Portable Low‐Field Magnetic Resonance Imaging in People With Human Immunodeficiency Virus
ABSTRACT Objective The aging population of people with HIV (PWH) raises heightened concerns regarding accelerated aging and dementia. Portable, low‐field MRI (LF‐MRI) is an innovative technology that could enhance access and facilitate routine monitoring of PWH.
Annabel Sorby‐Adams +14 more
wiley +1 more source
Life in cold blood: Exploring the cryptic diversity of species of <i>Haemogregarina</i> in Southern Africa's terrapins. [PDF]
Barnard M +5 more
europepmc +1 more source
Insights Into the Antigenic Repertoire of Unclassified Synaptic Antibodies
ABSTRACT Objective We sought to characterize the sixth most common finding in our neuroimmunological laboratory practice (tissue assay‐observed unclassified neural antibodies [UNAs]), combining protein microarray and phage immunoprecipitation sequencing (PhIP‐Seq). Methods Patient specimens (258; 133 serums; 125 CSF) meeting UNA criteria were profiled;
Michael Gilligan +22 more
wiley +1 more source
Identification of a cytosol-to-nucleus feedback loop that regulates neuronal microtubule nucleation. [PDF]
Kumar N +7 more
europepmc +1 more source
Nuclear Transportation of Diacylglycerol Kinase γ and Its Possible Function in the Nucleus
Takehiro Matsubara +12 more
openalex +1 more source
Differential effects of immediate posttraining sulphide microinfusions into the nucleus accumbens shell and core on Morris water maze retention [PDF]
Barry Setlow, James L. McGaugh
openalex +1 more source
ABSTRACT Mutations in myelin regulatory factor (MYRF) are linked to demyelinating disorders. We report a 38‐year‐old male who developed acute symmetric leukoencephalopathy mimicking a stroke following an influenza A virus infection. While clinical symptoms markedly improved with corticosteroids, MRI revealed persistent white matter lesions, contrasting
Jinghan Hu +5 more
wiley +1 more source
Mechanochemical interactions in cancer cells: The role of substrate stiffness in cell behavior and drug response. [PDF]
Ramezani SR +2 more
europepmc +1 more source
Exploratory Analysis of ELP1 Expression in Whole Blood From Patients With Familial Dysautonomia
ABSTRACT Background Familial dysautonomia (FD) is a hereditary neurodevelopmental disorder caused by aberrant splicing of the ELP1 gene, leading to a tissue‐specific reduction in ELP1 protein expression. Preclinical models indicate that increasing ELP1 levels can mitigate disease manifestations.
Alejandra González‐Duarte +13 more
wiley +1 more source
Paediatric auditory brainstem implant: How we do it. [PDF]
Kullar PJ +7 more
europepmc +1 more source

