-to-date literary data about the role of tissue and circulating stem cells in the processes of regeneration and carcinogenesis of gastric mucosa and intestine and development of liver and pancreatic fibrosis. The paper also presents the novel methods of treatment of common gastrointestinal diseases with the use of cell and gene technologies.
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Gharzai, Laila A., and Michelle L. Mierzwa. "Radiotherapy in Cutaneous Squamous Cell and Basal Cell Carcinoma." Facial Plastic Surgery 36, no. 02 (2020): 180–85. http://dx.doi.org/10.1055/s-0040-1709119.

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AbstractRadiotherapy is a key component in the multidisciplinary treatment of skin cancers, used in definitive management of selected nonmelanomatous skin cancers and as an adjunct treatment in high-risk cases. Understanding the role of radiotherapy in nonmelanoma skin cancers is increasingly important as their incidence continues to rise. This article provides an overview of risk factors associated with nonmelanomatous skin cancers and the principles of both definitive and adjuvant radiotherapy.
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Tomita, Mariko, Takehiro Matsuda, Hirochika Kawakami, et al. "THIS ARTICLE HAS BEEN RETRACTED Curcumin targets Akt cell survival signaling pathway in HTLV-I-infected T-cell lines." Cancer Science 97, no. 4 (2006): 322–27. http://dx.doi.org/10.1111/j.1349-7006.2006.00175.x.

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Tomita, Mariko, Takehiro Matsuda, Hirochika Kawakami, et al. "This article has been retracted: Curcumin targets Akt cell survival signaling pathway in HTLV-I-infected T-cell lines." Cancer Science 102, no. 2 (2010): 498. http://dx.doi.org/10.1111/j.1349-7006.2010.01830.x.

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Tomita, Mariko, Takehiro Matsuda, Hirochika Kawakami, et al. "This article has been retracted: Curcumin targets Akt cell survival signaling pathway in HTLV-I-infected T-cell lines." Cancer Science 102, no. 2 (2010): 499. http://dx.doi.org/10.1111/j.1349-7006.2010.01831.x.

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Thum, Meen-Yau, Shree Bhaskaran, Hossam I. Abdalla, Brian Ford, Nazira Sumar, and Amolak Bansal. "ORIGINAL ARTICLE: Prednisolone Suppresses NK Cell Cytotoxicity In Vitro in Women With a History of Infertility and Elevated NK Cell Cytotoxicity." American Journal of Reproductive Immunology 59, no. 3 (2008): 259–65. http://dx.doi.org/10.1111/j.1600-0897.2007.00574.x.

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Chopp, Michael, Gary K. Steinberg, Douglas Kondziolka, et al. "Article Commentary: Who's in Favor of Translational Cell Therapy for Stroke: STEPS Forward Please?" Cell Transplantation 18, no. 7 (2009): 691–93. http://dx.doi.org/10.3727/096368909x470883.

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Mienville, J. M. "Feature Article: Cajal-Retzius Cell Physiology: Just in Time to Bridge the 20th Century." Cerebral Cortex 9, no. 8 (1999): 776–82. http://dx.doi.org/10.1093/cercor/9.8.776.

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SCHLIWA, MANFRED. "Review Article: Permeabilized Cell Models for the Study of Granule Transport in Pigment Cells." Pigment Cell Research 1, no. 2 (1987): 65–68. http://dx.doi.org/10.1111/j.1600-0749.1987.tb00391.x.

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