-
1دورية أكاديمية
المؤلفون: Paula Quintero-Ronderos, Karen Marcela Jiménez, Clara Esteban-Pérez, Diego A. Ojeda, Sandra Bello, Dora Janeth Fonseca, María Alejandra Coronel, Harold Moreno-Ortiz, Diana Carolina Sierra-Díaz, Elkin Lucena, Sandrine Barbaux, Daniel Vaiman, Paul Laissue
المصدر: Molecular Medicine, Vol 25, Iss 1, Pp 1-8 (2019)
مصطلحات موضوعية: Therapeutics. Pharmacology, RM1-950, Biochemistry, QD415-436
وصف الملف: electronic resource
العلاقة: http://link.springer.com/article/10.1186/s10020-019-0104-3Test; https://doaj.org/toc/1076-1551Test; https://doaj.org/toc/1528-3658Test
-
2دورية أكاديمية
المؤلفون: Paula Quintero-Ronderos, Eric Mercier, Jean-Christophe Gris, Clara Esteban-Perez, Harold Moreno-Ortiz, Dora Janeth Fonseca, Elkin Lucena, Daniel Vaiman, Paul Laissue
المصدر: Reproductive Biology and Endocrinology, Vol 15, Iss 1, Pp 1-5 (2017)
مصطلحات موضوعية: Recurrent pregnancy loss, THBD, Molecular marker, Female infertility, Gynecology and obstetrics, RG1-991, Reproduction, QH471-489
وصف الملف: electronic resource
العلاقة: http://link.springer.com/article/10.1186/s12958-017-0311-0Test; https://doaj.org/toc/1477-7827Test
-
3دورية أكاديمية
المؤلفون: Paula Quintero-Ronderos, Eric Mercier, Michiko Fukuda, Ronald González, Carlos Fernando Suárez, Manuel Alfonso Patarroyo, Daniel Vaiman, Jean-Christophe Gris, Paul Laissue
المصدر: PLoS ONE, Vol 12, Iss 10, p e0186149 (2017)
وصف الملف: electronic resource
العلاقة: http://europepmc.org/articles/PMC5634651?pdf=renderTest; https://doaj.org/toc/1932-6203Test
-
4دورية أكاديمية
المؤلفون: Paula Quintero-Ronderos, Gladis Montoya-Ortiz
المصدر: Autoimmune Diseases, Vol 2012 (2012)
مصطلحات موضوعية: Immunologic diseases. Allergy, RC581-607
وصف الملف: electronic resource
-
5
المؤلفون: Dora Janeth Fonseca, Clara Esteban-Pérez, Sandrine Barbaux, María Alejandra Coronel, Elkin Lucena, Diego A. Ojeda, Diana Carolina Sierra-Diaz, Karen Marcela Jiménez, Paul Laissue, Sandra Bello, Daniel Vaiman, Paula Quintero-Ronderos, Harold Moreno-Ortiz
المصدر: Molecular Medicine, Vol 25, Iss 1, Pp 1-8 (2019)
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario
Molecular Medicineمصطلحات موضوعية: 0301 basic medicine, Pregnancy disorder, Plgf gene, Pathogenesis, Repeated implantation failure, Gene sequence, Gene mutation, Bioinformatics, Gene, Plasmid, Cohort Studies, 0302 clinical medicine, Pre-Eclampsia, Pregnancy, Placental growth factor, In vitro fertilization, lcsh:QD415-436, Promoter Regions, Genetic, Genetics (clinical), Priority journal, Reimplantation, Fetal Growth Retardation, Genetic transcription, Sequence analysis, Forkhead Transcription Factors, Phenotype, Colombian, 030220 oncology & carcinogenesis, Molecular Medicine, Female, Human, Adult, Infertility, Abortion, Habitual, Genotype, Complement component C3, Short Report, Major clinical study, Biology, Polymorphism, Single Nucleotide, Article, Preeclampsia, lcsh:Biochemistry, 03 medical and health sciences, Genetic screening, Genetics, medicine, Humans, Genetic Predisposition to Disease, Molecular Biology, Fetus, Genetic regulation, Gene deletion, lcsh:RM1-950, In vitro study, Frenchman, FOXD1 gene, Intrauterine growth retardation, medicine.disease, C3 gene, 030104 developmental biology, lcsh:Therapeutics. Pharmacology, Gene identification, Mutation, Genetic variability, Controlled study
وصف الملف: text; application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3e6cb15e50b18b0da7ec32c3cfaf10bTest
http://link.springer.com/article/10.1186/s10020-019-0104-3Test -
6
المصدر: Handbook of Tumor Syndromes ISBN: 9781351187435
Handbook of Tumor Syndromesمصطلحات موضوعية: medicine.medical_specialty, business.industry, medicine, Juvenile polyposis syndrome, medicine.disease, business, Dermatology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::e4115f390f647900b4cefd647fb5145bTest
https://doi.org/10.1201/9781351187435-19Test -
7
المؤلفون: Paul Laissue, Paula Quintero-Ronderos
المصدر: Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosarioمصطلحات موضوعية: 0301 basic medicine, FOXD1 protein, Unclassified drug, Molecular biology, Basic science, Organogenesis, Protein function, Pathogenesis, Review, Disease, Scientist, Signal transduction, Winged Helix, Embryo development, Retina development, Disease predisposition, Pregnancy, Drug Discovery, Forkhead box D1 protein, Antibody specificity, Cell proliferation, Genetics (clinical), Retina ganglion cell, Gene expression regulation, Forkhead Transcription Factors, Immunohistochemistry, Implantation, Recurrent pregnancy loss, Organ Specificity, Molecular Medicine, Female, Disease Susceptibility, Cancer aetiology, Signal Transduction, Human, Kidney development, Embryonic Development, Kidney morphogenesis, Computational biology, Biology, 03 medical and health sciences, Genetics, Animals, Humans, Gene, Transcription factor, FOXD1, Forkhead transcription factor, Body patterning, Animal, Microarray analysis, Recurrent abortion, Reproductive success, Nonhuman, Human genetics, Malignant neoplasm, Metabolism, 030104 developmental biology, Gene Expression Regulation, Central nervous system, Physician, Protein protein interaction, Protein structure, Gene expression, Risk factor
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41a1729c68f2d3bbd1177c2ec9b5b962Test
https://doi.org/10.1007/s00109-018-1665-2Test -
8
المؤلفون: Daniel Vaiman, Clara Esteban-Pérez, Paula Quintero-Ronderos, Dora Janeth Fonseca, Jean-Christophe Gris, Harold Moreno-Ortiz, Elkin Lucena, Paul Laissue, Eric Mercier
المساهمون: Center For Research in Genetics and Genomics-CIGGUR [Bogotá, Colombia] (GENIUROS Research Group), School of Medicine and Health Sciences [Bogotá, Colombia]-Universidad del Rosario [Bogotá, Colombia], Service d'Hématologie [CHRU Nîmes], Centre Hospitalier Universitaire de Nîmes (CHU Nîmes), Caractéristiques féminines des dysfonctions des interfaces cardio-vasculaires (EA 2992), Université Montpellier 1 (UM1)-Université de Montpellier (UM), Department of Reproductive Genetics [Bogotá, Colombia], The Colombian Center of Fertility and Sterility [Bogotá, Colombia] (CECOLFES), 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), This study was supported by the Universidad del Rosario (grant: CS/ABN062/GENIUROS 017)., BMC, BMC
المصدر: Reproductive Biology and Endocrinology, Vol 15, Iss 1, Pp 1-5 (2017)
Reproductive Biology and Endocrinology
Reproductive Biology and Endocrinology, BioMed Central, 2016, 15 (1), pp.92. ⟨10.1186/s12958-017-0311-0⟩
Reproductive Biology and Endocrinology, 2016, 15 (1), pp.92. ⟨10.1186/s12958-017-0311-0⟩
Reproductive Biology and Endocrinology : RB&E
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosarioمصطلحات موضوعية: single nucleotide, 0301 basic medicine, Candidate gene, Pregnancy disorder, Thrombomodulin, [SDV]Life Sciences [q-bio], THBD, Mestizo, Gene sequence, 030204 cardiovascular system & hematology, Gene mutation, Molecular marker, Bioinformatics, Gene, Computational biology, chemistry.chemical_compound, 0302 clinical medicine, Endocrinology, Gene Frequency, Pregnancy, habitual, Databases, Genetic, Coding region, lcsh:Reproduction, Female infertility, Thbd protein, Thbd, Obstetrics and Gynecology, Thbd gene, Polymerase chain reaction, [SDV] Life Sciences [q-bio], Recurrent pregnancy loss, Female, Adult, Abortion, Habitual, lcsh:QH471-489, Short Communication, Case control study, Genetic database, Genetic predisposition to disease, Single-nucleotide polymorphism, Major clinical study, Case-control studies, Caucasian, Biology, Polymorphism, Single Nucleotide, lcsh:Gynecology and obstetrics, Article, Databases, 03 medical and health sciences, Genetics, Genetic predisposition, Humans, Genetic Predisposition to Disease, Genetic variation, human, Polymorphism, Allele frequency, lcsh:RG1-991, Spontaneous abortion, Abortion, Computational Biology, Genetic Variation, Recurrent abortion, Gene frequency, Single nucleotide polymorphism, 030104 developmental biology, Reproductive Medicine, chemistry, Case-Control Studies, genetic, Controlled study, Developmental Biology
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5b097e14a5ce9be13f4434fe86d7f26Test
http://link.springer.com/article/10.1186/s12958-017-0311-0Test -
9
المؤلفون: Paul Laissue, Paula Quintero-Ronderos
المصدر: Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosarioمصطلحات موضوعية: 0301 basic medicine, Candidate gene, Abortion, Habitual, Disease, Computational biology, Biology, Miscarriage, DNA sequencing, Transcriptome, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, Pregnancy, Next generation sequencing, Exome Sequencing, Humans, Molecular implantation, Genetic Association Studies, Sanger sequencing, 030219 obstetrics & reproductive medicine, Massive parallel sequencing, Translational medicine, Obstetrics and Gynecology, Genetic Variation, High-Throughput Nucleotide Sequencing, Recurrent pregnancy loss, 030104 developmental biology, Pregnancy Maintenance, symbols, Female
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6963b494417b9a56de1399c9ef27d36Test
https://pubmed.ncbi.nlm.nih.gov/30879428Test -
10
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