Epigenomic Studies of Facioscapulohumeral Muscular Dystrophy (FSHD)

被引：0
|
作者：
Zeng, Weihua [1 ]
de Greef, Jessica C. [2 ]
Chen, Yen-yun [1 ]
Chien, Richard [1 ]
Kong, Xiangduo [1 ]
Winokur, Sara T. [1 ]
Ball, Alexander R., Jr. [1 ]
van der Maarel, Silvere M. [2 ]
Yokomori, Kyoko [1 ]
机构：
[1] Univ Calif Irvine, Irvine, CA USA
[2] Leiden Univ, Med Ctr, Leiden, Netherlands
来源：
FASEB JOURNAL | 2010年 / 24卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
引用
收藏
页数：1
相关论文
共 50 条
  • [31] CRISPR screen identifies therapeutic target for Facioscapulohumeral Muscular Dystrophy (FSHD)
    Dengler, V. L.
    GENETICS IN MEDICINE, 2020, 22 (06) : 982 - 982
  • [32] Genetic Counseling and Testing for FSHD (Facioscapulohumeral Muscular Dystrophy) in the Israeli Population
    Yanoov-Sharav, Miri
    Leshinsky-Silver, Esther
    Cohen, Sarit
    Vinkler, Chana
    Michelson, Marina
    Lerman-Sagie, Tally
    Ginzberg, Mira
    Sadeh, Menahem
    Lev, Dorit
    JOURNAL OF GENETIC COUNSELING, 2012, 21 (04) : 557 - 563
  • [33] Electrostimulation of shoulder girdle muscles in facioscapulohumeral muscular dystrophy (FSHD) patients
    Sacconi, S.
    Tanant, V.
    Colson, S.
    Desnuelle, C.
    EUROPEAN JOURNAL OF NEUROLOGY, 2008, 15 : 17 - 18
  • [34] ISOLATION AND MAPPING OF REARRANGEMENTS ASSOCIATED WITH FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD)
    WEIFFENBACH, B
    SCHUTTE, B
    DUBOIS, J
    MANNING, S
    MA, N
    JACOBSEN, SJ
    TAWIL, R
    GRIGGS, RC
    ALTHERR, M
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (03) : 1370 - 1370
  • [35] Respiratory function and trajectories in facioscapulohumeral muscular dystrophy (FSHD): a clinical audit
    Robinson, E.
    Lees, E.
    Moat, D.
    Michell-Sodhi, J.
    Richardson, M.
    Wong, K.
    Grover, E.
    Schiava, M.
    Bolano, C.
    Salman, D.
    Guglieri, M.
    Elseed, M.
    McCallum, M.
    Diaz-Manera, J.
    James, M.
    Straub, V.
    Bettolo, C. Marini
    Pace, F.
    Muni-Lofra, R.
    Tasca, G.
    NEUROMUSCULAR DISORDERS, 2024, 43
  • [36] The diagnostic role of Next generation sequencing on Facioscapulohumeral muscular dystrophy (FSHD)
    Yavuzcan, Beyza
    Kaptan, Manar
    Eraslan, Serpil
    Eren, Sahin Avci Ilker
    Yunisova, Gulshan
    Demirhan, Mehmet
    Oflazer, Piraye
    Kayserili, Hulya
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 1533 - 1534
  • [37] French National Protocol for diagnosis and care of facioscapulohumeral muscular dystrophy (FSHD)
    Attarian, Shahram
    Beloribi-Djefaflia, Sadia
    Bernard, Rafaelle
    Nguyen, Karine
    Cances, Claude
    Gavazza, Carole
    Echaniz-Laguna, Andoni
    Espil, Caroline
    Evangelista, Teresinha
    Feasson, Leonard
    Audic, Frederique
    Zagorda, Berenice
    De Bovis, Virginie Milhe
    Stojkovic, Tanya
    Sole, Guilhem
    Salort-Campana, Emmanuelle
    Sacconi, Sabrina
    JOURNAL OF NEUROLOGY, 2024, 271 (08) : 5378 - 5391
  • [38] Wireless Sensors to Measure Walking in Patients with Facioscapulohumeral Muscular Dystrophy (FSHD)
    Huisinga, Jessie
    Bruetsch, Adam
    Currence, Melissa
    Herbelin, Laura
    Jawdat, Omar
    Pasnoor, Mamatha
    Dimachkie, Mazen
    Barohn, Richard
    Statland, Jeffrey
    NEUROLOGY, 2016, 86
  • [39] Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): Validation of the differential double digestion for FSHD
    Upadhyaya, M
    Maynard, J
    Rogers, MT
    Lunt, PW
    Jardine, P
    Ravine, D
    Harper, PS
    JOURNAL OF MEDICAL GENETICS, 1997, 34 (06) : 476 - 479
  • [40] Absence of anticipation in large at-risk sibships with facioscapulohumeral muscular dystrophy (FSHD)
    Coffeen, C
    Tawil, R
    McDermott, M
    Flanigan, KM
    NEUROMUSCULAR DISORDERS, 2001, 11 (6-7) : 617 - 617
12345