Cargando…

Characterization of Two ENU-Induced Mutations Affecting Mouse Skeletal Morphology

Using the N-ethyl-N-nitrosourea (ENU) mutagenesis screen, we have identified two skeletal morphology mutants, Skm1 and Skm2. Positional cloning and candidate gene sequencing localized the causative point mutations within the genes coding for natriuretic peptide receptor C (NPR-C) and filamin b (FLNB...

Descripción completa

Detalles Bibliográficos
Autores principales:	Dauphinee, Shauna M., Eva, Megan M., Yuki, Kyoko E., Herman, Melissa, Vidal, Silvia M., Malo, Danielle
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Genetics Society of America 2013
Materias:	Investigations
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789799/ https://www.ncbi.nlm.nih.gov/pubmed/23979929 http://dx.doi.org/10.1534/g3.113.007310

Ejemplares similares

Mouse ENU Mutagenesis to Understand Immunity to Infection: Methods, Selected Examples, and Perspectives
por: Caignard, Grégory, et al.
Publicado: (2014)

Suppression of Hepcidin Expression and Iron Overload Mediate Salmonella Susceptibility in Ankyrin 1 ENU-Induced Mutant
por: Yuki, Kyoko E., et al.
Publicado: (2013)

Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse
por: Sun, Miao, et al.
Publicado: (2012)

Characterization of Highper, an ENU-induced mouse mutant with abnormal psychostimulant and stress responses
por: Eisener-Dorman, Amy F., et al.
Publicado: (2012)

An ENU-induced splicing mutation reveals a role for Unc93b1 in early immune cell activation following Influenza A H1N1 infection
por: Lafferty, Erin I, et al.
Publicado: (2014)

Chromoanasynthetic Genomic Rearrangement Identified in a N-Ethyl-N-Nitrosourea (ENU) Mutagenesis Screen in Caenorhabditis elegans
por: Itani, Omar A., et al.
Publicado: (2015)

Functional annotation and ENU
por: Gunn, Teresa M
Publicado: (2012)

Gnaq(M1J): An ENU induced mutant allele affecting pigmentation in the mouse
por: Pratt, C. Herbert, et al.
Publicado: (2016)

Mutational pattern and frequency of induced nucleotide changes in mouse ENU mutagenesis
por: Takahasi, K Ryo, et al.
Publicado: (2007)

Whole exome sequencing of ENU-induced thrombosis modifier mutations in the mouse
por: Tomberg, Kärt, et al.
Publicado: (2018)

The Mouse MC13 Mutant Is a Novel ENU Mutation in Collagen Type II, Alpha 1
por: Cionni, Megan, et al.
Publicado: (2014)

Identification of Mouse Cytomegalovirus Resistance Loci by ENU Mutagenesis
por: Crozat, Karine, et al.
Publicado: (2009)

New insights into behaviour using mouse ENU mutagenesis
por: Oliver, Peter L., et al.
Publicado: (2012)

N-Ethyl-N-Nitrosourea (ENU) Mutagenesis Reveals an Intronic Residue Critical for Caenorhabditis elegans 3′ Splice Site Function in Vivo
por: Itani, Omar A., et al.
Publicado: (2016)

A mouse model of hereditary coproporphyria identified in an ENU mutagenesis screen
por: Conway, Ashlee J., et al.
Publicado: (2017)

A Mutation in Synaptojanin 2 Causes Progressive Hearing Loss in the ENU-Mutagenised Mouse Strain Mozart
por: Manji, Shehnaaz S. M., et al.
Publicado: (2011)

ENU-induced phenovariance in mice: inferences from 587 mutations
por: Arnold, Carrie N, et al.
Publicado: (2012)

An ENU-Mutagenesis Screen in the Mouse: Identification of Novel Developmental Gene Functions
por: Wansleeben, Carolien, et al.
Publicado: (2011)

A mouse chromosome 4 balancer ENU-mutagenesis screen isolates eleven lethal lines
por: Boles, Melissa K, et al.
Publicado: (2009)

An ENU-induced p.C225S missense mutation in the mouse Tgfb1 gene does not cause Camurati-Engelmann disease-like skeletal phenotypes
por: Ichimura, Satoki, et al.
Publicado: (2016)

Pla2g12b and Hpn Are Genes Identified by Mouse ENU Mutagenesis That Affect HDL Cholesterol
por: Aljakna, Aleksandra, et al.
Publicado: (2012)

Contribution of increased ISG15, ISGylation and deregulated Type I IFN signaling in Usp18 mutant mice during the course of bacterial infections
por: Dauphinee, Shauna M., et al.
Publicado: (2014)

Three Novel Pigmentation Mutants Generated by Genome-Wide Random ENU Mutagenesis in the Mouse
por: Tsipouri, Vicky, et al.
Publicado: (2004)

Measurement of the pi --> e.nu branching ratio
por: Bryman, D A, et al.
Publicado: (1994)

High resolution mapping and positional cloning of ENU-induced mutations in the Rw region of mouse chromosome 5
por: Ching, Yung-Hao, et al.
Publicado: (2010)

Probability of phenotypically detectable protein damage by ENU-induced mutations in the Mutagenetix database
por: Wang, Tao, et al.
Publicado: (2018)

New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis
por: Sabrautzki, Sibylle, et al.
Publicado: (2012)

A novel ENU-induced Cpox mutation causes microcytic hypochromic anemia in mice
por: Miyasaka, Yuki, et al.
Publicado: (2022)

Characterization of ENU-induced Mutations in Red Blood Cell Structural Proteins
por: Kildey, Katrina, et al.
Publicado: (2013)

Search for W --> e.nu decays
por: Givernaud, Alain
Publicado: (1983)

Search for W --> enu in UA2
por: Mapelli, Livio P
Publicado: (1983)

Erratum to: New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis
por: Sabrautzki, Sibylle, et al.
Publicado: (2014)

Search for massive neutrinos in the pi-e.nu decay
por: Numao, T, et al.
Publicado: (1984)

Mouse Chromosome 4 Is Associated with the Baseline and Allergic IgE Phenotypes
por: Kanagaratham, Cynthia, et al.
Publicado: (2017)

Constraints on massive neutrinos in pi --> e.nu decay
por: Azuelos, Georges, et al.
Publicado: (1986)

An ENU mutagenesis screen identifies novel and known genes involved in epigenetic processes in the mouse
por: Daxinger, Lucia, et al.
Publicado: (2013)

Identification of a Novel ENU-Induced Mutation in Mouse Tbx1 Linked to Human DiGeorge Syndrome
por: Chen, Jiaofeng, et al.
Publicado: (2016)

Discovery of Candidate Disease Genes in ENU–Induced Mouse Mutants by Large-Scale Sequencing, Including a Splice-Site Mutation in Nucleoredoxin
por: Boles, Melissa K., et al.
Publicado: (2009)

A Novel ENU-Induced Mutation in Myo6 Causes Vestibular Dysfunction and Deafness
por: Wong, Elaine Y. M., et al.
Publicado: (2016)

A new Otogelin ENU mouse model for autosomal-recessive nonsyndromic moderate hearing impairment
por: El Hakam Kamareddin, Carole, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_fupu4ulvsip8099g7qn4f59058