Search Results - Arbones, M.L.

  • Showing 1 - 11 results of 11
Refine Results
  1. 1
    Alterations in the phenotype of neocortical pyramidal cells in the Dyrk1A+/− mouse

    Alterations in the phenotype of neocortical pyramidal cells in the Dyrk1A+/− mouse by Benavides-Piccione, R., Dierssen, M., Ballesteros-Yáñez, I., Martínez de Lagrán, M., Arbonés, M.L., Fotaki, V., DeFelipe, J., Elston, G.N.

    Get full text
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene

    Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene by RABIONET, R, ZELANTE, L, LOPEZ-BIGAS, N, D'AGRUMA, L, MELCHIONDA, S, RESTAGNO, G, ARBONES, M. L, GASPARINI, P, ESTIVILL, X

    Published in Human genetics
    Get full text
    Items that cite this one
    Article
    Save to List
    Saved in:
  3. 3
    [P1.27]: Dyrk1A gene dosage controls developmental cell death of the mesencephalic dopaminergic neurons

    [P1.27]: Dyrk1A gene dosage controls developmental cell death of the mesencephalic dopaminergic neurons by Barallobre, M.J., Laguna, A., Ramirez‐Bautista, E., Arbones, M.L.

    Get full text
    Article
    Save to List
    Saved in:
  4. 4
    [P1.04]: The protein kinase Dyrk1A regulates cell number during the development of the central nervous system

    [P1.04]: The protein kinase Dyrk1A regulates cell number during the development of the central nervous system by Barallobre, M.J., Laguna, A., Ramirez‐Bautista, E., Arbonés, M.L.

    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  5. 5
    Mutations in the Mitochondrial tRNA Ser(UCN) and in the GJB2 (Connexin 26) Gene Are Not Modifiers of the Age at Onset or Severity of Hearing Loss in Spanish Patients with the 12S rRNA A1555G Mutation

    Mutations in the Mitochondrial tRNA Ser(UCN) and in the GJB2 (Connexin 26) Gene Are Not Modifiers of the Age at Onset or Severity of Hearing Loss in Spanish Patients with the 12S r... by López-Bigas, N., Rabionet, R., Martinez, E., Bravo, O., Girons, J., Borragan, A., Pellicer, M., Arbonés, M.L., Estivill, X.

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  6. 6
    Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment

    Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment by López-Bigas, N., Melchionda, S., de Cid, R., Grifa, A., Zelante, L., Govea, N., Arbonés, M.L., Gasparini, P., Estivill, X.

    Published in Human mutation
    Get full text
    Items that cite this one
    Article
    Save to List
    Saved in:
  7. 7
    Erratum: Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment

    Erratum: Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment by López-Bigas, N., Melchionda, S., de Cid, R., Grifa, A., Zelante, L., Govea, N., Arbonés, M.L., Gasparini, P., Estivill, X.

    Published in Human mutation
    Get full text
    Items that cite this one
    Article
    Save to List
    Saved in:
  8. 8
    Erratum: Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment: MUTATIONS IN BRIEF

    Erratum: Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment: MUTATIONS IN BRIEF by López-Bigas, N., Melchionda, S., de Cid, R., Grifa, A., Zelante, L., Govea, N., Arbonés, M.L., Gasparini, P., Estivill, X.

    Published in Human mutation
    Get full text
    Article
    Save to List
    Saved in:
  9. 9
    Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment: Mutations in Brief

    Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment: Mutations in Brief by López-Bigas, N., Melchionda, S., de Cid, R., Grifa, A., Zelante, L., Govea, N., Arbonés, M.L., Gasparini, P., Estivill, X.

    Published in Human mutation
    Get full text
    Article
    Save to List
    Saved in:
  10. 10
    Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene

    Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene by Rabionet, R., Zelante, L., López-Bigas, N., D'Agruma, L., Melchionda, S., Restagno, G., Arbonés, M.L., Gasparini, P., Estivill, X.

    Published in Human genetics
    Get full text
    Items that cite this one
    Article
    Save to List
    Saved in:
  11. 11
    Industrially Processed Vacuum-Packed Peeled Kennebec Potatoes: Process Optimization, Sensory Evaluation, and Consumer Response

    Industrially Processed Vacuum-Packed Peeled Kennebec Potatoes: Process Optimization, Sensory Evaluation, and Consumer Response by Montouto-Graña, M., Cabanas-Arias, S., Vázquez-Odériz, M.L., Arbones-Maciñeira, E., Romero-Rodríguez, M.A.

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:

Search Tools: