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Showing 1 to 4 of 4 for “"Sox family"”.

  1. Approach to the identification of sex-determining genes in the tilapia genome by genetic mapping and comparative positional cloning

    … human. A few genes such as a DEAD box protein, Sox family, and a LIM/homeobox, seem to be good candidates for sex-determining genes, and will need further study. AFLP (amplified fragment length polymorphism)/BSA (Bulked segregant analysis) technique was performed to add more markers in the …

    unh-thes Repository record for Approach to the identification of sex-determining genes in the tilapia genome by genetic mapping and comparative positional cloning (opens in a new tab)

  2. Functional studies of <i>Ci-Gsx</i> gene in the developing central nervous system of <i>Ciona intestinalis</i>

    Gsx genes encode for members of ParaHox family of transcription factor and are highly conserved throughout the animal kingdom. They are expressed mainly in the developing CNS in members of all major groups of metazoans. Gsx function, in the few organisms in which it has been investigated, is …

    the-open-u Repository record for Functional studies of <i>Ci-Gsx</i> gene in the developing central nervous system of <i>Ciona intestinalis</i> (opens in a new tab)

  3. Biochemical and Functional Investigations into the Contribution of SOX17 Mutations to the Pathogenesis of Pulmonary Arterial Hypertension

    … of patients, rare heterozygous variants in the SOX17 gene, predicted to be functionally deleterious, were significantly associated with PAH. SOX17 is an essential transcription factor involved in the development of the pulmonary vasculature and is highly expressed in endothelial cells. The aims …

    cambridge Repository record for Biochemical and Functional Investigations into the Contribution of SOX17 Mutations to the Pathogenesis of Pulmonary Arterial Hypertension (opens in a new tab)

  4. Funtional Analysis of the Murine Genes, MOCS1 and Sox15

    … wurden die Funktionen der Mausgene, MOCS1 und Sox15, untersucht. Molybdän Cofaktor-Defizienz ist eine seltene und schwere autosomal-rezessive Krankheit beim Menschen, für die keine Therapie bekannt ist. Das Fehlen von aktiver Sulfitoxidase, die ein Molybdän Cofaktor-abhängiges Enzym ist, führt …

    goettingen Repository record for Funtional Analysis of the Murine Genes, MOCS1 and Sox15 (opens in a new tab)