Results 141 to 150 of about 1,500 (175)

Human fetal kidney organoids model early human nephrogenesis and Notch-driven cell fate. [PDF]

open access: yesEMBO J
Namestnikov M   +18 more
europepmc   +1 more source

The genetic landscape of pediatric postural orthostatic tachycardia syndrome. [PDF]

open access: yesClin Auton Res
Qu H   +13 more
europepmc   +1 more source

Distinct adaptive strategies to cisplatin, vinblastine and gemcitabine in a panel of chemoresistant bladder cancer cell lines. [PDF]

open access: yesCancer Drug Resist
Cuprych-Belter M   +5 more
europepmc   +1 more source

Prevalence and characteristics of genetic disease in adult kidney stone formers. [PDF]

open access: yesNephrol Dial Transplant
Anderegg MA   +10 more
europepmc   +1 more source

In silico analysis of SLC3A1 and SLC7A9 mutations in Iranian patients with Cystinuria [PDF]

open access: yesMolecular Biology Reports, 2018
Cystinuria is an autosomal recessive defect in reabsorptive transport of cystine and the dibasic amino acids ornithine, arginine, and lysine from renal tubule and small intestine. Mutations in two genes: SLC3A1, encoding the heavy chain rbAT of the renal cystine transport system and SLC7A9, the gene of its light chain b0, + AT have a crucial role in ...
Manijeh Mahdavi Mazdeh   +2 more
exaly   +4 more sources

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