Laura M Mitchell
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Explore the profile of Laura M Mitchell including associated specialties, affiliations and a list of published articles.
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4
Citations
218
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Recent Articles
1.
Carpenter D, Mitchell L, Armour J
Hum Genomics
. 2017 Feb;
11(1):2.
PMID: 28219410
Background: Salivary amylase in humans is encoded by the copy variable gene AMY1 in the amylase gene cluster on chromosome 1. Although the role of salivary amylase is well established,...
2.
Carpenter D, Dhar S, Mitchell L, Fu B, Tyson J, Shwan N, et al.
Hum Mol Genet
. 2015 Mar;
24(12):3472-80.
PMID: 25788522
The human salivary amylase genes display extensive copy number variation (CNV), and recent work has implicated this variation in adaptation to starch-rich diets, and in association with body mass index....
3.
Leidenroth A, Clapp J, Mitchell L, Coneyworth D, Dearden F, Iannuzzi L, et al.
Chromosoma
. 2012 Aug;
121(5):489-97.
PMID: 22903800
Macrosatellites are large polymorphic tandem arrays. The human subtelomeric macrosatellite D4Z4 has 11-150 repeats, each containing a copy of the intronless DUX4 gene. DUX4 is linked to facioscapulohumeral muscular dystrophy,...
4.
Clapp J, Mitchell L, Bolland D, Fantes J, Corcoran A, Scotting P, et al.
Am J Hum Genet
. 2007 Aug;
81(2):264-79.
PMID: 17668377
Facioscapulohumeral muscular dystrophy (FSHD) is caused by deletions within the polymorphic DNA tandem array D4Z4. Each D4Z4 repeat unit has an open reading frame (ORF), termed "DUX4," containing two homeobox...