Results 301 to 310 of about 27,273,409 (393)

Unraveling the Molecular Mechanisms of Glioma Recurrence: A Study Integrating Single‐Cell and Spatial Transcriptomics

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Glioma recurrence severely impacts patient prognosis, with current treatments showing limited efficacy. Traditional methods struggle to analyze recurrence mechanisms due to challenges in assessing tumor heterogeneity, spatial dynamics, and gene networks.
Lei Qiu, Yinjiao Fei, Jiaxuan Ding, Kexin Shi, Jinyan Luo, Yuchen Zhu, Xingjian Sun, Gefei Jiang, Yuandong Cao, Weilin Xu, Shu Zhou   +10 more
wiley   +1 more source

Machine-learning model for 30-day mortality in sepsis-associated delirium patients: A retrospective MIMIC-IV cohort study. [PDF]

Medicine (Baltimore)
Yin J, Pan X, Chen D, Zhang J, Jin G.
europepmc   +1 more source

A consistent approach for coupling lumped-parameter and phase-field models for in-vessel corium to thermodynamic databases.

, 2019
V. Tiwari
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

Public critical care databases for clinical research: challenges and opportunities. [PDF]

Crit Care
Cao Y, Wu B, Liu J, Tan H, Zhang Y, Gao W.   +5 more
europepmc   +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

Activity-type dependent conductance relationships in a model neuron database

BMC Neuroscience, 2009
Prinz Astrid A, Hudson Amber E
doaj   +1 more source

ChEBI: re-engineered for a sustainable future. [PDF]

Nucleic Acids Res
Malik A, Arsalan M, Moreno C, Mosquera J, Félix E, Kizilören T, Muthukrishnan V, Zdrazil B, Leach AR, O'Boyle NM.   +9 more
europepmc   +1 more source

Transport-based transfer learning on Electronic Health Records: application to detection of treatment disparities. [PDF]

J Am Med Inform Assoc
Li W, Ahmed S, Park YP, Dao Duc K.
europepmc   +1 more source

CellMap: precision mapping of cellular landscape in spatial transcriptomics. [PDF]

Nucleic Acids Res
Liu H, Li H, Sharma A, Tang G, Xie Z, Shen Y, Li Q, Gong C, Sun X, Luo K, Liu H.   +10 more
europepmc   +1 more source