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Anthony J. Bleyer

Wake Forest University
First Faculty of Medicine, Charles University in Prague

184

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9297

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A mutation in the SAA1 promoter causes hereditary amyloid A amyloidosis.

2021 Kidney International
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An intermediate effect size variant in UMOD confers risk for chronic kidney disease

2021 medRxiv
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Figure 2. [Illustration of the mechanism by...].

2021
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POLRMT mutations impair mitochondrial transcription causing neurological disease.

2021 Nature Communications
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Mitochondriopathy Manifesting as Inherited Tubulointerstitial Nephropathy Without Symptomatic Other Organ Involvement.

2021 Kidney International Reports
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Ultrabright plasmonic fluor nanolabel-enabled detection of a urinary ER stress biomarker in autosomal dominant tubulointerstitial kidney disease.

2021 American Journal of Physiology-renal Physiology
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Safety and Efficacy of Tenapanor for Long-term Serum Phosphorus Control in Maintenance Dialysis: A 52-Week Randomized Phase 3 Trial (PHREEDOM)

2021 Kidney
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Autosomal dominant tubulointerstitial kidney disease: more than just HNF1β.

2021 Pediatric Nephrology
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Sexual Dysfunction in Patients With Urinary Bladder Stones but no Bladder Outlet Obstruction.

2021 Frontiers of Medicine in China
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Elucidation of a novel mechanism for faulty protein retention and a therapeutic strategy for facilitated lysosomal removal

2021 The FASEB Journal
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