Auswahl der wissenschaftlichen Literatur zum Thema „Ligaen“
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Zeitschriftenartikel zum Thema "Ligaen"
Hendrati, Diana, Erianti Siska Purnamasari, Syulastri Effendi und Santhy Wyantuti. „Pemantapan Proses Sintesis Ligan Dibutilditiokarbamat (DBDTK) Sebagai Pengekstrak Logam Tanah Jarang Berdasarkan Desain Eksperimen“. ALCHEMY Jurnal Penelitian Kimia 14, Nr. 1 (15.02.2018): 195. http://dx.doi.org/10.20961/alchemy.14.1.15006.195-203.
Der volle Inhalt der QuelleHendrati, Diana, Erianti Siska Purnamasari, Syulastri Effendi und Santhy Wyantuti. „Pemantapan Proses Sistesis Ligan Dibutilditiokarbamat (DBDTK) sebagai Pengekstrak Logam Tanah Jarang berdasarkan Desain Eksperimen“. ALCHEMY Jurnal Penelitian Kimia 14, Nr. 1 (15.02.2018): 84. http://dx.doi.org/10.20961/alchemy.14.1.15006.84-99.
Der volle Inhalt der QuelleHendrati, Diana, Erianti Siska Purnamasari, Syulastri Effendi und Santhy Wyantuti. „Pemantapan Proses Sintesis Ligan Dibutilditiokarbamat (DBDTK) Sebagai Pengekstrak Logam Tanah Jarang Berdasarkan Desain Eksperimen“. ALCHEMY Jurnal Penelitian Kimia 14, Nr. 2 (03.09.2018): 219. http://dx.doi.org/10.20961/alchemy.14.2.15006.219-235.
Der volle Inhalt der QuelleAziz, Fitri Kusvila, Cantika Nukitasari, Fauziyah Ardli Oktavianingrum, Lita Windy Aryati und Broto Santoso. „Hasil In Silico Senyawa Z12501572, Z00321025, SCB5631028 dan SCB13970547 dibandingkan Turunan Zerumbon terhadap Human Liver Glycogen Phosphorylase (1l5Q) sebagai Antidiabetes“. Jurnal Kimia VALENSI 2, Nr. 2 (30.11.2016): 120–24. http://dx.doi.org/10.15408/jkv.v2i2.4170.
Der volle Inhalt der QuelleChoirunisa, Farra, Wahyuni Wahyuni und Halim Mardianto. „PENATALAKSANAAN FISIOTERAPI PADA POST OP ACLR : CASE REPORT“. Journal of Innovation Research and Knowledge 3, Nr. 1 (18.06.2023): 4811–16. http://dx.doi.org/10.53625/jirk.v3i1.5813.
Der volle Inhalt der QuelleMiao, Yinglong, Apurba Bhattarai und Jinan Wang. „Ligand Gaussian Accelerated Molecular Dynamics (LiGaMD): Characterization of Ligand Binding Thermodynamics and Kinetics“. Journal of Chemical Theory and Computation 16, Nr. 9 (21.07.2020): 5526–47. http://dx.doi.org/10.1021/acs.jctc.0c00395.
Der volle Inhalt der QuelleArifin, Ibrahim, Handini Widya Prameswari Sabandar und Hari Purnomo. „Molecular Docking Senyawa Jambu Biji (Psidium guajava L.) terhadap Reseptor Estrogen Alfa Sebagai Model Kandidat Antikanker Payudara“. Jurnal Ilmu Farmasi dan Farmasi Klinik, Nr. 1 (30.08.2023): 19. http://dx.doi.org/10.31942/jiffk.v0i1.9379.
Der volle Inhalt der QuelleBare, Yohanes, Mansur S, Sri Sulystyaningsih Natalia Daeng Tiring, Dewi Ratih Tirto Sari und Andri Maulidi. „Virtual Screening: Prediksi potensi 8-shogaol terhadap c-Jun N-Terminal Kinase (JNK)“. Jurnal Penelitian dan Pengkajian Ilmu Pendidikan: e-Saintika 4, Nr. 1 (05.03.2020): 1. http://dx.doi.org/10.36312/e-saintika.v4i1.157.
Der volle Inhalt der QuelleNauli, Tigor. „PENENTUAN SISI AKTIF SELULASE ASPERGILLUS NIGER DENGAN DOCKING LIGAN“. Jurnal Kimia Terapan Indonesia 16, Nr. 2 (10.12.2014): 94–100. http://dx.doi.org/10.14203/jkti.v16i2.14.
Der volle Inhalt der QuelleKoentjoro, Maharani Pertiwi, Adyan Donastin und Endry Nugroho Prasetyo. „POTENSI SENYAWA BIOAKTIF TANAMAN KELOR PENGHAMBAT INTERAKSI ANGIOTENSIN-CONVERTING ENZYME 2 PADA SINDROMA SARS-COV-2“. Jurnal Bioteknologi & Biosains Indonesia (JBBI) 7, Nr. 2 (29.12.2020): 259–70. http://dx.doi.org/10.29122/jbbi.v7i2.4156.
Der volle Inhalt der QuelleDissertationen zum Thema "Ligaen"
Nandakumar, Jayakrishnan. „Discrimination of RNA versus DNA by an RNA ligase and distinct modes of substrate recognition by DNA ligases /“. Access full-text from WCMC:, 2007. http://proquest.umi.com/pqdweb?did=1428838891&sid=13&Fmt=2&clientId=8424&RQT=309&VName=PQD.
Der volle Inhalt der QuelleFan, Jun. „Investigating the crosstalk between Nedd4 ubiquitin ligases and PIAS3 SUMO ligase“. Thesis, Queen Mary, University of London, 2017. http://qmro.qmul.ac.uk/xmlui/handle/123456789/31791.
Der volle Inhalt der QuelleNakatsubo, Tomoyuki. „Characterization of O-methyltransferases and pinoresinol reductases involved in lignin and lignan biosynthesis“. Kyoto University, 2008. http://hdl.handle.net/2433/123964.
Der volle Inhalt der Quelle0048
新制・課程博士
博士(農学)
甲第14173号
農博第1734号
新制||農||964(附属図書館)
学位論文||H20||N4412(農学部図書室)
UT51-2008-N490
京都大学大学院農学研究科応用生命科学専攻
(主査)教授 梅澤 俊明, 教授 宮川 恒, 教授 矢﨑 一史
学位規則第4条第1項該当
Wang, Shao-Fang. „Biochemical and biophysical studies of MDM2-ligand interactions“. Thesis, University of Edinburgh, 2012. http://hdl.handle.net/1842/9527.
Der volle Inhalt der QuelleLotte, Romain. „Caractérisation des interactions moléculaires entre la GTPase Rac1 et son régulateur HACE1 : perspectives en infectiologie et en cancérologie“. Electronic Thesis or Diss., Université Côte d'Azur (ComUE), 2017. http://www.theses.fr/2017AZUR4087.
Der volle Inhalt der QuelleThe small GTPase Rac1 plays a key role in various intracellular signaling pathways including cell proliferation. Our laboratory has shown that the CNF1 toxin, produced by pathogenic Escherichia coli, catalyzes the activation of Rac1. We also identified the role of the E3 ubiquitin-ligase HACE1, a tumor suppressor, in the regulation by ubiquitylation of active Rac1. If the activated form of Rac1 is proved to be a target of HACE1, the mode of interaction between these two proteins remains to be define as well as the role of these interactions in infection and cancer. The aim of my work was to characterize the molecular interactions between HACE1 and Rac1. We tested the hypothesis that HACE1 point mutations identified in cancers could interfere with its interaction with Rac1 and its ability to control cell growth. We showed that 13 cancer-associated somatic mutations of HACE1, led to a defective control of cell proliferation. Moreover, the study of these mutations allowed us to identify a group of amino acids, located on the ankyrin-repeats 5 to 7 of HACE1, which controls the interaction of HACE1 with Rac1 and thus its ubiquitylation. We also identified a role for the intermediate domain of HACE1 (MID) in conferring the specificity of association of HACE1 to the active form of Rac1. Ultimately, the characterization of interaction mutants between HACE1 and Rac1 as well as the effect of the CNF1 toxin on this signaling axis will give us more insight on this regulatory pathway in cancer and infection
Lelievre, Chloé. „Formation de liaisons amides par réactions enzymatiques détournées ATP Regeneration System in Chemoenzymatic Amide Bond Formation with Thermophilic CoA Ligase“. Thesis, université Paris-Saclay, 2020. http://www.theses.fr/2020UPASF026.
Der volle Inhalt der QuelleThe amide function is widespread in nature and also in many synthetic products such as pharmaceuticals and polymers. Numerous approaches have been developed to provide reliable synthesis methods. The most common approach in conventional chemistry is the acylation of an amine by activated carboxylic acid. Activation requires the use of either coupling reagents resulting in low atom economy, or expensive catalysts sometimes used under drastic conditions. Biocatalytic approaches are therefore interesting alternatives for economic and environmental reasons. Different enzymes can be used such as hydrolases, nitrile hydratases and transglutaminases that activate the acid in acyl-enzyme form to promote the nucleophilic addition of the amine. In recent years, interest in ATP-dependent enzymes has increased.In this project, we focused on CoA ligases that catalyze the formation of activated acid as acyl-adenylate and then acyl-thioester. We have thus demonstrated that by diverting the reaction by scavenging activated intermediate with an amine, we obtain the amide. The use of thermophilic CoA ligases allows us to work at a high temperature and thus facilitate the uncatalyzed addition of the amine. This system therefore dispenses with the use of expensive HSCoA. For a better system, we have also successfully integrated an ATP regeneration system with a Polyphosphate Kinase 2 (Class III) and an inorganic pyrophosphatase. The efficiency of this cascade was illustrated by the lab-scale chemo-enzymatic synthesis of N-methylbutyrylamide in 77 % yield using low enzyme loading.Biodiversity exploration using a genomic approach based on sequence comparison allowed us to identify several thermophilic CoA ligases active towards ω-amino acid substrates. K6Q029 from Thermaerobacter subterraneus was further studied. In particular, this enzyme is active towards ω-amino acid substrates, functionalized or not, with more or less long carbon chains, as well as on various carboxylic acids such as aromatics.Thanks to the structural resolution of A4YDT1, a promiscuous CoA ligase from the literature, we have identified, in collaboration with a team of crystallographers from theUniversity of Groningen (Netherlands), the residues involved in its substrate specificity to modify them by a rational approach. Variants of this enzyme have thus allowed to obtain δ-valerolactam and Ɛ-caprolactam
El, Hachem Najla. „Rôle pro-tumorigénique de HACE1 dans le mélanome“. Thesis, Université Côte d'Azur (ComUE), 2017. http://www.theses.fr/2017AZUR4035.
Der volle Inhalt der QuelleMelanoma incidence has considerably increased over the last thirty years, with a doubling every ten years. Melanoma accounts for only 5% of cutaneous cancers but causes more than 80% of deaths, which is a major public health problem. Indeed, this tumor is extremely aggressive and has a high metastatic potential. After the onset of metastases, the prognosis becomes highly unfavorable. Despite major therapeutic advances, many patients are still refractory to these new treatments. Understanding the mechanisms involved in the development of this tumor and the identification of new therapies remain a major issue. The sequencing of exomes led to the identification of a mutation in the RAC1 gene (P29S) constituting one of the most frequent somatic mutations in melanoma (after the BRAFV600, NRASQ61 and NF1 mutations). RAC1 is a small GTPase that is involved in several key cellular processes. Under physiological conditions, the activity of RAC1 is mainly controlled by GTPase activating proteins (GAPs) and Nucleotide Exchange (GEF) exchange factors. GAPs and GEFs control the level of RAC1- GTP and thus regulate its activity. The activity of RAC1 is also dependent on its protein level of expression which is controlled by E3 ubiquitin ligases, including HACE1. HACE1 is considered a tumor suppressor. Unexpectedly, our data clearly show that HACE1 promotes migratory and tumorigenic properties of melanoma cells. Indeed, inhibition of HACE1 alters migration of melanoma cells in vitro, as well as in vivo pulmonary colonization in mice. Transcriptomic analysis of 4 melanoma cell lines demonstrated that HACE1 suppression inhibits ITGAV and ITGB1 expression
El, Hachem Najla. „Rôle pro-tumorigénique de HACE1 dans le mélanome“. Electronic Thesis or Diss., Université Côte d'Azur (ComUE), 2017. http://www.theses.fr/2017AZUR4035.
Der volle Inhalt der QuelleMelanoma incidence has considerably increased over the last thirty years, with a doubling every ten years. Melanoma accounts for only 5% of cutaneous cancers but causes more than 80% of deaths, which is a major public health problem. Indeed, this tumor is extremely aggressive and has a high metastatic potential. After the onset of metastases, the prognosis becomes highly unfavorable. Despite major therapeutic advances, many patients are still refractory to these new treatments. Understanding the mechanisms involved in the development of this tumor and the identification of new therapies remain a major issue. The sequencing of exomes led to the identification of a mutation in the RAC1 gene (P29S) constituting one of the most frequent somatic mutations in melanoma (after the BRAFV600, NRASQ61 and NF1 mutations). RAC1 is a small GTPase that is involved in several key cellular processes. Under physiological conditions, the activity of RAC1 is mainly controlled by GTPase activating proteins (GAPs) and Nucleotide Exchange (GEF) exchange factors. GAPs and GEFs control the level of RAC1- GTP and thus regulate its activity. The activity of RAC1 is also dependent on its protein level of expression which is controlled by E3 ubiquitin ligases, including HACE1. HACE1 is considered a tumor suppressor. Unexpectedly, our data clearly show that HACE1 promotes migratory and tumorigenic properties of melanoma cells. Indeed, inhibition of HACE1 alters migration of melanoma cells in vitro, as well as in vivo pulmonary colonization in mice. Transcriptomic analysis of 4 melanoma cell lines demonstrated that HACE1 suppression inhibits ITGAV and ITGB1 expression
Orts, Julien. „Caractérisation des interactions entre ligands et protéines par RMN en solution“. Grenoble, 2010. http://www.theses.fr/2010GRENY011.
Der volle Inhalt der QuelleIn the process of structure-based drug design, the provision of the binding mode of ligands to the cellular receptor of interest is essential. This can suffer from limited access to protein/ligand structures, especially for the low affinity ligands that are commonly obtained from high throughput screening or fragment based lead discovery. In a common scenario crystal structures are available for one or several ligands but not for all chemical series of actual interest. Here, we present a new, NMR-based approach that allows overcoming this limitation. In the INPHARMA method interligand NOEs (Nuclear Overhauser Enhancement) are utilized to determine relative orientations of different chemical fragments binding competitively to a common receptor site. This novel methodology opens the way to the application of structure-based drug design already in an early stage of drug development, when structural information via crystallography is of difficult access
Gupta, S. K. „Isolation, cloning and characterization of lignin biosynthesis pathway gene(s) 4-coumarate co a ligase (4cl) from leucaena leucocephala“. Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2008. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2705.
Der volle Inhalt der QuelleBücher zum Thema "Ligaen"
Ġang. Ligden sudulul. Ku̇lu̇n Buyir Qota: Ȯbȯr Mongġol-un Keblel-u̇n Bȯlu̇glel, Ȯbȯr Mongġol-un Soyol-un Keblel-u̇n Qoriy-a, 2016.
Den vollen Inhalt der Quelle findenThylin, Stefan. Premier League: Första ligan. Västerås: Sportförlaget, 2010.
Den vollen Inhalt der Quelle findenLigden. Ligden-u̇ ȯgu̇lelge-yin songġomal. [Kȯkqota]: Ȯbȯr Mongġol-un Arad-un Keblel-u̇n Qoriy-a, 1985.
Den vollen Inhalt der Quelle findenWhiteside, Leo A. Ligament Balancing. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18689-9.
Der volle Inhalt der QuelleZimmermann, Timo. Management von Ligen in Individualsportarten. Wiesbaden: Springer Fachmedien Wiesbaden, 2019. http://dx.doi.org/10.1007/978-3-658-24919-9.
Der volle Inhalt der QuelleSociety, Ligden Poetry, Hrsg. Pulsar: Poems from Ligden Poetry Society. Swindon: Ligden Publishers, 2000.
Den vollen Inhalt der Quelle findenLandvreugd, Hermine. Margaretha bleef het langst liggen: Verhalen. Amsterdam: Bezige Bij, 1996.
Den vollen Inhalt der Quelle findenHösl, Florian. Wettbewerbsfähigkeit nationaler Ligen im europäischen Profifußball. Wiesbaden: Springer Fachmedien Wiesbaden, 2020. http://dx.doi.org/10.1007/978-3-658-32326-4.
Der volle Inhalt der QuelleGzoyan, Ēdita. Hayastani aṛajin hanrapetutʻyuně ev Azgeri ligan. Erevan: HH GAA "Gitutʻyun" hratarakchʻutʻyun, 2013.
Den vollen Inhalt der Quelle findenNienhaus, G. Ulrich. Protein-Ligand Interactions. New Jersey: Humana Press, 2005. http://dx.doi.org/10.1385/1592599125.
Der volle Inhalt der QuelleBuchteile zum Thema "Ligaen"
Dirks, Tineke, und Annelies Diesfeldt. „Liggen“. In Als je kind het zelf niet kan, 36–52. Houten: Bohn Stafleu van Loghum, 2001. http://dx.doi.org/10.1007/978-90-313-9512-5_3.
Der volle Inhalt der QuelleLewis, Norman G., Laurence B. Davin und Simo Sarkanen. „Lignin and Lignan Biosynthesis: Distinctions and Reconciliations“. In ACS Symposium Series, 1–27. Washington, DC: American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0697.ch001.
Der volle Inhalt der QuelleSharma, Swati, Abhishek Sharma, Sikandar I. Mulla, Deepak Pant, Tanvi Sharma und Ashok Kumar. „Lignin as Potent Industrial Biopolymer: An Introduction“. In Lignin, 1–15. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-40663-9_1.
Der volle Inhalt der QuelleBhat, Rajeev, Aziz Ahmad und Ivi Jõudu. „Applications of Lignin in the Agri-Food Industry“. In Lignin, 275–98. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-40663-9_10.
Der volle Inhalt der QuelleLu, Yong-Chao, Yao Lu und Xing Fan. „Structure and Characteristics of Lignin“. In Lignin, 17–75. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-40663-9_2.
Der volle Inhalt der QuelleAhuja, Vishal, und Raya Roy. „Lignin Synthesis and Degradation“. In Lignin, 77–113. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-40663-9_3.
Der volle Inhalt der QuelleNayak, Kush Kumar, Piyush Parkhey und Reecha Sahu. „Analysis of Lignin Using Qualitative and Quantitative Methods“. In Lignin, 115–38. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-40663-9_4.
Der volle Inhalt der QuelleLopez-Camas, Karen, Muhammad Arshad und Aman Ullah. „Chemical Modification of Lignin by Polymerization and Depolymerization“. In Lignin, 139–80. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-40663-9_5.
Der volle Inhalt der QuelleGhozali, Muhammad, Evi Triwulandari, Witta Kartika Restu, Sri Fahmiati und Yenny Meliana. „Lignin and Its Composites“. In Lignin, 181–202. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-40663-9_6.
Der volle Inhalt der QuelleKumar, Raj, Abhishek Gupta, Mohit Chawla, Keshaw Ram Aadil, Sunil Dutt, Vijay Bhooshan Kumar und Abhishek Chaudhary. „Advances in Nanotechnology based Strategies for Synthesis of Nanoparticles of Lignin“. In Lignin, 203–29. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-40663-9_7.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Ligaen"
Chandra, S., und V. Kumar. „Thermodynamic Properties of LiGaS2 and LiGaSe2 using First-Principle Calculations“. In 2018 5th IEEE Uttar Pradesh Section International Conference on Electrical, Electronics and Computer Engineering (UPCON). IEEE, 2018. http://dx.doi.org/10.1109/upcon.2018.8596990.
Der volle Inhalt der QuellePalermo, G., G. Accordi, D. Gadioli, Y. Zhang, E. Vitali, B. Guindani, D. Ardagna et al. „LIGATE - LIgand Generator and portable drug discovery platform AT Exascale“. In CF '24: 21st ACM International Conference on Computing Frontiers. New York, NY, USA: ACM, 2024. http://dx.doi.org/10.1145/3637543.3656335.
Der volle Inhalt der QuelleJelínek, Michal, Václav Kubeček, Ondřej Novák, Jaroslav Huynh, Martin Cimrman, Michal Chyla, Martin Smrž und Tomáš Mocek. „Difference Frequency Generation in BaGa4Se7, LiGaSe2, or LiGaS2 with Output Energy up to 100 μJ Tunable in a 5 to 13 μm Range Pumped by a 1.03 μm, 1.8 ps Laser“. In Advanced Solid State Lasers. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/assl.2022.jw3b.15.
Der volle Inhalt der QuelleChandra, Satish, V. Kumar und Yadvendra Singh. „First-principle calculations of Debye temperature of optoelectronic LiGaS2 and LiGaSe2 semiconductors under different pressures“. In Optical Components and Materials XVI, herausgegeben von Michel J. Digonnet und Shibin Jiang. SPIE, 2019. http://dx.doi.org/10.1117/12.2506878.
Der volle Inhalt der QuelleZhou, Lu, Ondřej Novák, Martin Smrž und Tomáš Mocek. „Study of Broadband Mid-infrared Optical Parametric Amplification in LiGaS2, LiGaSe2, LiInS2, and LiInSe2 Crystals“. In Compact EUV & X-ray Light Sources. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/euvxray.2022.jw5a.17.
Der volle Inhalt der QuelleSilva, Alessandro Márcio Hakme Da, Alessandro Fraga Farah, Abimael Caleb Ribeiro, Alexandre José Ribeiro und Jonas De Carvalho. „MODELO COMPUTACIONAL DE ANÁLISE DO COMPORTAMENTO MECÂNICO DA LIGA TI-6AL-4V EM COMPARAÇÃO A LIGA Ti-20Nb“. In IV Simpósio de Tecnologias da Fatec de Sertãozinho (SITEFA/Stz). Fatec Sertãozinho, 2022. http://dx.doi.org/10.33635/sitefa.v4i1.163.
Der volle Inhalt der QuelleLim, Manko, Timothy A. Jackson und Philip A. Anfinrud. „Ultrafast Near-IR Spectroscopy of Carbonmonoxymyoglobin: the Dynamics of Protein Relaxation“. In International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1992. http://dx.doi.org/10.1364/up.1992.thb3.
Der volle Inhalt der QuelleSunkesula, Sai Praneeth Reddy, Rishabh Dabral und Ganesh Ramakrishnan. „LIGHTEN“. In MM '20: The 28th ACM International Conference on Multimedia. New York, NY, USA: ACM, 2020. http://dx.doi.org/10.1145/3394171.3413778.
Der volle Inhalt der QuelleNEVES NETO, DURVAL NOLASCO DAS, Guilherme Sousa Ferreira LAGARES, Layre Araujo Abreu, Maria Karina Lima Lagares, Rone Fontoura Abreu und Vinicius Barroso de Sousa. „ESTUDO EPIDEMIOLÓGICO DE FEBRE CHIKUNGUNYA NO TOCANTINS, 2017 A 2021“. In Anais do Encontro Regional de Ligas Acadêmicas - Ligas Day. Recife, Brasil: Even3, 2023. http://dx.doi.org/10.29327/1314101.1-2.
Der volle Inhalt der QuelleSousa, Vinicius Barroso de, Maria Karina Lima Lagares, André Anderson Soares Souza, Rone Fontoura Abreu, Rone Antônio Alves de Abreu und Rômulo Antônio Fontoura Abreu. „ANÁLISE RETROSPECTIVA DA MORTALIDADE DE PACIENTES EM PÓS OPERATÓRIO DE CIRURGIAS ONCOLÓGICAS NO HOSPITAL REGIONAL DE ARAGUAÍNA, 2010 A 2021.“ In Anais do Encontro Regional de Ligas Acadêmicas - Ligas Day. Recife, Brasil: Even3, 2023. http://dx.doi.org/10.29327/1314101.1-1.
Der volle Inhalt der QuelleBerichte der Organisationen zum Thema "Ligaen"
Lalvani, S. B. Lignin-assisted coal depolymerization. Office of Scientific and Technical Information (OSTI), Januar 1991. http://dx.doi.org/10.2172/5795190.
Der volle Inhalt der QuelleChung-Jui Tsai, Mark F. Davis und Vincent L. Chiang. Genetic Augmentation of Syringyl Lignin in Low-lignin Aspen Trees, Final Report. Office of Scientific and Technical Information (OSTI), November 2004. http://dx.doi.org/10.2172/883338.
Der volle Inhalt der QuelleRaj, Ganesh V. Targeting Ligand Dependent and Ligand Independent Androgen Receptor Signaling in Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, Oktober 2014. http://dx.doi.org/10.21236/ada613818.
Der volle Inhalt der QuelleRaj, Ganesh V. Targeting Ligand-Dependent and Ligand-Independent Androgen Receptor Signaling in Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, Oktober 2013. http://dx.doi.org/10.21236/ada604653.
Der volle Inhalt der QuelleDilworth, G. L. Biochemical genetics of Lignin degradation. Office of Scientific and Technical Information (OSTI), Februar 1997. http://dx.doi.org/10.2172/471447.
Der volle Inhalt der QuelleLewis, N. G. Unravelling lignin formation and structure. Office of Scientific and Technical Information (OSTI), Januar 1991. http://dx.doi.org/10.2172/6001554.
Der volle Inhalt der QuelleCarlson, John E. ''The control of lignin synthesis''. Office of Scientific and Technical Information (OSTI), April 2005. http://dx.doi.org/10.2172/838425.
Der volle Inhalt der QuelleTaylor, Dean C., und Richard C. Mather III. Anterior Cruciate Ligament (ACL) Reconstruction. Touch Surgery Simulations, Mai 2014. http://dx.doi.org/10.18556/touchsurgery/2014.s0022.
Der volle Inhalt der QuelleShanoski, Jennifer E. Ligand Rearrangements of Organometallic Complexes inSolution. Office of Scientific and Technical Information (OSTI), Januar 2006. http://dx.doi.org/10.2172/883798.
Der volle Inhalt der QuelleGladysz, J. A. Ligand intermediates in metal-catalyzed reactions. Office of Scientific and Technical Information (OSTI), September 1991. http://dx.doi.org/10.2172/5977342.
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