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Showing 1 to 6 of 6 for “"Wfs1"”.

  1. Molecular and Functional Characterization of Pyramidal Cell Types in the Frontal Cortex of Mouse Brain

    … 2 of neocortex defined by genes Ntf3, Pdyn and Wfs1, corticostriatal neurons in layer 5a of lateral cortex expressing Etv1 and corticothalamic neurons in layer 6 of neocortex defined by Ntsr1 and Syt6. We generated translation profiles of actively translated mRNAs in the targeted cell types with …

    rockefeller Repository record for Molecular and Functional Characterization of Pyramidal Cell Types in the Frontal Cortex of Mouse Brain (opens in a new tab)

  2. Exploring the Grey Zone between Type 1 and Type 2 Diabetes

    … VNTR, TCF7L2 (study II), PPARG, KCNJ11, IGF2BP2, WFS1, CDKAL1, JAZF1, CDKN2A/2B, HHEX, SLC30A8 and FTO (study III) and MODY genes- HNF-4 , GCK, HNF-1 and HNF-1ß, formerly TCF2 (study IV), measured islet antibodies (ICA, IA-2A and GADA) and C-peptide (marker of beta-cell function instead of …

    lund Repository record for Exploring the Grey Zone between Type 1 and Type 2 Diabetes (opens in a new tab)

  3. Genetics of Type 2 Diabetes and Metabolic Syndrome: From Genome Wide Linkage Scan and Candidate Genes to Genome Wide Association Studies

    … in candidate genes for T2D (TCF7L2, WFS1, IGF2BP2) and obesity (FTO) predicted development of MetS and the risk to develop MetS seemed to be driven by associations with the previously reported phenotypes. These data do not support the view that the different components of MetS share a …

    lund Repository record for Genetics of Type 2 Diabetes and Metabolic Syndrome: From Genome Wide Linkage Scan and Candidate Genes to Genome Wide Association Studies (opens in a new tab)

  4. The genetics of non-syndromic hearing impairment in South Africa

    … variants were identified in the genes: WFS1 (c.A2141), MITF (cT918A), ADGRV1(c.G564T, c.A17450G, c.A11298C), PDSS1(c.C641T, NEU1(c.C1069T, c.G754C), c.G727A), TBC1D24(c.G1514A), MYO15A(c.C1378T, TMPRSS3(c.205+6t>A), c.9303+5G>A, c.G6634A), USH2A(c.T9437A, c.G2990T, c.G101A), …

    cape-town Repository record for The genetics of non-syndromic hearing impairment in South Africa (opens in a new tab)