Greagory Guzauskas

Summary

Affiliation: Greenwood Genetic Center
Country: USA

Publications

  1. pmc Microarray data integration for genome-wide analysis of human tissue-selective gene expression
    Liangjiang Wang
    Department of Genetics and Biochemistry, Clemson University, Clemson, SC 29634, USA
    BMC Genomics 11:S15. 2010
  2. pmc Sequence feature-based prediction of protein stability changes upon amino acid substitutions
    Shaolei Teng
    Department of Genetics and Biochemistry, Clemson University, Clemson, SC 29634, USA
    BMC Genomics 11:S5. 2010
  3. pmc The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains
    A K Srivastava
    J C Self Research Institute of Human Genetics, Greenwood Genetic Center, SC 29646, USA
    Proc Natl Acad Sci U S A 94:13069-74. 1997
  4. ncbi request reprint Integrated STS/YAC physical, genetic, and transcript map of human Xq21.3 to q23/q24 (DXS1203-DXS1059)
    A K Srivastava
    J C Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, South Carolina, 29646, USA
    Genomics 58:188-201. 1999
  5. ncbi request reprint Ectodysplasin-A1 is sufficient to rescue both hair growth and sweat glands in Tabby mice
    A K Srivastava
    J C Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, SC 29646, USA
    Hum Mol Genet 10:2973-81. 2001
  6. pmc AGTR2 in brain development and function
    Virginie S Vervoort
    Greenwood Genetic Center, J C Self Research Institute of Human Genetics, Greenwood, South Carolina 29646, USA
    Am J Med Genet A 140:419-20. 2006
  7. doi request reprint Intellectual disability, midface hypoplasia, facial hypotonia, and Alport syndrome are associated with a deletion in Xq22.3
    Jayson D Rodriguez
    JC Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, South Carolina, USA
    Am J Med Genet A 152:713-7. 2010

Research Grants

  1. CLONING GENES THAT CAUSE MENTAL RETARDATION
    Anand Srivastava; Fiscal Year: 2002
  2. CLONING GENES THAT CAUSE MENTAL RETARDATION
    Anand Srivastava; Fiscal Year: 2007
  3. CLONING GENES THAT CAUSE MENTAL RETARDATION
    Anand K Srivastava; Fiscal Year: 2010

Collaborators

  • R E Stevenson
  • I Thesleff
  • J Pispa
  • S Mumm
  • M S Ko
  • M L Mikkola
  • R Nagaraja
  • Tadahito Shimada
  • Anand Srivastava
  • Anand K Srivastava
  • Liangjiang Wang
  • Charles E Schwartz
  • A K Srivastava
  • Shaolei Teng
  • Jayson D Rodriguez
  • Virginie S Vervoort
  • D Schlessinger
  • Barbara R DuPont
  • Alessandra Renieri
  • Ilaria Meloni
  • Sydney Ladd
  • Nancy D Leslie
  • Shambhu S Bhat
  • Emanuel O Doyne
  • A J Hartung
  • John Archie
  • D M Donovan
  • L V Ouzts
  • J Hudson
  • C Y Cui
  • M C Durmowicz
  • C Jermak
  • S McMillan
  • M Shomaker
  • S A Copeland-Yates
  • K Sossey-Alaoui
  • J Kere
  • Y Du
  • S Ezer
  • M Pekkanen
  • T Jenks

Detail Information

Publications7

  1. pmc Microarray data integration for genome-wide analysis of human tissue-selective gene expression
    Liangjiang Wang
    Department of Genetics and Biochemistry, Clemson University, Clemson, SC 29634, USA
    BMC Genomics 11:S15. 2010
    ..The expression profiles contain valuable information for understanding human gene expression patterns. However, the effective use of public microarray data requires integrating the expression profiles from heterogeneous sources...
  2. pmc Sequence feature-based prediction of protein stability changes upon amino acid substitutions
    Shaolei Teng
    Department of Genetics and Biochemistry, Clemson University, Clemson, SC 29634, USA
    BMC Genomics 11:S5. 2010
    ....
  3. pmc The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains
    A K Srivastava
    J C Self Research Institute of Human Genetics, Greenwood Genetic Center, SC 29646, USA
    Proc Natl Acad Sci U S A 94:13069-74. 1997
    ..The longest Ta cDNA encodes a 391-residue transmembrane protein, ectodysplasin-A, containing 19 Gly-Xaa-Yaa repeats. The isoforms of ectodysplasin-A may correlate with differential roles during embryonic development...
  4. ncbi request reprint Integrated STS/YAC physical, genetic, and transcript map of human Xq21.3 to q23/q24 (DXS1203-DXS1059)
    A K Srivastava
    J C Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, South Carolina, 29646, USA
    Genomics 58:188-201. 1999
    ..Combined with high-density STS landmarks, the multiple YAC clone coverage and integrated genetic, radiation hybrid, and transcript map provide resources to further disease gene searches and sequencing...
  5. ncbi request reprint Ectodysplasin-A1 is sufficient to rescue both hair growth and sweat glands in Tabby mice
    A K Srivastava
    J C Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, SC 29646, USA
    Hum Mol Genet 10:2973-81. 2001
    ....
  6. pmc AGTR2 in brain development and function
    Virginie S Vervoort
    Greenwood Genetic Center, J C Self Research Institute of Human Genetics, Greenwood, South Carolina 29646, USA
    Am J Med Genet A 140:419-20. 2006
  7. doi request reprint Intellectual disability, midface hypoplasia, facial hypotonia, and Alport syndrome are associated with a deletion in Xq22.3
    Jayson D Rodriguez
    JC Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, South Carolina, USA
    Am J Med Genet A 152:713-7. 2010
    ....

Research Grants9

  1. CLONING GENES THAT CAUSE MENTAL RETARDATION
    Anand Srivastava; Fiscal Year: 2002
    ..abstract_text> ..
  2. CLONING GENES THAT CAUSE MENTAL RETARDATION
    Anand Srivastava; Fiscal Year: 2007
    ..abstract_text> ..
  3. CLONING GENES THAT CAUSE MENTAL RETARDATION
    Anand K Srivastava; Fiscal Year: 2010
    ....