Results 21 to 30 of about 8,390 (226)

LncRNA RASAL2-AS1 promotes METTL14-mediated m6A methylation in the proliferation and progression of head and neck squamous cell carcinoma [PDF]

open access: yesCancer Cell International
Background Long non-coding RNAs (lncRNAs) are key regulators of the 6-methyladenosine (m6A) epigenetic modification, playing a role in the initiation and progression of tumors.
Meiting Rong   +8 more
doaj   +2 more sources

Binding of microtubule-associated protein 1B to LIS1 affects the interaction between dynein and LIS1 [PDF]

open access: greenBiochemical Journal, 2005
For neuronal migration to occur, the cell must undergo morphological changes that require modifications of the cytoskeleton. Several different MAPs (microtubule-associated proteins) or actin-binding proteins are proposed to be involved in the migration of neurons. Therefore we have specifically analysed how two members of the MAP family, MAP1B and LIS1
Eva M. Jiménez‐Mateos   +4 more
openalex   +4 more sources

A de novo microdeletion involving PAFAH1B (LIS1) related to lissencephaly phenotype

open access: goldData in Brief, 2015
Lissencephaly is a type of the congenital malformation of the brain. Due to the impairments of neuronal migration, patients show absence of brain convolution manifesting smooth brain surfaces.
Keiko Shimojima   +2 more
doaj   +2 more sources

Total callosotomy ameliorates epileptic activity and improves cognitive function in a patient with Miller-Dieker syndrome [PDF]

open access: yesEpilepsy & Behavior Reports
Miller-Dieker syndrome (MDS) is characterized by facial abnormalities and lissencephaly and is caused by a microdeletion in the region containing the LIS1 gene at chromosome 17p13.3.
Masataka Fukuoka   +9 more
doaj   +2 more sources

NudC-like protein 2 regulates the LIS1/dynein pathway by stabilizing LIS1 with Hsp90 [PDF]

open access: greenProceedings of the National Academy of Sciences, 2010
The type I lissencephaly gene product LIS1, a key regulator of cytoplasmic dynein, is critical for cell proliferation, survival, and neuronal migration. However, little is known about the regulation of LIS1. Here, we identify a previously uncharacterized mammalian homolog of Aspergillus NudC, NudCL2 (NudC-like ...
Yuehong Yang   +5 more
openalex   +4 more sources

Lis1 Regulates Dynein as a Molecular Wedge [PDF]

open access: bronzeBiophysical Journal, 2014
Cytoplasmic dynein walks along microtubules by coupling cycles of ATP hydrolysis in its motor domain with cycles of microtubule binding and release at its microtubule-binding domain. Unlike the other cytoskeletal motors--kinesin and myosin--that have achieved functional diversity through molecular diversity, a single isoform of cytoplasmic dynein is ...
Sirui Zou   +4 more
  +6 more sources

LIS1 and dynein motor function in neuronal migration and development [PDF]

open access: goldGenes & Development, 2001
Neuronal migration has been studied extensively for over 30 years in diverse mammalian species from the mouse to human. The sequence of events that occurs during cortical development is shared by all of these species (for reviews, see Gleeson and Walsh 2000; Walsh and Goffinet 2000).
Anthony Wynshaw‐Boris   +1 more
openalex   +4 more sources

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