Kendrah Kidd
Overview
Explore the profile of Kendrah Kidd including associated specialties, affiliations and a list of published articles.
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Articles
30
Citations
408
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Recent Articles
1.
Schott C, Arnaldi M, Baker C, Wang J, McIntyre A, Colaiacovo S, et al.
Kidney Int Rep
. 2025 Feb;
10(2):574-590.
PMID: 39990878
Introduction: Genetic kidney disease (GKD) accounts for 10% to 20% of chronic kidney disease (CKD). Genetic testing using gene panel or targeted exome sequencing (ES) can confirm GKD; however, integration...
2.
Bazua-Valenti S, Brown M, Zavras J, Riedl Khursigara M, Grinkevich E, Sidhom E, et al.
J Clin Invest
. 2024 Dec;
134(24).
PMID: 39680459
The trafficking dynamics of uromodulin (UMOD), the most abundant protein in human urine, play a critical role in the pathogenesis of kidney disease. Monoallelic mutations in the UMOD gene cause...
3.
Elhassan E, Kmochova T, Benson K, Fennelly N, Baresova V, Kidd K, et al.
Kidney Int Rep
. 2024 Jul;
9(7):2209-2226.
PMID: 39081747
Introduction: Monoallelic variants in the gene encoding asparagine-linked glycosylation protein 5 homolog (ALG5) have been recently shown to disrupt polycystin-1 (PC1) maturation and trafficking via underglycosylation, causing an autosomal dominant...
4.
Fages V, Bourre F, Larrue R, Wenzel A, Gibier J, Bonte F, et al.
Kidney Int Rep
. 2024 May;
9(5):1451-1457.
PMID: 38707821
Introduction: Patients with autosomal dominant tubulointerstitial kidney disease (ADTKD) usually present with nonspecific progressive chronic kidney disease (CKD) with mild to negative proteinuria and a family history. ADTKD- leads to...
5.
Kim Y, Li C, Gu C, Fang Y, Tycksen E, Puri A, et al.
Nat Commun
. 2023 Oct;
14(1):6493.
PMID: 37838725
Misfolded protein aggregates may cause toxic proteinopathy, including autosomal dominant tubulointerstitial kidney disease due to uromodulin mutations (ADTKD-UMOD), a leading hereditary kidney disease. There are no targeted therapies. In our...
6.
Jorge S, Kidd K, Vyletal P, Nogueira E, Martin L, Howard K, et al.
Kidney Int Rep
. 2023 May;
8(5):1112-1116.
PMID: 37180515
No abstract available.
7.
Airik M, Arbore H, Childs E, Huynh A, Phua Y, Chen C, et al.
Antioxidants (Basel)
. 2023 Apr;
12(4).
PMID: 37107275
Karyomegalic interstitial nephritis (KIN) is a genetic adult-onset chronic kidney disease (CKD) characterized by genomic instability and mitotic abnormalities in the tubular epithelial cells. KIN is caused by recessive mutations...
8.
de Haan A, van Eerde A, Eijgelsheim M, Rump P, Van der Zwaag B, Hennekam E, et al.
Kidney Int
. 2023 Apr;
103(5):986-989.
PMID: 37085259
No abstract available.
9.
Kim Y, Li C, Gu C, Tycksen E, Puri A, Pietka T, et al.
bioRxiv
. 2023 Jan;
PMID: 36711449
Misfolded protein aggregates may cause toxic proteinopathy, including autosomal dominant tubulointerstitial kidney disease due to uromodulin mutations (ADTKD- ), one of the leading hereditary kidney diseases, and Alzheimer’s disease etc....
10.
Al-Bataineh M, Kinlough C, Marciszyn A, Lam T, Ye L, Kidd K, et al.
J Biol Chem
. 2023 Jan;
299(3):102925.
PMID: 36682497
Polymorphism of the gene encoding mucin 1 (MUC1) is associated with skeletal and dental phenotypes in human genomic studies. Animals lacking MUC1 exhibit mild reduction in bone density. These phenotypes...