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Showing 1 to 3 of 3 for “"SCA5"”.

  1. Molecular and genetic characterization of spinocerebellar ataxia type 5 (SCA5)

    Spinocerebellar ataxia type 5 (SCA5) is a progressive neurodegenerative disorder, which primarily affects the cerebellum. The disease is inherited in an autosomal dominant pattern, with onset typically occurring in the 3rd or 4th decade of life. In 1994, SCA5 was mapped to the centromeric region of …

    umn Repository record for Molecular and genetic characterization of spinocerebellar ataxia type 5 (SCA5) (opens in a new tab)

  2. Estudio de la rickettsiosis transmitida por garrapatas en zonas rurales del departamento del Cauca y la importancia de Amblyomma patinoi en la epidemiología de la enfermedad

    … la búsqueda de genes rickettsiales (gltA, sca5, htrA) y bajo condiciones experimentales se realizaron ensayos de competencia vectorial de A. patinoi y un acercamiento del efecto de la infección de Rickettsia rickettsii sobre genes seleccionados del sistema inmune en esta garrapata. Se …

    javeriana Repository record for Estudio de la rickettsiosis transmitida por garrapatas en zonas rurales del departamento del Cauca y la importancia de Amblyomma patinoi en la epidemiología de la enfermedad (opens in a new tab)

  3. Elucidating the reversibility of ataxia

    … are implicated in spinocerebellar ataxia type 5 (SCA5) and spectrin-associated autosomal recessive cerebellar ataxia type 1 (SPARCA1), respectively. Our mouse model, lacking b-III spectrin (KO), mimics the progressive human phenotype displaying motor deficiencies as well as reduced Purkinje cell …

    edinburgh Repository record for Elucidating the reversibility of ataxia (opens in a new tab)