نتائج البحث - "Ronald Gonzalez"

المصدر: Repositorio Institucional UDCA
Universidad de Ciencias Aplicadas y Ambientales U.D.C.A
instacron:Universidad de Ciencias Aplicadas y Ambientales U.D.C.A
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario

مصطلحات موضوعية: Luteinizing hormone, Signal peptide, single nucleotide, Granulosa cell, Genome-wide association study, Gene mutation, Primary Ovarian Insufficiency, Gene, 0302 clinical medicine, Models, Protein stability, Cell differentiation, Ovary insufficiency, Referral and Consultation, Exome sequencing, Cell proliferation, Expert system, 030219 obstetrics & reproductive medicine, Estradiol, Oocitos, Molecular etiology, Polygenic disease, Bmpr1b gene, Patient referral, Bone morphogenetic protein receptors, Multicenter study, Clinical trial, Retrospective study, Intercellular Signaling Peptides and Proteins, Cohort analysis, Human, Bioinformatics, Single-nucleotide polymorphism, Expert Systems, Major clinical study, Primary ovarian insufficiency, Molecular dynamics, Article, 03 medical and health sciences, Molecular dynamics simulation, Exome Sequencing, Genetic predisposition, Frameshift mutation, Genetics, Humans, Polymorphism, Biology, Premature ovarian failure, Gene mapping, Bone Morphogenetic Protein Receptors, Type I, Retrospective Studies, Granulosa cell differentiation, Sustitución de Aminoácidos, Whole exome sequencing, Computational Biology, Gene frequency, Retrospective studies, 030104 developmental biology, Granullosa Cells, Reproductive Medicine, Células de la Granulosa, Mutation, Estudios de Cohortes, 0301 basic medicine, Models, Molecular, Candidate gene, Gene locus, Computational biology, Cohort Studies, Expert systems, Ovarian Follicle, Ovary follicle development, Missense mutation, Female infertility, Grem1 protein, Sanger sequencing, Nonsense mutation, Protein Stability, Folículo Ovárico, Rehabilitation, Obstetrics and Gynecology, Referral and consultation, Bone morphogenetic protein receptor 1, Meiosis, Chemistry, Whole-exome sequencing, symbols, Female, Intercellular signaling peptides and proteins, France, Bmpr1b protein, Ovulation, Adult, Adolescent, Receptores de Proteínas Morfogenéticas Óseas de Tipo 1, Genetic predisposition to disease, Molecular Dynamics Simulation, Polymorphism, Single Nucleotide, Molecular model, symbols.namesake, Young Adult, Genetic Predisposition to Disease, molecular, Grem1 gene, type i, Follitropin, Single nucleotide polymorphism, Young adult, Metabolism, Amino Acid Substitution, Oocytes, Genetic variability, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c869e5368507c83a5e34bd9707c9935Test
https://academic.oup.com/humrep/article/32/7/1512/3823627Test

9

Novel genes and mutations in patients affected by recurrent pregnancy loss

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.A

مصطلحات 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

10

Nucleobindins: Bioactive precursor proteins encoding putative endocrine factors?

المؤلفون: Suraj Unniappan, Ronald Gonzalez, Haneesha Mohan

المصدر: General and Comparative Endocrinology. 176:341-346

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::656750f81681afb627e660dbc8d0d430Test
https://doi.org/10.1016/j.ygcen.2011.11.021Test

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