Existencias: Novel genes and mutations in patients affected by recurrent pregnancy loss

Novel genes and mutations in patients affected by recurrent pregnancy loss

Recurrent pregnancy loss is a frequently occurring human infertility-related disease affecting ~1% of women. It has been estimated that the cause remains unexplained in >50% cases which strongly suggests that genetic factors may contribute towards the phenotype. Concerning its molecular aetio...

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Detalles Bibliográficos
Autores Principales:	Quintero-Ronderos, Paula, Mercier, Eric, Fukuda, Michiko, González, Ronald, Suarez Martinez, Carlos Fernando, Alfonso Patarroyo, Manuel, Vaiman, Daniel, Gris, Jean-Christophe, Laissue, Paul
Formato:	Artículo (Article)
Lenguaje:	Inglés (English)
Publicado:	2017
Materias:	Fibrinógeno Secundario Estromelisina 2 Habitual Humano Molecular Fibrinógeno Alphac Proteína Mmp1 Fragmento de péptido Gen Adams1 Amn gen Bioinformática Gen Bmp7 Caucásico Gen Cdh1 Gen Cdh11 Artículo Clínico Gen Col6A3 Gen Cr1 Modificación de ADN Gen Epas1 Gen F5 Gen Fga Gen Fgfr2 Gen Flt1 Gen Función del gen Mutación genética Secuencia de genes Código genético Estabilidad Genética Variabilidad genética Variación genética Gen Ido2 Gen lifr Gen Mmp1 Gen Mmp9 Gen Ncoa1 Secuenciación de próxima generación Fenotipo Aborto Recurrente Secuenciación de Sangre Gen Thbd Gen Tlr3 Gen Tnc Gen Traf3Ip1 Creer gen Secuenciación del exoma completo Aborto Biología Química Exoma La expresión génica Genética Genotipo Secuenciación de alto rendimiento Metabolismo Modelo molecular Mutación Fisiopatología El embarazo Dominio de proteínas Estructura secundaria de proteínas Teoría cuántica Termodinámica Biología Computacional Secuenciación de nucleótidos de alto rendimiento Matriz metaloproteinasa 1 Modelos Fragmentos de péptidos Dominios y motivos de interacción de proteínas Estructura de la proteína Enfermedades Enfermedades del aparato genital Infertilidad Reproducción Tro Gene Protein Structure Peptide Fragments Protein Interaction Domains And Motifs Matrix Metalloproteinase 1 Humans Models Computational Biology High-Throughput Nucleotide Sequencing Thermodynamics Quantum Theory Protein Secondary Structure Protein Domain Pregnancy Pathophysiology Mutation Molecular Model Metabolism High Throughput Sequencing Genotype Genetics Gene Expression Exome Chemistry Biology Abortion Whole Exome Sequencing Traf3Ip1 Gene Tlr3 Gene Thbd Gene Sanger Sequencing Recurrent Abortion Phenotype Next Generation Sequencing Ncoa1 Gene Mmp1 Gene Mmp9 Gene Lifr Gene Ido2 Gene Genetic Variation Genetic Variability Genetic Code Genetic Stability Gene Sequence Gene Mutation Gene Function Gene Flt1 Gene Fgfr2 Gene F5 Gene Fga Gene Dna Modification Epas1 Gene Cr1 Gene Col6A3 Gene Clinical Article Cdh11 Gene Cdh1 Gene Caucasian Bmp7 Gene Amn Gene Bioinformatics Adamts1 Gene Peptide Fragment Mmp1 Protein Fibrinogen Alphac Human Stromelysin 2 Secondary Fibrinogen
Acceso en línea:	http://repository.urosario.edu.co/handle/10336/19029 https://doi.org/10.1371/journal.pone.0186149

Internet

http://repository.urosario.edu.co/handle/10336/19029
https://doi.org/10.1371/journal.pone.0186149

Novel genes and mutations in patients affected by recurrent pregnancy loss

Internet

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