Using protein complexes to predict phenotypic effects of gene mutation

被引：0
|
作者：
Hunter B Fraser
Joshua B Plotkin
机构：
[1] Broad Institute of Harvard and MIT,Department of Biology
[2] University of Pennsylvania,undefined
来源：
Genome Biology | / 8卷
关键词：
Gene Pair; Disease Gene; Additional Data File; Human Protein Reference Database; Human Disease Gene;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 50 条
  • [1] Using protein complexes to predict phenotypic effects of gene mutation
    Fraser, Hunter B.
    Plotkin, Joshua B.
    GENOME BIOLOGY, 2007, 8 (11)
  • [2] A SIMPLE WAY TO VISUALIZE ALTERATIONS IN PROTEIN-STRUCTURE AND THE CONSEQUENTIAL PHENOTYPIC EFFECTS CAUSED BY A MUTATION IN A GENE
    DAY, M
    JOURNAL OF BIOLOGICAL EDUCATION, 1994, 28 (02) : 86 - 89
  • [3] Location and type of mutation in the LIS1 gene do not predict phenotypic severity
    Uyanik, G.
    Morris-Rosendahl, D. J.
    Stiegler, J.
    Klapecki, J.
    Gross, C.
    Berman, Y.
    Martin, P.
    Dey, L.
    Spranger, S.
    Korenke, G. C.
    Schreyer, I.
    Hertzberg, C.
    Neumann, T. E.
    Burkart, P.
    Spaich, C.
    Meng, N.
    Holthausen, H.
    Ades, L.
    Seidel, J.
    Mangold, E.
    Buyse, G.
    Meinecke, P.
    Schara, U.
    Zeschnigk, C.
    Muller, D.
    Helland, G.
    Schulze, B.
    Wright, M. L.
    Kortge-Jung, S.
    Hehr, A.
    Bogdahn, U.
    Schuierer, G.
    Kohlhase, J.
    Aigner, L.
    Wolff, G.
    Hehr, U.
    Winkler, J.
    NEUROLOGY, 2007, 69 (05) : 442 - 447
  • [4] Phenotypic Heterogeneity in a Brazilian Family with Mutation in the Codon 102 of the Prion Protein Gene
    Smid, Jerusa
    Landemberger, Michele C.
    Martins, Vilma R.
    Schultz, Rodrigo
    Rosemberg, Sergio
    Chimelli, Leila
    Nitrini, Ricardo
    PRION, 2011, 5 : 65 - 65
  • [5] Phenotypic heterogeneity in a Brazilian family with a mutation in codon 102 of the prion protein gene
    Smid, J.
    Landemberger, M. C.
    Martins, V. R.
    Schultz, R. R.
    Rosemberg, S.
    Chimelli, L.
    Nitrini, R.
    BRAIN PATHOLOGY, 2014, 24 : 16 - 16
  • [6] Phenotypic heterogeneity in AAAS gene mutation
    Barat, P
    Goizet, C
    Tullio-Pelet, A
    Puel, O
    Labessan, C
    Barthelemy, A
    ACTA PAEDIATRICA, 2004, 93 (09) : 1257 - 1259
  • [7] Phenotypic variation in a family with MPZ gene mutation
    Mechler, F
    Szabó, A
    Siska, É
    Züchner, S
    Molnár, MJ
    NEUROMUSCULAR DISORDERS, 2003, 13 (7-8) : 653 - 654
  • [8] A novel method to predict protein complexes based on Gene Ontology in PPI networks
    Luo, J. (luojiawei@hnu.edu.cn), 1600, Binary Information Press, P.O. Box 162, Bethel, CT 06801-0162, United States (09):
  • [9] ProAffiMuSeq: sequence-based method to predict the binding free energy change of protein-protein complexes upon mutation using functional classification
    Jemimah, Sherlyn
    Sekijima, Masakazu
    Gromiha, M. Michael
    BIOINFORMATICS, 2020, 36 (06) : 1725 - 1730
  • [10] Phenotypic Variability in a Family with a New SHOX Gene Mutation
    Festa, Adalgisa
    Grandone, Anna
    Luongo, Caterina
    Sasso, Marcella
    Mariani, Michela
    Del Giudice, Emanuele Miraglia
    Minari, Roberta
    Vottero, Alessandra
    Perrone, Laura
    HORMONE RESEARCH IN PAEDIATRICS, 2016, 86 : 449 - 450
12345