Academic literature on the topic 'PFM39'

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Journal articles on the topic "PFM39"

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Lunggani, Arina Tri, Wahyu Aji Mahardhika, Adi Budi Utomo, and Endang Kusdiyantini. "Molecular Characterization Of Phylloplane Mold From Avicennia marina Leaves." Bioma : Berkala Ilmiah Biologi 24, no. 1 (June 16, 2022): 61–65. http://dx.doi.org/10.14710/bioma.24.1.61-65.

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Mangroves are a habitat for organisms and microorganisms, including phylloplane molds. Phylloplane molds are known to have various potentials such as antimicrobial, enzyme, and pigment-producing. PFM19 is an orange pigment-producing phylloplane mold. Identification of the mold is needed to determine the species of the fungus so that it can be used for further research. This study aims to identify molecularly the PFM19 mold that produces orange pigment using ITS markers. The methods used in this study included the rejuvenation of isolates, DNA extraction, DNA amplification, and phylogenetic analysis. The results obtained that PFM19 has similarities with Talaromyces islandicus CBS 388.48 by 100% based on ITS markers.
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Abildgaard, N., A. M. Rojek, H. E. Møller, C. T. Hansen, N. B. Palstrøm, L. M. Rasmussen, H. C. Beck, and N. Marcussen. "PF639 IMMUNE ELECTRON MICROSCOPY AND MASS SPECTROMETRY FOR CLASSIFICATION OF AMYLOID DEPOSITS." HemaSphere 3, S1 (June 2019): 272–73. http://dx.doi.org/10.1097/01.hs9.0000560840.32000.6d.

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BATSUREN, Amgalanbat, Kenta TOMIDA, Toru HATAMURA, Hirokazu MASUI, and Mengu CHO. "Erratum for “Laboratory Tests to Standardize Environment Test Conditions of Micro/Nano Satellite Units” [Trans. JSASS Aerospace Tech. Japan Vol. 12, No. ists29, pp. Pf_1-Pf_10, 2014]." TRANSACTIONS OF THE JAPAN SOCIETY FOR AERONAUTICAL AND SPACE SCIENCES, AEROSPACE TECHNOLOGY JAPAN 12, ists29 (2014): Pf_39—Pf_40. http://dx.doi.org/10.2322/tastj.12.pf_39.

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Rao, Venkatarama K., Joan A. Whitlock, and Ann Progulske-Fox. "Development of a Genetic System for Eikenella corrodens: Transfer of Plasmids pFM739 and pLES2." Plasmid 30, no. 3 (November 1993): 289–95. http://dx.doi.org/10.1006/plas.1993.1062.

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Blotman, F., J. Branco, H. Barros, E. Thomas, C. Taieb, and E. Myon. "PFM3 CROSS-SURVEY OF FRENCH AND PORTUGUESE GENERAL PRACTITIONERS GLOBAL MANAGEMENT OF FIBROMYALGIA." Value in Health 8, no. 6 (November 2005): A50—A51. http://dx.doi.org/10.1016/s1098-3015(10)67294-4.

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Kunz, J., S. Lobitz, J. Andrea, G. Regine, H. Cario, L. Oevermann, D. Hakimeh, et al. "PF739 SICKLE CELL DISEASE IN GERMANY IS HETEROGENEOUS AND RESULTS IN SEVERE MORBIDITY: ANALYSES FROM A NATIONAL REGISTRY." HemaSphere 3, S1 (June 2019): 323–24. http://dx.doi.org/10.1097/01.hs9.0000561240.27342.da.

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Peris, I., E. Martínez-Balsalobre, E. Arriazu, N. Marcotegui, A. Torres-López, N. Areizaga, M. C. Mateos, M. L. Cayuela, M. D. Odero, and C. Vicente. "PF239 COMBINED TARGETING OF BCL-2 AND SET-PP2A INTERACTION INDUCES POTENT AND SYNERGISTIC ANTI-LEUKEMIC EFFECTS ON ACUTE MYELOID LEUKEMIA." HemaSphere 3, S1 (June 2019): 72. http://dx.doi.org/10.1097/01.hs9.0000559172.09663.83.

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Templeton, Thomas J., Hisashi Fujioka, Masamichi Aikawa, Kenneth C. Parker, and David C. Kaslow. "Plasmodium falciparum Pfs40, renamed Pf39, is localized to an intracellular membrane-bound compartment and is not sexual stage-specific." Molecular and Biochemical Parasitology 90, no. 1 (December 1997): 359–65. http://dx.doi.org/10.1016/s0166-6851(97)00164-3.

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Wernersbach, J., S. Khan, A. Bhatti, M. Theobald, and U. Hartwig. "PF439 EXPLORING THE THERAPEUTIC POTENTIAL OF T-CELL-RECEPTOR REDIRECTED CD3+ NATURAL KILLER CELLS FOR ADOPTIVE CELLULAR THERAPY TO ACUTE MYELOID LEUKEMIA." HemaSphere 3, S1 (June 2019): 172–73. http://dx.doi.org/10.1097/01.hs9.0000559968.36666.57.

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Lozano, M. L., M. E. Mingot, M. Perera, I. Jarque, R. Campos, T. J. González, G. Carreño, et al. "PF339 BIOLOGICAL AND CLINICAL FACTORS THAT FAVOR THE USE OF A SPECIFIC TPO-RA IN ITP PATIENTS. RESULTS FROM A SPANISH MULTICENTER STUDY." HemaSphere 3, S1 (June 2019): 121–22. http://dx.doi.org/10.1097/01.hs9.0000559568.66584.f4.

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Dissertations / Theses on the topic "PFM39"

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GABRIELLI, ANNALISA, and MAURIZIO TADDEI. "Synthesis of small molecules active on tumor relevant cellular signaling pathways." Doctoral thesis, Università di Siena, 2017. http://hdl.handle.net/11365/1004864.

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This PhD project is focused on the improvable potency of small molecules to restore and reactivate the physiological functions of specific cellular signaling pathways involved in the development of serious and degenerative diseases, such as skin cancer, leukemia, neurodegenerative diseases. Hence, here is reported the synthesis and the biological evaluation of the Hedgehog pathway's agonists and antagonists, as well as the MRN Complex inhibitors. Moreover, we worked in the field of the bioconjugation with the synthesis of the so called molecular linkers, which have been then used to conjugate some known cytotoxic agents. The resulting payloads have been sent to prepare new Antibody Drug Conjugates (ADC) using specific monoclonal antibodies (mAbs)
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Conference papers on the topic "PFM39"

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Nissa, Prihartini Khoirun, Fauzi Bakri, and Dewi Muliyati. "PENGEMBANGAN BUKU FISIKA BERDASARKAN KERANGKA KERJA TPACK PADA TOPIK FLUIDA STATIS." In SEMINAR NASIONAL FISIKA 2016 UNJ. PRODI Pendidikan Fisika dan Fisika UNJ, 2023. http://dx.doi.org/10.21009/03.1102.pf39.

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Pezzoli, M., L. Lodola, M. Manghisoni, F. Morsani, L. Ratti, V. Re, E. Riceputi, and G. Traversi. "Characterization of PFM3, a 32×32 readout chip for PixFEL X-ray imager." In 2019 IEEE Nuclear Science Symposium and Medical Imaging Conference (NSS/MIC). IEEE, 2019. http://dx.doi.org/10.1109/nss/mic42101.2019.9059651.

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