Publications by authors named "Alison May"

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CFTR function in alveolar type 1 cells drives lung liquid secretion and host defense.
Sayahi Suthakaran, Sonya Homami, Deebly Chavez, Stephanie Tang, Sarah K L Moore, Alison J May

bioRxiv· March 2025

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Rescue of alveolar wall liquid secretion blocks fatal lung injury due to influenza-staphylococcal coinfection.
Stephanie Tang, Ana Cassandra De Jesus, Deebly Chavez, Sayahi Suthakaran, Sarah Kl Moore, Alison J May

J Clin Invest· October 2023

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Long-term functional regeneration of radiation-damaged salivary glands through delivery of a neurogenic hydrogel.
Jianlong Li, Sonia Sudiwala, Lionel Berthoin, Seayar Mohabbat, Eliza A Gaylord, Alison J May

Sci Adv· December 2022

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Neuronal-epithelial cross-talk drives acinar specification via NRG1-ERBB3-mTORC2 signaling.
Alison J May, Aaron J Mattingly, Eliza A Gaylord, Nathan Griffin, Sonia Sudiwala

Dev Cell· November 2022

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A mechanism of gene evolution generating mucin function.
Petar Pajic, Shichen Shen, Jun Qu, Alison J May, Sarah Knox

Sci Adv· August 2022

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Phenotypic spectrum of the recurrent TRPM3 p.(Val837Met) substitution in seven individuals with global developmental delay and hypotonia.
Matthew A Lines, Paula Goldenberg, Ashley Wong, Siddharth Srivastava, Allan Bayat, Alison May

Am J Med Genet A· June 2022

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Comparison of Cosyntropin, Vigabatrin, and Combination Therapy in New-Onset Infantile Spasms in a Prospective Randomized Trial.
Kelly G Knupp, Jason Coryell, Rani K Singh, William D Gaillard, Renée A Shellhaas, Alison May

J Child Neurol· March 2022

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Septum submucosal glands exhibit aberrant morphology and reduced mucin production in chronic rhinosinusitis.
Onyekachi Ezinna Nnabue, Steven D Pletcher, Jose G Gurrola, Andrew N Goldberg, Kristiana M Jordan, Alison J May

Int Forum Allergy Rhinol· October 2021

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Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome.
Margot A Cousin, Blake A Creighton, Keith A Breau, Rebecca C Spillmann, Erin Torti, Alison S May

Nat Genet· July 2021

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A DNA repair disorder caused by de novo monoallelic DDB1 variants is associated with a neurodevelopmental syndrome.
Susan M White, Elizabeth Bhoj, Christoffer Nellåker, Augusta M A Lachmeijer, Aren E Marshall, Alison S May

Am J Hum Genet· April 2021

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Functional Specialization of Human Salivary Glands and Origins of Proteins Intrinsic to Human Saliva.
Marie Saitou, Eliza A Gaylord, Erica Xu, Alison J May, Lubov Neznanova

Cell Rep· November 2020

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FGF10 is an essential regulator of tracheal submucosal gland morphogenesis.
Alison J May, Tathyane H N Teshima, Alistair Noble, Abigail S Tucker

Dev Biol· July 2019

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Diverse progenitor cells preserve salivary gland ductal architecture after radiation-induced damage.
Alison J May, Noel Cruz-Pacheco, Elaine Emmerson, Eliza A Gaylord, Kerstin Seidel

Development· November 2018

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Home Visiting: Improving Children's and Families' Well-Being.
Courtney L Harrison, Alison May

NCSL Legisbrief· August 2018

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Salivary glands regenerate after radiation injury through SOX2-mediated secretory cell replacement.
Elaine Emmerson, Alison J May, Lionel Berthoin, Noel Cruz-Pacheco, Sara Nathan

EMBO Mol Med· March 2018

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SOX2 regulates acinar cell development in the salivary gland.
Elaine Emmerson, Alison J May, Sara Nathan, Noel Cruz-Pacheco, Carlos O Lizama

Elife· June 2017

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FGF and EDA pathways control initiation and branching of distinct subsets of developing nasal glands.
Alison J May, Denis Headon, David P Rice, Alistair Noble, Abigail S Tucker

Dev Biol· November 2016

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A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemia.
Daniel A Lichtenstein, Andrew W Crispin, Anoop K Sendamarai, Dean R Campagna, Klaus Schmitz-Abe, Alison May

Blood· October 2016

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Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9.
Klaus Schmitz-Abe, Szymon J Ciesielski, Paul J Schmidt, Dean R Campagna, Fedik Rahimov, Alison May

Blood· December 2015

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EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.
Joanne Traeger-Synodinos, Cornelis L Harteveld, John M Old, Mary Petrou, Renzo Galanello, Alison May

Eur J Hum Genet· April 2015

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Understanding the development of the respiratory glands.
Alison May, Abigail Tucker

Dev Dyn· April 2015

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EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.
Joanne Traeger-Synodinos, Cornelis L Harteveld, John M Old, Mary Petrou, Renzo Galanello, Alison May

Eur J Hum Genet· April 2015

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Neuro-behçet disease in an african american adolescent.
Alexander E Merkler, Carolina B Maciel, Alison S May, Wendy S Vargas, Kaleb Yohay

Neurohospitalist· January 2015

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Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD).
Pranesh K Chakraborty, Klaus Schmitz-Abe, Erin K Kennedy, Hapsatou Mamady, Turaya Naas, Alison May

Blood· October 2014

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Infection of the optic apparatus and hypothalamus by Mycobacterium haemophilum.
Alexander E Merkler, George Parlitsis, Sarju Patel, Cristiano Oliveira, Ehud Lavi, Alison May

Neurology· August 2014

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