Cargando…
Bioinformatics Analysis and High-Throughput Sequencing to Identify Differentially Expressed Genes in Nebulin Gene (NEB) Mutations Mice
BACKGROUND: High-throughput sequencing of the pathological tissue of 59 patients with thyroid cancer was compared with the normal population. It was found that the mutation frequency of the Nebulin gene (NEB) at amino acid 1133 locus of thyroid cancer patients was much higher than that of the normal...
Autores principales: | Wang, Haoyong, Nie, Xiaoyue, Li, Xin, Fang, Yi, Wang, Dandan, Wang, William, Hu, Yong, Liu, Zijing, Cao, Cheng |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241215/ https://www.ncbi.nlm.nih.gov/pubmed/32390000 http://dx.doi.org/10.12659/MSM.922953 |
Ejemplares similares
-
neb: a zebrafish model of nemaline myopathy due to nebulin mutation
por: Telfer, William R., et al.
Publicado: (2012) -
Variants in Nebulin (NEB) Are Linked to the Development of Familial Primary Angle Closure Glaucoma in Basset Hounds
por: Ahram, Dina F., et al.
Publicado: (2015) -
Novel mutations in NEB cause abnormal nebulin expression and markedly impaired muscle force generation in severe nemaline myopathy
por: Lawlor, Michael W, et al.
Publicado: (2011) -
Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in Neb
por: Laitila, Jenni M., et al.
Publicado: (2020) -
Usher syndrome and Nebulin‐associated myopathy in a single patient due to variants in MYO7A and NEB
por: Maia, Nuno, et al.
Publicado: (2020)