Detalhe da pesquisa
1.
In vivo base editing rescues primary hyperoxaluria type 1 in rats.
Kidney Int
; 105(3): 496-507, 2024 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-38142039
2.
Ureterocele with duplex collecting systems and febrile urinary tract infection risk.
Pediatr Surg Int
; 39(1): 200, 2023 May 16.
Artigo
Inglês
| MEDLINE | ID: mdl-37191737
3.
A comparison of the clinical characteristics of pediatric urolithiasis patients with positive and negative molecular diagnoses.
World J Urol
; 40(5): 1211-1216, 2022 May.
Artigo
Inglês
| MEDLINE | ID: mdl-35149915
4.
Lipidomics characterization of the lipid metabolism profiles in a cystinuria rat model: Precalculus damage in the kidney of cystinuria.
Prostaglandins Other Lipid Mediat
; 162: 106651, 2022 10.
Artigo
Inglês
| MEDLINE | ID: mdl-35680078
5.
Generation and characterization of a novel rat model of primary hyperoxaluria type 1 with a nonsense mutation in alanine-glyoxylate aminotransferase gene.
Am J Physiol Renal Physiol
; 320(3): F475-F484, 2021 03 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33491567
6.
Integration of exome sequencing and metabolic evaluation for the diagnosis of children with urolithiasis.
World J Urol
; 39(7): 2759-2765, 2021 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-32936332
7.
Amelioration of an Inherited Metabolic Liver Disease through Creation of a De Novo Start Codon by Cytidine Base Editing.
Mol Ther
; 28(7): 1673-1683, 2020 07 08.
Artigo
Inglês
| MEDLINE | ID: mdl-32413280
8.
CRISPR/Cas9-mediated metabolic pathway reprogramming in a novel humanized rat model ameliorates primary hyperoxaluria type 1.
Kidney Int
; 98(4): 947-957, 2020 10.
Artigo
Inglês
| MEDLINE | ID: mdl-32464217
9.
Cas9-nickase-mediated genome editing corrects hereditary tyrosinemia in rats.
J Biol Chem
; 293(18): 6883-6892, 2018 05 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29507093
10.
Identification of 8 novel gene variants in primary hyperoxaluria in 21 Chinese children with urinary stones.
World J Urol
; 37(8): 1713-1721, 2019 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-30488096
11.
Nine novel HOGA1 gene mutations identified in primary hyperoxaluria type 3 and distinct clinical and biochemical characteristics in Chinese children.
Pediatr Nephrol
; 34(10): 1785-1790, 2019 10.
Artigo
Inglês
| MEDLINE | ID: mdl-31123811
12.
Predictive Factors of Contralateral Operation after Initial Pyeloplasty in Children with Antenatally Detected Bilateral Hydronephrosis Due to Ureteropelvic Junction Obstruction.
Urol Int
; 100(3): 322-326, 2018.
Artigo
Inglês
| MEDLINE | ID: mdl-29518792
13.
Placental pathology and hypospadias.
Pediatr Res
; 81(3): 489-495, 2017 03.
Artigo
Inglês
| MEDLINE | ID: mdl-27855149
14.
Curcumin improves tendon healing in rats: a histological, biochemical, and functional evaluation.
Connect Tissue Res
; 57(1): 20-7, 2016.
Artigo
Inglês
| MEDLINE | ID: mdl-26540017
15.
Correction: Cas9-nickase-mediated genome editing corrects hereditary tyrosinemia in rats.
J Biol Chem
; 294(21): 8348, 2019 May 24.
Artigo
Inglês
| MEDLINE | ID: mdl-31127060
16.
Primary Hyperoxaluria.
N Engl J Med
; 376(15): e33, 2017 Apr 13.
Artigo
Inglês
| MEDLINE | ID: mdl-28402768
17.
Combined effect of ligament stem cells and umbilical-cord-blood-derived CD34+ cells on ligament healing.
Cell Tissue Res
; 362(3): 587-95, 2015 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-26224540
18.
Diacylglycerol kinase κ (DGKK) variants and hypospadias in Han Chinese: association and meta-analysis.
BJU Int
; 116(4): 634-40, 2015 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-25327554
19.
[Relationship between anogenital distance and cryptorchidism in human newborns].
Zhonghua Nan Ke Xue
; 21(5): 432-5, 2015 May.
Artigo
Chinês
| MEDLINE | ID: mdl-26117942
20.
Extracorporeal shock wave lithotripsy is effective in treating single melamine induced urolithiasis in infants and young children.
J Urol
; 189(4): 1498-502, 2013 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-23201375