G8: a novel domain associated with polycystic kidney disease and non-syndromic hearing loss
暂无分享,去创建一个
Qiang Li | David J. Studholme | Quan-Yuan He | Xiang-Hua Liu | Song-Ping Liang | Xuan-Wen Li | D. Studholme | Xiang-Hua Liu | S. Liang | Xuanshe Li | Quan-Yuan He | Qiang Li | Xuan-Wen Li
[1] Robert D. Finn,et al. Pfam: clans, web tools and services , 2005, Nucleic Acids Res..
[2] Yusuke Nakamura,et al. Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters' cells and the fibrocytes, as the cause of nonsyndromic hearing loss , 2003, Journal of Human Genetics.
[3] Carsten Bergmann,et al. PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD) , 2004, Human mutation.
[4] P. Comoglio,et al. A splicing variant of the RON transcript induces constitutive tyrosine kinase activity and an invasive phenotype , 1996, Molecular and cellular biology.
[5] R. C. Dickson,et al. Assembly of bacteriophage T4 tail fibers. IV. Subunit composition of tail fibers and fiber precursors. , 1973, Journal of molecular biology.
[6] Long Yu,et al. GG: A domain involved in phage LTF apparatus and implicated in human MEB and non‐syndromic hearing loss diseases , 2006, FEBS letters.
[7] Roser Torra,et al. A complete mutation screen of PKHD1 in autosomal-recessive polycystic kidney disease (ARPKD) pedigrees. , 2003, Kidney international.
[8] P. Wilson,et al. Polycystic kidney disease. , 2004, The New England journal of medicine.
[9] Peer Bork,et al. SMART 5: domains in the context of genomes and networks , 2005, Nucleic Acids Res..
[10] B J Keats,et al. Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2. , 2000, Gene.
[11] Geoffrey J. Barton,et al. JPred : a consensus secondary structure prediction server , 1999 .
[12] Leo Goodstadt,et al. CHROMA: consensus-based colouring of multiple alignments for publication , 2001, Bioinform..
[13] W B Wood,et al. Assembly of bacteriophage T4 tail fibers. II. Isolation and characterization of tail fiber precursors. , 1970, Journal of molecular biology.
[14] M. Bedford,et al. The FF domain: a novel motif that often accompanies WW domains. , 1999, Trends in biochemical sciences.
[15] J. Thompson,et al. The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. , 1997, Nucleic acids research.
[16] Izumi Horikawa,et al. Upregulation of the KIAA1199 gene is associated with cellular mortality. , 2006, Cancer letters.
[17] Vicente E. Torres,et al. The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein , 2002, Nature Genetics.