Dra. Paola Krall Opazo

paola-krall

Dra. Paola Krall Opazo

Líneas de investigación

Diagnóstico genético de enfermedades renales hereditarias, modelos animales de nefropatías
Investigación FAME UACh: http://medicina.uach.cl/investigacion/
Google Scholar: https://scholar.google.cl/citations?user=ytBBPEcAAAAJ&hl=en

 

Publicaciones

1-. S Mezzano, ADroguett, C Lavoz, P Krall, J Egido and M Ruiz-Ortega. Gremlin and Renal Diseases. Ready to jump the fence to clinical utility? Accepted in NDT. (2017).

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2-. Canales C, Krall P, Kairath P, Pérez I, Fragoso M, Carmona-Mora P, Ruiz P, Reiser J, Young J y Walz K. “Characterization of a Trpc6 transgenic mouse associated with early onset FSGS”. British Journal of Medicine & Medical Research 5(10): 1198-1212. (2015)

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3-. P Krall, C Pineda, P Ruiz, L Ejarque, T Vendrell, JA Camacho, S Mendizabal, A Oliver, J Ballarin, R Torra, E Ars. Cost-effective PKHD1 genetic testing for autosomal recessive polycystic kidney disease. Pediatr Nephrol; 29(2):223-34. doi: 10.1007/s00467-013-2657-7. (2014).

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4-. A Droguett, P Krall, ME Burgos, G Valderrama, D Carpio. L Ardiles. R Rodrígues-Diez. B Kerr. K Walz. M Ruiz-Ortega. J Egido. S Mezzano. Tubular overexpression of Gremlin induces renal damage susceptibility in mice. PLoS One. Jul 18;9(7):e101879. (2014)

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5-. P KrallCP Canales, P Kairath, P Carmona-Mora, J Molina, JD Carpio, SA Mezzano, J Li, C Wei, J Reiser, JI Young, K Walz. Podocyte-specific expression of wildtype or mutant Trpc6 is sufficient to cause severe glomerular disease. PLoS One;20;5(9):e12859. (2010)

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