A N Shelling
Overview
Explore the profile of A N Shelling including associated specialties, affiliations and a list of published articles.
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Articles
38
Citations
446
Followers
0
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Recent Articles
1.
Earle N, Poppe K, Pilbrow A, Cameron V, Troughton R, Skinner J, et al.
Am Heart J
. 2015 Mar;
169(4):579-86.e3.
PMID: 25819866
Background: There is a genetic contribution to the risk of ventricular arrhythmias in survivors of acute coronary syndromes (ACS). We wished to explore the role of 33 candidate single nucleotide...
2.
Foulkes W, Shelling A
Methods Mol Med
. 2011 Feb;
39:273-90.
PMID: 21340782
This chapter is an overview, from a technical perspective, of the approaches that can be used to analyze genetic changes in ovarian cancers. Traditional gene localization methods are discussed, followed...
3.
Dudding T, Lawrence O, Winship I, Froyen G, Vandewalle J, Scott R, et al.
Hum Reprod
. 2010 Oct;
25(12):3159-60.
PMID: 20952765
No abstract available.
4.
Leong I, Skinner J, Shelling A, Love D
Acta Physiol (Oxf)
. 2010 Mar;
199(3):257-76.
PMID: 20331541
Congenital long QT syndrome (LQT) is a group of cardiac disorders associated with the dysfunction of cardiac ion channels. It is characterized by prolongation of the QT-interval, episodes of syncope...
5.
Dhaene B, Nevado J, Pugeat M, Pierquin G, Lowry R, Reardon W, et al.
Hum Mutat
. 2010 Mar;
31(5):E1332-47.
PMID: 20232352
Blepharophimosis Syndrome (BPES) is an autosomal dominant developmental disorder of the eyelids with or without ovarian dysfunction caused by FOXL2 mutations. Overall, FOXL2deletions represent 12% of all genetic defects in...
6.
Gladding P, Evans C, Crawford J, Chung S, Vaughan A, Webster D, et al.
Heart Rhythm
. 2010 Feb;
7(4):481-6.
PMID: 20167303
Background: Molecular autopsy in sudden unexplained death in the young (SUDY) victims cannot usually be performed if tissue suitable for DNA extraction is not retained at autopsy. Objective: The purpose...
7.
Chand A, Harrison C, Shelling A
Hum Reprod Update
. 2009 Sep;
16(1):39-50.
PMID: 19752047
Background: Elucidation of the causes of premature ovarian failure (POF) is difficult due to the heterogeneity of the condition. Inhibin is a potential candidate gene for POF based on its...
8.
Ferguson L, Browning B, Huebner C, Petermann I, Shelling A, Demmers P, et al.
Dig Liver Dis
. 2008 Apr;
40(9):723-30.
PMID: 18394979
Background: Human Paneth cell alpha-defensins, especially DEFA5, are involved in maintaining homeostasis of the human microbial microflora. Since breakdown of normal mucosal antibacterial defence occurs in inflammatory bowel disease (IBD),...
9.
Grant V, Irwin R, Standley N, Shelling A, Chamley L
Biol Reprod
. 2008 Jan;
78(5):812-5.
PMID: 18184920
Although the sex of the offspring in mammals is commonly viewed as a matter of chance (depending on whether an X or a Y chromosome-bearing spermatozoon reaches the ovum first),...
10.
Browning B, Annese V, Barclay M, Bingham S, Brand S, Buning C, et al.
J Med Genet
. 2007 Aug;
45(1):36-42.
PMID: 17693570
Background: DLG5 p.R30Q has been reported to be associated with Crohn disease (CD), but this association has not been replicated in most studies. A recent analysis of gender-stratified data from...