Subaashini Natarajan
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Explore the profile of Subaashini Natarajan including associated specialties, affiliations and a list of published articles.
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10
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555
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Recent Articles
1.
Srihar K, Gusnanto A, Richman S, West N, Galvin L, Bottomley D, et al.
Sci Rep
. 2024 Sep;
14(1):21870.
PMID: 39300198
Microsatellite instability (MSI) occurs across a number of cancers and is associated with different clinical characteristics when compared to microsatellite stable (MSS) cancers. As MSI cancers have different characteristics, routine...
2.
Abdelhamed Z, Abdelmottaleb D, El-Asrag M, Natarajan S, Wheway G, Inglehearn C, et al.
Sci Rep
. 2019 Apr;
9(1):5446.
PMID: 30931988
Primary cilia defects result in a group of related pleiotropic malformation syndromes known as ciliopathies, often characterised by cerebellar developmental and foliation defects. Here, we describe the cerebellar anatomical and...
3.
Wheway G, Schmidts M, Mans D, Szymanska K, Nguyen T, Racher H, et al.
Nat Cell Biol
. 2015 Jul;
17(8):1074-1087.
PMID: 26167768
Defects in primary cilium biogenesis underlie the ciliopathies, a growing group of genetic disorders. We describe a whole-genome siRNA-based reverse genetics screen for defects in biogenesis and/or maintenance of the...
4.
Abdelhamed Z, Natarajan S, Wheway G, Inglehearn C, Toomes C, Johnson C, et al.
Dis Model Mech
. 2015 Jun;
8(6):527-41.
PMID: 26035863
Ciliopathies are a group of developmental disorders that manifest with multi-organ anomalies. Mutations in TMEM67 (MKS3) cause a range of human ciliopathies, including Meckel-Gruber and Joubert syndromes. In this study...
5.
Logan C, Szabadkai G, Sharpe J, Parry D, Torelli S, Childs A, et al.
Nat Genet
. 2013 Dec;
46(2):188-93.
PMID: 24336167
Mitochondrial Ca(2+) uptake has key roles in cell life and death. Physiological Ca(2+) signaling regulates aerobic metabolism, whereas pathological Ca(2+) overload triggers cell death. Mitochondrial Ca(2+) uptake is mediated by...
6.
Ding V, Lew Q, Chu K, Natarajan S, Rajasegaran V, Gurumurthy M, et al.
PLoS One
. 2013 Aug;
8(8):e72823.
PMID: 23977357
Hexamethylene bisacetamide inducible protein 1 (HEXIM1) is best known as the inhibitor of positive transcription elongation factor b (P-TEFb), which is composed of cyclin-dependent kinase 9 (CDK9)/cyclin T1. P-TEFb is...
7.
Wheway G, Abdelhamed Z, Natarajan S, Toomes C, Inglehearn C, Johnson C
Dev Biol
. 2013 Mar;
377(1):55-66.
PMID: 23454480
Meckel-Gruber syndrome (MKS) is an embryonic lethal ciliopathy resulting from mutations in genes encoding proteins localising to the primary cilium. Mutations in the basal body protein MKS1 account for 7%...
8.
Abdelhamed Z, Wheway G, Szymanska K, Natarajan S, Toomes C, Inglehearn C, et al.
Hum Mol Genet
. 2013 Jan;
22(7):1358-72.
PMID: 23283079
The ciliopathies are a group of heterogeneous diseases with considerable variations in phenotype for allelic conditions such as Meckel-Gruber syndrome (MKS) and Joubert syndrome (JBTS) even at the inter-individual level...
9.
Ding V, Boersema P, Foong L, Preisinger C, Koh G, Natarajan S, et al.
PLoS One
. 2011 Mar;
6(3):e17538.
PMID: 21437283
The role of fibroblast growth factor-2 (FGF-2) in maintaining undifferentiated human embryonic stem cells (hESC) was investigated using a targeted phosphoproteomics approach to specifically profile tyrosine phosphorylation events following FGF-2...
10.
Ding V, Ling L, Natarajan S, Yap M, Cool S, Choo A
J Cell Physiol
. 2010 May;
225(2):417-28.
PMID: 20506199
Fibroblast growth factor-2 (FGF-2) is widely used to culture human embryonic stem cells (hESC) and induced pluripotent stem (iPS) cells. Despite its importance in maintaining undifferentiated hESC phenotype, a lack...