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Pathogenic Variants of
SLC22A12
(URAT1) and
SLC2A9
(GLUT9) in Spanish Patients with Renal Hypouricemia: Founder Effect of
SLC2A9
Variant c.374C>T; p.(T125M).
Not available
S-EPMC10179447
|
biostudies-literature
Cite
Circulating levels of mitochondrial oxidative stress-related peptides MOTS-c and Romo1 in stable COPD: A cross-sectional study.
Not available
S-EPMC9944395
|
biostudies-literature
Cite
Splicing Analysis of Exonic OCRL Mutations Causing Lowe Syndrome or Dent-2 Disease.
Not available
S-EPMC5793168
|
biostudies-literature
Cite
The 372 T/C genetic polymorphism of TIMP-1 as a biomarker of mortality in patients with sepsis.
Not available
S-EPMC4014811
|
biostudies-literature
Cite
Novel missense mutation affecting the LIM-A domain of LMX1B in a family with Nail-Patella syndrome.
Not available
S-EPMC6409120
|
biostudies-literature
Cite
The androgen receptor expression and its activity have different relationships with prognosis in hepatocellular carcinoma.
Not available
S-EPMC7744520
|
biostudies-literature
Cite
Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations.
Not available
S-EPMC6325764
|
biostudies-literature
Cite
New
SLC22A12
(URAT1) Variant Associated with Renal Hypouricemia Identified by Whole-Exome Sequencing Analysis and Bioinformatics Predictions.
Not available
S-EPMC10530539
|
biostudies-literature
Cite
Sex differences in the prognostic value of urinary albumin-to-creatinine ratio for coronary artery disease and cardiovascular events in people with type 2 diabetes and normoalbuminuria.
Not available
S-EPMC12590722
|
biostudies-literature
Cite
Klotho expression in peripheral blood circulating cells is associated with vascular and systemic inflammation in atherosclerotic vascular disease.
Not available
S-EPMC9120199
|
biostudies-literature
Cite
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