المؤلفون: Xian Wu, Liuyi Dong, Chuanying Dai, Mingqi Hou, Jin Qian, Jiaqiang Sun

المصدر: Biomedicine & Pharmacotherapy, Vol 124, Iss, Pp 109923-(2020)

مصطلحات موضوعية: 0301 basic medicine, Polygonum, RM1-950, 03 medical and health sciences, 0302 clinical medicine, Traditional Chinese medicine, Glucosides, Polygonummultiflorum, Stilbenes, Animals, Humans, Medicine, Chinese Traditional, Pharmacology, biology, Traditional medicine, Chemistry, General Medicine, biology.organism_classification, Tetrahydroxystilbene, Pharmacological action, Extraction Purification, 030104 developmental biology, Pharmacological activities, 030220 oncology & carcinogenesis, Fallopia multiflora, Therapeutics. Pharmacology, 2 3 5 4 tetrahydroxystilbene 2 o β d glucoside

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5caf9136677301121adaef56b3877808Test
http://www.sciencedirect.com/science/article/pii/S075333222030113XTest

المؤلفون: Samuel Meignan, Abigaëlle Gros, Tiphaine Rogez-Florent, Amélie Lansiaux, Catherine Foulon, Jean François Goossens, Raphaël Frédérick, Sebastien Gluszok, Bernard Masereel, Laurence Goossens, Perrine Six, Claudiu T. Supuran, Christine Bal-Mahieu, Andrea Scozzafava, Patrick Depreux

المساهمون: UCL - SSS/LDRI - Louvain Drug Research Institute, Groupe de Recherche Interdiscipinaire Innovation et Optimisation Thérapeutique - EA 4481 (GRIIOT), Université de Lille, Droit et Santé, Institut pour la Recherche sur le Cancer de Lille (U837 INSERM - IRCL), Institut pour la recherche sur le cancer de Lille [Lille] (IRCL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre de Recherche Jean-Pierre AUBERT - Neurosciences et Cancer -JPArc [Lille], Institut de Chimie Pharmaceutique Albert Lespagnol (ICPAL), Laboratorio di Chimica Bioinorganica (LCBI), Università degli Studi di Firenze = University of Florence [Firenze] (UNIFI), Laboratorio di Chimica Bioinorganica, Université de Namur [Namur] (UNamur), EA 4481 Groupe de Recherche Interdiscipinaire (GRIIOT), Faculté des Sciences Pharmaceutiques et Biologiques, Università degli Studi di Firenze = University of Florence [Firenze], Université de Namur [Namur], Plasticité Cellulaire et Cancer (CPAC) - U908 (CPAC), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille, Centre de Recherche en Cancérologie de Marseille (CRCM), Aix Marseille Université (AMU)-Institut Paoli-Calmettes, Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Université Catholique de Louvain (UCL), Génétique moléculaire et approches thérapeutiques des hémopathies malignes, IRCL-Institut National de la Santé et de la Recherche Médicale (INSERM)

المصدر: Bioorganic & Medicinal Chemistry
Bioorganic & Medicinal Chemistry : the tetrahedron journal for research at the interface of chemistry and biology, Vol. 21, no. 6, p. 1451-1464 (2013)
Bioorganic & Medicinal Chemistry; Vol 21
Bioorganic and Medicinal Chemistry
Bioorganic and Medicinal Chemistry, Elsevier, 2013, 21 (6), pp.1451-1464. ⟨10.1016/j.bmc.2012.10.029⟩

مصطلحات موضوعية: 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (4 bromophenyl) 1h pyrazole, Carbonate dehydratase ix inhibitor, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (2 phenantryl) 1h pyrazole, Unclassified drug, Clinical Biochemistry, Cell, Pharmaceutical Science, Drug structure, Antiproliferative activity, 1 (3 aminosulfonylphenyl) 3 hydroxymethyl 5 phenyl 1h pyrazole, 01 natural sciences, Biochemistry, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (4 methoxyphenyl) 1h pyrazole, 1 (4 aminosulfonylphenyl) 4 hydroxymethyl 5 (2 naphthyl) 1h pyrazole, Breast cancer, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (5 bromo 6 methoxynaphtalen 2 yl) 1h pyrazole, Catalytic Domain, Drug Discovery, Cytotoxicity, Hypoxia, Carbonic Anhydrase Inhibitors, ComputingMilieux_MISCELLANEOUS, Enzyme active site, Carbonic Anhydrases, chemistry.chemical_classification, 0303 health sciences, Sulfonamides, Carbonic anhydrase, biology, Chemistry, Aryl sulfonamide inhibitors, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (2 methoxyphenyl) 1h pyrazole, Carbonate dehydratase IX, 3. Good health, 1 (3 aminosulfonylphenyl) 3 hydroxymethyl 5 (6 methoxy 2 naphthalenyl) 1h pyrazole, Molecular Docking Simulation, Enzyme inhibition, medicine.anatomical_structure, Drug screening, Drug selectivity, Molecular Medicine, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (6 methoxynaphtalen 2 yl) 1h pyrazole, Simulation, medicine.drug, 1 (4 aminosulfonylphenyl) 5 hydroxymethyl 3 phenyl 1h pyrazole, Protein Binding, 1 (3 aminosulfonylphenyl) 3 hydroxymethyl 5 naphthyl 1h pyrazole, Drug cytotoxicity, 1 (4 aminosulfonylphenyl) 5 hydroxymethyl 3 (2 naphthyl) 1h pyrazole, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 pyridinyl 1h pyrazole, Drug binding, Sulfonamide, Article, Molecular model, 03 medical and health sciences, Drug synthesis, Structure-Activity Relationship, Drug potency, [CHIM.ANAL]Chemical Sciences/Analytical chemistry, Antigens, Neoplasm, Cell Line, Tumor, medicine, Humans, Doxorubicin, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (1 naphthyl) 1h pyrazole, 1 (4 aminosulfonylphenyl) 4 hydroxymethyl 5 phenyl 1h pyrazole, Carbonic Anhydrase IX, Molecular Biology, 1 (4 aminosulfonylphenyl) 3 hydroxyethyl 5 phenyl 1h pyrazole, 030304 developmental biology, Cell Proliferation, 1 (4 aminosulfonylphenyl) 4 hydroxymethyl 5 (6 methoxy 2 naphtalenyl) 1h pyrazole, Carbonate dehydratase inhibitor, Cell strain MDA MB 231, Binding Sites, 010405 organic chemistry, Organic Chemistry, Active site, In vitro, 0104 chemical sciences, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (2 naphthyl) 1h pyrazole, Kinetics, Enzyme, Binding kinetics, Tumor progression, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (4 tolyl) 1h pyrazole, Pyrazole, biology.protein, Pyrazoles, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (3 methoxyphenyl) 1h pyrazole, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 phenyl 1h pyrazole, Cell line, 4 (5 aryl 2 hydroxymethyl pyrazol 1 yl)benzenesulfonamide

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d24fc0ffbfbf6b174096e2e6e1a78a94Test

المؤلفون: Ze-qi Chen, Yang Wang, Zhe Wang, Yucheng Cao, Wei Gong, Zian Xia, Nan-xiang Su, Weijun Peng, Chenxia Sheng

المصدر: BMC Complementary and Alternative Medicine

مصطلحات موضوعية: 0301 basic medicine, Oncology, medicine.medical_specialty, Disease, Mice, 03 medical and health sciences, Cognition, 0302 clinical medicine, Glucosides, Alzheimer Disease, Internal medicine, Stilbenes, Animals, Humans, Medicine, Cognitive decline, 2, 3, 5, 4′-tetrahydroxystilbene-2-O-β-D-glucoside, business.industry, Cognitive deficits, Rodent model, General Medicine, medicine.disease, Rats, Disease Models, Animal, 030104 developmental biology, Complementary and alternative medicine, Strictly standardized mean difference, Systematic review, Retention memory, 2 3 5 4 tetrahydroxystilbene 2 o β d glucoside, Alzheimer's disease, business, Alzheimer’s disease, 030217 neurology & neurosurgery, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::704bd2c8424c989b16be381caef92eb4Test
https://doi.org/10.1186/s12906-016-1313-8Test

المؤلفون: Mukeshd Doble, Ponnurengam Malliappan Sivakumar

المصدر: Medicinal Chemistry. 4:110-115

مصطلحات موضوعية: Models, Molecular, Steric effects, Quantitative structure–activity relationship, Binding Sites, Cyclooxygenase 2 Inhibitors, biology, Chemistry, Stereochemistry, Hydrogen bond, Binding energy, Quantitative Structure-Activity Relationship, Active site, Hydrogen Bonding, Interaction energy, 1 (4 fluorophenyl) 2 [(4 methylsulfonyl)phenyl]cyclopentene, 4 [5 (4 bromophenyl) 3 trifluoromethyl 1h pyrazol 1 yl]benzenesulfonamide, 5 (4 fluorophenyl) 1 [(4 methylsulfonyl)phenyl] 3 trifluoromethylpyrazole, 5 bromo 2 (4 fluorophenyl) 3 (4 methylsulfonylphenyl)thiophene, celecoxib, cyclooxygenase 2, cyclooxygenase 2 inhibitor, l 768 277, n (2 cyclohexyloxy 4 nitrophenyl)methanesulfonamide, nimesulide, prostaglandin synthase inhibitor, rofecoxib, sc 58451, valdecoxib, binding affinity, binding site, blood brain barrier, computer model, computer prediction, drug penetration, drug protein binding, drug structure, enzyme activity, IC 50, mathematical computing, priority journal, quantitative analysis, structure activity relation, chemical structure, chemistry, human, hydrogen bond, protein binding, quantitative structure activity relation, solubility, Blood-Brain Barrier, Cyclooxygenase 2, Humans, Inhibitory Concentration 50, Protein Binding, Solubility, Drug Discovery, biology.protein, Molecule, HOMO/LUMO

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee361189381f7e3d39df02cbddbe431bTest
https://doi.org/10.2174/157340608783789112Test

المؤلفون: Mario Cazzola, Clive P. Page, Paola Rogliani, Maria Gabriella Matera

المساهمون: Cazzola, M., Matera, Maria Gabriella, Rogliani, P., Page, C.

المصدر: Trends in Pharmacological Sciences. 28:544-550

مصطلحات موضوعية: muscle atrophy, Pathology, antioxidant, Heart disease, Phosphodiesterase Inhibitors, Settore MED/10 - Malattie dell'Apparato Respiratorio, gastrointestinal symptom, Angiotensin-Converting Enzyme Inhibitors, heart disease, oxygen therapy, systemic disease, heparin, Toxicology, Bioinformatics, Systemic inflammation, Antioxidants, PPAR agonist, hydroxymethylglutaryl coenzyme A reductase inhibitor, rosiglitazone, low drug dose, Pulmonary Disease, Chronic Obstructive, irbesartan, Adrenal Cortex Hormones, dipeptidyl carboxypeptidase inhibitor, pioglitazone, simvastatin, COPD, combination chemotherapy, beta 2 adrenergic receptor stimulating agent, Pulmonary inflammation, 4 (4 fluorophenyl) 2 (4 methylsulfinylphenyl) 5 (4 pyridyl)imidazole, 4 [4 (4 fluorophenyl) 1 (3 phenylpropyl) 5 (4 pyridinyl) 1h imidazol 2 yl] 3 butyn 1 ol, 4 [4 (4 fluorophenyl) 5 (2 methoxy 4 pyrimidinyl) 1 imidazolyl]cyclohexanol, acetylcysteine, angiotensin 2 receptor antagonist, bronchodilating agent, corticosteroid, doramapimod, enoxaparin, etanercept, glutathione derivative, glycosaminoglycan, infliximab, mevinolin, muscarinic receptor blocking agent, phosphodiesterase IV inhibitor, selenium derivative, superoxide dismutase, theophylline, antiinflammatory activity, atherosclerosis, cardiovascular risk, chronic obstructive lung disease, comorbidity, corticosteroid therapy, disease control, drug activity, drug efficacy, drug fatality, heart arrhythmia, human, nonhuman, pneumonia, priority journal, pulmonary rehabilitation, review, smoking cessation, thrombosis, Bronchodilator Agents, Drug Therapy, Combination, Humans, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Inflammation, PPAR gamma, Smoking Cessation, medicine.anatomical_structure, Combination, medicine.symptom, Chronic Obstructive, medicine.medical_specialty, chronic obstructive pulmonary disease, statins, Pulmonary Disease, Drug Therapy, ACE inhibitor, medicine, Pharmacology, Lung, Angiotensin II receptor type 1, business.industry, medicine.disease, inflammation, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c94a862bcc65f8429411a120b5e3968Test
https://doi.org/10.1016/j.tips.2007.09.006Test

المؤلفون: Ling, Shuang, Xu, Jin-Wen

المصدر: Oxidative Medicine and Cellular Longevity, Vol 2016 (2016)
Oxidative Medicine and Cellular Longevity

مصطلحات موضوعية: 0301 basic medicine, Aging, Vascular fibrosis, Ischemia, Review Article, Disease, Pharmacology, Biochemistry, law.invention, 03 medical and health sciences, 0302 clinical medicine, Glucosides, law, Stilbenes, Active component, Animals, Humans, Hypoglycemic Agents, Medicine, lcsh:QH573-671, Cellular Senescence, Neuroinflammation, Plants, Medicinal, business.industry, lcsh:Cytology, Cardiovascular Agents, Lipid metabolism, Cell Biology, General Medicine, medicine.disease, Disease Models, Animal, Neuroprotective Agents, 030104 developmental biology, Gene Expression Regulation, Fallopia multiflora, 2 3 5 4 tetrahydroxystilbene 2 o β d glucoside, business, Phytotherapy, 030217 neurology & neurosurgery, Drugs, Chinese Herbal, Signal Transduction

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8459dbc26db587fbcaf92d60a9d4e4b8Test
https://doaj.org/article/2bd65ca2f9ad4733b41aff75c05d93baTest

المؤلفون: Serena Ammendola, Maria Lucibello, Lionel N. J.L. Marlier, Persio Dello Sbarba, Nicola Zambrano, Paolo Bonini, Enrico Garaci, Tommaso Russo, Giovanna De Chiara, Federico Cozzolino, Danilo Labardi, Anna Teresa Palamara, Maria Torcia, Paolo Rosini, Lucia Nencioni

المساهمون: Torcia, M, De Chiara, G, Nencioni, L, Ammendola, S, Labardi, D, Lucibello, M, Rosini, P, Marlier, Ln, Bonini, P, Dello Sbarba, P, Palamara, At, Zambrano, Nicola, Russo, Tommaso, Garaci, E, Cozzolino, F.

المصدر: 276 (2001): 39027–39036.
info:cnr-pdr/source/autori:Torcia M., De Chiara G., Nencioni L., Ammendola S., Labardi D., Lucibello M., Rosini P., Marlier L.NJL., Bonini P., Dello Sbarba P.D., Palamara A.T., Zambrano N., Russo T., Garaci E., Cozzolino F./titolo:Nerve growth factor inhibits apoptosis in memory B lymphocytes via inactivation of p38 MAPK, prevention of Bcl-2 phosphorylation, and cytochrome c release./doi:/rivista:/anno:2001/pagina_da:39027/pagina_a:39036/intervallo_pagine:39027–39036/volume:276
Università degli studi di Firenze-IRIS

مصطلحات موضوعية: mitogen activated protein kinase p38, MAPK/ERK pathway, MAP Kinase Kinase 4, Pyridines, Apoptosis, animal cell, stress activated protein kinase, Biochemistry, Cytosol, mitochondrion, Enzyme Inhibitors, Cells, Cultured, serodiagnosis, Cultured, mitogen activated protein kinase, phosphorylation, Kinase, Cytochrome c, protein function, cytochrome c, priority journal, protein transport, Bioassay, Cells, Enzymes, Mutagenesis, Nerve growth factor (NGF), 4 (4 fluorophenyl) 2 (4 methylsulfinylphenyl) 5 (4 pyridyl)imidazole, Janus kinase, nerve growth factor, protein bcl 2, serine, synaptophysin, threonine, DNA fragment, enzyme inhibitor, imidazole derivative, mitogen activated protein kinase kinase, mitogen activated protein kinase kinase 4, pyridine derivative, recombinant protein, apoptosis, article, autocrine effect, B lymphocyte, cell survival, controlled study, enzyme activation, enzyme inactivation, human, human cell, immunoprecipitation, in vitro study, in vivo study, memory cell, molecular biology, nonhuman, protein phosphorylation, protein secretion, animal, cell culture, cell nucleus, chemistry, cytosol, drug antagonism, fluorescence microscopy, immunological memory, metabolism, pathology, physiology, protein binding, rat, time, Animalia, Janus, Animals, B-Lymphocytes, Cell Nucleus, Cytochrome c Group, DNA Fragmentation, Humans, Imidazoles, Immunologic Memory, JNK Mitogen-Activated Protein Kinases, Microscopy, Fluorescence, Mitochondria, Mitogen-Activated Protein Kinase Kinases, Mitogen-Activated Protein Kinases, Nerve Growth Factor, p38 Mitogen-Activated Protein Kinases, Phosphorylation, Precipitin Tests, Protein Binding, Protein Transport, Proto-Oncogene Proteins c-bcl-2, Rats, Recombinant Proteins, Serine, Threonine, Time Factors, p38 mitogen-activated protein kinases, Fluorescence, Protein kinase A, Molecular Biology, NGF, apoptosis, B lymphocytes, Microscopy, biology, Settore MED/07 - Microbiologia e Microbiologia Clinica, Autocrine signalling, Cell Biology, Molecular biology, Nerve growth factor, biology.protein

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9638ba3340c20fa3404d10801c31cd5eTest
https://doi.org/10.1074/jbc.m102970200Test

المؤلفون: John O. Trent, Jason Chesney, Sucheta Telang, Brian F. Clem, Umesh Goswami, Abdullah Yalcin, Sengodagounder Arumugam, Amy L. Clem

المساهمون: Uludağ Üniversitesi/Veterinerlik Fakültesi/Biyokimya Anabilim Dalı., Yalçın, Abdullah, ABI-4164-2020, A-5261-2016

المصدر: Oncogene

مصطلحات موضوعية: Cancer Research, Choline kinase, Unclassified drug, Mouse, Biochemistry & molecular biology, Signal transduction, Mitogen activated protein kinase, Steady state, Computational biology, Hela cells, chemistry.chemical_compound, Mice, 0302 clinical medicine, n (3,5 dimethylphenyl) 2 [[5 (4 ethylphenyl) 1h 1,2,4 triazol 3 yl]sulfanyl] acetamide, Computer model, Acetamides, Phosphatidic acid, Second messenger, Cancer inhibition, Enzyme activity, Phosphorylation, Mitogen-activated protein kinases, Cell proliferation, Phosphocholine, Priority journal, Phosphatidic-acid, 0303 health sciences, Extracellular signal-regulated MAP kinases, Genetics & heredity, Enzyme inhibitors, Molecular interaction, Enzyme inhibitor, 3. Good health, Cell biology, Biochemistry, Oncology, Protein conformation, 030220 oncology & carcinogenesis, Female, Models, molecular, Phosphatidylinositol 3-kinases, Choline Kinase, Phosphoethanolamine, N Acetylaspartic Acid, Xenograft model antitumor assays, Human, Prostate-cancer, Phosphorylcholine, Choline kinase alpha, Biology, Protein targeting, Article, 03 medical and health sciences, Protein kinase B, Genetics, Chemotherapy, Animals, Humans, Animal model, Animal experiment, Protein kinase A, Molecular Biology, Lung tumor, 030304 developmental biology, MAP kinase kinase kinase, Inhibitors, In silico, Phospholipase-D, Proto-oncogene proteins c-akt, Ras activation, Triazoles, Nonhuman, Raf-1, Actins, MAP kinase signaling system, Proto-oncogene proteins p21(ras), Phosphatidylcholine, Metabolism, chemistry, P-31, Human cell, Breast-cancer-cells, Protein expression, Cyclin-dependent kinase 9, Tumor xenograft, Cell membrane, Controlled study, Phosphatidylinositol 3 kinase, Growth-factors

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a4c80b6dd975991bdaafb743d0952b0Test
http://hdl.handle.net/11452/22749Test

المؤلفون: Salamone, G.V., Petracca, Y., Bass, J.I.F., Rumbo, M., Nahmod, K.A., Gabelloni, M.L., Vermeulen, M.E., Matteo, M.J., Geffner, J.R., Trevani, A.S.

المصدر: Lab. Invest. 2010;90(7):1049-1059
Biblioteca Digital (UBA-FCEN)
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN

مصطلحات موضوعية: mitogen activated protein kinase p38, Salmonella typhimurium, Neutrophils, Apoptosis, flagellin, fluorescence microscopy, toll like receptor 5, flagellum, immunology, leukocyte activation, caspase 3, phosphatidylinositol 3 kinase, enzyme phosphorylation, Cells, Cultured, drug effect, article, NF-kappa B, neutrophil, 2 (2 amino 3 methoxyphenyl)chromone, wortmannin, immunoglobulin enhancer binding protein, priority journal, Proto-Oncogene Proteins c-bcl-2, myeloid cell leukemia sequence 1 protein, Flagella, Salmonella Infections, protein degradation, cytokine production, wild type, signal transduction, protein bcl 2, salmonellosis, Cell Survival, MAP Kinase Signaling System, enzymology, interleukin 8, protein mcl 1, 3 (4 methylphenylsulfonyl) 2 propenenitrile, bacterium mutant, 4 (4 fluorophenyl) 2 (4 methylsulfinylphenyl) 5 (4 pyridyl)imidazole, Humans, controlled study, human, protein expression, cell culture, Helicobacter pylori, flow cytometry, human cell, mitogen activated protein kinase 3, mitogen activated protein kinase 1, physiology, protein kinase B, I kappa B alpha, metabolism

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od______3056::b7dde45b933cc71d79e723e81199d6c9Test

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/ İç Hastalıkları Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Kadın Hastalıkları ve Doğum Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Pediatri Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Genetik Anabilim Dalı., Ali, Rıdvan, Özkalemkaş, Fahir, Kimya, Yalçın, Köksal, Nligün, Özkocaman, Vildan, Gülten, Tuna, Yorulmaz, Hakan, Tunalı, Ahmet Semih, AAH-1854-2021, AAG-8495-2021, AAG-8393-2021

مصطلحات موضوعية: Male, Fetus risk, Blood sampling, Leukocytosis, Child growth, Review, Treatment response, Drug milk level, Piperazines, Infant, newborn, Targeted therapy, Issues, BCR ABL protein, Umbilical cord blood, Drug blood level, Teratogenicity, Pregnancy, hemic and lymphatic diseases, Antineoplastic agents, Hydroxyurea, Obstetrics & gynecology, Disease course, Treatment outcome, Cml, Child development, Vaginal delivery, Cancer, Drug tolerability, Prenatal drug exposure, 2 [2 methyl 5 [4 (1 piperazinylmethyl)benzamido]anilino] 4 (3 pyridyl)pyrimidine, Patient, Chronic myeloid leukemia, Anemia, Puerperium, Infant peripheral blood, Prognosis, Management, Amnion fluid, Female, Safety, Human, Adult, Breast milk, Fetus echography, Maternal blood, Breast feeding, Leukemia, myeloid, chronic-phase, Milk, human, Cytogenetics, Case report, Mesylate, Humans, Leukapheresis, Apgar score, neoplasms, Chronic myeloid-leukemia, Spontaneous abortion, Fetus growth, Gestational age, Philadelphia chromosome positive cell, Leukemia remission, Labor induction, Chronic Myeloid Leukemia, Imatinib, Thrombocythemia, Pyrimidines, Pregnancy complications, neoplastic, Drug determination, Drug tolerance, High performance liquid chromatography

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od______9458::058a8c3f7f625c3492c6b8261cde5ab5Test
http://hdl.handle.net/11452/22815Test