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1 n regard to the common urinary glycoprotein, uromodulin.
2 /80(+) and CD11c(+) kidney cells phagocytize uromodulin.
3 esponsible for the physiological cleavage of uromodulin.
4 by mutations in the UMOD gene, which encodes Uromodulin, a glycosylphosphatidylinositol-anchored prot
5 hin the kidneys under high concentrations of uromodulin, a kidney-specific protein and that PyV-haufe
6 is due to immune system activation by mutant uromodulin, a mouse strain with a homologous cysteine to
8 ividuals with mutations in the gene encoding uromodulin (ADTKD-UMOD), consistent with MUC1 haploinsuf
9 t baseline, hepsin-deficient mice accumulate uromodulin, along with hyperactivated NKCC2, resulting i
11 expand the physiological role of hepsin and uromodulin and highlight the importance of hepsin-mediat
12 correlation found between urinary levels of uromodulin and markers of UTIs in the general population
15 ted aggregated uromodulin, resulting in anti-uromodulin antibodies and circulating uromodulin contain
17 Common variants in the UMOD gene encoding uromodulin, associated with risk of hypertension and CKD
22 Here, we delineate the latest discoveries in uromodulin biology and its emerging roles in modulating
25 ase UMOD expression and urinary excretion of uromodulin, causing salt-sensitive hypertension and rena
26 enle's loop cells with wild-type and mutated uromodulin cDNA were evaluated to test this hypothesis.
28 set, we tested the genotype association with uromodulin concentration in the Atherosclerosis Risk in
30 dy, we investigated the association of serum uromodulin concentration with cardiovascular biomarkers
31 itro experiments of the next step, only high uromodulin concentrations (>=1.25 mg/mL) aggregated PyV,
37 n contrast, in voided urine samples (n = 59) uromodulin concentrations were below aggregation concent
41 n anti-uromodulin antibodies and circulating uromodulin containing immune complexes with glomerular d
43 factor, ammonium, alpha 1 microglobulin, and uromodulin correlated with the increment of TScr and tub
45 nal release and subsequent polymerization of uromodulin depend on its cleavage mediated by the serine
47 itro abnormalities and to be the only mutant Uromodulin detected in conditioned medium from transfect
48 ssociated with intracellular accumulation of uromodulin, endoplasmic reticulum-stress and signs of tu
50 esearch studies have gradually revealed that uromodulin exists in multiple forms and has important ro
52 ion among DDAH1 expression, NO activity, and uromodulin expression supported by data from both animal
54 importance of hepsin-mediated processing of uromodulin for kidney tubule homeostasis and salt sensit
59 e, a GWAS signal mapped to the gene encoding uromodulin has been shown to affect blood pressure by in
61 allele, driving higher urinary excretion of uromodulin, has been kept at a high frequency because of
62 dexed to creatinine (uUCR) urinary levels of uromodulin in 29,315 individuals of European ancestry fr
64 itation of monoclonal free light chains with uromodulin in the distal tubules, defining light chain c
69 e zona pellucida sperm binding proteins, and uromodulin, In addition, there is a repeat of a motif ca
76 y organized filaments, whereas non-polymeric uromodulin is detected both in urine and in the circulat
80 Tamm-Horsfall protein (THP), also known as uromodulin, is a kidney-specific protein produced by cel
82 In the third investigative step, none of 11 uromodulin-/- knockout mice (0%) with histologic signs o
86 associated with renal function, and urinary uromodulin levels may be a biomarker for kidney disease.
87 ers of a G allele of this variant had higher uromodulin levels than noncarriers did (geometric means
89 CKD and an intermediate reduction of urinary uromodulin levels, in line with an intermediate traffick
98 ant tubulointerstitial kidney disease due to uromodulin mutations (ADTKD-UMOD), a leading hereditary
100 Activation of NLRP3 required phagocytosis of uromodulin particles into lysosomes, cathepsin leakage,
103 ach, including extensive characterisation of uromodulin processing in cellular models and in specific
105 ells to demonstrate that hepsin influence on uromodulin processing is an important modulator of salt
107 In conditions of high salt intake, defective uromodulin processing predisposes hepsin-deficient mice
109 we generated a transgenic mouse in which the uromodulin promoter controlled expression of human HO-1.
110 tions in the UMOD gene, resulting in altered uromodulin protein in the gout-associated disorders fami
113 netic studies of urate transportation and of uromodulin-related nephropathy emphasize the pivotal imp
116 al cells to secrete IL-1beta may explain why uromodulin remains immunologically inert inside the lumi
119 els of intracellular and secreted aggregated uromodulin, resulting in anti-uromodulin antibodies and
120 n the region of the UMOD gene, which encodes uromodulin (Tamm-Horsfall protein), associate with chron
121 r CKD is clear, because the encoded protein, uromodulin (Tamm-Horsfall protein), is exclusively produ
122 ut not the prevalent soluble urinary protein uromodulin (Tamm-Horsfall protein), potently inhibited g
123 dies suggest that pathologic accumulation of uromodulin/Tamm-Horsfall glycoprotein (THP) occurs in th
125 The kidney-specific gene UMOD encodes for uromodulin, the most abundant protein excreted in normal
127 cation, provide insights into the biology of uromodulin, the role of keratins in the kidney, and the
128 ivo human urine models, NETs interacted with uromodulin to form large webs that entrapped the bacteri
130 ry with roles for proteolytic degradation of uromodulin (UMOD) and several collagens, including COL1A
131 impairment attributable to mutations of the uromodulin (UMOD) gene is associated with reduced uromod
132 disease (UAKD) is caused by mutations in the uromodulin (UMOD) gene that result in a misfolded form o
135 cyte chemoattractant protein 1 (MCP-1/CCL2), uromodulin (UMOD), and YKL-40 (CHI3L1) were measured in
136 and reported three urinary biomarkers namely Uromodulin (UMOD), Osteopontin (OPN), and Interleukin-9
140 atio of CKD per 1-SD higher concentration of uromodulin was 1.72 (95% confidence interval 1.07 to 2.7
141 isfolded proteins in the kidney (mucin 1 and uromodulin), we outline the general principles of protei
144 investigative step showed colocalization of uromodulin with aggregated PyV (1) in 10 kidneys with Py