FGF and EDA pathways control initiation and branching of distinct subsets of developing nasal glands

por May, Alison J., Headon, Denis, Rice, David P., Noble, Alistair, Tucker, Abigail S.
Publicado 2016

A mechanism of gene evolution generating mucin function

por Pajic, Petar, Shen, Shichen, Qu, Jun, May, Alison J., Knox, Sarah, Ruhl, Stefan, Gokcumen, Omer
Publicado 2022

EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies

por Traeger-Synodinos, Joanne, Harteveld, Cornelis L, Old, John M, Petrou, Mary, Galanello, Renzo, Giordano, Piero, Angastioniotis, Michael, De la Salle, Barbara, Henderson, Shirley, May, Alison
Publicado 2015

SOX2 regulates acinar cell development in the salivary gland

por Emmerson, Elaine, May, Alison J, Nathan, Sara, Cruz-Pacheco, Noel, Lizama, Carlos O, Maliskova, Lenka, Zovein, Ann C, Shen, Yin, Muench, Marcus O, Knox, Sarah M
Publicado 2017

Salivary glands regenerate after radiation injury through SOX2‐mediated secretory cell replacement

por Emmerson, Elaine, May, Alison J, Berthoin, Lionel, Cruz‐Pacheco, Noel, Nathan, Sara, Mattingly, Aaron J, Chang, Jolie L, Ryan, William R, Tward, Aaron D, Knox, Sarah M
Publicado 2018

Functional Specialization of Human Salivary Glands and Origins of Proteins Intrinsic to Human Saliva

por Saitou, Marie, Gaylord, Eliza A., Xu, Erica, May, Alison J., Neznanova, Lubov, Nathan, Sara, Grawe, Anissa, Chang, Jolie, Ryan, William, Ruhl, Stefan, Knox, Sarah M., Gokcumen, Omer
Publicado 2020

Rescue of alveolar wall liquid secretion blocks fatal lung injury due to influenza-staphylococcal coinfection

por Tang, Stephanie, De Jesus, Ana Cassandra, Chavez, Deebly, Suthakaran, Sayahi, Moore, Sarah K.L., Suthakaran, Keshon, Homami, Sonya, Rathnasinghe, Raveen, May, Alison J., Schotsaert, Michael, Britto, Clemente J., Bhattacharya, Jahar, Hook, Jaime L.
Publicado 2023

Long-term functional regeneration of radiation-damaged salivary glands through delivery of a neurogenic hydrogel

por Li, Jianlong, Sudiwala, Sonia, Berthoin, Lionel, Mohabbat, Seayar, Gaylord, Eliza A., Sinada, Hanan, Cruz Pacheco, Noel, Chang, Jiun Chiun, Jeon, Oju, Lombaert, Isabelle M.A., May, Alison J., Alsberg, Eben, Bahney, Chelsea S., Knox, Sarah M.
Publicado 2022

Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome

por Cousin, Margot A., Creighton, Blake A., Breau, Keith A., Spillmann, Rebecca C., Torti, Erin, Dontu, Sruthi, Tripathi, Swarnendu, Ajit, Deepa, Edwards, Reginald J., Afriyie, Simone, Bay, Julia C., Harper, Kathryn M., Beltran, Alvaro A., Munoz, Lorena J., Rodriguez, Liset Falcon, Stankewich, Michael C., Person, Richard E., Si, Yue, Normand, Elizabeth A., Blevins, Amy, May, Alison S., Bier, Louise, Aggarwal, Vimla, Mancini, Grazia M. S., van Slegtenhorst, Marjon A., Cremer, Kirsten, Becker, Jessica, Engels, Hartmut, Aretz, Stefan, MacKenzie, Jennifer J., Brilstra, Eva, van Gassen, Koen L. I., van Jaarsveld, Richard H., Oegema, Renske, Parsons, Gretchen M., Mark, Paul, Helbig, Ingo, McKeown, Sarah E., Stratton, Robert, Cogne, Benjamin, Isidor, Bertrand, Cacheiro, Pilar, Smedley, Damian, Firth, Helen V., Bierhals, Tatjana, Kloth, Katja, Weiss, Deike, Fairley, Cecilia, Shieh, Joseph T., Kritzer, Amy, Jayakar, Parul, Kurtz-Nelson, Evangeline, Bernier, Raphael A., Wang, Tianyun, Eichler, Evan E., van de Laar, Ingrid M. B. H., McConkie-Rosell, Allyn, McDonald, Marie T., Kemppainen, Jennifer, Lanpher, Brendan C., Schultz-Rogers, Laura E., Gunderson, Lauren B., Pichurin, Pavel N., Yoon, Grace, Zech, Michael, Jech, Robert, Winkelmann, Juliane, Beltran, Adriana S., Zimmermann, Michael T., Temple, Brenda, Moy, Sheryl S., Klee, Eric W., Tan, Queenie K.-G., Lorenzo, Damaris N.
Publicado 2021