Detalhe da pesquisa
1.
Sleep Deprivation Impairs Intestinal Mucosal Barrier by Activating Endoplasmic Reticulum Stress in Goblet Cells.
Am J Pathol
; 194(1): 85-100, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37918798
2.
GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tract.
Hum Genomics
; 18(1): 41, 2024 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38654324
3.
Invariant natural killer T cells drive hepatic homeostasis in nonalcoholic fatty liver disease via sustained IL-10 expression in CD170+ Kupffer cells.
Eur J Immunol
; 53(11): e2350474, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37489253
4.
Crosstalk between Interleukin-1 Receptor-Like 1 and Transforming Growth Factor-ß Receptor Signaling Promotes Renal Fibrosis
Am J Pathol
; 193(8): 1029-1045, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37236504
5.
Phlorizin, an Important Glucoside: Research Progress on Its Biological Activity and Mechanism.
Molecules
; 29(3)2024 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38338482
6.
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
Am J Hum Genet
; 107(4): 727-742, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32891193
7.
Phenotype and genotype spectra of a Chinese cohort with nephronophthisis-related ciliopathy.
J Med Genet
; 59(2): 147-154, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33323469
8.
Diagnosis delay a family of Galloway-Mowat Syndrome caused by a classical splicing mutation of Lage3.
BMC Nephrol
; 24(1): 29, 2023 02 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36755238
9.
Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency.
Kidney Int
; 102(3): 604-612, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35643375
10.
Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy.
Kidney Int
; 102(3): 592-603, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35483523
11.
Genetic spectrum of CAKUT and risk factors for kidney failure: a pediatric multicenter cohort study.
Nephrol Dial Transplant
; 2022 Dec 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-36549658
12.
PPARα agonist exerts protective effects in podocyte injury via inhibition of the ANGPTL3 pathway.
Exp Cell Res
; 407(2): 112753, 2021 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34499887
13.
Reduction in peritonitis rates: 18-year results from the most active pediatric peritoneal dialysis center in China.
Pediatr Nephrol
; 37(10): 2437-2448, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35166916
14.
Comparative proteomic analysis of children FSGS FFPE tissues.
BMC Pediatr
; 22(1): 707, 2022 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36503536
15.
Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome.
J Am Soc Nephrol
; 32(3): 580-596, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33593823
16.
Design, Synthesis, and Bioactivity of Eighteen Novel 2H-1,4-Benzoxazin-3(4H)-one Containing a Propanolamine Moiety.
Chem Biodivers
; 19(11): e202200567, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36008877
17.
Effect of cooking methods on the edible, nutritive qualities and volatile flavor compounds of rabbit meat.
J Sci Food Agric
; 102(10): 4218-4228, 2022 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35038172
18.
[Research progress on muscle spindle morphology].
Sheng Li Xue Bao
; 74(6): 1039-1047, 2022 Dec 25.
Artigo
em Zh
| MEDLINE | ID: mdl-36594392
19.
Diagnostic and clinical utility of genetic testing in children with kidney failure.
Pediatr Nephrol
; 36(11): 3653-3662, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34031707
20.
Pediatric kidney transplantation in China: an analysis from the IPNA Global Kidney Replacement Therapy Registry.
Pediatr Nephrol
; 36(3): 685-692, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32929532