Results 171 to 180 of about 5,030,093 (326)
Guiding Similarity Search in Chemical Fragment Spaces with Weighted Fingerprints. [PDF]
Lübbers J +4 more
europepmc +1 more source
Discovery and Targeted Proteomic Studies Reveal Striatal Markers Validated for Huntington's Disease
ABSTRACT Objective Clinical trials for Huntington's disease (HD) enrolling persons before clinical motor diagnosis (CMD) lack validated biomarkers. This study aimed to conduct an unbiased discovery analysis and a targeted examination of proteomic biomarkers scrutinized by clinical validation. Methods Cerebrospinal fluid was obtained from PREDICT‐HD and
Daniel Chelsky +8 more
wiley +1 more source
A framework for privacy-preserving similarity search of massive multi-party genomic data. [PDF]
Liu J +5 more
europepmc +1 more source
ABSTRACT Objective Accurate localization of epileptogenic tubers (ETs) in patients with tuberous sclerosis complex (TSC) is essential but challenging, as these tubers lack distinct pathological or genetic markers to differentiate them from other cortical tubers.
Tinghong Liu +11 more
wiley +1 more source
A novel pairwise sequence alignment algorithm for similarity search in massive datasets. [PDF]
Masoudi-Sobhanzadeh Y, Omidi Y.
europepmc +1 more source
ABSTRACT Objective People with epilepsy (PWE) may experience cognitive deficits but fail to undergo formal evaluation. This study compares cognitive status between PWE and healthy controls in the West African Republic of Guinea. Methods A cross‐sectional, case–control study was conducted in sequential recruitment phases (July 2024–July 2025) at Ignace ...
Maya L. Mastick +14 more
wiley +1 more source
jdispatcher-viewers: interactive visualizations of sequence similarity search results and domain predictions. [PDF]
Madeira F +5 more
europepmc +1 more source
SIMBSIG: Similarity search and clustering for biobank-scale data
Adamer MF +3 more
europepmc +1 more source
ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi +2 more
wiley +1 more source
Leveraging a foundation model zoo for cell similarity search in oncological microscopy across devices. [PDF]
Kalweit G +16 more
europepmc +1 more source

