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ProteomicsMosaic PKHD1 variants in polycystic kidney caused aberrant protein profiling of mitochondria and lysosomes
Autosomal recessive polycystic kidney disease (ARPKD) is a severe renal cystic disease mainly caused by PKHD1. However, its genetic cause, pathological features, and mechanism remained unsolved. Our findings may provide new insight on the pathophysiology of the polycystic kidney due to PKHD1 deficie...
ORGANISM(S): Homo Sapiens 
PXD028042 |
ProteomicsProteomics analysis in normal and blue light-exposed ARPE-19 cells
Proteomics analysis to identify the differential expression of proteins in normal and blue light-exposed ARPE-19 cells
ORGANISM(S): Homo Sapiens 
2020-01-22 | PXD017259 |
UnknownDeep learning algorithms for identifying developmental dysplasia of the hip based on sonographic images: a retrospective, prospective, multicenter study in China.

Background

Hip ultrasound is the first-line tool to identify developmental dysplasia of the hip (DDH) among suspected infants, yet it has limitations including poor reproducibility and high diagnostic error rates. This study aims to develop and validate a deep convolutional neural network al...
S-EPMC12547208 | biostudies-literature
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