Cargando…
A single nucleotide mutation in Nppc is associated with a long bone abnormality in lbab mice
BACKGROUND: The long bone abnormality (lbab) mouse is a new autosomal recessive mutant characterized by overall smaller body size with proportionate dwarfing of all organs and shorter long bones. Previous linkage analysis has located the lbab mutation on chromosome 1 between the markers D1Mit9 and D...
Autores principales: | Jiao, Yan, Yan, Jian, Jiao, Feng, Yang, HongBin, Donahue, Leah Rae, Li, Xinmin, Roe, Bruce A, Stuart, John, Gu, Weikuan |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1867825/ https://www.ncbi.nlm.nih.gov/pubmed/17439653 http://dx.doi.org/10.1186/1471-2156-8-16 |
Ejemplares similares
-
The Mature COC Promotes the Ampullary NPPC Required for Sperm Release from Porcine Oviduct Cells
por: Wu, Zhanying, et al.
Publicado: (2023) -
Insulin Infusion Is Linked to Increased NPPC Expression in Muscle and Plasma C-type Natriuretic Peptide in Male Dogs
por: Gregory, Justin M, et al.
Publicado: (2021) -
Genotype-Phenotype Correlation of 2q37 Deletions Including NPPC Gene Associated with Skeletal Malformations
por: Tassano, Elisa, et al.
Publicado: (2013) -
De novo 2q36.3q37.1 deletion encompassing TRIP12 and NPPC yields distinct phenotypes
por: Kondo, Yuto, et al.
Publicado: (2020) -
Genome Wide Analysis of Sex Difference in Gene Expression Profiles of Bone Formations Using sfx Mice and BXD RI Strains
por: Huang, Yue, et al.
Publicado: (2014)