Results 81 to 90 of about 2,827 (178)

Characterization of Primary Cilia Formation in Human ESC-Derived Retinal Organoids

open access: yesStem Cells International, 2023
Objectives. Primary cilia are conserved organelles found in polarized mammalian cells that regulate neuronal growth, migration, and differentiation. Proper cilia formation is essential during eye development. Our previous reports found that both amacrine
Ke Ning   +8 more
doaj   +1 more source

Loss of STARD7 Triggers Metabolic Reprogramming and Cell Cycle Arrest in Breast Cancer

open access: yesAdvanced Science, Volume 12, Issue 31, August 21, 2025.
Breast cancer cells undergo metabolic and transcriptomic reprogramming to support aberrant cell proliferation. Their mitochondria rely on the transfer of phosphatidylcholine from the endoplasmic reticulum to their membranes by STARD7, a candidate upregulated in breast cancer, to be functional.
Ewelina Dondajewska   +18 more
wiley   +1 more source

MyGene2 automated match report: ARL13B

open access: yes, 2016
MyGene2.org is free, public, searchable & browsable website. Families with rare genetic conditions, clinicians, and researchers families who are interested in sharing health and genetic information can create MyGene2 profiles and use these to connect with other families, clinicians, and researchers who may have or be studying the same condition. If
openaire   +1 more source

The Kinesin Motor Kif9 Disrupts Primary Cilia Length by Mispositioning Centriolar Satellites

open access: yesThe FASEB Journal, Volume 39, Issue 14, 31 July 2025.
The primary cilium is a small organelle that functions as a cell signaling hub, with its assembly, disassembly, and length tightly regulated. Centriolar satellites (CS), granules around the centrosome, regulate both centrosomal and ciliary functions.
Juan Jesus Vicente   +3 more
wiley   +1 more source

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2019
Objective: We present prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 3.
Chih-Ping Chen   +8 more
doaj   +1 more source

Role for the IFT-A Complex in Selective Transport to the Primary Cilium

open access: yesCell Reports, 2016
Intraflagellar transport sub-complex A (IFT-A) is known to regulate retrograde IFT in the cilium. To rigorously assess its other possible roles, we knocked out an IFT-A subunit, IFT121/WDR35, in mammalian cells and screened the localization of more than ...
Wenxiang Fu   +4 more
doaj   +1 more source

ARL13B regulates juxtaposed cilia-cilia elongation in BBSome dependent manner in Caenorhabditis elegans

open access: goldiScience
The interaction of cilia with various cellular compartments, such as axons, has emerged as a new form of cellular communication. Cilia often extend in proximity to cilia from neighboring cells. However, the mechanisms driving this process termed juxtaposed cilia-cilia elongation (JCE) remain unclear. We use fluorescence-based visualization to study the
Merve G. Turan   +3 more
openalex   +4 more sources

CEP162: A critical regulator of ciliary transition zone assembly and its implications in ciliopathies

open access: yesJournal of Cell Communication and Signaling, Volume 19, Issue 2, June 2025.
Abstract CEP162, a 162‐kDa centrosome protein, is a crucial centrosomal adapter, mediating cell differentiation and polarization. CEP162 maintains mitosis by dynamically stabilizing microtubules. CEP162 promotes the transition zone (TZ) assembly in the basal body through interaction with CEP131, CEP290, and axoneme microtubules as well as the distal ...
Jun Yin   +7 more
wiley   +1 more source

IMPDH2's Central Role in Cellular Growth and Diseases: A Potential Therapeutic Target

open access: yesCell Proliferation, Volume 58, Issue 6, June 2025.
IMPDH2 is a rate‐limiting enzyme in guanine nucleotide biosynthesis. It plays diverse roles in various physiological and pathological processes: nucleotide metabolism, inflammation, immune function, ribosomal stress. Structural or regulatory alterations in IMPDH2 are linked to significant health issues, and critical relevance in disease progression. We
Zheng Li   +8 more
wiley   +1 more source

Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice

open access: yesG3: Genes, Genomes, Genetics, 2016
We have previously described a forward genetic screen in mice for abnormalities of brain development. Characterization of two hydrocephalus mutants by whole-exome sequencing after whole-genome SNP mapping revealed novel recessive mutations in Dnaaf1 and ...
Seungshin Ha   +3 more
doaj   +1 more source

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