Search details
1.
The choroid plexus links innate immunity to CSF dysregulation in hydrocephalus.
Cell
; 186(4): 764-785.e21, 2023 02 16.
Article
in English
| MEDLINE | ID: mdl-36803604
2.
Small Molecule Targets TMED9 and Promotes Lysosomal Degradation to Reverse Proteinopathy.
Cell
; 178(3): 521-535.e23, 2019 07 25.
Article
in English
| MEDLINE | ID: mdl-31348885
3.
Pathogenic variants in autism gene KATNAL2 cause hydrocephalus and disrupt neuronal connectivity by impairing ciliary microtubule dynamics.
Proc Natl Acad Sci U S A
; 121(27): e2314702121, 2024 07 02.
Article
in English
| MEDLINE | ID: mdl-38916997
4.
Role of ecto-5'-nucleotidase in bladder function.
FASEB J
; 38(2): e23416, 2024 01 31.
Article
in English
| MEDLINE | ID: mdl-38198186
5.
TRIM71 mutations cause a neurodevelopmental syndrome featuring ventriculomegaly and hydrocephalus.
Brain
; 2024 Jun 04.
Article
in English
| MEDLINE | ID: mdl-38833623
6.
A novel SMARCC1 BAFopathy implicates neural progenitor epigenetic dysregulation in human hydrocephalus.
Brain
; 147(4): 1553-1570, 2024 Apr 04.
Article
in English
| MEDLINE | ID: mdl-38128548
7.
ADAR regulates APOL1 via A-to-I RNA editing by inhibition of MDA5 activation in a paradoxical biological circuit.
Proc Natl Acad Sci U S A
; 119(44): e2210150119, 2022 11.
Article
in English
| MEDLINE | ID: mdl-36282916
8.
Reduced surface pH and upregulated AE2 anion exchange in SLC26A3-deleted polarized intestinal epithelial cells.
Am J Physiol Cell Physiol
; 326(3): C829-C842, 2024 Mar 01.
Article
in English
| MEDLINE | ID: mdl-38223928
9.
Blockade of the mineralocorticoid receptor improves markers of human endothelial cell dysfunction and hematological indices in a mouse model of sickle cell disease.
FASEB J
; 37(8): e23092, 2023 08.
Article
in English
| MEDLINE | ID: mdl-37482902
10.
A neural stem cell paradigm of pediatric hydrocephalus.
Cereb Cortex
; 33(8): 4262-4279, 2023 04 04.
Article
in English
| MEDLINE | ID: mdl-36097331
11.
Apolipoprotein L1 (APOL1) cation current in HEK-293 cells and in human podocytes.
Pflugers Arch
; 475(3): 323-341, 2023 03.
Article
in English
| MEDLINE | ID: mdl-36449077
12.
OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasis.
Genet Med
; 25(3): 100351, 2023 03.
Article
in English
| MEDLINE | ID: mdl-36571463
13.
Magnesium homeostasis in deoxygenated sickle erythrocytes is modulated by endothelin-1 via Na+ /Mg2+ exchange.
FASEB J
; 36(12): e22638, 2022 12.
Article
in English
| MEDLINE | ID: mdl-36331552
14.
DGAT2 Inhibition Potentiates Lipid Droplet Formation To Reduce Cytotoxicity in APOL1 Kidney Risk Variants.
J Am Soc Nephrol
; 33(5): 889-907, 2022 05.
Article
in English
| MEDLINE | ID: mdl-35232775
15.
The erythroid K-Cl cotransport inhibitor [(dihydroindenyl)oxy]acetic acid blocks erythroid Ca2+-activated K+ channel KCNN4.
Am J Physiol Cell Physiol
; 323(3): C694-C705, 2022 09 01.
Article
in English
| MEDLINE | ID: mdl-35848620
16.
Purinergic signaling is essential for full Psickle activation by hypoxia and by normoxic acid pH in mature human sickle red cells and in vitro-differentiated cultured human sickle reticulocytes.
Pflugers Arch
; 474(5): 553-565, 2022 05.
Article
in English
| MEDLINE | ID: mdl-35169901
17.
Recruitment of APOL1 kidney disease risk variants to lipid droplets attenuates cell toxicity.
Proc Natl Acad Sci U S A
; 116(9): 3712-3721, 2019 02 26.
Article
in English
| MEDLINE | ID: mdl-30733285
18.
Trpv1 and Trpa1 are not essential for Psickle-like activity in red cells of the SAD mouse model of sickle cell disease.
Blood Cells Mol Dis
; 92: 102619, 2021 12.
Article
in English
| MEDLINE | ID: mdl-34768199
19.
Plasma Mucin-1 (CA15-3) Levels in Autosomal Dominant Tubulointerstitial Kidney Disease due to MUC1 Mutations.
Am J Nephrol
; 52(5): 378-387, 2021.
Article
in English
| MEDLINE | ID: mdl-34098564
20.
Genomics of human congenital hydrocephalus.
Childs Nerv Syst
; 37(11): 3325-3340, 2021 11.
Article
in English
| MEDLINE | ID: mdl-34232380