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Artykuły w czasopismach na temat "GABA"

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Akasu, Takashi, Yoshikazu Munakata, Masashi Tsurusaki, and Hiroshi Hasuo. "Role of GABAA and GABAC Receptors in the Biphasic GABA Responses in Neurons of the Rat Major Pelvic Ganglia." Journal of Neurophysiology 82, no. 3 (1999): 1489–96. http://dx.doi.org/10.1152/jn.1999.82.3.1489.

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The role of γ-aminobutyric acid-A (GABAA) and GABAC receptors in the GABA-induced biphasic response in neurons of the rat major pelvic ganglia (MPG) were examined in vitro. Application of GABA (100 μM) to MPG neurons produced a biphasic response, an initial depolarization (GABAd) followed by a hyperpolarization (GABAh). The input resistance of the MPG neurons was decreased during the GABAd, whereas it was increased during the GABAh. The GABAd could be further separated into the early component (early GABAd) with a duration of 27 ± 5 s (mean ± SE; n = 11) and the late component (late GABAd) wit
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Qian, H., and J. E. Dowling. "GABAA and GABAC receptors on hybrid bass retinal bipolar cells." Journal of Neurophysiology 74, no. 5 (1995): 1920–28. http://dx.doi.org/10.1152/jn.1995.74.5.1920.

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1. gamma-Aminobutyric acid (GABA) responses from solitory hybrid bass retinal bipolar cells were studied with the use of conventional and perforated whole cell patch-clamp recording. 2. GABA elicited a chloride current in bipolar cells that had both transient and sustained components. The transient component was sensitive to bicuculline and resembled GABAA-mediated currents, whereas the more sustained component was resistant to bicuculline and resembled the responses mediated by GABAC receptors. 3. The bicuculline-resistant GABA responses recorded from the bipolar cells could not be modulated
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Jackel, C., W. Krenz, and F. Nagy. "BICUCULLINE/BACLOFEN-INSENSITIVE GABA RESPONSE IN CRUSTACEAN NEURONES IN CULTURE." Journal of Experimental Biology 191, no. 1 (1994): 167–93. http://dx.doi.org/10.1242/jeb.191.1.167.

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Neurones were dissociated from thoracic ganglia of embryonic and adult lobsters and kept in primary culture. When gamma-aminobutyric acid (GABA) was applied by pressure ejection, depolarizing or hyperpolarizing responses were produced, depending on the membrane potential. They were accompanied by an increase in membrane conductance. When they were present, action potential firing was inhibited. The pharmacological profile and ionic mechanism of GABA-evoked current were investigated under voltage-clamp with the whole-cell patch-clamp technique. The reversal potential of GABA-evoked current depe
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Zhang, J., and M. M. Slaughter. "Preferential suppression of the ON pathway by GABAC receptors in the amphibian retina." Journal of Neurophysiology 74, no. 4 (1995): 1583–92. http://dx.doi.org/10.1152/jn.1995.74.4.1583.

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1. Electrophysiological recordings were obtained from neurons in the amphibian intact retina and retinal slice preparations. The effects of gamma-aminobutyric acid (GABA) were evaluated in the presence of bicuculline or SR95531, which block the GABAA receptor, and baclofen, which saturates the GABAB receptor. 2. Under these conditions, GABA preferentially reduced ON light responses in amacrine and ganglion cells, apparently through a presynaptic mechanism that reduced bipolar cell input. GABA also produced a small hyperpolarization in the resting membrane potential of ganglion cells. 3. Picrot
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Naffaa, Moawiah M., David E. Hibbs, Mary Chebib та Jane R. Hanrahan. "Pharmacological Effect of GABA Analogues on GABA-ϱ2 Receptors and Their Subtype Selectivity". Life 12, № 1 (2022): 127. http://dx.doi.org/10.3390/life12010127.

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GABAϱ receptors are distinctive GABAergic receptors from other ionotropic GABAA and metabotropic GABAB receptors in their pharmacological, biochemical, and electrophysiological properties. Although GABA-ϱ1 receptors are the most studied in this subfamily, GABA-ϱ2 receptors are widely distributed in the brain and are considered a potential target for treating neurological disorders such as stroke. The structure of GABA-ϱ2 receptors and their pharmacological features are poorly studied. We generated the first homology model of GABA-ϱ2 channel, which predicts similar major interactions of GABA wi
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ROTOLO, THOMAS C., and RAMON F. DACHEUX. "Two neuropharmacological types of rabbit ON-alpha ganglion cells express GABAC receptors." Visual Neuroscience 20, no. 4 (2003): 373–84. http://dx.doi.org/10.1017/s095252380320403x.

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The major inhibitory neurotransmitters GABA and glycine provide the bulk of input to large-field ganglion cells in the retina. Whole-cell patch-clamp recordings were used to characterize the glycine- and GABA-activated currents for morphologically identified ON-α ganglion cells in the rabbit retina. Cells identified as ON-α cells by light evoked currents were intracellularly stained and examined by light microscopy which revealed dendritic stratification in the vitreal half of the inner plexiform layer and confirmed their physiological identity. All Ca2+-mediated synaptic influences were aboli
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Han, Y., D. Cao, X. Li та ін. "Attenuation of γ-aminobutyric acid (GABA) transaminase activity contributes to GABA increase in the cerebral cortex of mice exposed to β-cypermethrin". Human & Experimental Toxicology 33, № 3 (2013): 317–24. http://dx.doi.org/10.1177/0960327113497770.

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The current study investigated the γ-aminobutyric acid (GABA) levels and GABA metabolic enzymes (GABA transaminase (GABAT) and glutamate decarboxylase (GAD)) activities at 2 and 4 h after treatment, using a high-performance liquid chromatography with ultraviolet detectors and colorimetric assay, in the cerebral cortex of mice treated with 20, 40 or 80 mg/kg β-cypermethrin by a single oral gavage, with corn oil as vehicle control. In addition, GABA protein (4 h after treatment), GABAT protein (2 h after treatment) and GABA receptors messenger RNA (mRNA) expression were detected by immunohistoch
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Absalom, Nathan, Izumi Yamamoto, David O'Hagan, Luke Hunter, and Mary Chebib. "Probing the Mode of Neurotransmitter Binding to GABA Receptors Using Selectively Fluorinated GABA Analogues." Australian Journal of Chemistry 68, no. 1 (2015): 23. http://dx.doi.org/10.1071/ch14456.

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Stereoselective fluorination is a useful technique for controlling the conformations of organic molecules. This concept has been exploited to create conformationally biased analogues of the neurotransmitter gamma-aminobutyric acid (GABA). Mono- and di-fluorinated GABA analogues are found to adopt different conformations, due to subtle stereoelectronic effects associated with the C–F bond. These conformationally biased GABA analogues exhibit different shape-dependent selectivity patterns towards GABAA, GABAB, and GABAC receptors, providing valuable information on the binding modes of the natura
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Liske, S., та M. E. Morris. "Extrasynaptic effects of GABA (γ-aminobutyric acid) agonists on myelinated axons of peripheral nerve". Canadian Journal of Physiology and Pharmacology 72, № 4 (1994): 368–74. http://dx.doi.org/10.1139/y94-054.

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Effects of the inhibitory neurotransmitter, GABA (γ-aminobutyric acid) on the excitability of myelinated fibers of isolated amphibian sciatic nerves and their dorsal and ventral spinal roots have been compared with those of a GABAA agonist, THIP (4,5,6,7-tetrahydroisoxazolo[5,4-c]pyridin-3-ol), and the GABAB agonist baclofen. Graded, prolonged increases in the amplitude of A-fiber half-maximal compound action potentials of Rana ballenderi sciatic nerves were evoked by GABA (Rmax = 49%, EC50 = 0.1 mM); responses to THIP were smaller (Rmax = 34%, EC50 = 1.1 mM) and with a different, distinctly b
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Fischer, Y., and I. Parnas. "Activation of GABAB receptors at individual release boutons of the crayfish opener neuromuscular junction produces presynaptic inhibition." Journal of Neurophysiology 75, no. 4 (1996): 1377–85. http://dx.doi.org/10.1152/jn.1996.75.4.1377.

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1. Presynaptic inhibition in crustaceans involves the activation of gamma-aminobutyric acid-A (GABAA) receptors that produce an increase in chloride conductance at excitatory axon terminals. Such inhibition produced by single inhibitory pulses is blocked by picrotoxin, a GABAA antagonist. 2. Presynaptic inhibition produced by bath application of GABA was not blocked by picrotoxin. Measurements of the membrane resistance of the excitatory axon terminals revealed that substantial presynaptic inhibition still persisted after 50 microM picrotoxin had completely blocked the increase in conductance
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Rozprawy doktorskie na temat "GABA"

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Kragler, Andrea. "GABA-Transporter." Diss., lmu, 2003. http://nbn-resolving.de/urn:nbn:de:bvb:19-9774.

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Picard, Raymonde. "Charakterisierung funktioneller Domänen für GABA und Furosemid auf GABAA-Rezeptoren." [S.l.] : [s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=971995141.

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Ong, Jennifer. "GABA and GABA-receptors in the enteric nervous system /." Title page, contents and summary only, 1985. http://web4.library.adelaide.edu.au/theses/09PH/09pho582.pdf.

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Davies, Martin. "The GABA transporter and the regulation of the GABA¦A receptor." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1993. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/nq23915.pdf.

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Aanesen, Arthur. "Gaba and human spermatozoa : characterization and regulation of gaba transport proteins /." Stockholm, 1998. http://diss.kib.ki.se/search/diss.se.cfm?19980925aane.

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Mendu, Suresh Kumar. "Role of GABA and GABAA Channels in T lymphocytes and Stem cells." Doctoral thesis, Uppsala universitet, Institutionen för neurovetenskap, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-172541.

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GABA (gamma-aminobutyric acid) is best known for its physiological function in the central nervous system.  In the brain GABA is the main inhibitory neurotransmitter where it decreases excitability of neurons and neuronal networks.  The balance between excitation evoked by glutamate and inhibition evoked by GABA is the base from where the brain works. It is fair to say that glutamate is like the gas-pedal and GABA the brake that keeps the brain running at a normal speed.  But, it is not only in the brain that GABA is taking a part in a physiological process vital to life. GABA is present in bl
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Gardner-Fortier, Catherine. "Développement d'un fromage fonctionnel renfermant un composé bioactif, l'acide gama-aminobutyrique (GABA)." Thesis, Université Laval, 2011. http://www.theses.ulaval.ca/2011/28143/28143.pdf.

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CHAMBON, JEAN-PIERRE. "Caracterisation de derives pyridazinyl-gaba comme ligands antagonistes du recepteur gaba-a." Université Louis Pasteur (Strasbourg) (1971-2008), 1987. http://www.theses.fr/1987STR13002.

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Chambon, Jean-Pierre. "Caractérisation de dérivés pyridazinyl-gaba comme ligands antagonistiques du récepteur gaba-A." Grenoble 2 : ANRT, 1987. http://catalogue.bnf.fr/ark:/12148/cb37603758b.

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Namwindwa, Ernest Sinvula. "GABA and glutamate mimetics." Thesis, University of Bath, 1987. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.376436.

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Książki na temat "GABA"

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J, Enna S., ed. GABA. Academic Press/Elsevier, 2006.

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Enna, S. J., and Hanns Möhler, eds. The GABA Receptors. Humana Press, 2007. http://dx.doi.org/10.1007/978-1-59745-465-0.

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Monti, Jaime M., Seithikurippu Ratnas Pandi-Perumal, and Hanns Möhler, eds. GABA and Sleep. Springer Basel, 2010. http://dx.doi.org/10.1007/978-3-0346-0226-6.

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Enna, S. J., and Norman G. Bowery, eds. The GABA Receptors. Humana Press, 1997. http://dx.doi.org/10.1007/978-1-4757-2597-1.

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J, Enna S., and Bowery N. G, eds. The GABA receptors. 2nd ed. Humana Press, 1997.

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J, Enna S., and Möhler Hanns, eds. The GABA receptors. 3rd ed. Humana Press, 2007.

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Ibrahim, Houmedgaba Maki. Gaba-caxxa =: Bâton. ILD, Gabbutíh Afitteh Maqhadá, 2008.

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Subai, Nadu. Al gaba al naimaa'. Centre essor et civilisation, 1993.

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Erdö, Sándor L., ed. GABA Outside the CNS. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-76915-3.

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International, Symposium on Peripheral GABAergic Mechanisms (1990 Rome Italy). GABA outside the CNS. Springer-Verlag, 1992.

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Części książek na temat "GABA"

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Manji, Husseini K., Jorge Quiroz, R. Andrew Chambers, et al. "GABA." In Encyclopedia of Psychopharmacology. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_444.

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Rey, Jose A. "GABA." In Encyclopedia of Clinical Neuropsychology. Springer New York, 2011. http://dx.doi.org/10.1007/978-0-387-79948-3_1765.

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Rey, Jose A. "GABA." In Encyclopedia of Clinical Neuropsychology. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-56782-2_1765-2.

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Rey, Jose A. "GABA." In Encyclopedia of Clinical Neuropsychology. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-57111-9_1765.

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King, Maedbh. "GABA." In Encyclopedia of Personality and Individual Differences. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-319-24612-3_752.

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King, Maedbh. "GABA." In Encyclopedia of Personality and Individual Differences. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-28099-8_752-1.

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Robinson, Timothy N., and Richard W. Olsen. "GABA." In Comparative Invertebrate Neurochemistry. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4615-9804-6_3.

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Murala, Sireesha, Anudeep Yelam, Mahmoud M. Ismail, and Pradeep C. Bollu. "GABA." In Neurochemistry in Clinical Practice. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-07897-2_4.

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Petroianu, Georg, and Peter Michael Osswald. "GABA-Rezeptor." In Anästhesie in Frage und Antwort. Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-662-05715-5_25.

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Petroianu, Georg, and Peter Michael Osswald. "GABA-Rezeptor." In Anästhesie in Frage und Antwort. Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-662-05717-9_36.

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Streszczenia konferencji na temat "GABA"

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Araujo, Wesna Simone B., Ricardo Cesar G. Landim, Thiago B. Da Silva Costa, Elvis Lira Da Silva, Gabriela Castellano, and Letícia Rittner. "Enhancing fMRS Data Quality and GABA Quantification Using SpectroViT: A Deep Learning Reconstruction Approach." In 2024 20th International Symposium on Medical Information Processing and Analysis (SIPAIM). IEEE, 2024. https://doi.org/10.1109/sipaim62974.2024.10783635.

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Asriany, Sherly, Adnan Sofyan, and Ridwan Ridwan. "Analisis Pencahayaan pada Material Lokal Gaba-gaba." In Temu Ilmiah IPLBI 2018. Ikatan Peneliti Lingkungan Binaan Indonesia, 2018. http://dx.doi.org/10.32315/ti.7.g048.

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Asriany, Sherly, and Adnan Sofyan. "Analisis Termal pada Material Alami Gaba-gaba (Pelepah Sagu) sebagai Bahan Alternatif Hemat Energi." In Temu Ilmiah Ikatan Peneliti Lingkungan Binaan Indonesia 6. Ikatan Peneliti Lingkungan Binaan Indonesia, 2017. http://dx.doi.org/10.32315/ti.6.h001.

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Akhmedov, R. R. "PRODUCTION OF WINES USING GAMMA-AMINOBUTYRIC ACID." In Innovative Technologies in Science and Education. ДГТУ-Принт, 2024. https://doi.org/10.23947/itse.2024.144-146.

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The production of wine with the addition of gamma-aminobutyric acid (GABA) represents an innovative direction in winemaking, aimed at creating functional products with enhanced health benefits. GABA, as an important neurotransmitter, helps reduce stress, improve sleep, and lower blood pressure. This article examines methods for increasing GABA content in wine, including the use of various strains of yeast and bacteria such as Lactobacillus hilgardii and Saccharomyces cerevisiae, as well as the optimization of fermentation conditions. Data analysis showed that the choice of strains and fermenta
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Dampf, Sara J., and Timothy M. Korter. "Low-frequency Vibrational Spectroscopy of $\gamma$-Aminobutyric Acid Derivatives: GABA Hydrochloride and $\beta$-Phenyl-GABA Hydrochloride." In 2020 45th International Conference on Infrared, Millimeter and Terahertz Waves (IRMMW-THz). IEEE, 2020. http://dx.doi.org/10.1109/irmmw-thz46771.2020.9370844.

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REBER, ANNIE, MARIE-HELENE LEROY, and BERNARD POITEVIN. "VISUO-VESTIBULAR REFLEXES ADJUSTMENT BY GABA ANTAGONISTS." In Proceedings of the International School of Biophysics. WORLD SCIENTIFIC, 1998. http://dx.doi.org/10.1142/9789812816887_0028.

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Tan, Chuanxin, Xiaohui Yan, Xiaoguang Wu, Chang Zhu, Mengxing Gou, and Xuejun Liu. "Research Progress of Gamma-Aminobutyric Acid(GABA)." In 2017 6th International Conference on Energy, Environment and Sustainable Development (ICEESD 2017). Atlantis Press, 2017. http://dx.doi.org/10.2991/iceesd-17.2017.114.

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Banerjee, Jyotirmoy, Aparna Dixit, P. Sarat Chandra, and Manjari Tripathi. "Targeting Gaba-A Receptors: Looking Beyond Benzodiazepine." In ECON 2023. Thieme Medical and Scientific Publishers Pvt. Ltd., 2023. http://dx.doi.org/10.1055/s-0044-1791456.

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Costa, Susana, Maria Fernandes та M. Sameiro Gonçalves. "Photocleavage Studies of γ-aminobutyric acid (GABA) Conjugates". У The 11th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2007. http://dx.doi.org/10.3390/ecsoc-11-01338.

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Azevedo, Ruan Ruan Gambardella Rosalina de, Adriel Rêgo Barbosa, Felipe Felipe Candeas Amorim, et al. "Atypical manifestation of Anti-Gaba-Br autoimmune encephalitis." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.583.

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Introduction: Anti-GABA-Br is an autoantibody associated with autoimmune encephalitis and small cell lung carcinoma. Clinical seizures, including status epilepticus, represent the most common feature of anti-GABA-Br related disorders. This case reports a previously healthy 40-year-old man with rapidly progressive dementia and Anti-GABA-Br positive cerebrospinal fluid (CSF). This is a case report based on retrospective analysis of a single patient’s medical record. Case report: From May 2019 to October 2020, the patient presented with dulling, decreased speech frequency and gait disturbance. He
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Raporty organizacyjne na temat "GABA"

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Koh, Wee Yin, Babak Rasti, Xiao Xian Lim, and Wan June Tan. GABA DACHO: Dark chocolate enriched with gamma-aminobutyric acid (GABA) and inulin as prebiotic. Peeref, 2023. http://dx.doi.org/10.54985/peeref.2306p1335975.

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Locy, Robert D., Hillel Fromm, Joe H. Cherry, and Narendra K. Singh. Regulation of Arabidopsis Glutamate Decarboxylase in Response to Heat Stress: Modulation of Enzyme Activity and Gene Expression. United States Department of Agriculture, 2001. http://dx.doi.org/10.32747/2001.7575288.bard.

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Most plants accumulate the nonprotein amino acid, g-aminobutyric acid (GABA), in response to heat stress. GABA is made from glutamate in a reaction catalyzed by glutamate decarboxylase (GAD), an enzyme that has been shown by the Israeli PI to be a calmodulin (CaM) binding protein whose activity is regulated in vitro by calcium and CaM. In Arabidopsis there are at least 5 GAD genes, two isoforms of GAD, GAD1 and GAD2, are known to be expressed, both of which appear to be calmodulin-binding proteins. The role of GABA accumulation in stress tolerance remains unclear, and thus the objectives of th
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Gee, Kelvin W. Dual Modulators of GABA-A and Alpha7 Nicotinic Receptors for Treating Autism. Defense Technical Information Center, 2014. http://dx.doi.org/10.21236/ada610984.

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Pastrana Arias, Ariel, Cesar Redondo Bermúdez, Jairo Mercado Camargo, and Karla Espinosa Ruiz. Evaluación de la neurotransmisión Gabaérgica en el núcleo accumbens de ratas durante la retirada de la cocaína. Universidad de Cartagena, 2014. https://doi.org/10.32997/11227/18478.

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Los psicoestimulantes como la cocaína por sus propiedades reforzadoras y hedónicas pueden conducir a la adicción. La suspensión del consumo de cocaína en adictos produce un síndrome de retirada que puede llevar a recaer en su consumo. Los enfoques farmacológicos disponibles no mejoran esta situación. Se investigó en un modelo de retirada de cocaína en ratas como se afectaron los niveles de GABA en el núcleo accumbens y como estos niveles fueron modificados durante esta retirada por el baclofén y la vigabatrina. CONCLUSIONES La administración repetida de cocaína y posterior retirada puede modif
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Fromm, Hillel, and Joe Poovaiah. Calcium- and Calmodulin-Mediated Regulation of Plant Responses to Stress. United States Department of Agriculture, 1993. http://dx.doi.org/10.32747/1993.7568096.bard.

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We have taken a molecular approach to clone cellular targets of calcium/calmodulin (Ca2+/CaM). A 35S-labeled recombinant CaM was used as a probe to screen various cDNA expression libraries. One of the isolated clones from petunia codes for the enzyme glutamate decarboxylase (GAD) which catalyzes the conversion of glutamate to g-aminobutyric acid (GABA). The activity of plant GAD has been shown to be dramatically enhanced in response to cold and heat shock, anoxia, drought, mechanical manipulations and by exogenous application of the stress phytohormone ABA in wheat roots. We have purified the
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Ron, Eliora, and Eugene Eugene Nester. Global functional genomics of plant cell transformation by agrobacterium. United States Department of Agriculture, 2009. http://dx.doi.org/10.32747/2009.7695860.bard.

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The aim of this study was to carry out a global functional genomics analysis of plant cell transformation by Agrobacterium in order to define and characterize the physiology of Agrobacterium in the acidic environment of a wounded plant. We planed to study the proteome and transcriptome of Agrobacterium in response to a change in pH, from 7.2 to 5.5 and identify genes and circuits directly involved in this change. Bacteria-plant interactions involve a large number of global regulatory systems, which are essential for protection against new stressful conditions. The interaction of bacteria with
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Kõlves, Kairi, and Luke Bayliss. Petani bunuh diri gara-gara perubahan iklim. Siapkah kita? Edited by Ria Ernunsari. Monash University, 2024. http://dx.doi.org/10.54377/4201-96ad.

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ทัศนาขจร, อัญชลี, วิเชียร ริมพณิชยกิจ та ศิราวุธ กลิ่นบุหงา. การวิเคราะห์ลักษณะและความแปรผันของไมโครแซเทลไลต์ในจีโนมของกุ้งกุลาดำและความเป็นไปได้ในการใช้จำแนกพันธุกรรม : รายงานวิจัยฉบับสมบูรณ์. จุฬาลงกรณ์์มหาวิทยาลัย, 2000. https://doi.org/10.58837/chula.res.2000.28.

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ไมโครแซเทลไลต์เป็นดีเอ็นเอที่มีการเรียงตัวของเบสซ้ำช่วงสั้นๆ ในหนึ่งหน่วยซ้ำประกอบด้วยลำดับเบส 1-6 คู่เบส พบกระจายอยู่ทั่วไปจีโนมของยูคาริโอต ความผันแปรของไมโครแซเทลไลต์เกิดจากการเพิ่มขึ้นหรือลดลงของจำนวนซ้ำและตรวจสอบได้โดยใช้เทคนิคพีซีอาร์ ไมโครแซเทลไลต์เป็นเครื่องหมายพันธุกรรมที่จำแนกความแตกต่างในสิ่งมีชีวิตต่างๆ ได้ดี เนื่องจากมีความผันแปรของจำนวนซ้ำสูงหรือมีความหลากหลายของจำนวนอัลลีลและมีอยู่มากหลายตำแหน่งในจีโนม ในงานวิจัยนี้ได้แยกไมโครแซเทลไลต์จากจีโนมของกุ้งกุลาดำ โดยการสร้างห้องสมุดยีนแล้วค้นหาโคลนที่มีไมโครแซเทลไลต์ชนิด tri- และ tetranucleotide repeats โดยวิธีโคโลนีไฮบริไดเซชั่น สามาร
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editorial team, 360info. Gaza: A year of escalation. Monash University, 2024. http://dx.doi.org/10.54377/cbd9-d3e2.

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Chaudhury, Saswata, and Sanchit S. Agarwal. Will Gaza jeopardise India's energy resilience? Edited by Bharat Bhushan and Chris Bartlett. Monash University, 2023. http://dx.doi.org/10.54377/3624-919a.

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