V N Subramaniam
Overview
Explore the profile of V N Subramaniam 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
27
Citations
524
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Landers K, Li H, Subramaniam V, Mortimer R, Richard K
Placenta
. 2013 Jun;
34(8):716-8.
PMID: 23735835
Normal fetal neurological development depends on a regulated supply of maternal thyroid hormone (TH). We have previously demonstrated that transthyretin (TTR) a TH binding protein, is synthesized, secreted and internalized...
2.
Jeffery J, Urquhart A, Subramaniam V, Parton R, Khanna K
Oncogene
. 2010 Mar;
29(18):2649-58.
PMID: 20190801
The proper function of the spindle is crucial to the high fidelity of chromosome segregation and is indispensable for tumor suppression in humans. Centrobin is a recently identified centrosomal protein...
3.
Subramaniam V, Wallace D, Dixon J, Fletcher L, Crawford D
Gut
. 2005 Jun;
54(7):1048-9.
PMID: 15951560
No abstract available.
4.
Wallace D, Summerville L, Lusby P, Subramaniam V
Gut
. 2005 Jun;
54(7):980-6.
PMID: 15951546
Background: Transferrin receptor 2 (TfR2) is a key molecule involved in the regulation of iron homeostasis. Mutations in humans cause type 3 haemochromatosis and a targeted mutation in mice leads...
5.
Wallace D, Browett P, Wong P, Kua H, Ameratunga R, Subramaniam V
Gut
. 2005 Mar;
54(4):567-8.
PMID: 15753550
No abstract available.
6.
Anderson G, Ramm G, Subramaniam V, Powell L
J Gastroenterol Hepatol
. 2004 May;
19(6):712.
PMID: 15151632
No abstract available.
7.
Arden K, Wallace D, Dixon J, Summerville L, Searle J, Anderson G, et al.
Gut
. 2003 Jul;
52(8):1215-7.
PMID: 12865285
Background: A severe form of iron overload with the clinicopathological features of haemochromatosis inherited in an autosomal dominant manner has been described in the Solomon Islands. The genetic basis of...
8.
Roy L, Bergeron J, Lavoie C, Hendriks R, Gushue J, Fazel A, et al.
Mol Biol Cell
. 2000 Aug;
11(8):2529-42.
PMID: 10930451
Transitional endoplasmic reticulum (tER) consists of confluent rough and smooth endoplasmic reticulum (ER) domains. In a cell-free incubation system, low-density microsomes (1.17 g cc(-1)) isolated from rat liver homogenates reconstitute...
9.
Powell L, Subramaniam V, Yapp T
J Hepatol
. 2000 Mar;
32(1 Suppl):48-62.
PMID: 10728794
Hereditary haemochromatosis (HHC) is a common inherited disorder of iron metabolism characterised by progressive iron loading of parenchymal cells of the liver, pancreas, heart and other organs ultimately leading to...
10.
Subramaniam V, Loh E, Horstmann H, Habermann A, Xu Y, Coe J, et al.
J Cell Sci
. 2000 Feb;
113 ( Pt 6):997-1008.
PMID: 10683148
Members of the syntaxin family play a fundamental role in vesicle docking and fusion of diverse transport events. We have molecularly characterized syntaxin 8, a novel member of the syntaxin...