Results 1 to 10 of about 3,545 (191)

LIS1 mediated Schwann cell reprogramming enhances perineural invasion by activating the serine/NMDAR/AKT signaling pathway in head and neck squamous carcinoma [PDF]

open access: yesCancer Cell International
Background Perineural invasion (PNI) has significant implications for the prognosis of patients with head and neck squamous cell carcinoma (HNSCC).
Jing Liu   +7 more
doaj   +2 more sources

Cryo-EM captures early intermediate steps in dynein activation by LIS1 [PDF]

open access: yesNature Communications
Cytoplasmic dynein-1 (dynein) is an essential molecular motor in eukaryotic cells. Dynein primarily exists in an autoinhibited Phi state and requires conformational changes to assemble with its cofactors and form active transport complexes.
Kendrick H. V. Nguyen   +4 more
doaj   +2 more sources

The Role of Hippocampal Interneuron Migration in Neurodevelopmental Disorders: A Systematic Review. [PDF]

open access: yesHippocampus
ABSTRACT Hippocampal abnormalities are frequently associated with neurodevelopmental disorders as interneurons are crucial in establishing the network connectivity of neurons. This systematic review analyzed primary literature with a focus on aberrant hippocampal interneuron migration as an etiology for neurodevelopmental disorders, summarizing the ...
Till MAC   +3 more
europepmc   +2 more sources

Cancer Stem Cells Shift Metabolite Acetyl-Coenzyme A to Abrogate the Differentiation of CD103<sup>+</sup> T Cells. [PDF]

open access: yesAdv Sci (Weinh)
Lei et al. demonstrate that cancer stem cells (CSCs) play a pivotal role in impairing the differentiation of CD103+ T cells in patients with non‐small‐cell lung cancer. The key mechanism involves CSC‐derived acetyl‐CoA, which disrupts CD103+ T cell differentiation by sequentially inducing acetylation and ubiquitination of the Blimp‐1 protein. Targeting
Lei J   +10 more
europepmc   +2 more sources

Post-LECA Origin and Diversification of an Axonemal Outer Arm Dynein Motor. [PDF]

open access: yesCytoskeleton (Hoboken)
ABSTRACT Dyneins were present in the last eukaryotic common ancestor (LECA) and play key roles in eukaryotic biology. Axonemal dyneins form the inner and outer arms that power ciliary beating, and it has long been recognized that outer arms in some organisms contain two different heavy chain motors, whereas those from other species contain a third unit
King SM.
europepmc   +2 more sources

Pt-LIS1 participates nuclear deformation and acrosome formation via regulating Dynein-1 during spermatogenesis in Portunus trituberculatus [PDF]

open access: yesScientific Reports
Spermatogenesis involves complex dynamic mechanisms. Dynein-1 is a key carrier in cellular cargo transport, participating in nuclear deformation and acrosome formation during spermatogenesis.
Le Chang   +6 more
doaj   +2 more sources

Deep learning-based identification of causative genes in lissencephaly using 3D-MRI volumetric datasets [PDF]

open access: yesNeuroImage: Reports
Background: This paper reports a genetic identification task using 3D convolutional neural network (3D-CNN) models applied to a proprietary 3D magnetic resonance imaging (MRI) dataset of patients with lissencephaly.
Naoki Takahashi   +3 more
doaj   +2 more sources

Gene-specific long-term course, neurodevelopmental outcome and quality of life in patients with LIS1/PAFAH1B1-, DCX-, DYNC1H1-, TUBA1A- and TUBG1-related lissencephaly [PDF]

open access: yesOrphanet Journal of Rare Diseases
Background Classic lissencephaly is a malformation of cortical development that includes agyria and pachygyria. The major clinical symptoms are developmental impairment, muscular hypotonia, and drug-resistant epilepsy.
Christiane R. Proepper   +33 more
doaj   +2 more sources

Structural and ensemble-based mechanistic insights into cytoplasmic dynein-1 [PDF]

open access: yesFrontiers in Molecular Biosciences
Cytoplasmic dynein-1 is a multi-subunit motor that transports diverse cargoes toward microtubule minus-ends, playing crucial roles in intracellular organisation and cell division.
Amit Kumawat
doaj   +2 more sources

Capturing disease severity in LIS1-lissencephaly reveals proteostasis dysregulation in patient-derived forebrain organoids [PDF]

open access: yesNature Communications
LIS1-lissencephaly is a neurodevelopmental disorder marked by reduced cortical folding and severe neurological impairment. Although all cases result from heterozygous mutations in the LIS1 gene, patients present a broad spectrum of severity. Here, we use
Lea Zillich   +21 more
doaj   +2 more sources

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