Cargando…
Cystine nephrolithiasis
Our understanding of the molecular basis of cystinuria has deepened as the result of the causative genes, SLC3A1 and SLC7A9, being identified. The proteins coded for by these genes form a heterodimer responsible for reabsorption of filtered cystine in the proximal tubule. Failure of this transport s...
Autores principales: | Fattah, Hasan, Hambaroush, Yasmin, Goldfarb, David S. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220544/ https://www.ncbi.nlm.nih.gov/pubmed/25383320 http://dx.doi.org/10.3978/j.issn.2223-4683.2014.07.04 |
Ejemplares similares
-
Accurate 24-h urine cystine quantification for patients on cystine-binding thiol drugs
por: Mikel, Charles C., et al.
Publicado: (2022) -
Pediatric Nephrolithiasis
por: Cao, Brent, et al.
Publicado: (2023) -
Significant differences in struvite and cystine stone frequency seen among Chinese nephrolithiasis patients living in North America compared to those living in China
por: Chi, Thomas, et al.
Publicado: (2016) -
Nutrition in calcium nephrolithiasis
por: Dogliotti, Elena, et al.
Publicado: (2013) -
Metabolic syndrome and nephrolithiasis
por: Ramaswamy, Krishna, et al.
Publicado: (2014)