Cargando…

oxi-1 and fshr-1 are required for neuromuscular signaling under normal and oxidative stress conditions in C. elegans

Detalles Bibliográficos
Autores principales:	Wei, Barry, Kowalski, Jennifer R.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Caltech Library 2018
Materias:	New Finding
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282492/ https://www.ncbi.nlm.nih.gov/pubmed/32550383 http://dx.doi.org/10.17912/pfyw-ft85

Ejemplares similares

C. elegans dkf-1 (Protein Kinase D1) mutants have age-dependent defects in locomotion and neuromuscular transmission
por: Johnson, James R., et al.
Publicado: (2023)

The HSN egg-laying command neurons are required for normal defecation frequency in Caenorhabditis elegans (II)
por: Garcia, Jessica, et al.
Publicado: (2019)

The autophagy gene product BEC-1 supports normal aging and neurodevelopment in Caenorhabditis elegans: Integration
por: Ashley, Nicholas, et al.
Publicado: (2019)

The autophagy gene product BEC-1 supports normal aging and neurodevelopment in Caenorhabditis elegans II
por: Ashley, Nicholas, et al.
Publicado: (2019)

The autophagy gene product BEC-1 supports normal aging and neurodevelopment in Caenorhabditis elegans III
por: Ashley, Nicholas, et al.
Publicado: (2019)

The autophagy gene product BEC-1 supports normal aging and neurodevelopment in Caenorhabditis elegans I
por: Ashley, Nicholas, et al.
Publicado: (2019)

Minimum number of synaptic vesicles for the initiation of a single action potential at C. elegans neuromuscular junction
por: Chen, Lili, et al.
Publicado: (2020)

C. elegans rab-18 mutants display reduced lipid content under fed and fasted conditions
por: Ratemi, Zakaria, et al.
Publicado: (2019)

DCAF-13 is required for C. elegans growth, development, and fertility
por: Durkan, Aidan, et al.
Publicado: (2022)

Differential effects on neuromuscular physiology between Sod1 loss-of-function mutation and paraquat-induced oxidative stress in Drosophila
por: Ueda, Atsushi, et al.
Publicado: (2021)

rol-6 and dpy-10 C. elegans mutants have normal mitochondrial function after normalizing to delayed development
por: Sparling, A. Clare, et al.
Publicado: (2023)

A C. elegans MAP kinase pathway is required for wild-type display of an L1-specific surface antigen (srf-6 is nsy-1 III)
por: Foley, Stephen J., et al.
Publicado: (2019)

The C-terminus of SPE-11 is required for proper embryonic development in C. elegans
por: Jaramillo-Lambert, Aimee, et al.
Publicado: (2020)

UNC-108/RAB-2 is required for C. elegans stress-induced sleep
por: Robinson, Bryan, et al.
Publicado: (2019)

The IFT20 homolog in Caenorhabditis elegans is required for ciliogenesis and cilia-mediated behavior
por: De-Castro, Ana R. G., et al.
Publicado: (2021)

A mutation linked to degt-1(ok3307) in C. elegans strain VC2633 affects rpm-1
por: Jin, Eugene Jennifer, et al.
Publicado: (2022)

Three C. elegans srf-6 mutants carry nsy-1 mutations (srf-6 is nsy-1 I)
por: Van Sciver, Nicholas D., et al.
Publicado: (2019)

Genetic interactions in a C. elegans sod-1 ALS model: glutamatergic neuron degeneration
por: Osborne, Jennifer F, et al.
Publicado: (2021)

Endogenous expression and localization of CAV-1::GFP in C. elegans
por: Sloan, Dillon E., et al.
Publicado: (2020)

Visualization of endogenous NID-1 and EMB-9 in C. elegans
por: Matsuo, Kanae, et al.
Publicado: (2019)

Left-right asymmetry in oxidative stress sensing neurons in C. elegans
por: Quintin, Sophie, et al.
Publicado: (2022)

LIR-1 and PDTF-1 regulate the permeability barrier function of the C. elegans cuticle
por: Sandhu, Anjali, et al.
Publicado: (2021)

Phase separation dynamics of the C. elegans PGL-1 P granule protein in oocytes are sensitive to heat stress
por: Watkins, Brooklynne, et al.
Publicado: (2021)

nu444 is a novel allele of pkc-1 in C. elegans
por: Wang, Han, et al.
Publicado: (2017)

A spontaneous TIR1 loss-of-function allele in C. elegans
por: Myles, Krista M., et al.
Publicado: (2023)

ICD-1/BTF3 antagonizes SKN-1-mediated endoderm specification in Caenorhabditis elegans
por: Ewe, Chee Kiang, et al.
Publicado: (2019)

Localization of tbg-1 mRNAs and GFP::TBG-1 protein in Early C. elegans Embryos
por: DeMeyer, Lauren, et al.
Publicado: (2017)

Low density lipoprotein receptors LRP-1 and LRP-2 in C. elegans
por: Minor, Paul J, et al.
Publicado: (2019)

LRP-2 controls the localization of C. elegans SYS-1/beta-catenin
por: Minor, Paul J, et al.
Publicado: (2019)

New allele of C. elegans gene pign-1, named as xyz11
por: Narimatsu, Tetsuya, et al.
Publicado: (2019)

Indirect Modulation by FLP-1 Peptides on Chemotaxis and Dispersal Behavior in C. elegans
por: Lynch, Michael J, et al.
Publicado: (2023)

A missense mutation in the C. elegans src-2 tyrosine-protein kinase reduces brood size and enhances embryonic morphogenesis defects in src-1(RNAi) conditions
por: Bai, Xiaofei, et al.
Publicado: (2023)

C. elegans mpk-1b long first intron enhances MPK-1B protein expression
por: Robinson-Thiewes, Sarah, et al.
Publicado: (2021)

Enhanced pentylenetetrazole sensitivity in a C. elegans mutant associated with DNM1 encephalopathy
por: Vaji, Madeline A., et al.
Publicado: (2020)

A C. elegans model for the rare human channelopathy, Timothy syndrome type 1
por: Lagoy, Ross, et al.
Publicado: (2018)

The Caenorhabditis elegans tmc-1 is involved in egg-laying inhibition in response to harsh touch
por: Kaulich, Eva, et al.
Publicado: (2021)

SGK-1 mediated inhibition of iron import is a determinant of lifespan in C. elegans
por: Wu, Gang, et al.
Publicado: (2023)

The C. elegans pseudogene sspt-16 (F55A3.7) is required to safeguard germ cells against reprogramming
por: Ofenbauer, Andreas, et al.
Publicado: (2021)

MFP1/MSD-1 and MFP2/NSPH-2 co-localize with MSP during C. elegans spermatogenesis
por: Morrison, Kayleigh N., et al.
Publicado: (2021)

pry-1 interacts with bar-1 to regulate vit-2 expression, lipid levels, and lifespan in Caenorhabditis elegans adults
por: De, Atreyee, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_uhb5nn3c3nglhjilp63lcm64lk