Identification and characterization of regulatory elements in the promoter of ACVR1, the gene mutated in Fibrodysplasia Ossificans Progressiva.
about
Molecular, phenotypic aspects and therapeutic horizons of rare genetic bone disorders.High-throughput screening for modulators of ACVR1 transcription: discovery of potential therapeutics for fibrodysplasia ossificans progressiva.Myositis ossificans in children: a review.The Horizon of a Therapy for Rare Genetic Diseases: A "Druggable" Future for Fibrodysplasia Ossificans Progressiva.
P2860
Identification and characterization of regulatory elements in the promoter of ACVR1, the gene mutated in Fibrodysplasia Ossificans Progressiva.
description
2013 nî lūn-bûn
@nan
2013 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Identification and characteriz ...... plasia Ossificans Progressiva.
@ast
Identification and characteriz ...... plasia Ossificans Progressiva.
@en
Identification and characteriz ...... plasia Ossificans Progressiva.
@nl
type
label
Identification and characteriz ...... plasia Ossificans Progressiva.
@ast
Identification and characteriz ...... plasia Ossificans Progressiva.
@en
Identification and characteriz ...... plasia Ossificans Progressiva.
@nl
prefLabel
Identification and characteriz ...... plasia Ossificans Progressiva.
@ast
Identification and characteriz ...... plasia Ossificans Progressiva.
@en
Identification and characteriz ...... plasia Ossificans Progressiva.
@nl
P2093
P2860
P50
P356
P1476
Identification and characteriz ...... splasia Ossificans Progressiva
@en
P2093
Francesca Giacopelli
Laura Tonachini
Marzia Mura
Roberto Ravazzolo
P2860
P2888
P356
10.1186/1750-1172-8-145
P577
2013-09-18T00:00:00Z
P5875
P6179
1004590007