J M Derry

Summary

Affiliation: Immunex Corporation
Country: USA

Publications

  1. ncbi Mutations in a delta 8-delta 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata. jderry@immunex.com
    J M Derry
    Immunex Corporation, Seattle, Washington 98101 2936, USA
    Nat Genet 22:286-90. 1999
  2. ncbi Transgenic rescue of the tattered phenotype by using a BAC encoding Ebp
    G D Means
    Immunex Corporation, Seattle, Washington 98101, USA
    Mamm Genome 12:323-5. 2001
  3. ncbi The mouse homolog of the Wiskott-Aldrich syndrome protein (WASP) gene is highly conserved and maps near the scurfy (sf) mutation on the X chromosome
    J M Derry
    Howard Hughes Medical Institute, Stanford University Medical Center, California 94305, USA
    Genomics 29:471-7. 1995
  4. ncbi WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia
    J M Derry
    Howard Hughes Medical Institute, Stanford University Medical Center, CA 94305, USA
    Hum Mol Genet 4:1127-35. 1995
  5. ncbi Dystroglycan: brain localisation and chromosome mapping in the mouse
    D C Gorecki
    Molecular Neurobiology Unit, Royal Free Hospital School of Medicine, London, UK
    Hum Mol Genet 3:1589-97. 1994
  6. ncbi Mapping of the glycine receptor alpha 2-subunit gene and the GABAA alpha 3-subunit gene on the mouse X chromosome
    J M Derry
    MRC Molecular Neurobiology Unit, MRC Centre, Cambridge, United Kingdom
    Genomics 10:593-7. 1991
  7. ncbi Molecular characterization of the human interleukin (IL)-17 receptor
    Z Yao
    Department of Molecular Biology, Immunex Corporation, Seattle, WA 98101, USA
    Cytokine 9:794-800. 1997
  8. ncbi Mapping of the phosphorylase kinase alpha subunit gene on the mouse X chromosome
    P J Barnard
    MRC Molecular Neurobiology Unit, Medical Research Council Centre, Cambridge, England
    Cytogenet Cell Genet 53:91-4. 1990
  9. ncbi RBM3, a novel human gene in Xp11.23 with a putative RNA-binding domain
    J M Derry
    Howard Hughes Medical Insitute, Stanford University Medical Center, CA 94305, USA
    Hum Mol Genet 4:2307-11. 1995
  10. ncbi Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization
    M Symons
    Onyx Pharmaceuticals, Richmond, California 94806, USA
    Cell 84:723-34. 1996

Collaborators

Detail Information

Publications15

  1. ncbi Mutations in a delta 8-delta 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata. jderry@immunex.com
    J M Derry
    Immunex Corporation, Seattle, Washington 98101 2936, USA
    Nat Genet 22:286-90. 1999
    ....
  2. ncbi Transgenic rescue of the tattered phenotype by using a BAC encoding Ebp
    G D Means
    Immunex Corporation, Seattle, Washington 98101, USA
    Mamm Genome 12:323-5. 2001
  3. ncbi The mouse homolog of the Wiskott-Aldrich syndrome protein (WASP) gene is highly conserved and maps near the scurfy (sf) mutation on the X chromosome
    J M Derry
    Howard Hughes Medical Institute, Stanford University Medical Center, California 94305, USA
    Genomics 29:471-7. 1995
    ..Northern analysis of sf tissue samples indicated the presence of WASP mRNA in liver and skin, presumably as a consequence of lymphocytic infiltration, but non abnormalities in the amount or size of mRNA present...
  4. ncbi WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia
    J M Derry
    Howard Hughes Medical Institute, Stanford University Medical Center, CA 94305, USA
    Hum Mol Genet 4:1127-35. 1995
    ..The distribution of eight missense mutations provides valuable information on amino acids which are essential for normal protein function, and suggests that sites in the first two exons are hot-spots for mutation...
  5. ncbi Dystroglycan: brain localisation and chromosome mapping in the mouse
    D C Gorecki
    Molecular Neurobiology Unit, Royal Free Hospital School of Medicine, London, UK
    Hum Mol Genet 3:1589-97. 1994
    ..Dystroglycan is also expressed in those brain areas where the dystrophin-related protein (utrophin) is present. Our results provide a basis for a future characterisation of the role of dystrophin-dystroglycan association in the brain...
  6. ncbi Mapping of the glycine receptor alpha 2-subunit gene and the GABAA alpha 3-subunit gene on the mouse X chromosome
    J M Derry
    MRC Molecular Neurobiology Unit, MRC Centre, Cambridge, United Kingdom
    Genomics 10:593-7. 1991
    ..This establishes the XF region of the mouse X chromosome as homologous with the Xp22.1-p22.3 region of the human X chromosome and indicates the presence of an evolutionary breakpoint in the region of Xp21.3...
  7. ncbi Molecular characterization of the human interleukin (IL)-17 receptor
    Z Yao
    Department of Molecular Biology, Immunex Corporation, Seattle, WA 98101, USA
    Cytokine 9:794-800. 1997
    ..Binding studies suggest that recombinant hIL-17 binds to the hIL-17R with low affinity...
  8. ncbi Mapping of the phosphorylase kinase alpha subunit gene on the mouse X chromosome
    P J Barnard
    MRC Molecular Neurobiology Unit, Medical Research Council Centre, Cambridge, England
    Cytogenet Cell Genet 53:91-4. 1990
    ....
  9. ncbi RBM3, a novel human gene in Xp11.23 with a putative RNA-binding domain
    J M Derry
    Howard Hughes Medical Insitute, Stanford University Medical Center, CA 94305, USA
    Hum Mol Genet 4:2307-11. 1995
    ..The homology of RMB3 in both sequence and size to an RNA binding protein from maize, AAIP , suggests that it functions in a fundamental pathway conserved from plants to mammals...
  10. ncbi Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization
    M Symons
    Onyx Pharmaceuticals, Richmond, California 94806, USA
    Cell 84:723-34. 1996
    ..The WASP sequence contains two novel domains that are homologous to other proteins involved in action organization...
  11. ncbi Cloning and characterization of a novel zinc finger gene in Xp11.2
    J M Derry
    Howard Hughes Medical Institute, Stanford University Medical School, California 94305, USA
    Genomics 30:361-5. 1995
    ..A fourth exon contains 12 zinc finger DNA binding motifs and finger linking regions characteristic of ZNF proteins of the Krüppel family. ZNF157 maps to the telomeric end of a cluster of ZNF genes that includes ZNF21, ZNF41, and ZNF81...
  12. ncbi Localization of monoamine oxidase A and B genes on the mouse X chromosome
    J M Derry
    MRC Molecular Neurobiology Unit, Medical Research Council Centre, Cambridge, UK
    Nucleic Acids Res 17:8403. 1989
  13. ncbi Mapping of a liver phosphorylase kinase alpha-subunit gene on the mouse X chromosome
    Y Geng
    MRC Molecular Neurobiology Unit, MRC Centre, Cambridge, United Kingdom
    Genomics 15:191-3. 1993
    ..This mapping position would suggest a location for the human liver alpha-subunit gene on the proximal short arm of the X chromosome, a region recently implicated in X-linked liver glycogenosis (XLG)...
  14. ncbi Isolation of a novel gene mutated in Wiskott-Aldrich syndrome
    J M Derry
    Howard Hughes Medical Institute, Beckman Center for Molecular and Genetic Medicine, Stanford, California
    Cell 78:635-44. 1994
    ..WASP encodes a 501 amino acid proline-rich protein that is likely to be a key regulator of lymphocyte and platelet function...
  15. ncbi Physical linkage of the A-raf-1, properdin, synapsin I, and TIMP genes on the human and mouse X chromosomes
    J M Derry
    MRC Molecular Neurobiology Unit, MRC Centre, Cambridge, United Kingdom
    Genomics 12:632-8. 1992
    ..Analysis of the corresponding region of the human X chromosome indicates a similar arrangement and in addition shows that the properdin gene lies within 5 kb of the 5' end of the synapsin I gene...