Developing senescence to remodel the embryo

por Storer, Mekayla, Keyes, William M
Publicado 2014

To regenerate or not to regenerate: Vertebrate model organisms of regeneration‐competency and ‐incompetency

por Aztekin, Can, Storer, Mekayla A.
Publicado 2022

Cellular and molecular mechanisms that regulate mammalian digit tip regeneration

por Storer, Mekayla A., Miller, Freda D.
Publicado 2020

Introductions to the community: Early-career researchers in the time of COVID-19

por Agudo, Judith, Cheng, Chia-Wei, Jones, Courtney L., Avgustinova, Alexandra, Rodriguez-Fraticelli, Alejo E., Storer, Mekayla
Publicado 2021

Interleukin-6 Regulates Adult Neural Stem Cell Numbers during Normal and Abnormal Post-natal Development

por Storer, Mekayla A., Gallagher, Denis, Fatt, Michael P., Simonetta, Jaclin V., Kaplan, David R., Miller, Freda D.
Publicado 2018

The senescence-associated secretory phenotype induces cellular plasticity and tissue regeneration

por Ritschka, Birgit, Storer, Mekayla, Mas, Alba, Heinzmann, Florian, Ortells, Mari Carmen, Morton, Jennifer P., Sansom, Owen J., Zender, Lars, Keyes, William M.
Publicado 2017

Peripheral Nerve Single-Cell Analysis Identifies Mesenchymal Ligands that Promote Axonal Growth

por Toma, Jeremy S., Karamboulas, Konstantina, Carr, Matthew J., Kolaj, Adelaida, Yuzwa, Scott A., Mahmud, Neemat, Storer, Mekayla A., Kaplan, David R., Miller, Freda D.
Publicado 2020

Restoration of hippocampal neural precursor function by ablation of senescent cells in the aging stem cell niche

por Fatt, Michael P., Tran, Lina M., Vetere, Gisella, Storer, Mekayla A., Simonetta, Jaclin V., Miller, Freda D., Frankland, Paul W., Kaplan, David R.
Publicado 2022

Schwann cell precursors contribute to skeletal formation during embryonic development in mice and zebrafish

por Xie, Meng, Kamenev, Dmitrii, Kaucka, Marketa, Kastriti, Maria Eleni, Zhou, Baoyi, Artemov, Artem V., Storer, Mekayla, Fried, Kaj, Adameyko, Igor, Dyachuk, Vyacheslav, Chagin, Andrei S.
Publicado 2019

Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations

por Stankiewicz, Paweł, Sen, Partha, Bhatt, Samarth S., Storer, Mekayla, Xia, Zhilian, Bejjani, Bassem A., Ou, Zhishuo, Wiszniewska, Joanna, Driscoll, Daniel J., Bolivar, Juan, Bauer, Mislen, Zackai, Elaine H., McDonald-McGinn, Donna, Nowaczyk, Małgorzata M.J., Murray, Mitzi, Shaikh, Tamim H., Martin, Vicki, Tyreman, Matthew, Simonic, Ingrid, Willatt, Lionel, Paterson, Joan, Mehta, Sarju, Rajan, Diana, Fitzgerald, Tomas, Gribble, Susan, Prigmore, Elena, Patel, Ankita, Shaffer, Lisa G., Carter, Nigel P., Cheung, Sau Wai, Langston, Claire, Shaw-Smith, Charles
Publicado 2009