N Ray Dunn
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Explore the profile of N Ray Dunn including associated specialties, affiliations and a list of published articles.
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36
Citations
1613
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Recent Articles
1.
Goh K, Lu H, Tan E, Lee Z, Wong A, Tran T, et al.
Biol Open
. 2024 Oct;
13(10).
PMID: 39387302
The generation of lung epithelial cells through the directed differentiation of human pluripotent stem cells (hPSCs) in vitro provides a platform to model both embryonic lung development and adult airway...
2.
Tomaz L, Liu B, Meroshini M , Ong S, Tan E, Tolwinski N, et al.
J Cell Sci
. 2022 Oct;
135(21).
PMID: 36217793
The gene mutated in colorectal cancer (MCC) encodes a coiled-coil protein implicated, as its name suggests, in the pathogenesis of hereditary human colon cancer. To date, however, the contributions of...
3.
Wu K, Yeo N, Ng C, Chioh F, Fan Q, Tian X, et al.
BMC Biol
. 2022 Feb;
20(1):47.
PMID: 35164755
Background: Polypoidal choroidal vasculopathy (PCV), a subtype of age-related macular degeneration (AMD), is a global leading cause of vision loss in older populations. Distinct from typical AMD, PCV is characterized...
4.
Alic I, Goh P, Murray A, Portelius E, Gkanatsiou E, Gough G, et al.
Mol Psychiatry
. 2021 Jul;
26(10):5789.
PMID: 34272490
No abstract available.
5.
Goh K, Tan E, Lu H, Roy S, Dunn N
Sci Rep
. 2021 Feb;
11(1):4712.
PMID: 33633173
Basal cells are multipotent stem cells responsible for the repair and regeneration of all the epithelial cell types present in the proximal lung. In mice, the elusive origins of basal...
6.
Trott J, Alpagu Y, Tan E, Shboul M, Dawood Y, Elsy M, et al.
Development
. 2020 Oct;
147(21).
PMID: 33033118
Mitchell-Riley syndrome (MRS) is caused by recessive mutations in the regulatory factor X6 gene () and is characterised by pancreatic hypoplasia and neonatal diabetes. To determine why individuals with MRS...
7.
Ong S, de Vos I, Meroshini M, Poobalan Y, Dunn N
Sci Rep
. 2020 Jul;
10(1):11801.
PMID: 32678226
Microfibril-associated glycoprotein 4 (MFAP4) is an extracellular matrix protein belonging to the fibrinogen-related protein superfamily. MFAP4 is produced by vascular smooth muscle cells and is highly enriched in the blood...
8.
Alic I, Goh P, Murray A, Portelius E, Gkanatsiou E, Gough G, et al.
Mol Psychiatry
. 2020 Jul;
26(10):5766-5788.
PMID: 32647257
A population of more than six million people worldwide at high risk of Alzheimer's disease (AD) are those with Down Syndrome (DS, caused by trisomy 21 (T21)), 70% of whom...
9.
PRDM15 loss of function links NOTCH and WNT/PCP signaling to patterning defects in holoprosencephaly
Mzoughi S, Di Tullio F, Low D, Motofeanu C, Ong S, Wollmann H, et al.
Sci Adv
. 2020 Jan;
6(2):eaax9852.
PMID: 31950080
Holoprosencephaly (HPE) is a congenital forebrain defect often associated with embryonic lethality and lifelong disabilities. Currently, therapeutic and diagnostic options are limited by lack of knowledge of potential disease-causing mutations....
10.
Chia C, Madrigal P, Denil S, Martinez I, Garcia-Bernardo J, El-Khairi R, et al.
Stem Cell Reports
. 2019 Jan;
12(1):57-70.
PMID: 30629940
Heterozygous de novo mutations in GATA6 are the most frequent cause of pancreatic agenesis in humans. In mice, however, a similar phenotype requires the biallelic loss of Gata6 and its...