Cargando…
A whole genome SNP genotyping by DNA microarray and candidate gene association study for kidney stone disease
BACKGROUND: Kidney stone disease (KSD) is a complex disorder with unknown etiology in majority of the patients. Genetic and environmental factors may cause the disease. In the present study, we used DNA microarray to genotype single nucleotide polymorphisms (SNP) and performed candidate gene associa...
Autores principales: | Rungroj, Nanyawan, Nettuwakul, Choochai, Sudtachat, Nirinya, Praditsap, Oranud, Sawasdee, Nunghathai, Sritippayawan, Suchai, Chuawattana, Duangporn, Yenchitsomanus, Pa-thai |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4031563/ https://www.ncbi.nlm.nih.gov/pubmed/24886237 http://dx.doi.org/10.1186/1471-2350-15-50 |
Ejemplares similares
-
Association between Human Prothrombin Variant (T165M) and Kidney Stone Disease
por: Rungroj, Nanyawan, et al.
Publicado: (2012) -
A novel loss-of-function mutation of PBK associated with human kidney stone disease
por: Nettuwakul, Choochai, et al.
Publicado: (2020) -
Impaired trafficking and instability of mutant kidney anion exchanger 1 proteins associated with autosomal recessive distal renal tubular acidosis
por: Deejai, Nipaporn, et al.
Publicado: (2022) -
Loss-of-function mutations of SCN10A encoding Na(V)1.8 α subunit of voltage-gated sodium channel in patients with human kidney stone disease
por: Nettuwakul, Choochai, et al.
Publicado: (2018) -
Genistein Sensitizes Human Cholangiocarcinoma Cell Lines to Be Susceptible to Natural Killer Cells
por: Chiawpanit, Chutipa, et al.
Publicado: (2022)