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Articoli di riviste sul tema "Stem cells"

Autore: Grafiati
Pubblicato: 4 giugno 2021
Ultima modifica: 31 luglio 2024

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1

CR, Thambidorai. "Stem Cells in Urethral Replacement". Journal of Embryology & Stem Cell Research 4, n. 1 (2020): 1–2. http://dx.doi.org/10.23880/jes-16000139.

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2

Aguilar-Gallardo, Cristóbal, e Carlos Simón. "Cells, Stem Cells, and Cancer Stem Cells". Seminars in Reproductive Medicine 31, n. 01 (17 gennaio 2013): 005–13. http://dx.doi.org/10.1055/s-0032-1331792.

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3

Srivastava, A. N., Neema Tiwari, Shailendra Yadav e Suryakant . "LUNG CANCER STEM CELLS-AN UPDATE". Era's journal of medical research 4, n. 1 (1 giugno 2017): 22–31. http://dx.doi.org/10.24041/ejmr2017.4.

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4

Yang, Junzheng. "Stem Cells Applications in Neurodegenerative Diseases". Epidemiology International Journal 7, n. 4 (2023): 1–6. http://dx.doi.org/10.23880/eij-16000267.

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Abstract (sommario):
Neurodegenerative diseases are a kind of diseases caused by progressive loss of neuronal structure and function and glial cell homeostasis imbalance, there are many kinds of neurodegenerative diseases include Alzheimer's disease (AD), Parkinson's disease (PD); Huntington's disease (HD) and amyotrophic lateral sclerosis (ALS). So far, due to the lack of ideal treatment methods, it seriously threats to human health especially the elder population. Recently, with the rapid development of regenerative medicine, stem cells rely on their advantages including self-renewing capability, low immunogenicity, migration and homing capabilities, and stem cell derivatives including stem cells derived extracellular vesicles and stem cell-derived organoids, it provides unlimited application possibilities for the treatment of neurodegenerative diseases. In this review, we will summarize the recent research progress on the preclinical and clinical applications of stem cells in neurodegenerative diseases, hope that the reviews may provide some useful clues for researchers.
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5

Weigel, Detlef, e Gerd Jürgens. "Stem cells that make stems". Nature 415, n. 6873 (febbraio 2002): 751–54. http://dx.doi.org/10.1038/415751a.

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6

J, Otsuka. "A Theoretical Study on the Cell Differentiation Forming Stem Cells in Higher Animals". Physical Science & Biophysics Journal 5, n. 2 (2021): 1–10. http://dx.doi.org/10.23880/psbj-16000191.

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The recent genome sequencing of multicellular diploid eukaryotes reveals an enlarged repertoire of protein genes for signal transmission but it is still difficult to elucidate the network of signal transmission to drive the life cycle of such an eukaryote only from biochemical and genetic studies. In the present paper, a theoretical study is carried out for the cell differentiation, the formation of stem cells and the growth from a child to the adult in the higher animal. With the intercellular and intracellular signal transmission in mind, the cell differentiation is theoretically derived from the process by the transition of proliferated cells from proliferation mode to differentiation mode and by both the long-range interaction between distinctive types of cells and the short-range interaction between the same types of cells. As the hierarchy of cell differentiation is advanced, the original types of self-reproducible cells are replaced by the self-reproducible cells returned from the cells differentiated already. The latter type of self-reproducible cells are marked with the signal specific to the preceding differentiation and become the stem cells for the next stage of cell differentiation. This situation is realized under the condition that the differentiation of cells occurs immediately after their proliferation in the development. The presence of stem cells in the respective lineages of differentiated cells strongly suggests another signal transmission for the growth of a child to a definite size of adult that the proliferation of stem cells in one lineage is activated by the signal from the differentiated cells in the other lineage(s) and is suppressed by the signal from the differentiated cells in its own lineage. This style of signal transmission also explains the metamorphosis and maturation of germ cells in higher animals.
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7

Challa, Stalin Reddy, e Swathi Goli. "Differentiation of Human Embryonic Stem Cells into Engrafting Myogenic Precursor Cells". Stem cell Research and Therapeutics International 1, n. 1 (16 aprile 2019): 01–05. http://dx.doi.org/10.31579/2643-1912/002.

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Degenerative muscle diseases affect muscle tissue integrity and function. Human embryonic stem cells (hESC) are an attractive source of cells to use in regenerative therapies due to their unlimited capacity to divide and ability to specialize into a wide variety of cell types. A practical way to derive therapeutic myogenic stem cells from hESC is lacking. In this study, we demonstrate the development of two serum-free conditions to direct the differentiation of hESC towards a myogenic precursor state. Using TGFß and PI3Kinase inhibitors in combination with bFGF we showed that one week of differentiation is sufficient for hESC to specialize into PAX3+/PAX7+ myogenic precursor cells. These cells also possess the capacity to further differentiate in vitro into more specialized myogenic cells that express MYOD, Myogenin, Desmin and MYHC, and showed engraftment in vivo upon transplantation in immunodeficient mice. Ex vivo myomechanical studies of dystrophic mouse hindlimb muscle showed functional improvement one month post-transplantation. In summary, this study describes a promising system to derive engrafting muscle precursor cells solely using chemical substances in serum-free conditions and without genetic manipulation.
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8

Garg, Minal. "MicroRNAs, stem cells and cancer stem cells". World Journal of Stem Cells 4, n. 7 (2012): 62. http://dx.doi.org/10.4252/wjsc.v4.i7.62.

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9

Li, Jia J., e Michael M. Shen. "Prostate Stem Cells and Cancer Stem Cells". Cold Spring Harbor Perspectives in Medicine 9, n. 6 (5 ottobre 2018): a030395. http://dx.doi.org/10.1101/cshperspect.a030395.

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10

Reya, Tannishtha, Sean J. Morrison, Michael F. Clarke e Irving L. Weissman. "Stem cells, cancer, and cancer stem cells". Nature 414, n. 6859 (novembre 2001): 105–11. http://dx.doi.org/10.1038/35102167.

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11

Soria, Bernat, Francisco J. Bedoya e Franz Martin. "Gastrointestinal Stem Cells I. Pancreatic stem cells". American Journal of Physiology-Gastrointestinal and Liver Physiology 289, n. 2 (agosto 2005): G177—G180. http://dx.doi.org/10.1152/ajpgi.00116.2005.

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Abstract (sommario):
The transplantation of islets isolated from donor pancreas has renewed the interest in cell therapy for the treatment of diabetes. In addition, the capacity that stem cells have to differentiate into a wide variety of cell types makes their use ideal to generate β-cells for transplantation therapies. Several studies have reported the generation of insulin-secreting cells from embryonic and adult stem cells that normalized blood glucose values when transplanted into diabetic animal models. Finally, although much work remains to be done, there is sufficient evidence to warrant continued efforts on stem cell research to cure diabetes.
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12

Bjerknes, Matthew, e Hazel Cheng. "Gastrointestinal Stem Cells. II. Intestinal stem cells". American Journal of Physiology-Gastrointestinal and Liver Physiology 289, n. 3 (settembre 2005): G381—G387. http://dx.doi.org/10.1152/ajpgi.00160.2005.

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Current views of the identity, distribution, and regulation of small intestinal epithelial stem cells and their immediate progeny are discussed. Recent works implicating Wnt signaling in stem and progenitor proliferation, the involvement of Notch signaling in epithelial lineage specification, and the role of hedgehog and bone morphogenetic protein families in crypt formation are integrated. We had the good fortune that many of these papers came in pairs from independent groups. We attempt to identify points of agreement, reinterpret each in the context of the other, and indicate directions for continued progress.
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13

Hill, Reginald, e Hong Wu. "PTEN, Stem Cells, and Cancer Stem Cells". Journal of Biological Chemistry 284, n. 18 (30 dicembre 2008): 11755–59. http://dx.doi.org/10.1074/jbc.r800071200.

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14

Nighojkar, Urvashi Rajeev, Dr Priya A. Lele e Mudita Agrawal. "Scope of Stem Cells in Periodontal Regeneration". International Journal of Scientific Research 2, n. 5 (1 giugno 2012): 428–31. http://dx.doi.org/10.15373/22778179/may2013/145.

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15

P, Pradeep. "Role of Stem Cells in Cerebral Infarction". Journal of Embryology & Stem Cell Research 2, n. 2 (2018): 1–8. http://dx.doi.org/10.23880/jes-16000112.

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16

Karunanithi Arulvizhi M, Arunagiri. "Stem Cells in Periodontal Regenerations - A Review". International Journal of Science and Research (IJSR) 13, n. 2 (5 febbraio 2024): 589–94. http://dx.doi.org/10.21275/sr24206105401.

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17

Ahmed Elkammar, Hala. "Effect of human bone marrow derived mesenchymal stem cells on squamous cell carcinoma cell line". International Journal of Academic Research 6, n. 1 (30 gennaio 2014): 110–16. http://dx.doi.org/10.7813/2075-4124.2014/6-1/a.14.

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18

M. Baghdadi, Houry. "Effect of stem cells on genetic mutations and proliferation in squamous cell carcinoma". International Journal of Academic Research 6, n. 1 (30 gennaio 2014): 192–97. http://dx.doi.org/10.7813/2075-4124.2014/6-1/a.25.

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19

MAS, Bezerra, Ferreira LAM, Kawasaki-Oyama RS, Nascimento MCA, Cuzziol CI, Castanhole-Nunes MMU, Pavarino EC, Maniglia JM e Goloni-Bertollo EM. "Effectiveness of Hypoxia-Induced Accumulation of Cancer Stem Cells in Head and Neck Squamous Cell Carcinoma". Cancer Medicine Journal 3, S1 (30 novembre 2020): 13–23. http://dx.doi.org/10.46619/cmj.2020.3.s1-1003.

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Abstract (sommario):
INTRODUCTION: The small number of cancer stem cells, which correspond to only 0.01% - 0.1% of total tumor cells, has been the biggest obstacle in understanding their biology and role in the origin and maintenance of tumors, their metastatic and recurrence potentials, and resistance to radio-chemotherapy. Therefore, promoting its accumulation will enable further studies and future advances in the diagnosis and treatment of head and neck cancer squamous cell carcinoma. OBJECTIVE: To induce cancer stem cell accumulation in primary cell cultures of head and neck squamous cell carcinoma using a hypoxia chamber. METHODS: Head and neck squamous cell carcinoma samples were cultured and subjected to hypoxia. Oxygen deprivation aimed to induce cancer stem cell accumulation. RESULTS: Immediately after hypoxia, the percentage of O2-deprived cancer stem cells increased 2-fold as compared to control. Surprisingly, new phenotyping performed 45 days after hypoxia showed a 9-fold increase in cancer stem cell percentage in cells that suffered hypoxia. Hypoxic cells showed an increase in spheroid formation when compared to control cells, as well as enhanced abilities in invasion and migration. CONCLUSION: Hypoxia was efficient in cancer stem cell accumulation. As cancer stem cells are a small number of cells within the tumor, promoting their accumulation will enable further studies and future advances in the diagnosis and treatment of head and neck cancer.
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20

Lebacqz, Karen, Carol Tauer, Glenn McGee e Arthur Caplan. "Stem Cells". Hastings Center Report 29, n. 4 (luglio 1999): 4. http://dx.doi.org/10.2307/3528057.

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21

Sargaiyan, Vinod, Rajveer S. Yadav, Saurabh S. Parihar, Makrand Sapat, Sateesh Bhatele e Archana H. Lanje. "Stem Cells". International Journal of Oral Care & Research 5, n. 4 (2017): 332–34. http://dx.doi.org/10.5005/jp-journals-10051-0126.

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22

Rafael, Hernando. "Stem Cells". Journal of Neurosurgery 108, n. 4 (aprile 2008): 841–42. http://dx.doi.org/10.3171/jns/2008/108/4/0841.

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23

Thakur, Madhukar. "Stem Cells". Malecular Imaging and Radionuclide Therapy 24, n. 1 (5 febbraio 2015): 37. http://dx.doi.org/10.4274/mirt.24.01.01.

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24

Moraczewski, Albert S. "Stem Cells". Ethics & Medics 28, n. 3 (2003): 1–2. http://dx.doi.org/10.5840/em20032834.

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25

Hodson, Richard. "Stem cells". Nature 597, n. 7878 (29 settembre 2021): S5. http://dx.doi.org/10.1038/d41586-021-02620-5.

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26

Lederman, Lynne. "Stem Cells". BioTechniques 42, n. 1 (gennaio 2007): 25–29. http://dx.doi.org/10.2144/000112337.

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27

Huang, B., C. Jiang, L. Qin, Y. Cui, J. Liu, M. Stimpfel, B. Cvjeticanin et al. "Stem cells". Human Reproduction 28, suppl 1 (1 giugno 2013): i366—i368. http://dx.doi.org/10.1093/humrep/det224.

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28

Bernstein, Daniel. "Stem cells". Current Opinion in Pediatrics 31, n. 5 (ottobre 2019): 617–22. http://dx.doi.org/10.1097/mop.0000000000000801.

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29

Murdoch, Barbara. "Stem Cells". American Biology Teacher 78, n. 2 (1 febbraio 2016): 174. http://dx.doi.org/10.1525/abt.2016.78.2.174.

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30

Thaller, Seth R., Sharon Elliot e Ernesto J. Arroyo. "Stem Cells". Journal of Craniofacial Surgery 31, n. 1 (2020): 4–5. http://dx.doi.org/10.1097/scs.0000000000005803.

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31

Oktem, Ozgur, e Kutluk Oktay. "Stem Cells". Annals of the New York Academy of Sciences 1127, n. 1 (aprile 2008): 20–26. http://dx.doi.org/10.1196/annals.1434.010.

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32

Kereiakes, Dean J. "Stem Cells". Circulation 107, n. 7 (25 febbraio 2003): 939–40. http://dx.doi.org/10.1161/01.cir.0000057607.03836.f8.

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33

Levi, Benjamin, Jason P. Glotzbach, Victor W. Wong, Emily R. Nelson, Jeong Hyun, Derrick C. Wan, Geoffrey C. Gurtner e Michael T. Longaker. "Stem Cells". Journal of Craniofacial Surgery 23, n. 1 (gennaio 2012): 319–23. http://dx.doi.org/10.1097/scs.0b013e318241dbaf.

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34

Behr, Björn, Sae Hee Ko, Victor W. Wong, Geoffrey C. Gurtner e Michael T. Longaker. "Stem Cells". Plastic and Reconstructive Surgery 126, n. 4 (ottobre 2010): 1163–71. http://dx.doi.org/10.1097/prs.0b013e3181ea42bb.

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35

Sinclair, Jan, e Gail Thompson. "Stem Cells". Neurology Now 4, n. 4 (luglio 2008): 9. http://dx.doi.org/10.1097/01.nnn.0000333834.11483.04.

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36

WEISSMAN, IRVING, GERALD SPANGRUDE, SHELLY HEIMFELD, LAURIE SMITH e NOBUKO UCHIDA. "Stem cells". Nature 353, n. 6339 (settembre 1991): 26. http://dx.doi.org/10.1038/353026a0.

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37

ISCOVE, NORMAN. "Stem cells". Nature 353, n. 6339 (settembre 1991): 26. http://dx.doi.org/10.1038/353026b0.

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38

Lomberk, Gwen. "Stem Cells". Pancreatology 7, n. 4 (settembre 2007): 314–16. http://dx.doi.org/10.1159/000105496.

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39

BAUM, RUDY M. "Stem Cells". Chemical & Engineering News 85, n. 49 (3 dicembre 2007): 3. http://dx.doi.org/10.1021/cen-v085n049.p003.

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40

Cheng, Li-Chun, Masoud Tavazoie e Fiona Doetsch. "Stem Cells". Neuron 46, n. 3 (maggio 2005): 363–67. http://dx.doi.org/10.1016/j.neuron.2005.04.027.

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41

Hucho, Ferdinand. "Stem cells". Molecular Aspects of Medicine 22, n. 3 (giugno 2001): 143–47. http://dx.doi.org/10.1016/s0098-2997(01)00005-x.

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42

Tuma, Rabiya S. "Stem cells". Oncology Times 4, n. 6 (giugno 2007): 15–17. http://dx.doi.org/10.1097/01434893-200706000-00019.

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43

Shalaby, Mohamed Adel. "Stem Cells". Al-Azhar Medical Journal 45, n. 1 (gennaio 2016): i—iii. http://dx.doi.org/10.12816/0026258.

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44

He, H., M. R. Emmett, A. G. Marshall, Y. Ji, C. A. Conrad, W. Priebe, H. Colman et al. "Stem Cells". Neuro-Oncology 12, Supplement 4 (21 ottobre 2010): iv119—iv127. http://dx.doi.org/10.1093/neuonc/noq116.s18.

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45

Joshi, K., S. Gupta, S. Mazumder, Y. Okemoto, B. Angenieux, H. Kornblum, I. Nakano et al. "STEM CELLS". Neuro-Oncology 13, suppl 3 (21 ottobre 2011): iii145—iii153. http://dx.doi.org/10.1093/neuonc/nor163.

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46

Cheng, L., Z. Huang, W. Zhou, Q. Wu, J. Rich, S. Bao, P. Baxter et al. "STEM CELLS". Neuro-Oncology 15, suppl 3 (1 novembre 2013): iii206—iii216. http://dx.doi.org/10.1093/neuonc/not190.

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47

GUDJONSSON, THORARINN, ALLAN RANDRUP THOMSEN, OLLI VAINIO e HELGA M. ÖGMUNDSDÓTTIR. "Stem cells". APMIS 113, n. 11-12 (novembre 2005): 725–26. http://dx.doi.org/10.1111/j.1600-0463.2005.apm_113-12.x.

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48

Fuchs, Elaine, e Julia A. Segre. "Stem Cells". Cell 100, n. 1 (gennaio 2000): 143–55. http://dx.doi.org/10.1016/s0092-8674(00)81691-8.

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49

Weissman, Irving L. "Stem Cells". Cell 100, n. 1 (gennaio 2000): 157–68. http://dx.doi.org/10.1016/s0092-8674(00)81692-x.

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50

Benfey, Philip N. "Stem cells:". Current Biology 9, n. 5 (marzo 1999): R171—R172. http://dx.doi.org/10.1016/s0960-9822(99)80105-5.

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