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Oktober 2020 / J Genet Genomics Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation X. Su Y. Feng S.A. Rahman S. Wu G. Li F. Rüschendorf L. Zhao H. Cui J. Liang L. Fang H. Hu S. Froehler Y. Yu G. Patone O. Hummel Q. Chen K. Raile F.C. Luft S. Bähring K. Hussain W. Chen J. Zhang M. Gong 01. Januar 2001 / Cytogenet Genome Res Assignment of the huntingtin (Hdh) gene, the huntingtin associated protein (Hap1) gene, and the huntingtin interacting protein (Hip1) gene to rat chromosomes 14, 10, and 12 by radiation hybrid mapping and fluorescent in situ hybridization H. Zimdahl C. Goesele G. Luetjens F. Gruetzner T. Kreitler K. Voss E.E. Wanker M. Knoblauch 01. August 1998 / Biochem Soc Trans Polyglutamine expansion and Huntington's disease G.P. Bates L. Mangiarini E.E. Wanker S.W. Davies 17. April 1998 / FEBS Lett HAP1-huntingtin interactions do not contribute to the molecular pathology in Huntington's disease transgenic mice F. Bertaux A.H. Sharp C.A. Ross H. Lehrach G.P. Bates E.E. Wanker 08. August 1997 / Cell Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation S.W. Davies M. Turmaine B.A. Cozens M. DiFiglia A.H. Sharp C.A. Ross E. Scherzinger E.E. Wanker L. Mangiarini G.P. Bates 01. Januar 1999 / Methods Enzymol Detection of polyglutamine aggregation in mouse models S.W. Davies K. Sathasivam C. Hobbs P. Doherty L. Mangiarini E. Scherzinger E.E. Wanker G.P. Bates 26. Mai 1998 / Proc Natl Acad Sci U S A Huntingtin aggregation monitored by dynamic light scattering Y. Georgalis E.B. Starikov B. Hollenbach R. Lurz E. Scherzinger W. Saenger H. Lehrach E.E. Wanker 06. Juni 2000 / Proc Natl Acad Sci U S A Inhibition of huntingtin fibrillogenesis by specific antibodies and small molecules: implications for Huntington's disease therapy V. Heiser E. Scherzinger A. Boeddrich E. Nordhoff R. Lurz N. Schugardt H. Lehrach E.E. Wanker 01. Januar 1998 / Mamm Genome IRS-PCR-based genetic mapping of the huntingtin interacting protein gene (HIP1) on mouse chromosome 5 H. Himmelbauer N. Wedemeyer T. Haaf E.E. Wanker L.C. Schalkwyk H. Lehrach 29. Juni 1999 / Philos Transact A Math Phys Eng Sci Aggregation of truncated GST-HD exon 1 fusion proteins containing normal range and expanded glutamine repeats B. Hollenbach E. Scherzinger K. Schweiger R. Lurz H. Lehrach E.E. Wanker Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Seite 4 … Nächste Seite Next › Letzte Seite Last »
28. Oktober 2020 / J Genet Genomics Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation X. Su Y. Feng S.A. Rahman S. Wu G. Li F. Rüschendorf L. Zhao H. Cui J. Liang L. Fang H. Hu S. Froehler Y. Yu G. Patone O. Hummel Q. Chen K. Raile F.C. Luft S. Bähring K. Hussain W. Chen J. Zhang M. Gong
01. Januar 2001 / Cytogenet Genome Res Assignment of the huntingtin (Hdh) gene, the huntingtin associated protein (Hap1) gene, and the huntingtin interacting protein (Hip1) gene to rat chromosomes 14, 10, and 12 by radiation hybrid mapping and fluorescent in situ hybridization H. Zimdahl C. Goesele G. Luetjens F. Gruetzner T. Kreitler K. Voss E.E. Wanker M. Knoblauch
01. August 1998 / Biochem Soc Trans Polyglutamine expansion and Huntington's disease G.P. Bates L. Mangiarini E.E. Wanker S.W. Davies
17. April 1998 / FEBS Lett HAP1-huntingtin interactions do not contribute to the molecular pathology in Huntington's disease transgenic mice F. Bertaux A.H. Sharp C.A. Ross H. Lehrach G.P. Bates E.E. Wanker
08. August 1997 / Cell Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation S.W. Davies M. Turmaine B.A. Cozens M. DiFiglia A.H. Sharp C.A. Ross E. Scherzinger E.E. Wanker L. Mangiarini G.P. Bates
01. Januar 1999 / Methods Enzymol Detection of polyglutamine aggregation in mouse models S.W. Davies K. Sathasivam C. Hobbs P. Doherty L. Mangiarini E. Scherzinger E.E. Wanker G.P. Bates
26. Mai 1998 / Proc Natl Acad Sci U S A Huntingtin aggregation monitored by dynamic light scattering Y. Georgalis E.B. Starikov B. Hollenbach R. Lurz E. Scherzinger W. Saenger H. Lehrach E.E. Wanker
06. Juni 2000 / Proc Natl Acad Sci U S A Inhibition of huntingtin fibrillogenesis by specific antibodies and small molecules: implications for Huntington's disease therapy V. Heiser E. Scherzinger A. Boeddrich E. Nordhoff R. Lurz N. Schugardt H. Lehrach E.E. Wanker
01. Januar 1998 / Mamm Genome IRS-PCR-based genetic mapping of the huntingtin interacting protein gene (HIP1) on mouse chromosome 5 H. Himmelbauer N. Wedemeyer T. Haaf E.E. Wanker L.C. Schalkwyk H. Lehrach
29. Juni 1999 / Philos Transact A Math Phys Eng Sci Aggregation of truncated GST-HD exon 1 fusion proteins containing normal range and expanded glutamine repeats B. Hollenbach E. Scherzinger K. Schweiger R. Lurz H. Lehrach E.E. Wanker