Literatura académica sobre el tema "Protein and mRNA levels"
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Artículos de revistas sobre el tema "Protein and mRNA levels"
Berger, Lloyd C., Jnanankur Bag y Bruce H. Sells. "Translation of poly(A)-binding protein mRNA is regulated by growth conditions". Biochemistry and Cell Biology 70, n.º 9 (1 de septiembre de 1992): 770–78. http://dx.doi.org/10.1139/o92-117.
Texto completoGerstenfeld, L. C., M. H. Finer y H. Boedtker. "Altered beta-actin gene expression in phorbol myristate acetate-treated chondrocytes and fibroblasts". Molecular and Cellular Biology 5, n.º 6 (junio de 1985): 1425–33. http://dx.doi.org/10.1128/mcb.5.6.1425-1433.1985.
Texto completoGerstenfeld, L. C., M. H. Finer y H. Boedtker. "Altered beta-actin gene expression in phorbol myristate acetate-treated chondrocytes and fibroblasts." Molecular and Cellular Biology 5, n.º 6 (junio de 1985): 1425–33. http://dx.doi.org/10.1128/mcb.5.6.1425.
Texto completoWillis, Dianna E., Erna A. van Niekerk, Yukio Sasaki, Mariano Mesngon, Tanuja T. Merianda, Gervan G. Williams, Marvin Kendall, Deanna S. Smith, Gary J. Bassell y Jeffery L. Twiss. "Extracellular stimuli specifically regulate localized levels of individual neuronal mRNAs". Journal of Cell Biology 178, n.º 6 (4 de septiembre de 2007): 965–80. http://dx.doi.org/10.1083/jcb.200703209.
Texto completoVeletza, S. V., K. V. Nichols, I. Gross, H. Lu, D. W. Dynia y J. Floros. "Surfactant protein C: hormonal control of SP-C mRNA levels in vitro". American Journal of Physiology-Lung Cellular and Molecular Physiology 262, n.º 6 (1 de junio de 1992): L684—L687. http://dx.doi.org/10.1152/ajplung.1992.262.6.l684.
Texto completoMaicas, E., F. G. Pluthero y J. D. Friesen. "The accumulation of three yeast ribosomal proteins under conditions of excess mRNA is determined primarily by fast protein decay". Molecular and Cellular Biology 8, n.º 1 (enero de 1988): 169–75. http://dx.doi.org/10.1128/mcb.8.1.169-175.1988.
Texto completoMaicas, E., F. G. Pluthero y J. D. Friesen. "The accumulation of three yeast ribosomal proteins under conditions of excess mRNA is determined primarily by fast protein decay." Molecular and Cellular Biology 8, n.º 1 (enero de 1988): 169–75. http://dx.doi.org/10.1128/mcb.8.1.169.
Texto completoChen, Xu-Qiao, Carlos A. Barrero, Rodrigo Vasquez-Del Carpio, E. Premkumar Reddy, Chiara Fecchio, Salim Merali, Alessia Deglincerti, Cheng Fang, Jack Rogers y Maria L. Maccecchini. "Posiphen Reduces the Levels of Huntingtin Protein through Translation Suppression". Pharmaceutics 13, n.º 12 (7 de diciembre de 2021): 2109. http://dx.doi.org/10.3390/pharmaceutics13122109.
Texto completoFortelny, Nikolaus, Christopher M. Overall, Paul Pavlidis y Gabriela V. Cohen Freue. "Can we predict protein from mRNA levels?" Nature 547, n.º 7664 (julio de 2017): E19—E20. http://dx.doi.org/10.1038/nature22293.
Texto completoWatkins, David C., Peter J. Rapiejko, Manuel Ros, Hsien-yu Wang y Craig C. Malbon. "G-Protein mRNA levels during adipocyte differentiation". Biochemical and Biophysical Research Communications 165, n.º 3 (diciembre de 1989): 929–34. http://dx.doi.org/10.1016/0006-291x(89)92692-2.
Texto completoTesis sobre el tema "Protein and mRNA levels"
Simion, Oana-Maria. "Uncoupling proteins mRNA levels in mice lacking acylation-stimulating protein". Thesis, McGill University, 2001. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=33018.
Texto completoIn male ASP-deficient mice mRNA levels were measured by semi-quantitative RT-PCR and the following changes were observed: UCP-1 decreased in all tested tissues, UCP-2 increased by 15% and 6 fold in muscle and white adipose tissue and UCP-3 increased 2.5 and 10 fold in muscle and epididymal adipose tissue, respectively. In female ASP-deficient mice UCP-1 decreased in all tissues, UCP-2 increased by 10% and 40% in inguinal and brown adipose tissue, respectively, and UCP-3 remained stable in all tissues. High fat diet nullified these differences, and decreased all wild-type UCP levels.
We propose that UCP-2 and 3 assume the role of UCP-1 in fuel utilization, thus helping mice face an increased energy load in the absence of ASP.
Byström, Jonas. "Eosinophil Cationic Protein : Expression Levels and Polymorphisms". Doctoral thesis, Uppsala University, Department of Medical Sciences, 2002. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-2059.
Texto completoThe eosinophil cationic protein (ECP) is usually associated with the eosinophil granulocyte. In this thesis the presence and production of this protein has been studied in two other cells. The circulating monocyte was found to contain ECP mRNA and small amounts of ECP, one thousand times less than that found in the eosinophil. The production decreased by differentiation of the myelomonoblastic cell line U937 into a macrophage phenotype. Submucosal lung macrophages did not stain for ECP and alveolar macrophages did not contain ECP mRNA. The circulating neutrophil contains ECP at a level hundred fold less than the eosinophil. We found that the protein is located to the primary granules of the neutrophil but could detect no ECP mRNA in the cell. It was shown in vitro that the protein was taken up by the cell and partly transported to the primary granules. The uptake did not seem to be receptor mediated. Upon stimulation of the neutrophils, ECP previously taken up, was re-secreted.
The ECP protein is heterogeneous both to molecular characteristics and to function. To evaluate if a genetic component is involved, the ECP gene was analysed in 70 individuals. Three single nucleotide polymorphisms (SNP´s) were found, denoted 277(C>T), 434(G>C) and 562(G>C). The two first were located to the mature peptide-coding region and would change the amino acids, arg45cys and arg97thr. The prevalence of the most common SNP, 434, was evaluated in two eosinophil-related diseases, allergy/asthma and Hodgkin Lymphoma (HL). Forty-three HL patients were evaluated and it was found that the 434GG was significantly more prevalent in patients having nodular sclerosis (NS) as compared to other histologies (p=0.03). Erythrocyte sedimentation rate was also related to the 434GG genotype (p=0.009). In 209 medical students 434GG was more common (p=0.002) in those who indicated allergy. The genotype was unrelated to the production of IgE antibodies to allergens. In analysis of 76 subjects with asthma it was found that the 434GG genotype was significantly more common among allergic asthmatics (p=0.04). Asthma and HL-NS are characterized by fibrosis and eosinophils and ECP has been suggested in fibrosis development.
Kachra, Zarin. "Regulation of insulin-like growth factor-I (IGF-I) and IGF-binding protein-1 (IGFBP-1) mRNA levels in cultured rat hepatocytes". Thesis, McGill University, 1993. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=41300.
Texto completoIGF-I mRNA levels were stimulated 2.0 to 2.5 fold by bovine growth hormone (bGH) and 1.8 to 2.0 fold by glucagon but on combining bGH and glucagon, a synergistic effect was observed and IGF-I mRNA level was augmented 10 to 12 fold. Octreotide blocked the hGH induced stimulation of IGF-I production in serum and hepatic IGF-I mRNA levels in hypophysectomized rats. This effect could have been partly due to the low levels of glucagon in serum when hypophysectomized rats were treated with hGH and octreotide. Octreotide was also found to inhibit GH stimulated IGF-I mRNA levels in rat hepatocytes.
The unique synergy observed with glucagon and bGH on IGF-I mRNA levels in hepatocytes was not reproduced by T$ sb3$, oPRL, dexamethasone, EGF or insulin when each was added in combination with bGH or glucagon. Like glucagon, the addition of IBMX or (Bu)$ sb2$cAMP stimulated IGF-I mRNA levels 1.8 to 2.0 fold, but in the presence of bGH, IGF-I mRNA levels were stimulated 10 to 12 fold. PMA stimulated IGF-I mRNA levels 1.2 to 1.4 fold but displayed no synergism when added with bGH. The stimulatory effect of bGH plus glucagon on IGF-I mRNA levels was inhibited in PKC depleted cells, in the presence of inhibitors of PKC and in the presence of cycloheximide. bGH had no posttranscriptional effect on IGF-I mRNA stability whereas glucagon or (Bu)$ sb2$cAMP stabilized IGF-I mRNA at a posttranscriptional level.
In summary, the major hormonal regulators of hepatic IGF-I mRNA levels appear to be GH and glucagon. Hepatic IGF-I mRNA levels are regulated by pathways involving protein kinase C and, protein kinase A as well as by synthesis of one or more protein(s).
Glucagon and dexamethasone each stimulated IGFBP-1 mRNA levels 3 to 4 fold whereas bGH and T$ sb3$ each inhibited IGFBP-1 mRNA levels 45 to 70%. Insulin, which inhibited IGFBP-1 mRNA levels 95%, was the most powerful inhibitor and was also found to inhibit IGFBP-1 mRNA levels in the presence of dexamethasone. IBMX and (Bu)$ sb2$cAMP stimulated IGFBP-1 mRNA levels 6 to 8 fold whereas PMA inhibited IGFBP-1 mRNA levels 40 to 50%. The inhibitory effect of bGH on IGFBP-1 mRNA levels was abolished in PKC depleted cells and also in the presence of inhibitors of PKC. In the presence of cycloheximide, IGFBP-1 mRNA was superinduced by bGH. bGH had no posttranscriptional effect on IGFBP-1 mRNA whereas glucagon and (Bu)$ sb2$cAMP stabilized IGFBP-1 mRNA at a postranscriptional level.
In summary, bGH, T$ sb3$ and insulin inhibited whereas dexamethasone and glucagon stimulated IGFBP-1 mRNA levels in hepatocytes. Effect of glucagon may be via elevation of cAMP levels, whereas the effect of bGH may be via activation of PKC levels. The inhibitory effect of bGH appears to require synthesis of one or more protein(s) besides stimulation of PKC levels.
Schwanhäußer, Björn. "Global analysis of cellular protein dynamics by pulse-labeling and quanti tati ve mass spectrometry". Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2011. http://dx.doi.org/10.18452/16305.
Texto completoThe first part of the thesis describes the establishment of a modified version of the classic SILAC approach routinely used in quantitative mass spectrometry (MS) to assay relative changes in protein levels. In the newly-devised approach termed pulsed SILAC (pSILAC) differentially treated cells are transferred to culture medium supplemented with different versions of stable-isotope labeled heavy amino acids. As MS-based relative quantification is exclusively based on the newly-synthesized heavy protein amounts the method enables the detection of differences in protein production resulting from the treatment. The second part of the thesis shows the use of pSILAC to globally quantify the impact of microRNAs onto the proteome. Ectopic over-expression or knock-down of a single microRNA both affected protein production of hundreds of proteins. pSILAC identified several target genes as exclusively translationally regulated as changes in corresponding transcript levels were virtually absent. Measuring newly-synthesized protein amounts with heavy amino acids in a pulsed-labeling fashion has also been used to determine turnover rates of individual proteins, described in the third part of the present work. Along with transcript turnover as well as mRNA and protein levels they are essential for a dynamic description of gene expression. Simultaneous application of the nucleoside analogue 4-thiouridine (4sU) and heavy amino acids (SILAC) to metabolically label newly-produced mRNAs and proteins in mouse fibroblasts resulted in the calculation of mRNA and protein lifetimes and absolute levels for approximately 5,000 genes. While mRNA and protein levels were overall well correlated, a correlation between mRNA and protein half-lives was virtually absent. Yet this seemingly chaotic distribution of mRNA and protein half-lives was highly instructive since specific gene subsets have obviously evolved distinct combinations of half-lives that relate to their biological functions.
Van, Rooyen Marina. "The modulating effect of myo-inositol and other antidepressants on the mRNA levels and protein expression of selected subcellular enzymes / Marina van Rooyen". Thesis, North-West University, 2005. http://hdl.handle.net/10394/504.
Texto completoThesis (M.Sc. (Pharmacology))--North-West University, Potchefstroom Campus, 2005.
Peter, Martina Andrea. "Growth hormone-dependent expression and regulation of insulin-like growth factor (IGF) I and IGF binding protein mRNA levels in rat tissues in vivo /". [S.l.] : [s.n.], 1993. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=10291.
Texto completoKogan, Cary. "The expression of neurofilament protein and mRNA levels in the lateral geniculate nucleus and area V1 of the developing and adult vervet monkey (Ceorcopithicus aethiops) /". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape10/PQDD_0028/MQ50807.pdf.
Texto completoBeyerle, Jolantha [Verfasser] y Heinz [Akademischer Betreuer] Schmeiser. "Assessment of mRNA, protein levels and activities of xenobiotic metabolizing enzymes in colon and rectal mucosa of colorectal cancer patients / Jolantha Beyerle ; Betreuer: Heinz Schmeiser". Heidelberg : Universitätsbibliothek Heidelberg, 2016. http://d-nb.info/1180736281/34.
Texto completoArslan, Sevki. "Effects Of Benzene On Liver, Kidney And Lung Cyp1a, Cyp2b4, Cyp2e1 And Cyp3a6 Mrna, Protein Level, And Drug Metabolizing Enzyme Activities And Toxicity In Diabetic Rabbits". Phd thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/3/12609446/index.pdf.
Texto completoBeresford, Guy William. "Control of glucokinase and mRNA levels in hepatocytes". Thesis, University of Newcastle Upon Tyne, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.386292.
Texto completoLibros sobre el tema "Protein and mRNA levels"
Lynne, Maquat, ed. Nonsense-mediated mRNA decay. Georgetown, Tex: Landes Bioscience, 2006.
Buscar texto completoBerry, Fred Brandon. Calmodulin protein and mRNA expression during postmatal development of the rat brain. Ottawa: National Library of Canada, 1995.
Buscar texto completoJ, Kay, Ballard F. J y Mayer R. J, eds. Gene expression: Regulation at the RNA and protein levels. London: Biochemical Society, 1989.
Buscar texto completoKovalchuke, Lyudmila. Regulation of Parkin Protein Levels by L-3,4-dihydroxyphenylalanine. [New York, N.Y.?]: [publisher not identified], 2018.
Buscar texto completoD, Takezawa y United States. National Aeronautics and Space Administration., eds. Calmodulin gene family in potato: Developmental and touch-induced expression of the mRNA encoding a novel isoform. [Washington, D.C: National Aeronautics and Space Administration, 1997.
Buscar texto completoNargolwalla, Cyra. Modulation of mRNA levels for tPA, PAI-1 & TGF-gbs in rat testicular somatic cells. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1991.
Buscar texto completoManzerra, Pasquale. Expression of constitutive hsc70 and stress-inducible hsp70 mRNA and protein in the rabbit central nervous system. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1997.
Buscar texto completoStevens, Miata Yvette. Corticotropin-releasing hormone receptor subtype 1 and subtype mRNA expression and protein localization in the myometruim in pregnanct. Ottawa: National Library of Canada, 1998.
Buscar texto completoMyllynen, Jenni Eileen. The effect of nerve-mediated activity on the expression of Muscle Regulatory Factor and Myosin Heavy Chain Protein mRNA transcripts. Sudbury, Ont: Laurentian University, Behavioural Neuroscience Program, 1997.
Buscar texto completoOwh, Phillip. Myelin basic protein up-regulates CD44 levels in an astrocytoma cell line in vitro. Ottawa: National Library of Canada, 1996.
Buscar texto completoCapítulos de libros sobre el tema "Protein and mRNA levels"
Matsumoto, Ayaka, Nariaki Matsuura y Miki Hieda. "Detection of SUN1 Splicing Variants at the mRNA and Protein Levels in Cancer". En The LINC Complex, 307–19. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-8691-0_21.
Texto completoArnoldi, Michele, Giulia Zarantonello, Stefano Espinoza, Stefano Gustincich, Francesca Di Leva y Marta Biagioli. "Design and Delivery of SINEUP: A New Modular Tool to Increase Protein Translation". En Methods in Molecular Biology, 63–87. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2010-6_4.
Texto completoZhou, Haiyan. "Design of Bifunctional Antisense Oligonucleotides for Exon Inclusion". En Methods in Molecular Biology, 53–62. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2010-6_3.
Texto completoSmeland, Erlend B., Tore Godal, Klaus Beiske, Rosemary Watt, Susan Pfeifer-Ohlsson y Rolf Ohlsson. "Regulation of c-myc mRNA and Protein Levels During Activation of Normal Human B Cells". En Current Topics in Microbiology and Immunology, 290–96. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71562-4_43.
Texto completoBradbury, Joshua J., Holly E. Lovegrove, Marta Giralt-Pujol y Shane P. Herbert. "Analysis of mRNA Subcellular Distribution in Collective Cell Migration". En Cell Migration in Three Dimensions, 389–407. New York, NY: Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-2887-4_22.
Texto completoMirlekar, Bhalchandra, Daniel Michaud y Yuliya Pylayeva-Gupta. "IL-35 Detection in B Cells at the mRNA and Protein Level". En Methods in Molecular Biology, 125–47. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1237-8_8.
Texto completoFawcett, Tony, William J. Simon, John Shanklin y Antoni R. Slabas. "Expression of MRNA and Steady-State Levels of Protein Isoforms of Enoyl-ACP Reductase From Brassica napus". En Plant Lipid Metabolism, 90–92. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-015-8394-7_25.
Texto completoBoudreau-Larivière, Céline, Roxanne Y. Y. Chan y Bernard J. Jasmin. "Activity-Linked Regulation of Acetylcholinesterase mRNA Levels Involves Distinct Molecular Mechanisms in Developing Versus Adult Skeletal Muscles". En Structure and Function of Cholinesterases and Related Proteins, 128–29. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4899-1540-5_26.
Texto completoLackner, K. J., W. März, G. Wolter, H. Sartor y W. Gross. "Anabolic Steroids do not Change mRNA Levels and Protein Secretion of Apolipoprotein A-I and B-100 in HepG2 Cells". En Recent Developments in Lipid and Lipoprotein Research, 151–56. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-84855-1_18.
Texto completoMatsuno, Akira, Yudo Ishii, Mineko Murakami, Katsumi Hoya, Shoko M. Yamada, Shinya Miyamoto, Jae-Hyun Son et al. "Quantum Dot-Based In Situ Hybridization and Immunohistochemistry to Detect mRNA and Protein at Subcellular Levels, Comparison with Studies Using Electron Microscopy". En In Situ Hybridization Methods, 417–25. New York, NY: Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2303-8_22.
Texto completoActas de conferencias sobre el tema "Protein and mRNA levels"
Ohlsson, M., A. J. W. Hsueh y T. Ny. "HORMONE REGULATION OF THE FIBRINOLYTIC SYSTEM IN THE OVARY". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644389.
Texto completoMsdcalf, R. L., E. K. O. Kruithof y W.-D. Schleuning. "TRANSIENT INDUCTION OF PLASMINOGEN ACTIVATOR INHIBITOR 2 (PAI-2) GENE TRANSCRIPTION BY THE TUMOUR PROMOTING PHORBOL ESTER PMA IN THE HUMAN MACROPHAGE-LIKE CELT, LINE U-937". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642857.
Texto completoApostolatos, Christopher, Tracess Smalley y Mildred A. Duncan. "Abstract 3934: Analysis of PKC-ζ protein and mRNA levels in normal and malignant breast tissue". En Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-3934.
Texto completoSchützle, H., M. Weis-Klemm, RE Gay, S. Gay y WK Aicher. "THU0049 Protein kinase inhibition enhances steady state mrna levels encoding il -16 but reduces il-18 encoding message levels in fibroblasts". En Annual European Congress of Rheumatology, Annals of the rheumatic diseases ARD July 2001. BMJ Publishing Group Ltd and European League Against Rheumatism, 2001. http://dx.doi.org/10.1136/annrheumdis-2001.846.
Texto completoAndreasen, P. A., A. Riccio, L. R. Lund, K. G. Welinder, F. Blasi y K. Danø. "PLASMINOGEN ACTIVATOR INHIBITOR TYPE 1: STUDIES ON STRUCTURE AND REGULATION". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642810.
Texto completoAntonacopoulou, A., A. Kottorou, V. Tzelepi, F. Dimitrakopoulos, T. Makatsoris, A. Koutras y H. Kalofonos. "PO-513 The alternative NF-κB pathway in colorectal cancer. from genetic polymorphisms through mRNA to protein levels". En 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-eacr25.1014.
Texto completoMedcalf, R. L., E. van den Berg y W.-D. Schleuning. "THE INFLUENCE OF GLUCOCORTICOID HORMONES ON THE GENE TRANSCRIPTION OF POUR COMPONENTS OF THE FIBRINOLYTIC SYSTEM". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644611.
Texto completoYou, Jun, Clare E. Yellowley, Henry J. Donahue y Christopher R. Jacobs. "Physiological Levels of Substrate Deformation Are Less Stimulatory to Bone Cells Compared to Fluid Flow". En ASME 1999 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 1999. http://dx.doi.org/10.1115/imece1999-0427.
Texto completoKillian, Megan L. y Tammy L. Haut Donahue. "Effect of Pathological and Physiological Loads on Interleukin-1α Protein Production in Porcine Menisci". En ASME 2008 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2008. http://dx.doi.org/10.1115/sbc2008-192145.
Texto completoWheeler, Sarah, Raja Seethala, Doris Siwak, Kathleen Cieply, Carol Sherer, Gordon Mills, Jennifer R. Grandis y Ann Marie Egloff. "Abstract 4646: Evaluation of EGFR gene amplification status, mRNA, protein, and phosphoprotein levels expression in head and neck cancer patient tissues". En 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.am10-4646.
Texto completoInformes sobre el tema "Protein and mRNA levels"
Barash, Itamar y Robert E. Rhoads. Translational Mechanisms that Govern Milk Protein Levels and Composition. United States Department of Agriculture, noviembre de 2004. http://dx.doi.org/10.32747/2004.7586474.bard.
Texto completoBarash, Itamar y Robert Rhoads. Translational Mechanisms Governing Milk Protein Levels and Composition. United States Department of Agriculture, 2006. http://dx.doi.org/10.32747/2006.7696526.bard.
Texto completoYoung, Erin, Cem Kuscu, Christine Watkins y Murat Dogan. Using CRISPR Gene Editing to Prevent Accumulation of Lipids in Hepatocytes. University of Tennessee Health Science Center, enero de 2022. http://dx.doi.org/10.21007/com.lsp.2022.0007.
Texto completoStern, David y Gadi Schuster. Manipulation of Gene Expression in the Chloroplast. United States Department of Agriculture, septiembre de 2000. http://dx.doi.org/10.32747/2000.7575289.bard.
Texto completoMeidan, Rina y Robert Milvae. Regulation of Bovine Corpus Luteum Function. United States Department of Agriculture, marzo de 1995. http://dx.doi.org/10.32747/1995.7604935.bard.
Texto completoChristopher, David A. y Avihai Danon. Plant Adaptation to Light Stress: Genetic Regulatory Mechanisms. United States Department of Agriculture, mayo de 2004. http://dx.doi.org/10.32747/2004.7586534.bard.
Texto completoAbcouwer, Steve P. Demonstration that a mRNA Binding Protein is Responsible for GADD45 mRNA Destabilization. Fort Belvoir, VA: Defense Technical Information Center, mayo de 2003. http://dx.doi.org/10.21236/ada418512.
Texto completoWoodson, William, Shimon Mayak y Haim Rabinowitch. Physiological and Molecular Characterization of the Response to Ethylene during Senescence of Carnation Genotypic Variants. United States Department of Agriculture, julio de 1995. http://dx.doi.org/10.32747/1995.7613011.bard.
Texto completoFunkenstein, Bruria y Cunming Duan. GH-IGF Axis in Sparus aurata: Possible Applications to Genetic Selection. United States Department of Agriculture, noviembre de 2000. http://dx.doi.org/10.32747/2000.7580665.bard.
Texto completoYaron, Zvi, Martin P. Schreibman, Abigail Elizur y Yonathan Zohar. Advancing Puberty in the Black Carp (Mylopharyngodon Piceus) and the Striped Bass (Morone Saxatilis). United States Department of Agriculture, agosto de 1993. http://dx.doi.org/10.32747/1993.7568102.bard.
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