Добірка наукової літератури з теми "Germ cells"

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Пов'язані теми наукових робіт:

Статті в журналах з теми "Germ cells":

1
Kerr, Candace, John Gearhart, Aaron Elliott, and Peter Donovan. "Embryonic Germ Cells: When Germ Cells Become Stem Cells." Seminars in Reproductive Medicine 24, no. 5 (November 2006): 304–13. http://dx.doi.org/10.1055/s-2006-952152.
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2
Wylie, Chris. "Germ Cells." Cell 96, no. 2 (January 1999): 165–74. http://dx.doi.org/10.1016/s0092-8674(00)80557-7.
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Wylie, Chris. "Germ cells." Current Opinion in Genetics & Development 10, no. 4 (August 2000): 410–13. http://dx.doi.org/10.1016/s0959-437x(00)00105-2.
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Wylie, Chris. "Introduction: Germ cells." Seminars in Developmental Biology 4, no. 3 (June 1993): 147–48. http://dx.doi.org/10.1006/sedb.1993.1017.
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Xu, HongYan, MingYou Li, JianFang Gui, and YunHan Hong. "Fish germ cells." Science China Life Sciences 53, no. 4 (April 2010): 435–46. http://dx.doi.org/10.1007/s11427-010-0058-8.
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Rossant, Janet. "Immortal germ cells?" Current Biology 3, no. 1 (January 1993): 47–49. http://dx.doi.org/10.1016/0960-9822(93)90148-h.
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Eppig, John, and Mary Ann Handel. "Germ Cells from Stem Cells." Biology of Reproduction 79, no. 1 (July 2008): 172–78. http://dx.doi.org/10.1095/biolreprod.108.070789.
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8
Stewart, Colin L., Inder Gadi, and Harshida Bhatt. "Stem Cells from Primordial Germ Cells Can Reenter the Germ Line." Developmental Biology 161, no. 2 (February 1994): 626–28. http://dx.doi.org/10.1006/dbio.1994.1058.
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Zhangab, Rong, Wancun Chang, and Jian-Yong Han. "Culture of Rabbit Embryonic Germ Cells Derived from Primordial Germ Cells." Journal of Applied Animal Research 26, no. 2 (December 2004): 61–66. http://dx.doi.org/10.1080/09712119.2004.9706509.
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Cinalli, Ryan M., Prashanth Rangan, and Ruth Lehmann. "Germ Cells Are Forever." Cell 132, no. 4 (February 2008): 559–62. http://dx.doi.org/10.1016/j.cell.2008.02.003.
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Дисертації з теми "Germ cells":

1
Hajkova, Petra. "Epigenetic reprogramming in mouse germ cells." DoctoralThesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2003. http://dx.doi.org/10.18452/15020.
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Bei Säugerkeimzellen, Zygoten und Embryos in frühen Stadien kommt der epigenetischen Neuprogammierung eine außergewöhnlich wichtige Rolle in der Regulation der Genomfunktionen in entscheidenden Entwicklungsstadien zu. Die epigenetische Neuprogrammierung in Keimzellen löscht zuerst die Imprinting-Markierungen und Epi-Mutationen und stellt dann geschlechtsspezifische Markierungen (genomische Prägung) wieder her. Die vorliegende Arbeit bezieht sich auf das Löschen epigenetischer Modifikationen in primordialen Mauskeimzellen (primordial germ cells (PGCs)) zwischen dem 10.5 bis 13.5 Tag nach der Befruchtung. Entgegen früheren Annahmen zeigen unsere Ergebnisse, daß primordiale Mauskeimzellen (PGCs) beim Eintritt in die embryonalen Keimdrüsen noch immer DNS Methylierungsmarker besitzen, die ähnlich dem Marker in somatischen Zellen sind. Kurz nach dem Eintritt in die Keimdrüsen werden die DNS Methylierungsmarker, die in Verbindung mit geprägten und nicht geprägten Genen stehen, gelöscht. Für die Mehrzahl der Gene beginnt die Löschung der Marker in männlichen und weiblichen Embryos gleichzeitig und ist innerhalb eines Entwicklungstages abgeschlossen. Diese Kinetik deutet auf einen aktiven Demethylierungsprozess hin, initiiert durch ein somatisches Signal, ausgehend von der embryonalen Keimdrüse. Der Zeitpunkt der Neuprogrammierung in den primordialen Keimzellen ist entscheidend, da er sicherstellt, daß Keimzellen beiden Geschlechts einen epigenetisch äquivalenten Status erhalten, bevor sie geschlechtsspezifisch ausdifferenzieren und anschließend neu elterlich geprägt werden. Vollständiges Verständnis des Prozesses der Neuprogrammierung der Keimzellen ist nicht nur im Hinblick auf genomisches Imprinting wichtig, sondern auch für die Erforschung von Mechanismen für die Wiederherstellung von omnipotenten Zellen bei Klonierung und Stammzellenerhaltung.
Epigenetic reprogramming in mammalian germ cells, zygote and early embryos, plays a crucial role in regulating genome functions at critical stages of development. Germ line epigenetic reprogramming assures erasure of all the imprinting marks and epi-mutations and establishment of new sex-specific gametic imprints. The presented work focuses on the erasure of epigenetic modifications that occur in mouse primordial germ cells (PGCs) between day 10.5 to 13.5 post coitum (dpc). Contrary to previous assumptions, our results show that as they enter the genital ridge the PGCs still possess DNA methylation marks comparable to those found in somatic cells. Shortly after the entry of PGCs into the gonadal anlagen the DNA methylation marks associated with imprinted and non-imprinted genes are erased. For most genes the erasure commences simultaneously in PGCs of both male and female embryos and is completed within only one day of development. The kinetics of this process indicates that is an active demethylation process initiated by a somatic signal emanating from the stroma of the genital ridge. The timing of reprogramming in PGCs is crucial since it ensures that germ cells of both sexes acquire an equivalent epigenetic state prior to the differentiation of the definitive male and female germ cells in which, new parental imprints are established subsequently. Complete understanding of the germline reprogramming processes is important not only in the light of genomic imprinting but also for resolving other mechanisms connected with restoring cellular totipotency, such as cloning and stem cell derivation.
2
Ono, Tetsuo. "Novel preservation method of germ cells and somatic cells." DAM, Kyoto University, 2003. http://hdl.handle.net/2433/120542.
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Li, Ying. "Transgenic birds from transformed primordial germ cells." Electronic Thesis or Dissertation, University of Reading, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.385118.
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Al-Thani, Rawda. "Primordial germ cells of the chick embryo." Electronic Thesis or Dissertation, University of Reading, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315524.
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Yoon, Christina Migyung 1970. "Idenficiation of the zebrafish primordial germ cells." Thesis, Massachusetts Institute of Technology, 1997. http://hdl.handle.net/1721.1/43551.
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Grabole, Nils. "Functional analysis of Prdm14 in primordial germ cells and stem cells." Electronic Thesis or Dissertation, University of Cambridge, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.608092.
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Vick, Lorraine Mary. "Genetic manipulation of fowl via primordial germ cells." Electronic Thesis or Dissertation, University of Reading, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317960.
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Seisenberger, Stefanie. "Reprogramming the epigenome of mouse primordial germ cells." Electronic Thesis or Dissertation, University of Cambridge, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.610019.
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9
Wigmore, Kip. "The primordial germ cells of the goat fetus." Electronic thesis or dissertation, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ43237.pdf.
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10
Pogool, Satian. "Factors controlling migration of avian primordial germ cells." Electronic Thesis or Dissertation, University of Manchester, 2002. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.531435.
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Анотація:
Avian embryos have played an important role in the study of vertebrate development but further understanding of their development may also benefit the commercial poultry industry. Manipulation and use of primordial germ cells (PGCs) as a vehicle for constructed genotypes will be increasingly important for future improvement of commercial poultry including the turkey. However, the manipulation and use of PGCs will depend on a basic understanding of PGC migration. PGCs are known to migrate considerable distances before colonising the gonad. Previous work in the chick and quail have suggested that avian PGCs arise from the ventral surface of the area pellucida before the blastoderm undergoes gastrulation, translocate to the germinal crescent during primitive streak stages and penetrate the extraembryonic blood vessels (stage 10) after they have formed. PGCs are subsequently carried by the blood stream into the embryo proper during stages 12-14 and then leave the blood vessels and migrate to the developing gonads. However, the factors controlling PGC migration are poorly understood. The developmental stages of older turkey embryos are not well documented. Therefore, this study started by classifying them. It was found that turkey embryos at stage 4 and younger were slightly different from chick embryos, but from stages 5 onwards, turkey embryos could be staged using criteria described for the chick (Hamburger and Hamilton, 1951). Avian PGCs can be recognized by their distinctive morphology being large cells with large and eccentrically placed nuclei, and a cytoplasm containing refractile granules. These characteristics were confirmed for turkey PGCs. In order to manipulate PGCs, cells need to be identified using appropriate markers. A panel of markers previously used for chick, quail, mouse, rat and rabbit were tested with turkey PGCs at different stages. It was found that turkey PGCs could be detected by the histochemical stains, periodic acid-Schiff (PAS) and alkaline phosphatase (AP) or using antibodies to stage-specific embryonic antigen-1 (SSEA-1), fucosylated polylactosamine carbohydrate groups (EMA-1) and ovomucin-like protein (OLP). At primitive streak stages, turkey PGCs were located in the area pellucida. During stages 11 - 15, they were found in the blood reaching maximal numbers at stage 14. After stage 15, most PGCs were located outside the circulatory system. From stage 18, PGCs began to settle in gonadal ridges and after stage 28, PGCs were found only in the gonads. Turkey PGCs were isolated from the blood with a micropipette, during visual selection under the microscope, and their Identity confirmed using the above markers. These PGCs could be cultured on a gonadal stromal cell layer or on coverslips coated with rat-tail collagen. Isolated PGCs adhered to coated coverslips were prepared and examined with scanning electron microscope (SEM). Such cells had typical features of PGCs seen in situ and some had the morphology of motile cells. PGC movement in vitro, in response to a variety of potential chemoattractants, was then studied. Conventional chemotaxis assays could not be used to study such small numbers of cells. Therefore, the assay was carried out using a Dunn chemotaxis chamber which allows direct observation of cells and detailed analysis of their movement from a timed series of images. A positive chemotactic response was observed with cells exposed to a gradient of medium conditioned by stromal cells or 10 ng/ml transforming growth factor beta-1 (TGFbeta1). Cells exposed to 100 ng/ml stem cell factor (SCF) or control medium showed no such response. These observations indicate that TGF?l can play a role in directed migration of PGCs in vitro, but further experiments are required to determine whether this factor is similarly involved in vivo.

Книги з теми "Germ cells":

1
Sassone-Corsi, Paolo, Margaret T. Fuller, and Robert Braun. Germ cells. Cold Spring Harbor, N.Y: Cold Spring Harbor Laboratory Press, 2011.
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2
Jacobsen, G. Krag. Atlas of germ cells tumours. Copenhagen: Munksgaard, 1989.
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3
Orwig, Kyle E. Male germline stem cells: Developmental regenerative potential. New York: Humana Press, 2011.
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4
Dadoune, Jean-Pierre. Histoire ordinaire et extraordinaire des cellules sexuelles. Paris: Hermann, 2011.
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5
Raghavan, Derek. Germ cell tumors. Hamilton [Ont.]: BC Decker, 2003.
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6
Germ, Cell Tumour Conference (4th 1997 Leeds England). Germ cell tumours IV: The proceedings of the fourth Germ Cell Tumour Conference, Leeds, November 1997. London: John Libbey, 1998.
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7
Goldstein, L. S. Radiation-induced germ cell mutations-- their detection and modification. Washington, DC: Defense Nuclear Agency, 1987.
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8
Goldstein, L. S. Radiation-induced germ cell mutations-- their detection and modification. Washington, DC: Defense Nuclear Agency, 1987.
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9
Goldstein, L. S. Radiation-induced germ cell mutations-- their detection and modification. Washington, DC: Defense Nuclear Agency, 1987.
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10
Symposium, on the Molecular and Cellular Biology of Fertilization (1984 University of California Davis). The molecular and cellular biology of fertilization. New York: Plenum Press, 1986.
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Частини книг з теми "Germ cells":

1
Wu, Ji, Zhuxia Zheng, Hu Wang, Xingxing Mei, Xingbao Ding, and Xiaoyong Li. "Primordial Germ Cells and Germ Line Stem Cells." In Translational Medicine Research, 3–28. Dordrecht: Springer Netherlands, 2015. http://dx.doi.org/10.1007/978-94-017-7273-0_1.
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2
Timson, David J., Richard J. Reece, James B. Thoden, Hazel M. Holden, Andrea L. Utz, Beverly M. K. Biller, Eugen-Matthias Strehle, et al. "Germ Cells Aplasia." In Encyclopedia of Molecular Mechanisms of Disease, 696. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_6809.
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3
Tagami, Takahiro, Daichi Miyahara, and Yoshiaki Nakamura. "Avian Primordial Germ Cells." In Advances in Experimental Medicine and Biology, 1–18. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-3975-1_1.
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Nagano, Makoto C. "Germ Line Stem Cells." In Stem Cells in Endocrinology, 23–47. Totowa, NJ: Humana Press, 2005. http://dx.doi.org/10.1385/1-59259-900-1:023.
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5
Labosky, Patricia A., and Brigid L. M. Hogan. "Mouse Primordial Germ Cells." In METHODS IN MOLECULAR BIOLOGY™, 187–99. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-483-8_12.
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Chang, M. C. "Fertilizability of Rabbit Germ Cells." In Ciba Foundation Symposium - Mammalian Germ Cells, 226–42. Chichester, UK: John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470718841.ch20.
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Popescu, P., Y. Rumpler, O. Gabriel-Robez, F. J. Ectors, and L. Koulischer. "Methods of Germ Cells Study." In Techniques in Animal Cytogenetics, 85–102. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-59711-4_4.
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McLaren, Anne. "Primordial Germ Cells in Mammals." In Organization of the Early Vertebrate Embryo, 1–9. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-1618-1_1.
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Gupta, Mukesh Kumar, and Hoon Taek Lee. "Differences Between Germ-Line Stem Cells and Multipotent Adult Germ-Line Stem Cells for MicroRNAs." In Stem Cells and Cancer Stem Cells, Volume 6, 113–29. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-2993-3_11.
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Mardanpour, Parisa, Kaomei Guan, Tamara Glaeser, Jae Ho Lee, Jessica Nolte, Gerald Wulf, Gerd Hasenfuss, Wolfgang Engel, Oliver Brüstle, and Karim Nayernia. "Reprogramming Male Germ Cells to Pluripotent Stem Cells." In Trends in Stem Cell Biology and Technology, 71–81. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-905-5_5.
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Тези доповідей конференцій з теми "Germ cells":

1
Hua, Jinlian, and Zhongying Dou. "Insulin-secreting cells differentiation derived from human embryonic germ cells." In 2010 3rd International Conference on Biomedical Engineering and Informatics (BMEI). IEEE, 2010. http://dx.doi.org/10.1109/bmei.2010.5640541.
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Morita, Ritsuko, Kazuhisa Nakao, Miho Ogawa, Yasumitsu Saji, Kentaro Ishida, and Takashi Tsuji. "Pluripotent stem cells developed into regenerated tooth by organ germ method in combination with tooth germ-derived epithelium." In 2007 International Symposium on Micro-NanoMechatronics and Human Science. IEEE, 2007. http://dx.doi.org/10.1109/mhs.2007.4420853.
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Papa, J. P., M. E. M. Gutierrez, R. Y. M. Nakamura, L. P. Papa, I. B. F. Vicentini, and C. A. Vicentini. "Automatic classification of fish germ cells through optimum-path forest." In 2011 33rd Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2011. http://dx.doi.org/10.1109/iembs.2011.6091259.
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Varghese, Shyni, Paranduangji Theprungsirikul, Angela Ferran, Nathaniel Hwang, Adam Canver, and Jennifer Elisseeff. "Chondrogenic differentiation of human embryonic germ cell derived cells in hydrogels." In Conference Proceedings. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2006. http://dx.doi.org/10.1109/iembs.2006.4397989.
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Varghese, Shyni, Paranduangji Theprungsirikul, Angela Ferran, Nathaniel Hwang, Adam Canver, and Jennifer Elisseeff. "Chondrogenic differentiation of human embryonic germ cell derived cells in hydrogels." In Conference Proceedings. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2006. http://dx.doi.org/10.1109/iembs.2006.259710.
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Schmidtová, S., K. Gerčáková, K. Kaláavská, M. Mego, and L. Kučerová. "PO-478 Chemosensitization of cisplatin-resistant testicular germ cell tumours cells." In Abstracts of the 25th Biennial Congress of the European Association for Cancer Research, Amsterdam, The Netherlands, 30 June – 3 July 2018. BMJ Publishing Group Ltd, 2018. http://dx.doi.org/10.1136/esmoopen-2018-eacr25.497.
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Huang, Tsung-Tao, Yu-Hsiang Tang, Ming-Hua Shiao, and Hung-Wei Liu. "Development and Application of Novel Microfluidic Culture Chips for Germ Cells." In 2019 IEEE 19th International Conference on Nanotechnology (IEEE-NANO). IEEE, 2019. http://dx.doi.org/10.1109/nano46743.2019.8993901.
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Bugao Li, Xiaohong Guo, and Li Zhang. "Characterization of a fertility candidate gene Ccdc79 in meiotic germ cells." In 2011 International Conference on Remote Sensing, Environment and Transportation Engineering (RSETE). IEEE, 2011. http://dx.doi.org/10.1109/rsete.2011.5966088.
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Looijenga, Leendert H. J., Hendrik Wermann, Ad Gillis, Friedemann Honecker, Ole Ammerpohl, Julie Richter, Wolter Oosterhuis, and Carsten Bokemeyer. "Abstract LB-67: Global DNA methylation in fetal human germ cells and germ cell tumors: correlation with differentiation and cisplatin resistance." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-lb-67.
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Bhartiya, J., and H. C. Bhartiya. "Impact of WR-2721 on X-ray induced alterations in germ cells of male mouse." In Proceedings of the Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 1988. http://dx.doi.org/10.1109/iembs.1988.95371.
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Звіти організацій з теми "Germ cells":

1
Braydich-Stolle, Laura K., Saber Hussain, John J. Schlager, and Marie-Claude Hofmann. Effect of Silver Nanoparticles on SRC Activity in Male Germ-line Stem Cells. Fort Belvoir, VA: Defense Technical Information Center, March 2006. http://dx.doi.org/10.21236/ada444778.
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2
Kwan, Amy, and Danish Mazhar. The management of advanced germ cell tumours. BJUI Knowledge, January 2020. http://dx.doi.org/10.18591/bjuik.0659.
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3
Foulkes, William D., Lesley Alpert, Louise Quenneville, and Gilles Tremblay. Is Breast Tissue from Women Who Carry Germ-Line BRCA1 or BRCA2 Mutations Normal"? - An Immuno-Histopathological Study". Fort Belvoir, VA: Defense Technical Information Center, August 2003. http://dx.doi.org/10.21236/ada419802.
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4
Foulkes, William D., L. Alpert, J. Deschenes, and G. Tremblay. Is Breast Tissue from Women Who Carry Germ-Line BRCA1 or BRCA2 Mutations Normal"? An Immuno-Histopathological Study". Fort Belvoir, VA: Defense Technical Information Center, August 2002. http://dx.doi.org/10.21236/ada409774.
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Pretlow, Thomas G. Prostatic Fluid Cells. Fort Belvoir, VA: Defense Technical Information Center, May 2005. http://dx.doi.org/10.21236/ada439716.
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Pretlow, Thomas G. Prostatic Fluid Cells. Fort Belvoir, VA: Defense Technical Information Center, April 2003. http://dx.doi.org/10.21236/ada415846.
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Pretlow, Thomas G. Prostatic Fluid Cells. Fort Belvoir, VA: Defense Technical Information Center, April 2002. http://dx.doi.org/10.21236/ada406134.
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Gur, Ilan. Nanocrystal Solar Cells. Office of Scientific and Technical Information (OSTI), January 2006. http://dx.doi.org/10.2172/922721.
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Pretlow, Thomas G. Prostatic Fluid Cells. Fort Belvoir, VA: Defense Technical Information Center, April 2004. http://dx.doi.org/10.21236/ada434468.
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Dooner, Mark, Jason M. Aliotta, Jeffrey Pimental, Gerri J. Dooner, Mehrdad Abedi, Gerald Colvin, Qin Liu, Heinz-Ulli Weier, Mark S. Dooner, and Peter J. Quesenberry. Cell Cycle Related Differentiation of Bone Marrow Cells into Lung Cells. Office of Scientific and Technical Information (OSTI), December 2007. http://dx.doi.org/10.2172/936517.
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