Navegar por término MeSH "Base Sequence"

Mostrando ítems 1-11 de 11

A novel mutation, outside of the candidate region for diagnosis, in the inverted formin 2 gene can cause focal segmental glomerulosclerosis

2013- Sánchez Ares, María; García Vidal, Marina; Espinosa Estévez, Antucho; Pardo Fernández, Julio; Vazquez Martul, Eduardo; [et al.]
Functional role of Tet-mediated RNA hydroxymethylcytosine in mouse ES cells and during differentiation.

2020- Lan, Jie; Rajan, Nicholas; Bizet, Martin; Penning, Audrey; Singh, Nitesh K; [et al.]
Genome of Rhodnius prolixus, an insect vector of Chagas disease, reveals unique adaptations to hematophagy and parasite infection

2015- Mesquita, R. D.; Vionette-Amaral, R. J.; Lowenberger, C.; Rivera-Pomar, R.; Monteiro, F. A.; [et al.]
Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene

2013- Melia, Maria J.; Kubota, Akatsuki; Ortolano, Saida; Vilchez, Juan J.; Gamez, Josep; [et al.]
Mapping genome variation of SARS-CoV-2 worldwide highlights the impact of COVID-19 super-spreaders

2020- Gómez Carballa, Alberto; Bello Paderne, Xabier; Pardo Seco, Jacobo José; Martinón Torres, Federico; Salas Ellacuriaga, Antonio [et al.]
Mosquito genomics. Highly evolvable malaria vectors: the genomes of 16 Anopheles mosquitoes

2015- Neafsey, D. E.; Waterhouse, R. M.; Abai, M. R.; Aganezov, S. S.; Alekseyev, M. A.; [et al.]
Nutritional, hormonal, and depot-dependent regulation of the expression of the small GTPase rab18 in rodent adipose tissue

2013- Pulido, M. R.; Rabanal-Ruiz, Y.; Almabouada, F.; Díaz-Ruiz, A.; Burrell, M. A.; [et al.]
Rheumatoid arthritis response to treatment across IgG1 allotype - anti-TNF incompatibility: a case-only study

2015- Montes Martínez, Ariana María; Pérez Pampín, Eva; Navarro-Sarabia, F.; Moreira, V.; de la Serna, A. R.; [et al.]
Septo-optic dysplasia caused by a novel FLNA splice site mutation: a case report

2019- Fernández Marmiesse, Ana; Pérez-Poyato, M. S.; Fontalba, A.; Marco de Lucas, E.; Martínez, M. T.; [et al.]
The Alu-rich genomic architecture of SPAST predisposes to diverse and functionally distinct disease-associated CNV alleles

2014- Boone, P. M.; Yuan, B.; Campbell, I. M.; Scull, J. C.; Withers, M. A.; [et al.]
Unraveling the effect of silent, intronic and missense mutations on VWF splicing: contribution of next generation sequencing in the study of mRNA

2019- Borràs N; Orriols G; Batlle Fonrodona, Francisco Javier; Perez Rodriguez, Almudena; Fidalgo T; [et al.]