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1دورية أكاديمية
المؤلفون: Quintero-Ronderos, Paula, Mercier, Eric, Gris, Jean-Christophe, Esteban-Perez, Clara, Moreno-Ortiz, Harold, Lucena, Elkin, Vaiman, Daniel, Fonseca-Mendoza, Dora Janeth, Laissue, Paul
المصدر: instname:Universidad del Rosario
مصطلحات موضوعية: Adult, Article, Caucasian, Controlled study, Female, Gene, Gene frequency, Gene mutation, Gene sequence, Human, Major clinical study, Mestizo, Polymerase chain reaction, Pregnancy disorder, Recurrent pregnancy loss, Single nucleotide polymorphism, Spontaneous abortion, Thbd gene, Biology, Case control study, Genetic database, Genetic predisposition, Genetic variation, Genetics, Pregnancy, Recurrent abortion, Thrombomodulin, Case-control studies, Computational biology, Genetic predisposition to disease
وصف الملف: application/pdf
العلاقة: https://repository.urosario.edu.co/handle/10336/22921Test; https://doi.org/10.1186/s12958-017-0311-0Test
الإتاحة: https://doi.org/10.1186/s12958-017-0311-0Test
https://repository.urosario.edu.co/handle/10336/22921Test -
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المؤلفون: Alexander Tolios, Johanna Gebhart, Stefanie Hofer, Dino Mehic, Ingrid Pabinger, Kate Downes, Matthias Haimel, Helmuth Haslacher, Cihan Ay
المصدر: Haemophilia : the official journal of the World Federation of Hemophilia. 27(6)
مصطلحات موضوعية: medicine.medical_specialty, business.industry, Thrombomodulin, Thrombin, Hematology, General Medicine, Plasma levels, Thbd gene, Blood Coagulation Disorders, medicine.disease, Hemorrhagic Disorders, Gastroenterology, Internal medicine, Cohort, Coagulopathy, medicine, Humans, In patient, Blood Coagulation Tests, Risk factor, business, Genetics (clinical), Plasma clot
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b66eb6902a9b6260cb4bacd0625c0172Test
https://pubmed.ncbi.nlm.nih.gov/34628704Test -
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المؤلفون: Eric Alamartine, Paula Vieira-Martins, Perrine Jullien, Veronique Fremeaux Bacchi, Nicolas Maillard, Christophe Mariat
المصدر: Nephrology Dialysis Transplantation. 36
مصطلحات موضوعية: Immunoglobulin A, Transplantation, biology, business.industry, Haplotype, Thbd gene, medicine.disease, Thrombomodulin, Nephropathy, Nephrology, Factor H, Immunology, Cohort, medicine, biology.protein, business, Allele frequency
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::935716218dce1cd24068247ff3494261Test
https://doi.org/10.1093/ndt/gfab104.0033Test -
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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 -
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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 -
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المؤلفون: Alexander P. Reiner, Nigel S. Key
المصدر: Blood. 127:1844-1845
مصطلحات موضوعية: 0301 basic medicine, Genetics, business.industry, Immunology, Ethnic group, Venous Thromboembolism, Cell Biology, Hematology, 030204 cardiovascular system & hematology, Thbd gene, Thrombomodulin, Polymorphism, Single Nucleotide, Biochemistry, Thrombosis and Hemostasis, Black or African American, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Risk Factors, Ethnicity, Humans, Medicine, Chromosome 20, business, Venous thromboembolism
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d00ae0838bdcf8a6b06eff93700b908Test
https://doi.org/10.1182/blood-2016-03-701698Test