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1دورية أكاديمية
المؤلفون: Cheng Xiao, Siliang Chen, Chunru Yang, Jieying Liu, Miao Yu
المصدر: Frontiers in Genetics, Vol 13 (2022)
مصطلحات موضوعية: WGCNA, metabolic dysfunction-associated fatty liver disease, polyunsaturated fatty acids, differentially expressed genes, ADAMTS1 gene, TGFβ3 gene, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fgene.2022.951224/fullTest; https://doaj.org/toc/1664-8021Test
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المؤلفون: Veniamin S. Fishman, S. A. Vasilyev, Oleg L. Serov, A. V. Vertinsky, Igor N. Lebedev, Evgeniia Sukhikh, A. A. Murashkina, Leonid Sukhikh, R. R. Savchenko
المصدر: Russian Journal of Genetics. 57:856-862
مصطلحات موضوعية: HeLa, ADAMTS1 Gene, Plasmid, biology, DNA repair, Cell culture, Micronucleus test, Genetics, Transfection, biology.organism_classification, Gene, Molecular biology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::531f7583d64b1c1f5f5d3b3bfac60c56Test
https://doi.org/10.1134/s1022795421070127Test -
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المؤلفون: Xiaofei Guo, Mingxing Chu, Ran Di, Qianqian Tang, Qiuyue Liu, Wenping Hu, Yan Yan, Zhuangbiao Zhang, Xiangyu Wang, Mei Jin, Jishun Tang, Yingjie Zhang, Pinqing Wang
المصدر: Veterinary Medicine and Science
مصطلحات موضوعية: ADAMTS1 Gene, Acetylserotonin O-Methyltransferase, Litter Size, media_common.quotation_subject, Single-nucleotide polymorphism, Biology, ASMT gene, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, reproduction, single nucleotide polymorphisms, ADAMTS1 Protein, Genotype, SNP, Animals, Allele, Gene, media_common, Genetics, General Veterinary, Goats, goat, Original Articles, Breed, Original Article, Female, Reproduction, ADAMTS1 gene, Polymorphism, Restriction Fragment Length
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a5ab26d8ac3dfe6dffebdec46d14976Test
http://europepmc.org/articles/PMC7738733Test -
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المؤلفون: Cheng Xiao, Siliang Chen, Chunru Yang, Jieying Liu, Miao Yu
مصطلحات موضوعية: Genetics, Genetic Engineering, Biomarkers, Developmental Genetics (incl. Sex Determination), Epigenetics (incl. Genome Methylation and Epigenomics), Gene Expression (incl. Microarray and other genome-wide approaches), Genome Structure and Regulation, Genomics, Genetically Modified Animals, Livestock Cloning, Gene and Molecular Therapy, WGCNA, metabolic dysfunction-associated fatty liver disease, polyunsaturated fatty acids, differentially expressed genes, ADAMTS1 gene, TGFβ3 gene
الإتاحة: https://doi.org/10.3389/fgene.2022.951224.s004Test
https://figshare.com/articles/dataset/Table1_Identification_of_polyunsaturated_fatty_acids_related_key_modules_and_genes_in_metabolic_dysfunction-associated_fatty_liver_disease_using_WGCNA_analysis_DOCX/21515655Test -
5دورية أكاديمية
المؤلفون: Mastronardi, Claudio Alberto, Paz-Filho, Gilberto, Zanoni, Martina, Arcos-Burgos, Mauricio, Licinio, Julio, Wong, Ma-Li, Molano-González, Nicolas
المصدر: instname:Universidad del Rosario
مصطلحات موضوعية: Endotoxin, Escherichia coli lipopolysaccharide, Sodium chloride, Interleukin 1beta converting enzyme, Lipopolysaccharide, Adamts1 gene, Adrenal gland, Animal experiment, Animal model, Animal tissue, Article, Caspase 1 gene, Controlled study, Correlation coefficient, Cxc motif ligand 1 gene, Cxc motif ligand 10 gene, Disintegrin like and metallopeptidase with thrombospondin type 1 motif 1 gene, Gene expression profiling, Gene inactivation, Gene interaction, Genetic association, Guanylate binding protein 2 gene, Hippocampus, Immune response gene, Immunogenetics, Inducible nitric oxide synthase gene, Inflammation, Injection, Interleukin 1 receptor antagonist gene, Lethality
وصف الملف: application/pdf
العلاقة: https://repository.urosario.edu.co/handle/10336/22651Test; https://doi.org/10.1159/000368310Test
الإتاحة: https://doi.org/10.1159/000368310Test
https://repository.urosario.edu.co/handle/10336/22651Test -
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المؤلفون: Qianqian Tang, Zhuangbiao Zhang, Xiangyu Wang, Qiuyue Liu, Xiaofei Guo, Jishun Tang, Yingjie Zhang, Pinqing Wang, Ran Di, Mingxing Chu, Wenping Hu, Yan Yan, Mei Jin
مصطلحات موضوعية: Litter (animal), ADAMTS1 Gene, Animal science, Biology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87ee83f13423977d420b05d307a13913Test
https://doi.org/10.1002/vms3.301/v3/response1Test -
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المؤلفون: Nicolás Molano-González, Gilberto Paz-Filho, Claudio A. Mastronardi, Mauricio Arcos-Burgos, Martina Zanoni, Julio Licinio, Ma-Li Wong
المصدر: Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosarioمصطلحات موضوعية: Male, Mouse, Interleukin 1beta converting enzyme, Caspase 1 gene, Real time polymerase chain reaction, Gene inactivation, Mice, 0302 clinical medicine, Endocrinology, Endotoxin, Gene expression, Coexpression, 0303 health sciences, Systemic Inflammatory Response Syndrome, Gene expression profiling, 3. Good health, CXCL1, Neurology, Deficiency, Cox2, Immunology, Caspase 1, Adrenal glands, Disease models, Article, 03 medical and health sciences, Interleukin 1 receptor antagonist gene, C57bl mouse, Genetics, Animal model, Animal experiment, Cxcl1, Lethality, Disease model, Endocrine and Autonomic Systems, medicine.disease, Mice, Inbred C57BL, Systemic inflammatory response syndrome, Correlation coefficient, chemistry, 030217 neurology & neurosurgery, Lipopolysaccharides, Injection, Chemokine, Lipopolysaccharide, Gene Expression, knockout, Hippocampus, Animal tissue, chemistry.chemical_compound, Chemically induced, Cxcl10, Adrenal Glands, Immune response gene, animal, Adamts1 gene, Inducible nitric oxide synthase gene, Priority journal, Mice, Knockout, Nerve cell plasticity, Cxc motif ligand 1 gene, Disintegrin like and metallopeptidase with thrombospondin type 1 motif 1 gene, Chemokines, inbred c57bl, medicine.symptom, Transcription, Nos2, Sodium chloride, Cxc motif ligand 10 gene, Guanylate binding protein 2 gene, Wild type, Gene interaction, Inflammation, Biology, Knockout mouse, T cell specific gtpase 1 gene, Immunogenetics, medicine, Animals, CXCL10, 030304 developmental biology, Adrenal gland, Escherichia coli lipopolysaccharide, Nonhuman, Adamts1, Disease Models, Animal, Metabolism, Prostaglandin endoperoxide synthase 2 gene, Genetic association, biology.protein, Controlled study, Spleen
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6310c39c486ef873f1ba1dfbb9dbf0a5Test
https://doi.org/10.1159/000368310Test -
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المؤلفون: Carlos F. Suárez, Eric Mercier, Manuel A. Patarroyo, Michiko Fukuda, Daniel Vaiman, Jean-Christophe Gris, Paula Quintero-Ronderos, Ronald Gonzalez, Paul Laissue
المساهمون: Caractéristiques féminines des dysfonctions des interfaces cardio-vasculaires (EA 2992), Université Montpellier 1 (UM1)-Université de Montpellier (UM), Centre Hospitalier Universitaire de Nîmes (CHU Nîmes), National Institute of Advanced Industrial Science and Technology (AIST), Institut Cochin (IC UM3 (UMR 8104 / U1016)), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Université de Montpellier (UM)-Université Montpellier 1 (UM1), Centre Hospitalier Régional Universitaire de Nîmes (CHRU Nîmes)
المصدر: PLoS ONE, Vol 12, Iss 10, p e0186149 (2017)
PLoS ONE
PLoS ONE, Public Library of Science, 2017, 12 (10), pp.e0186149. ⟨10.1371/journal.pone.0186149⟩
Larsen, E.C., Christiansen, O.B., Kolte, A.M., Macklon, N., New insights into mechanisms behind miscarriage (2013) BMC Med, 11, p. 154., https://doi.org/10.1186/1741-7015-11-154Test, https://doi.org/10.1186/1741-7015-11-154Test PMID: 23803387
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario
Repositorio Institucional UDCA
Universidad de Ciencias Aplicadas y Ambientales U.D.C.A
instacron:Universidad de Ciencias Aplicadas y Ambientales U.D.C.Aمصطلحات موضوعية: Caucásico, Gene Mutation, Secondary, Gene mutation, Pathology and Laboratory Medicine, Gene, Biochemistry, Models, Pregnancy, Fgfr2 Gene, Proteína Mmp1, Thbd Gene, Modificación de ADN, Genetic Stability, Exome sequencing, Clinical Article, Gen Col6A3, Thrombin, High-Throughput Nucleotide Sequencing, Gen F5, Genomics, Col6A3 Gene, Mmp1 Gene, Secuenciación de alto rendimiento, Fibrinogen Alphac, Factor V Deficiency, Ncoa1 Gene, Protein Structure, Genotype, Tro Gene, Adamts1 Gene, Variación genética, Amn gen, Creer gen, Gen Flt1, 03 medical and health sciences, Protein Domains, Gen Mmp9, Enfermedades del aparato genital, Gen Ncoa1, Genetics, Teoría cuántica, Molecular Biology Assays and Analysis Techniques, lcsh:R, Abortion, Biology and Life Sciences, Computational Biology, Proteins, Gen Mmp1, Enfermedades, Fga Gene, Peptide Fragments, Secuenciación de próxima generación, Epas1 Gene, 030104 developmental biology, Quantum Theory, lcsh:Q, Gen Bmp7, Genotipo, Estructura de la proteína, Models, Molecular, Etiology, La expresión génica, Gene Expression, lcsh:Medicine, Bmp7 Gene, Whole Exome Sequencing, Database and Informatics Methods, Gen Fgfr2, Gen Thbd, Medicine and Health Sciences, Gen Cdh11, Multidisciplinary, Gen, Lifr Gene, Deficiencia de Factor V, Deletion Mutation, Phenotype, Cr1 Gene, Función del gen, Factor Xa, Amino Acid Analysis, Thermodynamics, Gen Adams1, Matrix Metalloproteinase 1, Transcriptome Analysis, Adult, Amn Gene, Mmp1 Protein, Gen Ido2, Protein Domain, Secundario, Aborto Recurrente, Pathophysiology, Variabilidad genética, medicine, Fragmento de péptido, Gen Traf3Ip1, Mutación genética, Molecular Model, Genome Analysis, Metabolism, Aborto, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology, Biología, Disease, Aborto Habitual, El embarazo, 0302 clinical medicine, Fisiopatología, DNA sequencing, Infertilidad, lcsh:Science, Exome, Mutation, 030219 obstetrics & reproductive medicine, Química, Tlr3 Gene, Estromelisina 2, Dominio de proteínas, 3. Good health, Genetic Variability, Fenotipo, Modelo molecular, Human, Next-Generation Sequencing, Abortion, Habitual, Bioinformatics, Secuenciación de nucleótidos de alto rendimiento, Gen Tlr3, Código genético, Gen Tnc, Humans, Protein Interaction Domains and Motifs, Humano, Biology, Secuenciación del exoma completo, Termodinámica, High Throughput Sequencing, Factor V, Molecular, Genetic Variation, Cdh11 Gene, medicine.disease, Habitual, Human genetics, Molecular biology techniques, Sanger Sequencing, Ido2 Gene, Cdh1 Gene, Estabilidad Genética, 0301 basic medicine, Molecular biology, Next Generation Sequencing, Mmp9 Gene, Dna Modification, Estructura secundaria de proteínas, medicine.disease_cause, Protein Structure, Secondary, Fibrinógeno Alphac, Sequencing techniques, Peptide Fragment, Flt1 Gene, Exoma, Fibrinógeno, Protein Secondary Structure, Artículo Clínico, Metabolismo, Dominios y motivos de interacción de proteínas, Traf3Ip1 Gene, Gen lifr, Matriz metaloproteinasa 1, Bioinformática, Protein Interaction Domains And Motifs, Chemistry, Genetic Code, Biología Computacional, Female, Research Article, Fragmentos de péptidos, Gene Sequence, F5 Gene, Gen Cr1, Caucasian, Research and Analysis Methods, Gen Cdh1, Matrix Metalloproteinase 10, Secuencia de genes, Secuenciación de Sangre, Mutación, Gen Fga, Modelos, Fibrinogen, Human Genetics, Reproducción, Genética, Gen Epas1, Recurrent Abortion, Gene Function, Stromelysin 2
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65f7d0de31680d2d2380888c26429ed7Test
http://europepmc.org/articles/PMC5634651?pdf=renderTest