Structural Studies of FOXC2 Protein and Inhibitor Complexes

被引：0
作者：
Li, Shichang [1 ]
Kashipathy, Maithri [1 ]
Castaneda, Maria [1 ]
Lee, Jiyong [1 ]
Nam, Hyun-Joo [1 ]
机构：
[1] Univ Texas Dallas, Dept Bioengn, Richardson, TX 75083 USA
来源：
ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES | 2017年 / 73卷
关键词：
D O I：
10.1107/S0108767317097872
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
引用
收藏
页码：A216 / A216
页数：1
相关论文
共 50 条
  • [41] Lymphedema-distichiasis syndrome and FOXC2 gene mutation
    Traboulsi, EI
    Al-Khayer, K
    Matsumoto, M
    Kimak, MA
    Crowe, S
    Wilson, SE
    Finegold, DN
    Ferrell, RE
    Meisler, DM
    AMERICAN JOURNAL OF OPHTHALMOLOGY, 2002, 134 (04) : 592 - 596
  • [42] The forkhead transcription factor Foxc2 stimulates osteoblast differentiation
    Kim, Se Hwa
    Cho, Kyoung-Won
    Choi, Han Seok
    Park, Su Jin
    Rhee, Yumie
    Jung, Han-Sung
    Lim, Sung-Kil
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2009, 386 (03) : 532 - 536
  • [43] Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development
    Smith, RS
    Zabaleta, A
    Kume, T
    Savinova, OV
    Kidson, SH
    Martin, JE
    Nishimura, DY
    Alward, WLM
    Hogan, BLM
    John, SWM
    HUMAN MOLECULAR GENETICS, 2000, 9 (07) : 1021 - 1032
  • [44] Foxc1 and Foxc2 deletion causes abnormal lymphangiogenesis and correlates with ERK hyperactivation
    Fatima, Anees
    Wang, Ying
    Uchida, Yutaka
    Norden, Pieter
    Liu, Ting
    Culver, Austin
    Dietz, William H.
    Culver, Ford
    Millay, Meredith
    Mukouyama, Yoh-suke
    Kume, Tsutomu
    JOURNAL OF CLINICAL INVESTIGATION, 2016, 126 (07) : 2437 - 2451
  • [45] Comparative lymphatic, ocular, and metabolic phenotypes of Foxc2 haploinsufficient and aP2-FOXC2 transgenic mice
    Noon, A.
    Hunter, R. J.
    Witte, M. H.
    Kriederman, B.
    Bernas, M.
    Rennels, M.
    Percy, D.
    Enerback, S.
    Erickson, R. P.
    LYMPHOLOGY, 2006, 39 (02) : 84 - 94
  • [46] Truncating mutations in FOXC2 cause multiple lymphedema syndromes
    Finegold, DN
    Kimak, MA
    Lawrence, EC
    Levinson, KL
    Cherniske, EM
    Pober, BR
    Dunlap, JW
    Ferrell, RE
    HUMAN MOLECULAR GENETICS, 2001, 10 (11) : 1185 - 1189
  • [47] A novel FOXC2 mutation in spinal extradural arachnoid cyst
    Yoji Ogura
    Shunsuke Fujibayashi
    Aritoshi Iida
    Ikuyo Kou
    Masahiro Nakajima
    Eijiro Okada
    Yoshiaki Toyama
    Akio Iwanami
    Ken Ishii
    Masaya Nakamura
    Morio Matsumoto
    Shiro Ikegawa
    Human Genome Variation, 2 (1)
  • [48] Identification of FOXC2 gene variations and metabolic interaction effects between FOXC2 T (-512),C and PPARγ2 Pro12AIa polymorphisms
    Machicao, F
    Staiger, H
    Fritsche, A
    Stumvoll, M
    Haering, HU
    DIABETES, 2003, 52 : A513 - A513
  • [49] Antisense lncRNA FOXC2-AS1 promotes doxorubicin resistance in osteosarcoma by increasing the expression of FOXC2
    Zhang, Chun-Lin
    Zhu, Kun-Peng
    Ma, Xiao-Long
    CANCER LETTERS, 2017, 396 : 66 - 75
  • [50] Forkhead transcription factors, Foxc1 and Foxc2, are required for the morphogenesis of the cardiac outflow tract
    Seo, Seungwoon
    Kume, Tsutomu
    DEVELOPMENTAL BIOLOGY, 2006, 296 (02) : 421 - 436
12345