Browse by UCL people
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Number of items: 5.
Article
Duncan, AJ;
Heales, SJR;
Mills, K;
Eaton, S;
Land, JM;
Hargreaves, IP;
(2005)
Determination of coenzyme Q(10) status in blood mononuclear cells, skeletal muscle, and plasma by HPLC with Di-propoxy-coenzyme Q(10) as an internal standard.
CLIN CHEM
, 51
(12)
2380 - 2382.
10.1373/clinchem.2005.054643.
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El-Khairi, R;
Parnaik, R;
Duncan, AJ;
Lin, L;
Gerrelli, D;
Dattani, MT;
Conway, GS;
(2012)
Analysis of LIN28A in early human ovary development and as a candidate gene for primary ovarian insufficiency.
Molecular and Cellular Endocrinology
, 351
(2)
pp. 264-268.
10.1016/j.mce.2011.12.016.
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Ishida, M;
Monk, D;
Duncan, AJ;
Abu-Amero, S;
Chong, J;
Ring, SM;
Pembrey, ME;
... Moore, GE; + view all
(2012)
Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weight.
The American Journal of Human Genetics
, 90
(4)
715 - 719.
10.1016/j.ajhg.2012.02.021.
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Suntharalingham, JP;
Buonocore, F;
Duncan, AJ;
Achermann, JC;
(2015)
DAX-1 (NR0B1) and steroidogenic factor-1 (SF-1, NR5A1) in human disease.
Best Practice & Research Clinical Endocrinology & Metabolism
, 29
(4)
pp. 607-619.
10.1016/j.beem.2015.07.004.
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Thomas, AC;
Williams, H;
Seto-Salvia, N;
Bacchelli, C;
Jenkins, D;
O'Sullivan, M;
Mengrelis, K;
... Stanier, PM; + view all
(2014)
Mutations in SNX14 cause a distinctive autosomal recessive cerebellar ataxia and intellectual disability syndrome.
The American Journal of Human Genetics
, 95
(5)
pp. 611-621.
10.1016/j.ajhg.2014.10.007.
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