Mutational analysis of the hSNF5/INI1 gene in rhabdoid tumor.

被引:0
|
作者
Chen, TTL [1 ]
Savla, J [1 ]
Timmons, CF [1 ]
Schneider, NR [1 ]
Tomlinson, GE [1 ]
机构
[1] Univ Texas Dallas, Dallas, TX 75230 USA
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
645
引用
收藏
页码:A122 / A122
页数:1
相关论文
共 50 条
  • [31] Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer
    Versteege, I
    Sévenet, N
    Lange, J
    Rousseau-Merck, MF
    Ambros, P
    Handgretinger, R
    Aurias, A
    Delattre, O
    NATURE, 1998, 394 (6689) : 203 - 206
  • [32] The tumor suppressor hSNF5/INI1 modulates cell growth and actin cytoskeleton organization
    Medjkane, S
    Novikov, E
    Versteege, I
    Delattre, O
    CANCER RESEARCH, 2004, 64 (10) : 3406 - 3413
  • [33] Pediatric embryonal tumor with epithelial immunophenotype showing absence of hSNF5/INI1 expression
    Keiichi Sakai
    Hiroaki Shigeta
    Yoshifumi Ogiso
    Kazuhiro Hongo
    Shigeaki Kobayashi
    Takanori Hirose
    Child's Nervous System, 2005, 21 : 150 - 155
  • [34] Pediatric embryonal tumor with epithelial immunophenotype showing absence of hSNF5/INI1 expression
    Sakai, K
    Shigeta, H
    Ogiso, Y
    Hongo, K
    Kobayashi, S
    Hirose, T
    CHILDS NERVOUS SYSTEM, 2005, 21 (02) : 150 - 155
  • [35] RhoA-Dependent regulation of cell migration by the tumor suppressor hSNF5/INI1
    Caramel, Julie
    Quignon, Frederique
    Delattre, Olivier
    CANCER RESEARCH, 2008, 68 (15) : 6154 - 6161
  • [36] HIGH PROPORTION AND POOR PROGNOSIS OF HSNF5/INI1 GERMLINE MUTATIONS
    Bourdeaut, F.
    Reynaud, S.
    Brugiere, L.
    Lequin, D.
    Dufour, C.
    Doz, F.
    Andre, N.
    Perel, Y.
    Sainte-Rose, C.
    Bergeron, C.
    Rialland, X.
    Stephan, J.
    Figarella-Branger, D.
    Varlet, P.
    Freneaux, P.
    Ranchere, D.
    Coupier, I.
    Gauthier-Villars, M.
    Pierron, G.
    Delattre, O.
    NEURO-ONCOLOGY, 2010, 12 (06) : II34 - II34
  • [37] Inherited predisposition to rhabdoid tumours - A new cancer predisposition syndrome caused by mutations in the chromatin remodelling gene hSNF5/INI1
    Sheridan, E
    Sevenet, N
    Delattre, O
    JOURNAL OF MEDICAL GENETICS, 1999, 36 : S19 - S19
  • [38] NMR and Fluorescence Studies of DNA Binding Domain of INI1/hSNF5
    Lee, Dongju
    Moon, Sunjin
    Yun, Jihye
    Kim, Eunhee
    Cheong, Chaejoon
    Lee, Weontae
    BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 2014, 35 (09): : 2753 - 2757
  • [39] No evidence of hSNF5/INI1 point mutations in choroid plexus papilloma
    Mueller, W
    Eum, JHD
    Lass, U
    Paulus, W
    Sarkar, C
    Bruck, W
    von Deimling, A
    NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 2004, 30 (03) : 304 - 307
  • [40] Spontaneous Regression of Atypical Teratoid Rhabdoid Tumor Without Therapy in a Patient With Uncommon Regional Inactivation of SMARCB1 (hSNF5/INI1)
    Peterson, Jo Elle G.
    Bavle, Abhishek
    Mehta, Vidya P.
    Rauch, Ronald A.
    Whitehead, William E.
    Mohila, Carrie A.
    Su, Jack M.
    Adesina, Adekunle M.
    PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 2019, 22 (02) : 161 - 165