نتائج البحث

المساهمون: Caggiari, Laura, Miolo, Gianmaria, Buonadonna, Angela, Basile, Debora, Santeufemia, Davide, Cossu, Antonio, Palmieri, Giuseppe, De Zorzi, Mariangela, Fornasarig, Mara, Alessandrini, Lara, Canzonieri, Vincenzo, Lo Re, Giovanni, Puglisi, Fabio, Steffan, Agostino, Cannizzaro, Renato, De Re, Valli

المصدر: International journal of molecular sciences (Online) (2018). doi:10.3390/ijms19010047
info:cnr-pdr/source/autori:Caggiari L, Miolo G, Buonadonna A, Basile D,? Santeufemia D, Cossu A, Palmieri G, De Zorzi M, Fornasarig M, Alessandrini L, Canzonieri V, Lo Re G,? Puglisi F, Steffan A, Cannizzaro R, De Re V/titolo:Characterizing metastatic HER2-positive gastric cancer at the CDH1 haplotype/doi:10.3390%2Fijms19010047/rivista:International journal of molecular sciences (Online)/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume
International Journal of Molecular Sciences; Volume 19; Issue 1; Pages: 47
International Journal of Molecular Sciences, Vol 19, Iss 1, p 47 (2017)

مصطلحات موضوعية: 0301 basic medicine, CDH1, E-cadherin, HER2, Metastatic gastric cancer, Rs16260, Rs1801552, Catalysis, Molecular Biology, Spectroscopy, Computer Science Applications1707 Computer Vision and Pattern Recognition, Physical and Theoretical Chemistry, Organic Chemistry, Inorganic Chemistry, medicine.medical_treatment, metastatic gastric cancer, rs16260, rs1801552, Context (language use), Targeted therapy, lcsh:Chemistry, 03 medical and health sciences, 0302 clinical medicine, Trastuzumab, In vivo, medicine, skin and connective tissue diseases, lcsh:QH301-705.5, biology, business.industry, Standard treatment, Haplotype, Cancer, General Medicine, medicine.disease, Computer Science Applications, 030104 developmental biology, lcsh:Biology (General), lcsh:QD1-999, Carcinoma gastrico, 030220 oncology & carcinogenesis, Cancer research, biology.protein, business, medicine.drug, CDH1 gene

وصف الملف: ELETTRONICO; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::253193e08cca3a75502e1d661c575453Test
https://www.mdpi.com/1422-0067/19/1/47Test

8

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

تنقيح النتائج