Characterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patient.
about
A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature reviewNovel Mutation of Cleidocranial Dysplasia-related Frameshift Runt-related Transcription Factor 2 in a Sporadic Chinese Case.Interpreting short tandem repeat variations in humans using mutational constraint.Intrinsic Disorder in Proteins with Pathogenic Repeat Expansions.Syringic acid, a phenolic acid, promotes osteoblast differentiation by stimulation of Runx2 expression and targeting of Smad7 by miR-21 in mouse mesenchymal stem cells.
P2860
Characterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patient.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Characterisation of novel RUNX ...... eidocranial dysplasia patient.
@en
type
label
Characterisation of novel RUNX ...... eidocranial dysplasia patient.
@en
prefLabel
Characterisation of novel RUNX ...... eidocranial dysplasia patient.
@en
P2093
P2860
P356
P1433
P1476
Characterisation of novel RUNX ...... eidocranial dysplasia patient.
@en
P2093
Akio Shibata
Atsuo Nakayama
Hiroshi Kitoh
Hitoshi Miyachi
Junichiro Machida
Kazuo Shimozato
Masaki Matsushita
Masashi Kimura
Naoki Ishiguro
Seishi Yamaguchi
P2860
P356
10.1093/MUTAGE/GEV057
P577
2015-07-28T00:00:00Z