المؤلفون: Anushree Kamath, Abhishek Sharma, Arpit Shukla, Paritosh Parmar, Dhara Patel

المصدر: Frontiers in Microbiology, Vol 15 (2025)

مصطلحات موضوعية: siderophore, plant growth-promoting rhizobacteria, leaf spot disease, plant defense, induced systemic resistance, Microbiology, QR1-502

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fmicb.2024.1492139/full; https://doaj.org/toc/1664-302X

URL الوصول: https://doaj.org/article/feed8373e39d498faa396477300b07f2

المؤلفون: Anushree Kamath, Dhara Patel, Arpit Shukla

المصدر: European Journal of Plant Pathology. 165:407-419

مصطلحات موضوعية: Plant Science, Horticulture, Agronomy and Crop Science

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::fdb0cf5ff13f42f7fd42c94204eef316
https://doi.org/10.1007/s10658-022-02618-3

المؤلفون: Dhara Patel, Dhruv Mamtora, Anushree Kamath, Arpit Shukla

المصدر: Marine pollution bulletin. 177

مصطلحات موضوعية: Biodegradation, Environmental, Polyethylene, Polymers, Aquatic Science, Oceanography, Polypropylenes, Pollution, Plastics

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebbc1175b08eb4ebe1a139e0fa757a29
https://pubmed.ncbi.nlm.nih.gov/35290835

المؤلفون: Anushree Kamath, Arpit Shukla, Dhara Patel

المصدر: Physiological and Molecular Plant Pathology. 123:101927

مصطلحات موضوعية: Genetics, Plant Science

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::96458a021145b3a2554301d1aac47849
https://doi.org/10.1016/j.pmpp.2022.101927

المؤلفون: Dhara Patel, Monika Polra, Nistha Jani, Anushree Kamath, Arpit Shukla

المصدر: Molecular biotechnology. 63(8)

مصطلحات موضوعية: 0106 biological sciences, Computer science, Potential candidate, Bioengineering, Computational biology, 01 natural sciences, Applied Microbiology and Biotechnology, Biochemistry, 03 medical and health sciences, Drug Delivery Systems, Genome editing, 010608 biotechnology, CRISPR, Animals, Humans, Molecular Biology, 030304 developmental biology, Flexibility (engineering), Gene Editing, 0303 health sciences, Mechanism (biology), Cas9, Drug Resistance, Multiple, Multiple drug resistance, CRISPR-Cas Systems, Genes, MDR, Biotechnology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8505fe8452c3ac151ff95e52f66d1102
https://pubmed.ncbi.nlm.nih.gov/34021472

المؤلفون: Michael Tong, Markus A. Seeliger, Anushree Kamath, Nicole S. Sampson, Kunal Kumar, Jian Cao, Iwao Ojima, Monaf Awwa, Vincent M. Alford, Xiaodong Ren, Qianwen Gan

المصدر: ACS Chemical Biology. 12:2788-2803

مصطلحات موضوعية: Models, Molecular, 0301 basic medicine, Matrix metalloproteinase inhibitor, Integrin alpha4beta1, Matrix Metalloproteinase Inhibitors, Matrix metalloproteinase, Biochemistry, Small Molecule Libraries, Focal adhesion, 03 medical and health sciences, 0302 clinical medicine, Protein Domains, Cell Movement, Hemopexin, Cell Line, Tumor, Neoplasms, Chlorocebus aethiops, Animals, Humans, Paxillin, Enzyme Precursors, Focal Adhesions, biology, Chemistry, CD44, Cell migration, General Medicine, Molecular biology, Cell biology, Hyaluronan Receptors, 030104 developmental biology, Matrix Metalloproteinase 9, 030220 oncology & carcinogenesis, COS Cells, biology.protein, Molecular Medicine, Chickens, Proto-oncogene tyrosine-protein kinase Src

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::786f4cc74b2697b69c17a2ce2b263268
https://doi.org/10.1021/acschembio.7b00758

المؤلفون: Christian Philouze, Anushree Kamath, Charles-Henry Fabritius, Philippe Delair

المصدر: Organic & Biomolecular Chemistry. 13:9834-9843

مصطلحات موضوعية: Models, Molecular, Aza Compounds, Molecular Structure, Acenaphthenes, Stereochemistry, Organic Chemistry, Stereoisomerism, Ether, Ring (chemistry), Biochemistry, Cycloaddition, chemistry.chemical_compound, chemistry, Cyclization, Stereoselectivity, Physical and Theoretical Chemistry, Mannich reaction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09fd175ea5681c41c91b1d8165a33123
https://doi.org/10.1039/c5ob01013f

المؤلفون: Ying-Jen Chen, Joshua D. Seitz, Edison S. Zuniga, Anushree Kamath, Jacob G. Vineberg, Iwao Ojima

المصدر: Journal of Medicinal Chemistry

مصطلحات موضوعية: Stereochemistry, Biotin, Breast Neoplasms, Article, Taxoid, Inhibitory Concentration 50, Mice, chemistry.chemical_compound, Cell Line, Tumor, Antineoplastic Combined Chemotherapy Protocols, Drug Discovery, medicine, Animals, Humans, Receptors, Growth Factor, Molecular Targeted Therapy, Microscopy, Confocal, Combination chemotherapy, Glutathione, 3. Good health, Microscopy, Fluorescence, chemistry, Cell culture, Cancer cell, Molecular Medicine, Camptothecin, Click Chemistry, Female, Taxoids, medicine.drug, Conjugate

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3d741a776fbb7136242247dd9941d8e
https://doi.org/10.1021/jm500631u

المؤلفون: Ranjan Datta, Dinesh Jagadeesan, Chidambar Kulkarni, Muthusamy Eswaramoorthy, Anushree Kamath, Kasibhatta Kumara Ramanatha Datta

المصدر: Angewandte Chemie. 123:4015-4019

مصطلحات موضوعية: Materials science, Mesoscale meteorology, chemistry.chemical_element, Nanotechnology, General Chemistry, General Medicine, Catalysis, Carbon, Nanostructures, Solutions, Order (biology), Transformation (function), chemistry, Chemical physics, Spectrophotometry, Ultraviolet, Porosity, Coloring Agents

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f7f05cb5c63bbe0f51401b604a04c2c
https://doi.org/10.1002/ange.201007031

المؤلفون: Anushree Kamath, Philippe Delair, Andrew E. Greene, Julien Smith

المصدر: ChemInform. 45

مصطلحات موضوعية: Chemistry, Stereochemistry, Total synthesis, Organic chemistry, General Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::17cca54ebfc6dc75453aae3130bc60d6
https://doi.org/10.1002/chin.201429217

المؤلفون: Anushree Kamath, Joshua D. Seitz, Iwao Ojima

المصدر: Natural Products in Medicinal Chemistry

مصطلحات موضوعية: Taxoid, business.industry, Cancer research, Medicine, Cancer, business, medicine.disease

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::c73ab2a5ec4c2df4fbc3638a20fa2fba
https://doi.org/10.1002/9783527676545.ch04

المؤلفون: Andrew E. Greene, Anushree Kamath, Julien Smith, Philippe Delair

المساهمون: Département de Chimie Moléculaire - Synthèse Et Réactivité en Chimie Organique (DCM - SeRCO), Département de Chimie Moléculaire (DCM), Université Joseph Fourier - Grenoble 1 (UJF)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université Joseph Fourier - Grenoble 1 (UJF)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)

المصدر: SYNLETT
SYNLETT, Georg Thieme Verlag, 2014, 25 (02), pp.209-212. ⟨10.1055/s-0033-1340107⟩

مصطلحات موضوعية: chemistry.chemical_classification, Flexibility (engineering), 010405 organic chemistry, Organic Chemistry, Enantioselective synthesis, Total synthesis, 010402 general chemistry, 01 natural sciences, Cycloaddition, 0104 chemical sciences, chemistry, Yield (chemistry), Enol ether, Organic chemistry, [CHIM]Chemical Sciences, Stereoselectivity, ComputingMilieux_MISCELLANEOUS

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd71c5c87f7b062b1bf931d05e7b36e9
https://hal.archives-ouvertes.fr/hal-01652512

المؤلفون: Christian Philouze, Amaël Veyron, Philippe Delair, Paidi Venkatram Reddy, Julien Smith, Anushree Kamath, Hélène Jamet, Andrew E. Greene, Peter Koos

المساهمون: Département de Chimie Moléculaire - Synthèse Et Réactivité en Chimie Organique (DCM - SeRCO), Département de Chimie Moléculaire (DCM), Université Joseph Fourier - Grenoble 1 (UJF)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université Joseph Fourier - Grenoble 1 (UJF)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Département de Chimie Moléculaire - Chimie Théorique (DCM - CT), Laboratoire d'études dynamiques et structurales de la sélectivité (LEDSS), Université Joseph Fourier - Grenoble 1 (UJF)-Centre National de la Recherche Scientifique (CNRS), Université Joseph Fourier - Grenoble 1 (UJF)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)

المصدر: Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2013, 78 (10), pp.4840-4849. ⟨10.1021/jo400386f⟩

مصطلحات موضوعية: Models, Molecular, Biological Products, 010405 organic chemistry, Organic Chemistry, Molecular Conformation, Ether, Stereoisomerism, Alkylation, 010402 general chemistry, 01 natural sciences, Cycloaddition, 0104 chemical sciences, 3. Good health, chemistry.chemical_compound, chemistry, Organic chemistry, [CHIM]Chemical Sciences, Stereoselectivity, Pyrrolizidine Alkaloids, ComputingMilieux_MISCELLANEOUS

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff2111deb1c3c8ee31a2cf14fde645a1
https://hal.archives-ouvertes.fr/hal-01652591

المؤلفون: Iwao Ojima, Anushree Kamath

المصدر: ChemInform. 44

مصطلحات موضوعية: Chemistry, Peptidomimetic, Synthon, Indolizidine, General Medicine, biochemical phenomena, metabolism, and nutrition, Combinatorial chemistry, chemistry.chemical_compound, Enantiopure drug, polycyclic compounds, Organic synthesis, Tabtoxin, Monobactams, Structural motif

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::2d1b8bd295f7ee44bd3aa452f08a321d
https://doi.org/10.1002/chin.201315235

المؤلفون: Anushree Kamath, Iwao Ojima

المصدر: Tetrahedron. 68(52)

مصطلحات موضوعية: Peptidomimetic, Organic Chemistry, Synthon, Enantioselective synthesis, Indolizidine, biochemical phenomena, metabolism, and nutrition, Biochemistry, Combinatorial chemistry, Article, chemistry.chemical_compound, Enantiopure drug, chemistry, Drug Discovery, polycyclic compounds, Organic chemistry, Organic synthesis, Structural motif, Monobactams

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1c3ebe25cb4e13ec8d197f4c78dea4b
https://pubmed.ncbi.nlm.nih.gov/23264702