Karl Murray
Overview
Explore the profile of Karl Murray including associated specialties, affiliations and a list of published articles.
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Articles
5
Citations
36
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0
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Recent Articles
1.
Vafaeva O, Namchaiw P, Murray K, Diaz E, Cheng H
STAR Protoc
. 2025 Mar;
6(1):103692.
PMID: 40085650
The neurosphere assay is the gold standard for assessing the proliferative and differentiation capacities of neural progenitor cells (NPCs). Here, we present a protocol for isolating, propagating, and maintaining hippocampal...
2.
Ferns M, van der List D, Vierra N, Lacey T, Murray K, Kirmiz M, et al.
J Neurosci
. 2025 Feb;
PMID: 39933932
Voltage-gated K channels of the Kv2 family are highly expressed in brain and play dual roles in regulating neuronal excitability and in organizing endoplasmic reticulum - plasma membrane (ER-PM) junctions....
3.
Vafaeva O, Namchaiw P, Murray K, Diaz E, Cheng H
bioRxiv
. 2024 Apr;
PMID: 38559117
The neurosphere assay is the gold standard for determining proliferative and differentiation potential of neural progenitor cells (NPCs) in neurogenesis studies . While several assays have been developed to model...
4.
Ferns M, van der List D, Vierra N, Lacey T, Murray K, Kirmiz M, et al.
bioRxiv
. 2024 Feb;
PMID: 38328147
Voltage-gated K channels of the Kv2 family are highly expressed in brain and play dual roles in regulating neuronal excitability and in organizing endoplasmic reticulum - plasma membrane (ER-PM) junctions....
5.
Selman L, Sutton E, Medeiros Mirra R, Stone T, Gilbert E, Rolston Y, et al.
Palliat Med
. 2022 Nov;
37(4):586-601.
PMID: 36337051
Background: Voluntary and community sector bereavement services are central to bereavement support in the UK. Aim: To determine service providers' perspectives on access to their support before and during the...
6.
Page N, Gandal M, Estes M, Cameron S, Buth J, Parhami S, et al.
Biol Psychiatry
. 2021 Jan;
89(9):896-910.
PMID: 33386132
Background: Maternal immune activation (MIA) is a proposed risk factor for multiple neuropsychiatric disorders, including schizophrenia. However, the molecular mechanisms through which MIA imparts risk remain poorly understood. A recently...
7.
Song L, Yu A, Murray K, Cortopassi G
Brain Res
. 2016 Dec;
1657:232-244.
PMID: 28027875
Inherited mitochondrial complex 1 deficiency causes Leber's hereditary Optic Neuropathy (LHON) and retinal ganglion cell (RGC) degeneration, and optic neuropathies are common in many inherited mitochondrial diseases. How mitochondrial defects...