User profiles for Barbara A Jennings

Barbara Jennings

Verified email at uea.ac.uk
Cited by 2176

[HTML][HTML] Drosophila–a versatile model in biology & medicine

BH Jennings - Materials today, 2011 - Elsevier
The fruit fly Drosophila melanogaster is a versatile model organism that has been used in
biomedical research for over a century to study a broad range of phenomena. There are many …

Clinical relevance of DPYD variants c. 1679T> G, c. 1236G> A/HapB3, and c. 1601G> A as predictors of severe fluoropyrimidine-associated toxicity: a systematic …

…, U Amstutz, CR Largiadèr, BA Jennings… - The Lancet …, 2015 - thelancet.com
Background The best-known cause of intolerance to fluoropyrimidines is dihydropyrimidine
dehydrogenase (DPD) deficiency, which can result from deleterious polymorphisms in the …

[HTML][HTML] The Groucho/TLE/Grg family of transcriptional co-repressors

BH Jennings, D Ish-Horowicz - Genome biology, 2008 - Springer
The Drosophila Groucho (Gro) protein was the founding member of the family of transcriptional
co-repressor proteins that now includes the transducin-like enhancer of split (TLE) and …

Macular pigment optical density is related to cognitive function in older people

…, TM Scott, SB Kritchevsky, BJ Jennings… - Age and …, 2014 - academic.oup.com
Background: the xanthophylls lutein (L) and zeaxanthin (Z) exist in relatively high concentration
in multiple central nervous tissues (eg cortex and neural retina). L + Z in macula (ie …

[PDF][PDF] Molecular recognition of transcriptional repressor motifs by the WD domain of the Groucho/TLE corepressor

BH Jennings, LM Pickles, SM Wainwright, SM Roe… - Molecular cell, 2006 - cell.com
The Groucho (Gro)/TLE/Grg family of corepressors operates in many signaling pathways (including
Notch and Wnt). Gro/TLE proteins recognize a wide range of transcriptional …

Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t (8; 13)(p11; q12) myeloproliferative syndrome

…, JM Hernandez, BA Jennings… - Blood, The Journal …, 1998 - ashpublications.org
The 8p11 myeloproliferative syndrome is a rare, aggressive condition associated with
reciprocal translocations of chromosome band 8p11, most commonly the t(8;13)(p11;q12). To …

[HTML][HTML] Retinitis pigmentosa associated with rhodopsin mutations: Correlation between phenotypic variability and molecular effects

A Iannaccone, D Man, N Waseem, BJ Jennings… - Vision research, 2006 - Elsevier
Similar retinitis pigmentosa (RP) phenotypes can result from mutations affecting different
rhodopsin regions, and distinct amino acid substitutions can cause different RP severity and …

[HTML][HTML] Peripheral arterial disease and methylenetetrahydrofolate reductase (MTHFR) C677T mutations: A case-control study and meta-analysis

…, YK Loke, AJA Wright, PM Finglas, BA Jennings - Journal of vascular …, 2009 - Elsevier
OBJECTIVE: Hyperhomocysteinaemia is associated with peripheral arterial disease (PAD).
There are inter-individual variations in the metabolism of homocysteine because of genetic …

[HTML][HTML] Circulating autoantibodies in age-related macular degeneration recognize human macular tissue antigens implicated in autophagy, immunomodulation, and …

…, AH Alhatem, I Neeli, NI Lenchik, BJ Jennings… - PloS one, 2015 - journals.plos.org
Background We investigated sera from elderly subjects with and without age-related
macular degeneration (AMD) for presence of autoantibodies (AAbs) against human macular …

The genetics of cholesteatoma. A systematic review using narrative synthesis

BA Jennings, P Prinsley, C Philpott… - Clinical …, 2018 - Wiley Online Library
Objective A cholesteatoma is a mass of keratinising epithelium in the middle ear. It is a rare
disorder that is associated with significant morbidity, and its causative risk factors are poorly …