Literatura académica sobre el tema "Chicken embryogenesis"

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Artículos de revistas sobre el tema "Chicken embryogenesis":

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Dunon, D., J. Salomonsen, K. Skjødt, J. Kaufman y B. A. Imhof. "Ontogenic Appearance of MHC Class I (B-F) Antigens During Chicken Embryogenesis". Developmental Immunology 1, n.º 2 (1990): 127–35. http://dx.doi.org/10.1155/1990/75158.

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Expression of chicken MHC class (B-F) antigens during ontogeny was determined by binding of anticlass antibody and appearance of B-F transcripts by Northern blotting in chicken organs during embryogenesis until 2 weeks after hatching. MHC class transcripts first become detectable in day 6.5 of embryogenesis. B-F cell-surface expression first becomes detectable in hemopoietic organs by day 10‑12 of embryogenesis and somewhat later in nonhemopoietic organs. Flow cytometry analysis of hemopoietic cells throughout embryogenesis revealed B-Fhi and B-F1 cell populations. The percentage of B-F cells in spleen and bone marrow decreased around hatching, which could reflect either cell flows in these organs during this period or the sensitivity of hemopoietic cells to hatching stress.
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Frolova, Elena I., Valentina M. Fokina y David C. Beebe. "The expression pattern of opticin during chicken embryogenesis". Gene Expression Patterns 4, n.º 3 (mayo de 2004): 335–38. http://dx.doi.org/10.1016/j.modgep.2003.10.002.

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Kaspers, B., I. Schranner y U. Lösch. "Distribution of Immunoglobulins During Embryogenesis in the Chicken*". Journal of Veterinary Medicine Series A 38, n.º 1-10 (12 de febrero de 1991): 73–79. http://dx.doi.org/10.1111/j.1439-0442.1991.tb00986.x.

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Xu, Xuehong, MengMeng Xu, Odell D. Jones, Xunzhang Chen, Li Yanfei, Guifang Yan, Yuexing Pan et al. "Liquid Crystal in Lung Development and Chicken Embryogenesis". Molecular Crystals and Liquid Crystals 547, n.º 1 (30 de junio de 2011): 164/[1854]—172/[1862]. http://dx.doi.org/10.1080/15421406.2011.572042.

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Venturini, Loretta y Sheldon B. Sparber. "Salicylate and cocaine: interactive toxicity during chicken mid-embryogenesis". Free Radical Biology and Medicine 30, n.º 2 (enero de 2001): 198–207. http://dx.doi.org/10.1016/s0891-5849(00)00455-x.

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Gabriel, J. E., L. E. Alvares, C. C. P. Paz, I. U. Packer y L. L. Coutinho. "Temporal expression pattern of myostatin transcripts during chicken embryogenesis". Arquivo Brasileiro de Medicina Veterinária e Zootecnia 58, n.º 5 (octubre de 2006): 940–43. http://dx.doi.org/10.1590/s0102-09352006000500033.

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Wunsch, Ann M. y Arthur L. Haas. "Ubiquitin-protein conjugates selectively distribute during early chicken embryogenesis". Developmental Dynamics 204, n.º 2 (octubre de 1995): 118–32. http://dx.doi.org/10.1002/aja.1002040203.

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Yang, Seo Yeong, Hong Jo Lee, Hyung Chul Lee, Young Sun Hwang, Young Hyun Park, Tamao Ono y Jae Yong Han. "The dynamic development of germ cells during chicken embryogenesis". Poultry Science 97, n.º 2 (febrero de 2018): 650–57. http://dx.doi.org/10.3382/ps/pex316.

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Samak, Dalia H., Yasser S. El-Sayed, Hazem M. Shaheen, Ali H. El-Far, Mohamed E. Abd El-Hack, Ahmed E. Noreldin, Karima El-Naggar et al. "Developmental toxicity of carbon nanoparticles during embryogenesis in chicken". Environmental Science and Pollution Research 27, n.º 16 (29 de noviembre de 2018): 19058–72. http://dx.doi.org/10.1007/s11356-018-3675-6.

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Hartley, Rebecca S., Everett Bandman y Zipora Yablonka-Reuveni. "Skeletal muscle satellite cells appear during late chicken embryogenesis". Developmental Biology 153, n.º 2 (octubre de 1992): 206–16. http://dx.doi.org/10.1016/0012-1606(92)90106-q.

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Tesis sobre el tema "Chicken embryogenesis":

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Snell, Daniel C. "Cell-surface molecules of developing chicken B cells". Thesis, University of Reading, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326977.

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Hamer, Marcus Justin. "The regulation of hepatic phosphofructokinase in the embryo and neonate chicken". Thesis, University of Manchester, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.252712.

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Bell, George W. "Geisha: A Gallus (chicken) EST and in situ hybridization approach for identifying genes expressed during early embryogenesis". Diss., The University of Arizona, 2003. http://hdl.handle.net/10150/298791.

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With ever-increased quality and quantity of vertebrate genomic sequences, gene finding remains problematic, and predicting gene function from sequence remains a tremendous challenge. Nevertheless, similarity of sequence and patterns of gene expression are rapid methods for providing insight into potential functional roles of novel genes. For developmental studies, microarrays offer a means for screening a large number of sequences for expression within defined tissues and/or organs, but each experiment profiles expression level for only one anatomical region at one specific developmental stage. Whole mount in situ hybridization (ISH) offers an alternative approach that gives precise spatial and temporal resolution of gene expression throughout an embryo. I predicted that combined high throughput analysis of expressed sequence tags (ESTs) and whole mount ISH analysis of novel clones would effectively identify novel developmentally regulated avian genes. 5' ESTs were generated from randomly chosen cDNA clones of a chick late gastrula endoderm-mesoderm library. Following screening to remove ubiquitously expressed clones, internal clustering, and comparison to GenBank sequences, remaining cDNAs (both similar and dissimilar to known genes) were screened for expression in HH stage 4-12 embryos by automated high throughput whole mount ISH. Comparison to GenBank sequences by blastn and blastx (e < 0.05) revealed that one quarter of all 955 ESTs represented novel genes. Of these novel clones, ISH showed that about one quarter (60 clones) exhibited patterned expression during embryogenesis. EST sequences, ISH images and corresponding blast reports were assembled into a freely accessible Web database at http://geisha.biosci.arizona.edu.
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Kocamis, Hakan. "Functional profiles of growth related genes during embryogenesis and postnatal development of chicken and mouse skeletal muscle". Morgantown, W. Va. : [West Virginia University Libraries], 2001. http://etd.wvu.edu/templates/showETD.cfm?recnum=2026.

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Thesis (Ph. D.)--West Virginia University, 2001.
Title from document title page. Document formatted into pages; contains ix, 109 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 88-104).
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Sarver, Amy G. "The ontogeny of myogenic regulatory factor expression during muscle differentiation in the biceps femoris and pectoralis major muscles of the chicken Appendix I. Isolation and characterization of microsatellite DNA in rainbow trout ; Appendix II. Analysis of myostatin expression during embryogenesis of the rainbow trout /". Morgantown, W. Va. : [West Virginia University Libraries], 2001. http://etd.wvu.edu/templates/showETD.cfm?recnum=2080.

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Thesis (M.S.)--West Virginia University, 2001.
Title from document title page. Document formatted into pages; contains vii, 78 p. : ill. (some col.). Vita. Includes abstract. Includes bibliographical references (p. 52-62).
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Johnson, Christopher Derek Martin. "Growth hormone in chick embryogenesis". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ28952.pdf.

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Leclerc, Benoît. "Studies on prolactin and its receptor during late embryogenesis in turkeys and chickens". Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=102673.

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Changes in the levels of expression of the prolactin receptor (PRLR) mRNA in the pituitary gland, hypothalamus, liver, pancreas, kidney and gonad from embryonic day (ED) 15 and ED21 to 1 day post-hatch, respectively, in chickens and turkeys were measured by real-time PCR. In both species, PRLR mRNA increased from low levels during the last week of ED to reach maxima at the peri-hatch period. Similarly, circulating levels of prolactin (PRL) also increased during this interval and were correlated with the observed increases in tissue content of PRLR mRNA. This suggested that PRL was up-regulating its own receptor during late embryogenesis. In support of this, in vitro stimulation of the pituitary gland of turkeys with VIP on ED24 resulted in a 4 fold and 3 fold increase in PRL and PRLR, respectively. Stimulation with VIP of either the hypothalamus or gonad had no effect on either levels of the PRLR transcript. This suggests that VIP acts indirectly through increased PRL to upregulate the number of receptors. In order to investigate the transcription of genes that may be induced/suppressed by PRL, suppressive subtractive hybridization (SSH) libraries from control or VIP stimulated ED24 turkey pituitary glands were constructed. Stimulation with VIP resulted in a 5.7 and 2.8 fold increase in media and pituitary content of PRL, respectively. The changes in PRL were consistent with endogenous levels of PRL observed just prior to hatch. Following sequence analysis of random clones (n=96) from each library, a total of 145 non-redundant putative genes were obtained. About 51% of the putative genes have as yet no assigned function, whereas, 15% were housekeeping genes and 34% had known functions within various pathways. Real-time PCR was used to confirm the differential expression of 21 of these genes in VIP treated and control pituitaries. Since the majority of these genes were expressed at levels consistent with the direction of subtraction, these data suggest that these libraries may be useful to study the direct and indirect effects of increasing levels of PRL on anterior pituitary function at about the time of hatch.
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Simon, Horst Hubertus. "Development of the efferent system in the segmented chick brainstem". Thesis, King's College London (University of London), 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307096.

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Myat, Anna. "Chick homologues of Notch, Delta and Serrate : their roles in the developing inner ear and elsewhere". Thesis, University of Oxford, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296937.

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Kim, Min Jung. "Characterization of agrin function in chicken and zebrafish embryogenesis". 2004. http://www.lib.ncsu.edu/theses/available/etd-06302004-214359/unrestricted/etd.pdf.

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Libros sobre el tema "Chicken embryogenesis":

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A. Sobolewska, G. Elminowska-Wenda, J. Bogucka, M. Szpinda, K. Walasik*, A. Dankowiakowska, W. Jóźwicki, H. Wiśniewska y M. Bednarczyk. The effect of two different green lighting schedules during embryogenesis on myogenesis in broiler chickens. Verlag Eugen Ulmer, 2019. http://dx.doi.org/10.1399/eps.2019.281.

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Capítulos de libros sobre el tema "Chicken embryogenesis":

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von Thülen, Berend, Reinhold Janocha y Jürgen Niessing. "Expression Profile of Two Homeoboxgenes during Chicken Embryogenesis". En Developmental Patterning of the Vertebrate Limb, 57–59. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3310-8_9.

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Actas de conferencias sobre el tema "Chicken embryogenesis":

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Aygün, Ali y Doğan Narinç. "The effects of thermal manipulations during embryogenesis of broiler chicks on growth of embryo and skeletal traits". En INTERNATIONAL CONFERENCE ON ADVANCES IN NATURAL AND APPLIED SCIENCES: ICANAS 2016. Author(s), 2016. http://dx.doi.org/10.1063/1.4945841.

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