Results 261 to 270 of about 6,545,298 (346)

A directed weighted network-based method for drug combinations identification using drug-target and inter-target regulation. [PDF]

BMC Bioinformatics
Xiao S, Li Y, Bai J, Shen Z, Huang C, Xiang R, Zhai Y, Jiang X.   +7 more
europepmc   +1 more source

Comparison of query performance in relational a non-relation databases

, 2019
Roman Čerešňák, Michal Kvet
openalex   +1 more source

Diagnostic Utility of the ATG9A Ratio in AP‐4–Associated Hereditary Spastic Paraplegia

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Adaptor protein complex 4–associated hereditary spastic paraplegia (AP‐4‐HSP), a childhood‐onset neurogenetic disorder and frequent mimic of cerebral palsy, is caused by biallelic variants in the adaptor protein complex 4 (AP‐4) subunit genes (AP4B1 [for SPG47], AP4M1 [for SPG50], AP4E1 [for SPG51], and AP4S1 [for SPG52]).
Habibah A. P. Agianda, Hyo‐Min Kim, Nicole Battaglia, Joshua Rong, Amy Tam, Enrique Gonzalez Saez‐Diez, Cornelius F. Boerkoel, Afshin Saffari, Vicente Quiroz, Luca Schierbaum, Zainab Zaman, Katerina Bernardi, Darius Ebrahimi‐Fakhari   +12 more
wiley   +1 more source

Construction of waste-to-resource knowledge graph for industrial symbiosis identification using large language models. [PDF]

Nat Commun
Zhao L, Sun Y, Ren J, Gao H, Xiao G.
europepmc   +1 more source

A Comparative Analysis in Relation to Informational Self-Determination and Privacy: : The Icelandic Health Sector Database Decision and The German Census Act Decision

, 2007
Anna Kristin Jack Ulfarsdottir
openalex   +1 more source

Clinically Relevant Outcome Measures in Women With Adrenoleukodystrophy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Adrenoleukodystrophy is a rare inherited peroxisomal disease caused by pathogenic variants in the ABCD1 gene located on the X chromosome. Although the most severe central nervous system and adrenal complications typically affect only men with adrenoleukodystrophy, the majority of women develop myeloneuropathy symptoms in adulthood.
Chenwei Yan, Elizabeth I. Pierpont, Amena S. Fine, Reena V. Kartha   +3 more
wiley   +1 more source

Gender and geographic disparities among DSM-5-TR authors in relation to financial conflicts of interest and industry payments: cross-sectional analysis. [PDF]

BMJ Ment Health
Diianni AT, Davis LC, Piper BJ.
europepmc   +1 more source

Meningovascular Inflammation in Cerebral Amyloid Angiopathy‐Related Cortical Superficial Siderosis

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT The role of inflammation in cortical superficial siderosis (cSS), a marker of cerebral amyloid angiopathy (CAA) linked to high hemorrhage risk, is unclear. We examined 15 patients with cSS using 3 T post‐contrast vessel wall MRI (VWI) and CSF analysis.
Philipp Arndt, Eya Khadhraoui, Sebastian J. Müller, Katja Neumann, Hendrik Mattern, Sven G. Meuth, Valentina Perosa, Andreas Charidimou, Stefanie Schreiber   +8 more
wiley   +1 more source

Νovel methylation biomarkers in liquid biopsy and classifying biosignatures for the clinical management of breast cancer. [PDF]

Breast Cancer Res
Panagopoulou M, Papadaki MA, Karaglani M, Theodosiou T, Michaelidou K, Baritaki S, Tsamardinos I, Kakolyris S, Agelaki S, Chatzaki E.   +9 more
europepmc   +1 more source