I H Still

Summary

Affiliation: Cleveland Clinic Foundation
Country: USA

Publications

  1. ncbi The third member of the transforming acidic coiled coil-containing gene family, TACC3, maps in 4p16, close to translocation breakpoints in multiple myeloma, and is upregulated in various cancer cell lines
    I H Still
    Center for Molecular Genetics, NB20, The Lerner Research Institute, Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, Ohio, 44195, USA
    Genomics 58:165-70. 1999
  2. ncbi Cloning of TACC1, an embryonically expressed, potentially transforming coiled coil containing gene, from the 8p11 breast cancer amplicon
    I H Still
    Center for Molecular Genetics, The Lerner Research Institute, Cleveland Clinic Foundation, Ohio 44195, USA
    Oncogene 18:4032-8. 1999
  3. ncbi Direct isolation of human transcribed sequences from yeast artificial chromosomes through the application of RNA fingerprinting
    I H Still
    Department of Neurosciences NC30, The Lerner Research Institute, Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH 44195, USA
    Proc Natl Acad Sci U S A 94:10373-8. 1997
  4. ncbi Identification of a novel gene (ADPRTL1) encoding a potential Poly(ADP-ribosyl)transferase protein
    I H Still
    Center for Molecular Genetics NB20, The Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA
    Genomics 62:533-6. 1999
  5. ncbi The Brn-3a transcription factor gene (POU4F1) maps close to the locus for the variant late infantile form of neuronal ceroid-lipofuscinosis
    I H Still
    Department of Neurosciences NC30, Cleveland Clinic Foundation, Ohio 44195, USA
    Cytogenet Cell Genet 74:225-6. 1996
  6. ncbi The t(8;13) atypical myeloproliferative disorder: further analysis of the ZNF198 gene and lack of evidence for multiple genes disrupted on chromosome 13
    I H Still
    Blood 92:1456-8. 1998

Detail Information

Publications6

  1. ncbi The third member of the transforming acidic coiled coil-containing gene family, TACC3, maps in 4p16, close to translocation breakpoints in multiple myeloma, and is upregulated in various cancer cell lines
    I H Still
    Center for Molecular Genetics, NB20, The Lerner Research Institute, Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, Ohio, 44195, USA
    Genomics 58:165-70. 1999
    ..Subsequently, this gene pair has undergone two successive rounds of gene duplication to give rise to the three FGFR/TACC gene pairs on chromosomes 4, 8, and 10...
  2. ncbi Cloning of TACC1, an embryonically expressed, potentially transforming coiled coil containing gene, from the 8p11 breast cancer amplicon
    I H Still
    Center for Molecular Genetics, The Lerner Research Institute, Cleveland Clinic Foundation, Ohio 44195, USA
    Oncogene 18:4032-8. 1999
    ....
  3. ncbi Direct isolation of human transcribed sequences from yeast artificial chromosomes through the application of RNA fingerprinting
    I H Still
    Department of Neurosciences NC30, The Lerner Research Institute, Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH 44195, USA
    Proc Natl Acad Sci U S A 94:10373-8. 1997
    ..This method, therefore, permits the simultaneous isolation and mapping of novel expressed sequences directly from whole YACs...
  4. ncbi Identification of a novel gene (ADPRTL1) encoding a potential Poly(ADP-ribosyl)transferase protein
    I H Still
    Center for Molecular Genetics NB20, The Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA
    Genomics 62:533-6. 1999
    ..We have subsequently refined the location of the ADPRTL1 genomic locus to 13q11, close to the recently cloned ZNF198 gene...
  5. ncbi The Brn-3a transcription factor gene (POU4F1) maps close to the locus for the variant late infantile form of neuronal ceroid-lipofuscinosis
    I H Still
    Department of Neurosciences NC30, Cleveland Clinic Foundation, Ohio 44195, USA
    Cytogenet Cell Genet 74:225-6. 1996
    ..As one of these YACs is only 320 kb long, this localises POU4F1 within the critical region defining the CLN5 locus, and raises the possibility that POU4F1 is a candidate gene for CLN5...
  6. ncbi The t(8;13) atypical myeloproliferative disorder: further analysis of the ZNF198 gene and lack of evidence for multiple genes disrupted on chromosome 13
    I H Still
    Blood 92:1456-8. 1998