Cargando…

The fasn-1(g14ts) allele is a Gly1830Arg missense mutation in C. elegans FASN-1

Detalles Bibliográficos
Autores principales:	Bai, Xiaofei, Woodbury, David, Golden, Andy
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Caltech Library 2020
Materias:	New Finding
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7252273/ https://www.ncbi.nlm.nih.gov/pubmed/32550489 http://dx.doi.org/10.17912/micropub.biology.000244

Ejemplares similares

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)

Conserved missense variant in ALDH1A3 ortholog impairs fecundity in C. elegans
por: Wong, Wan-Rong, et al.
Publicado: (2021)

A novel null allele of C. elegans gene ceh-14
por: Bayer, Emily, et al.
Publicado: (2018)

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)

copa-1 mutants experience heightened endoplasmic reticulum stress sensitivity in a C. elegans COPA Syndrome model
por: Larkin, Kerry A., et al.
Publicado: (2023)

Pharyngeal pumping phenotypes of common fluorescently-tagged C. elegans strains
por: Bauer, Rosemary, et al.
Publicado: (2020)

Using CRISPR knock-in of fluorescent tags to examine isoform-specific expression of EGL-19 in C. elegans
por: McDonald, Kara, et al.
Publicado: (2023)

New allele of C. elegans gene pign-1, named as xyz11
por: Narimatsu, Tetsuya, 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)

Suppression of him-14(it44ts) by a transgene insertion expressing GFP::COSA-1
por: Girard, Chloé, et al.
Publicado: (2021)

Caenorhabditis elegans che-5 is allelic to gcy-22
por: Kunitomo, Hirofumi, et al.
Publicado: (2020)

Effects of ASD-associated daf-18/PTEN missense variants on C. elegans dauer development
por: González-Cavazos, Carolina, et al.
Publicado: (2019)

Two Deletion Alleles in the C. elegans mir-49 gene.
por: Delich, Cassandra, et al.
Publicado: (2020)

Two novel alleles in C. elegans mir-1822 gene.
por: Anderson, Marcy, et al.
Publicado: (2020)

Molecular lesions in alleles of the Caenorhabditis elegans lin-11 gene
por: Young, Adrie F., et al.
Publicado: (2022)

C. elegans Gene Regulatory Alleles and Reporter Bashing Studies
por: Froehlich, Jonathan J, et al.
Publicado: (2023)

Generation of a C. elegans tdp-1 null allele and humanized TARDBP containing human disease-variants.
por: Lins, Jeremy, et al.
Publicado: (2023)

Loss of proteasome subunit RPN-12 causes an increased mean lifespan at a higher temperature in C. elegans
por: Fernando, Lourds, et al.
Publicado: (2020)

Two new CRISPR-generated alleles in the C. elegans mir-1022 gene.
por: Horn, Connor, et al.
Publicado: (2020)

A null allele in the wdfy-3 selective autophagy gene of C. elegans .
por: Buddell, Tyler, et al.
Publicado: (2022)

Volume of the thalamus and hypothalamus in the Ts1Rhr and Ms1Rhr mouse models relevant to Down syndrome
por: Arthun, Jocelyn, et al.
Publicado: (2023)

Novel deletion alleles of a C. elegans gene Y48E1C.1, named as tm5468, tm5625 and tm5626
por: Hori, Sayaka, et al.
Publicado: (2017)

Novel deletion alleles of a C. elegans gene Y73E7A.1, named as tm6429 and tm6475
por: Suehiro, Yuji, et al.
Publicado: (2017)

Identification of Acetylation Sites of Fatty Acid Synthase (FASN) by Mass Spectrometry and FASN Activity Assay
por: Miao, Ting, et al.
Publicado: (2023)

New deletion alleles for Caenorhabditis elegans Hedgehog pathway-related genes wrt-6 and wrt-10
por: Sherry, Tessa, et al.
Publicado: (2019)

Three alleles in the pat-3 locus of Caenorhabditis elegans: mutations in the membrane-distal NPxY phosphotyrosine motif
por: Hanna, Jacob, et al.
Publicado: (2020)

New allele of C. elegans gene spch-3 (T27A3.4), called xc2
por: Munoz, Nicholas R., et al.
Publicado: (2018)

Canavanine resistance mutation can1-1 in Schizosaccharomyces pombe is a missense mutation in the ubiquitin ligase adaptor gene any1
por: Yang, Yu-Sheng, et al.
Publicado: (2022)

om92 , a glp-1 enhancer mutation, is an allele of ekl-1
por: Stein, Samantha A., et al.
Publicado: (2022)

Novel deletion alleles of a C. elegans gene C38D4.9, named as tm4476 and tm4561
por: Yoshina, Sawako, et al.
Publicado: (2017)

New alleles of C. elegans gene cls-2 (R107.6), called xc3, xc4, and xc5
por: Munoz, Nicholas R., et al.
Publicado: (2017)

Difference in phenotypic severity of presumed null alleles of capg-1
por: VanDiepenbos, Sarah, et al.
Publicado: (2020)

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)

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

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)

Cannot write session to /tmp/vufind_sessions/sess_q9nq3ejucn01ak2vpk2iu27jcj