Littérature scientifique sur le sujet « Ligaen »
Créez une référence correcte selon les styles APA, MLA, Chicago, Harvard et plusieurs autres
Sommaire
Consultez les listes thématiques d’articles de revues, de livres, de thèses, de rapports de conférences et d’autres sources académiques sur le sujet « Ligaen ».
À côté de chaque source dans la liste de références il y a un bouton « Ajouter à la bibliographie ». Cliquez sur ce bouton, et nous générerons automatiquement la référence bibliographique pour la source choisie selon votre style de citation préféré : APA, MLA, Harvard, Vancouver, Chicago, etc.
Vous pouvez aussi télécharger le texte intégral de la publication scolaire au format pdf et consulter son résumé en ligne lorsque ces informations sont inclues dans les métadonnées.
Articles de revues sur le sujet "Ligaen"
Hendrati, Diana, Erianti Siska Purnamasari, Syulastri Effendi et Santhy Wyantuti. « Pemantapan Proses Sintesis Ligan Dibutilditiokarbamat (DBDTK) Sebagai Pengekstrak Logam Tanah Jarang Berdasarkan Desain Eksperimen ». ALCHEMY Jurnal Penelitian Kimia 14, no 1 (15 février 2018) : 195. http://dx.doi.org/10.20961/alchemy.14.1.15006.195-203.
Texte intégralHendrati, Diana, Erianti Siska Purnamasari, Syulastri Effendi et Santhy Wyantuti. « Pemantapan Proses Sistesis Ligan Dibutilditiokarbamat (DBDTK) sebagai Pengekstrak Logam Tanah Jarang berdasarkan Desain Eksperimen ». ALCHEMY Jurnal Penelitian Kimia 14, no 1 (15 février 2018) : 84. http://dx.doi.org/10.20961/alchemy.14.1.15006.84-99.
Texte intégralHendrati, Diana, Erianti Siska Purnamasari, Syulastri Effendi et Santhy Wyantuti. « Pemantapan Proses Sintesis Ligan Dibutilditiokarbamat (DBDTK) Sebagai Pengekstrak Logam Tanah Jarang Berdasarkan Desain Eksperimen ». ALCHEMY Jurnal Penelitian Kimia 14, no 2 (3 septembre 2018) : 219. http://dx.doi.org/10.20961/alchemy.14.2.15006.219-235.
Texte intégralAziz, Fitri Kusvila, Cantika Nukitasari, Fauziyah Ardli Oktavianingrum, Lita Windy Aryati et 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, no 2 (30 novembre 2016) : 120–24. http://dx.doi.org/10.15408/jkv.v2i2.4170.
Texte intégralChoirunisa, Farra, Wahyuni Wahyuni et Halim Mardianto. « PENATALAKSANAAN FISIOTERAPI PADA POST OP ACLR : CASE REPORT ». Journal of Innovation Research and Knowledge 3, no 1 (18 juin 2023) : 4811–16. http://dx.doi.org/10.53625/jirk.v3i1.5813.
Texte intégralMiao, Yinglong, Apurba Bhattarai et Jinan Wang. « Ligand Gaussian Accelerated Molecular Dynamics (LiGaMD) : Characterization of Ligand Binding Thermodynamics and Kinetics ». Journal of Chemical Theory and Computation 16, no 9 (21 juillet 2020) : 5526–47. http://dx.doi.org/10.1021/acs.jctc.0c00395.
Texte intégralArifin, Ibrahim, Handini Widya Prameswari Sabandar et 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, no 1 (30 août 2023) : 19. http://dx.doi.org/10.31942/jiffk.v0i1.9379.
Texte intégralBare, Yohanes, Mansur S, Sri Sulystyaningsih Natalia Daeng Tiring, Dewi Ratih Tirto Sari et Andri Maulidi. « Virtual Screening : Prediksi potensi 8-shogaol terhadap c-Jun N-Terminal Kinase (JNK) ». Jurnal Penelitian dan Pengkajian Ilmu Pendidikan : e-Saintika 4, no 1 (5 mars 2020) : 1. http://dx.doi.org/10.36312/e-saintika.v4i1.157.
Texte intégralNauli, Tigor. « PENENTUAN SISI AKTIF SELULASE ASPERGILLUS NIGER DENGAN DOCKING LIGAN ». Jurnal Kimia Terapan Indonesia 16, no 2 (10 décembre 2014) : 94–100. http://dx.doi.org/10.14203/jkti.v16i2.14.
Texte intégralKoentjoro, Maharani Pertiwi, Adyan Donastin et 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, no 2 (29 décembre 2020) : 259–70. http://dx.doi.org/10.29122/jbbi.v7i2.4156.
Texte intégralThèses sur le sujet "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.
Texte intégralFan, 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.
Texte intégralNakatsubo, Tomoyuki. « Characterization of O-methyltransferases and pinoresinol reductases involved in lignin and lignan biosynthesis ». Kyoto University, 2008. http://hdl.handle.net/2433/123964.
Texte intégral0048
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.
Texte intégralLotte, 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.
Texte intégralThe 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.
Texte intégralThe 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.
Texte intégralMelanoma 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.
Texte intégralMelanoma 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.
Texte intégralIn 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.
Texte intégralLivres sur le sujet "Ligaen"
Ġang. Ligden sudulul. Ku̇lu̇n Buyir Qota : Ȯbȯr Mongġol-un Keblel-u̇n Bȯlu̇glel, Ȯbȯr Mongġol-un Soyol-un Keblel-u̇n Qoriy-a, 2016.
Trouver le texte intégralThylin, Stefan. Premier League : Första ligan. Västerås : Sportförlaget, 2010.
Trouver le texte intégralLigden. Ligden-u̇ ȯgu̇lelge-yin songġomal. [Kȯkqota] : Ȯbȯr Mongġol-un Arad-un Keblel-u̇n Qoriy-a, 1985.
Trouver le texte intégralWhiteside, Leo A. Ligament Balancing. Berlin, Heidelberg : Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18689-9.
Texte intégralZimmermann, Timo. Management von Ligen in Individualsportarten. Wiesbaden : Springer Fachmedien Wiesbaden, 2019. http://dx.doi.org/10.1007/978-3-658-24919-9.
Texte intégralSociety, Ligden Poetry, dir. Pulsar : Poems from Ligden Poetry Society. Swindon : Ligden Publishers, 2000.
Trouver le texte intégralLandvreugd, Hermine. Margaretha bleef het langst liggen : Verhalen. Amsterdam : Bezige Bij, 1996.
Trouver le texte intégralHösl, Florian. Wettbewerbsfähigkeit nationaler Ligen im europäischen Profifußball. Wiesbaden : Springer Fachmedien Wiesbaden, 2020. http://dx.doi.org/10.1007/978-3-658-32326-4.
Texte intégralGzoyan, Ēdita. Hayastani aṛajin hanrapetutʻyuně ev Azgeri ligan. Erevan : HH GAA "Gitutʻyun" hratarakchʻutʻyun, 2013.
Trouver le texte intégralNienhaus, G. Ulrich. Protein-Ligand Interactions. New Jersey : Humana Press, 2005. http://dx.doi.org/10.1385/1592599125.
Texte intégralChapitres de livres sur le sujet "Ligaen"
Dirks, Tineke, et Annelies Diesfeldt. « Liggen ». Dans 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.
Texte intégralLewis, Norman G., Laurence B. Davin et Simo Sarkanen. « Lignin and Lignan Biosynthesis : Distinctions and Reconciliations ». Dans ACS Symposium Series, 1–27. Washington, DC : American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0697.ch001.
Texte intégralSharma, Swati, Abhishek Sharma, Sikandar I. Mulla, Deepak Pant, Tanvi Sharma et Ashok Kumar. « Lignin as Potent Industrial Biopolymer : An Introduction ». Dans Lignin, 1–15. Cham : Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-40663-9_1.
Texte intégralBhat, Rajeev, Aziz Ahmad et Ivi Jõudu. « Applications of Lignin in the Agri-Food Industry ». Dans Lignin, 275–98. Cham : Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-40663-9_10.
Texte intégralLu, Yong-Chao, Yao Lu et Xing Fan. « Structure and Characteristics of Lignin ». Dans Lignin, 17–75. Cham : Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-40663-9_2.
Texte intégralAhuja, Vishal, et Raya Roy. « Lignin Synthesis and Degradation ». Dans Lignin, 77–113. Cham : Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-40663-9_3.
Texte intégralNayak, Kush Kumar, Piyush Parkhey et Reecha Sahu. « Analysis of Lignin Using Qualitative and Quantitative Methods ». Dans Lignin, 115–38. Cham : Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-40663-9_4.
Texte intégralLopez-Camas, Karen, Muhammad Arshad et Aman Ullah. « Chemical Modification of Lignin by Polymerization and Depolymerization ». Dans Lignin, 139–80. Cham : Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-40663-9_5.
Texte intégralGhozali, Muhammad, Evi Triwulandari, Witta Kartika Restu, Sri Fahmiati et Yenny Meliana. « Lignin and Its Composites ». Dans Lignin, 181–202. Cham : Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-40663-9_6.
Texte intégralKumar, Raj, Abhishek Gupta, Mohit Chawla, Keshaw Ram Aadil, Sunil Dutt, Vijay Bhooshan Kumar et Abhishek Chaudhary. « Advances in Nanotechnology based Strategies for Synthesis of Nanoparticles of Lignin ». Dans Lignin, 203–29. Cham : Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-40663-9_7.
Texte intégralActes de conférences sur le sujet "Ligaen"
Chandra, S., et V. Kumar. « Thermodynamic Properties of LiGaS2 and LiGaSe2 using First-Principle Calculations ». Dans 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.
Texte intégralPalermo, 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 ». Dans CF '24 : 21st ACM International Conference on Computing Frontiers. New York, NY, USA : ACM, 2024. http://dx.doi.org/10.1145/3637543.3656335.
Texte intégralJelínek, Michal, Václav Kubeček, Ondřej Novák, Jaroslav Huynh, Martin Cimrman, Michal Chyla, Martin Smrž et 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 ». Dans Advanced Solid State Lasers. Washington, D.C. : Optica Publishing Group, 2022. http://dx.doi.org/10.1364/assl.2022.jw3b.15.
Texte intégralChandra, Satish, V. Kumar et Yadvendra Singh. « First-principle calculations of Debye temperature of optoelectronic LiGaS2 and LiGaSe2 semiconductors under different pressures ». Dans Optical Components and Materials XVI, sous la direction de Michel J. Digonnet et Shibin Jiang. SPIE, 2019. http://dx.doi.org/10.1117/12.2506878.
Texte intégralZhou, Lu, Ondřej Novák, Martin Smrž et Tomáš Mocek. « Study of Broadband Mid-infrared Optical Parametric Amplification in LiGaS2, LiGaSe2, LiInS2, and LiInSe2 Crystals ». Dans Compact EUV & X-ray Light Sources. Washington, D.C. : Optica Publishing Group, 2022. http://dx.doi.org/10.1364/euvxray.2022.jw5a.17.
Texte intégralSilva, Alessandro Márcio Hakme Da, Alessandro Fraga Farah, Abimael Caleb Ribeiro, Alexandre José Ribeiro et Jonas De Carvalho. « MODELO COMPUTACIONAL DE ANÁLISE DO COMPORTAMENTO MECÂNICO DA LIGA TI-6AL-4V EM COMPARAÇÃO A LIGA Ti-20Nb ». Dans IV Simpósio de Tecnologias da Fatec de Sertãozinho (SITEFA/Stz). Fatec Sertãozinho, 2022. http://dx.doi.org/10.33635/sitefa.v4i1.163.
Texte intégralLim, Manko, Timothy A. Jackson et Philip A. Anfinrud. « Ultrafast Near-IR Spectroscopy of Carbonmonoxymyoglobin : the Dynamics of Protein Relaxation ». Dans International Conference on Ultrafast Phenomena. Washington, D.C. : Optica Publishing Group, 1992. http://dx.doi.org/10.1364/up.1992.thb3.
Texte intégralSunkesula, Sai Praneeth Reddy, Rishabh Dabral et Ganesh Ramakrishnan. « LIGHTEN ». Dans MM '20 : The 28th ACM International Conference on Multimedia. New York, NY, USA : ACM, 2020. http://dx.doi.org/10.1145/3394171.3413778.
Texte intégralNEVES NETO, DURVAL NOLASCO DAS, Guilherme Sousa Ferreira LAGARES, Layre Araujo Abreu, Maria Karina Lima Lagares, Rone Fontoura Abreu et Vinicius Barroso de Sousa. « ESTUDO EPIDEMIOLÓGICO DE FEBRE CHIKUNGUNYA NO TOCANTINS, 2017 A 2021 ». Dans Anais do Encontro Regional de Ligas Acadêmicas - Ligas Day. Recife, Brasil : Even3, 2023. http://dx.doi.org/10.29327/1314101.1-2.
Texte intégralSousa, Vinicius Barroso de, Maria Karina Lima Lagares, André Anderson Soares Souza, Rone Fontoura Abreu, Rone Antônio Alves de Abreu et Rômulo Antônio Fontoura Abreu. « ANÁLISE RETROSPECTIVA DA MORTALIDADE DE PACIENTES EM PÓS OPERATÓRIO DE CIRURGIAS ONCOLÓGICAS NO HOSPITAL REGIONAL DE ARAGUAÍNA, 2010 A 2021. » Dans Anais do Encontro Regional de Ligas Acadêmicas - Ligas Day. Recife, Brasil : Even3, 2023. http://dx.doi.org/10.29327/1314101.1-1.
Texte intégralRapports d'organisations sur le sujet "Ligaen"
Lalvani, S. B. Lignin-assisted coal depolymerization. Office of Scientific and Technical Information (OSTI), janvier 1991. http://dx.doi.org/10.2172/5795190.
Texte intégralChung-Jui Tsai, Mark F. Davis et Vincent L. Chiang. Genetic Augmentation of Syringyl Lignin in Low-lignin Aspen Trees, Final Report. Office of Scientific and Technical Information (OSTI), novembre 2004. http://dx.doi.org/10.2172/883338.
Texte intégralRaj, Ganesh V. Targeting Ligand Dependent and Ligand Independent Androgen Receptor Signaling in Prostate Cancer. Fort Belvoir, VA : Defense Technical Information Center, octobre 2014. http://dx.doi.org/10.21236/ada613818.
Texte intégralRaj, Ganesh V. Targeting Ligand-Dependent and Ligand-Independent Androgen Receptor Signaling in Prostate Cancer. Fort Belvoir, VA : Defense Technical Information Center, octobre 2013. http://dx.doi.org/10.21236/ada604653.
Texte intégralDilworth, G. L. Biochemical genetics of Lignin degradation. Office of Scientific and Technical Information (OSTI), février 1997. http://dx.doi.org/10.2172/471447.
Texte intégralLewis, N. G. Unravelling lignin formation and structure. Office of Scientific and Technical Information (OSTI), janvier 1991. http://dx.doi.org/10.2172/6001554.
Texte intégralCarlson, John E. ''The control of lignin synthesis''. Office of Scientific and Technical Information (OSTI), avril 2005. http://dx.doi.org/10.2172/838425.
Texte intégralTaylor, Dean C., et Richard C. Mather III. Anterior Cruciate Ligament (ACL) Reconstruction. Touch Surgery Simulations, mai 2014. http://dx.doi.org/10.18556/touchsurgery/2014.s0022.
Texte intégralShanoski, Jennifer E. Ligand Rearrangements of Organometallic Complexes inSolution. Office of Scientific and Technical Information (OSTI), janvier 2006. http://dx.doi.org/10.2172/883798.
Texte intégralGladysz, J. A. Ligand intermediates in metal-catalyzed reactions. Office of Scientific and Technical Information (OSTI), septembre 1991. http://dx.doi.org/10.2172/5977342.
Texte intégral