Michael A Gray
Overview
Explore the profile of Michael A Gray including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
61
Citations
1152
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Frueh J, Shu P, Vennard T, Gray M, Phillips S
J AOAC Int
. 2024 May;
107(4):693-704.
PMID: 38704865
Background: Infant formulas, and pediatric and adult nutritional products, are being fortified with bovine lactoferrin (bLF) due to its beneficial impacts on immune development and gut health. Lactoferrin supplementation into...
2.
Delpiano L, Rodenburg L, Burke M, Nelson G, Amatngalim G, Beekman J, et al.
Proc Natl Acad Sci U S A
. 2023 Nov;
120(47):e2307551120.
PMID: 37967223
In cystic fibrosis (CF), defects in the CF transmembrane conductance regulator (CFTR) channel lead to an acidic airway surface liquid (ASL), which compromises innate defence mechanisms, predisposing to pulmonary failure....
3.
Vennard T, Meredith N, Maria S, Brink L, Shah N, Morrow A, et al.
J Pharm Biomed Anal
. 2023 Nov;
238:115817.
PMID: 37939550
Glycerol monolaurate (GML), a monoglyceride found in human milk (HM), has antimicrobial properties against a broad spectrum of bacteria, viruses, and fungi. In this study, an LC-MS/MS method was developed...
4.
A Cell-Based Optimised Approach for Rapid and Efficient Gene Editing of Human Pluripotent Stem Cells
Cuevas-Ocana S, Yang J, Aushev M, Schlossmacher G, Bear C, Hannan N, et al.
Int J Mol Sci
. 2023 Jun;
24(12).
PMID: 37373413
Introducing or correcting disease-causing mutations through genome editing in human pluripotent stem cells (hPSCs) followed by tissue-specific differentiation provide sustainable models of multiorgan diseases, such as cystic fibrosis (CF). However,...
5.
Rodenburg L, Delpiano L, Railean V, Centeio R, Pinto M, Smits S, et al.
Int J Mol Sci
. 2022 Oct;
23(20).
PMID: 36293514
Individuals with cystic fibrosis (CF) suffer from severe respiratory disease due to a genetic defect in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which impairs airway epithelial ion and...
6.
Lin J, Gettings S, Talbi K, Schreiber R, Taggart M, Preller M, et al.
Pflugers Arch
. 2022 Oct;
475(2):167-179.
PMID: 36205782
The cystic fibrosis transmembrane conductance regulator (CFTR) anion channel and the epithelial Na channel (ENaC) play essential roles in transepithelial ion and fluid transport in numerous epithelial tissues. Inhibitors of...
7.
Jo S, Centeio R, Park J, Ousingsawat J, Jeon D, Talbi K, et al.
FASEB J
. 2022 Oct;
36(11):e22534.
PMID: 36183361
The solute carrier 26 family member A9 (SLC26A9) is an epithelial anion transporter that is assumed to contribute to airway chloride secretion and surface hydration. Whether SLC26A9 or CFTR is...
8.
Saint-Criq V, Guequen A, Philp A, Villanueva S, Apablaza T, Fernandez-Moncada I, et al.
Elife
. 2022 May;
11.
PMID: 35635440
Bicarbonate secretion is a fundamental process involved in maintaining acid-base homeostasis. Disruption of bicarbonate entry into airway lumen, as has been observed in cystic fibrosis, produces several defects in lung...
9.
Pereira C, Mazein A, Farinha C, Gray M, Kunzelmann K, Ostaszewski M, et al.
Sci Rep
. 2021 Nov;
11(1):22223.
PMID: 34782688
Cystic fibrosis (CF) is a life-threatening autosomal recessive disease caused by more than 2100 mutations in the CF transmembrane conductance regulator (CFTR) gene, generating variability in disease severity among individuals...
10.
Saint-Criq V, Wang Y, Delpiano L, Lin J, Sheppard D, Gray M
J Cyst Fibros
. 2021 May;
20(5):843-850.
PMID: 34020896
Background: The clinical response to cystic fibrosis transmembrane conductance regulator (CFTR) modulators varies between people with cystic fibrosis (CF) of the same genotype, in part through the action of solute...