Search Results - Sara K. Young-Baird

  • Showing 1 - 9 results of 9
Refine Results
  1. 1
    Novel pathogenic EIF2S3 missense variants causing clinically variable MEHMO syndrome with impaired eIF2γ translational function, and literature review

    Novel pathogenic EIF2S3 missense variants causing clinically variable MEHMO syndrome with impaired eIF2γ translational function, and literature review by Kotzaeridou, Urania, Young‐Baird, Sara K., Suckow, Vanessa, Thornburg, Alexis G., Wagner, Matias, Harting, Inga, Christ, Stine, Strom, Tim, Dever, Thomas E., Kalscheuer, Vera M.

    Published in Clinical genetics
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    Polyamine Control of Translation Elongation Regulates Start Site Selection on Antizyme Inhibitor mRNA via Ribosome Queuing

    Polyamine Control of Translation Elongation Regulates Start Site Selection on Antizyme Inhibitor mRNA via Ribosome Queuing by Ivanov, Ivaylo P., Shin, Byung-Sik, Loughran, Gary, Tzani, Ioanna, Young-Baird, Sara K., Cao, Chune, Atkins, John F., Dever, Thomas E.

    Published in Molecular cell
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  3. 3
    Pumping the brakes: A noncanonical RNA-binding domain in FMRP stalls elongating ribosomes

    Pumping the brakes: A noncanonical RNA-binding domain in FMRP stalls elongating ribosomes by Young-Baird, Sara K.

    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  4. 4
    The Drosophila ribonucleoprotein Clueless is required for ribosome biogenesis in vivo

    The Drosophila ribonucleoprotein Clueless is required for ribosome biogenesis in vivo by Sen, Aditya, Rodriguez-Martinez, Ambar, Young-Baird, Sara K., Cox, Rachel T.

    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  5. 5
    Suppression of MEHMO Syndrome Mutation in eIF2 by Small Molecule ISRIB

    Suppression of MEHMO Syndrome Mutation in eIF2 by Small Molecule ISRIB by Young-Baird, Sara K., Lourenço, Maíra Bertolessi, Elder, Megan K., Klann, Eric, Liebau, Stefan, Dever, Thomas E.

    Published in Molecular cell
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  6. 6
    Studies of a mosaic patient with DBA and chimeric mice reveal erythroid cell–extrinsic contributions to erythropoiesis

    Studies of a mosaic patient with DBA and chimeric mice reveal erythroid cell–extrinsic contributions to erythropoiesis by Doty, Raymond T., Fan, Xing, Young, David J., Liang, Jialiu, Singh, Komudi, Pakbaz, Zahra, Desmond, Ronan, Young-Baird, Sara K., Chandrasekharappa, Settara C., Donovan, Frank X., Phelps, Susan R., Winkler, Thomas, Dunbar, Cynthia E., Abkowitz, Janis L.

    Published in Blood
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  7. 7
    Impaired EIF2S3 function associated with a novel phenotype of X-linked hypopituitarism with glucose dysregulation

    Impaired EIF2S3 function associated with a novel phenotype of X-linked hypopituitarism with glucose dysregulation by Gregory, Louise C., Ferreira, Carolina B., Young-Baird, Sara K., Williams, Hywel J., Harakalova, Magdalena, van Haaften, Gijs, Rahman, Sofia A., Gaston-Massuet, Carles, Kelberman, Daniel, GOSgene, Qasim, Waseem, Camper, Sally A., Dever, Thomas E., Shah, Pratik, Robinson, Iain C.A.F., Dattani, Mehul T.

    Published in EBioMedicine
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  8. 8
    MEHMO syndrome mutation EIF2S3-I259M impairs initiator Met-tRNAiMet binding to eukaryotic translation initiation factor eIF2

    MEHMO syndrome mutation EIF2S3-I259M impairs initiator Met-tRNAiMet binding to eukaryotic translation initiation factor eIF2 by Young-Baird, Sara K, Shin, Byung-Sik, Dever, Thomas E

    Published in Nucleic acids research
    Request full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  9. 9
    Impaired EIF2S3 function associated with a novel phenotype of X-linked hypopituitarism with glucose dysregulationResearch in context

    Impaired EIF2S3 function associated with a novel phenotype of X-linked hypopituitarism with glucose dysregulationResearch in context by Louise C. Gregory, Carolina B. Ferreira, Sara K. Young-Baird, Hywel J. Williams, Magdalena Harakalova, Gijs van Haaften, Sofia A. Rahman, Carles Gaston-Massuet, Daniel Kelberman, GOSgene, Waseem Qasim, Sally A. Camper, Thomas E. Dever, Pratik Shah, Iain C.A.F. Robinson, Mehul T. Dattani

    Published in EBioMedicine
    Get full text
    Article
    Save to List
    Saved in:

Search Tools: