Ontology highlight
ABSTRACT:
INSTRUMENT(S):
ORGANISM(S): Homo Sapiens (human)
SUBMITTER: Marcello Manfredi
LAB HEAD: Marcello Manfredi
PROVIDER: PXD053349 | Pride | 2025-07-21
REPOSITORIES: Pride
Action | DRS | |||
---|---|---|---|---|
FGR2_Ip_Hela_NT_2_20092021_LIB2.mgf | Mgf | |||
FGR2_Ip_Hela_NT_2_20092021_LIB3.mgf | Mgf | |||
File_peak.zip | Other | |||
File_raw.zip | Other | |||
HeLaDoxoRipa_1_conc_30102023_Lib1.mgf | Mgf |
Items per page: 5 1 - 5 of 5 |
Salsi Valentina V Losi Francesca F Fosso Bruno B Ferrarini Marco M Pini Sara S Manfredi Marcello M Vattemi Gaetano G Mongini Tiziana T Maggi Lorenzo L Pesole Graziano G Henras Anthony K AK Kaufman Paul D PD McStay Brian B Tupler Rossella R
Nucleic acids research 20250701 13
Facioscapulohumeral muscular dystrophy (FSHD) is a hereditary myopathy linked to deletions of the tandemly arrayed D4Z4 macrosatellite at human chromosome 4q35. These deletions cause local chromatin changes and anomalous expression of nearby transcripts FRG2A, DBET, and D4Z4. We discovered that FRG2A is part of a family of long noncoding RNAs (lncRNAs) expressed in skeletal muscle cells, with levels varying among patients. FRG2A localizes in the nucleolus and associates with repetitive DNA at ri ...[more]