Search details
1.
Endotoxemia Correlates with Kidney Function and Length of Stay in Critically Ill Patients.
Blood Purif
; 53(1): 30-39, 2024.
Article
in English
| MEDLINE | ID: mdl-37918364
2.
Krüppel-like factor 6-mediated loss of BCAA catabolism contributes to kidney injury in mice and humans.
Proc Natl Acad Sci U S A
; 118(23)2021 06 08.
Article
in English
| MEDLINE | ID: mdl-34074766
3.
Transcriptional regulation of proximal tubular metabolism in acute kidney injury.
Pediatr Nephrol
; 38(4): 975-986, 2023 04.
Article
in English
| MEDLINE | ID: mdl-36181578
4.
Loss of proximal tubular transcription factor Krüppel-like factor 15 exacerbates kidney injury through loss of fatty acid oxidation.
Kidney Int
; 100(6): 1250-1267, 2021 12.
Article
in English
| MEDLINE | ID: mdl-34634362
5.
Autosomal dominant osteopetrosis associated with renal tubular acidosis is due to a CLCN7 mutation.
Am J Med Genet A
; 170(11): 2988-2992, 2016 11.
Article
in English
| MEDLINE | ID: mdl-27540713
6.
Receptor-mediated endocytosis and endosomal acidification is impaired in proximal tubule epithelial cells of Dent disease patients.
Proc Natl Acad Sci U S A
; 110(17): 7014-9, 2013 Apr 23.
Article
in English
| MEDLINE | ID: mdl-23572577
7.
Roles of Krüppel-Like Transcription Factors KLF6 and KLF15 in Proximal Tubular Metabolism.
Nephron
; 147(12): 766-768, 2023.
Article
in English
| MEDLINE | ID: mdl-37263229
8.
Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism.
Hum Mol Genet
; 19(10): 2028-38, 2010 May 15.
Article
in English
| MEDLINE | ID: mdl-20190276
9.
Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21.
Hum Genet
; 129(1): 51-8, 2011 Jan.
Article
in English
| MEDLINE | ID: mdl-20976470
10.
Proximal Tubular Transcription Factors in Acute Kidney Injury: Recent Advances.
Nephron
; 144(12): 613-615, 2020.
Article
in English
| MEDLINE | ID: mdl-32645697
11.
Genetic background influences tumour development in heterozygous Men1 knockout mice.
Endocr Connect
; 9(5): 426-437, 2020 May.
Article
in English
| MEDLINE | ID: mdl-32348957
12.
An N-Ethyl-N-Nitrosourea (ENU)-Induced Tyr265Stop Mutation of the DNA Polymerase Accessory Subunit Gamma 2 (Polg2) Is Associated With Renal Calcification in Mice.
J Bone Miner Res
; 34(3): 497-507, 2019 03.
Article
in English
| MEDLINE | ID: mdl-30395686
13.
Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis.
J Bone Miner Res
; 34(7): 1324-1335, 2019 07.
Article
in English
| MEDLINE | ID: mdl-30830987
14.
Podocyte-Specific Loss of Krüppel-Like Factor 6 Increases Mitochondrial Injury in Diabetic Kidney Disease.
Diabetes
; 67(11): 2420-2433, 2018 11.
Article
in English
| MEDLINE | ID: mdl-30115650
15.
An N-Ethyl-N-Nitrosourea (ENU) Mutagenized Mouse Model for Autosomal Dominant Nonsyndromic Kyphoscoliosis Due to Vertebral Fusion.
JBMR Plus
; 2(3): 154-163, 2018 May.
Article
in English
| MEDLINE | ID: mdl-30283900
16.
A mouse model for inherited renal fibrosis associated with endoplasmic reticulum stress.
Dis Model Mech
; 10(6): 773-786, 2017 06 01.
Article
in English
| MEDLINE | ID: mdl-28325753
17.
Cinacalcet corrects hypercalcemia in mice with an inactivating Gα11 mutation.
JCI Insight
; 2(20)2017 10 19.
Article
in English
| MEDLINE | ID: mdl-29046478
18.
Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy.
JCI Insight
; 2(3): e91103, 2017 02 09.
Article
in English
| MEDLINE | ID: mdl-28194447
19.
Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Signaling Pathway.
PLoS One
; 11(12): e0167916, 2016.
Article
in English
| MEDLINE | ID: mdl-27959934
20.
Identification of a G-Protein Subunit-α11 Gain-of-Function Mutation, Val340Met, in a Family With Autosomal Dominant Hypocalcemia Type 2 (ADH2).
J Bone Miner Res
; 31(6): 1207-14, 2016 06.
Article
in English
| MEDLINE | ID: mdl-26818911