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Genomics|October 15, 1996
Cloning of human lymphocyte-specific interferon regulatory factor (hLSIRF/hIRF4) and mapping of the gene to 6p23-p25A Grossman, H W Mittrücker, J Nicholl, et al.
Parkinsonism & Related Disorders|January 31, 2015
Novel GCH1 variant in Dopa-responsive dystonia and Parkinson's diseaseA J Lewthwaite, T D Lambert, E B Rolfe, et al.
Nutrients|August 29, 2024
Effects of Dietary Nitrate Supplementation on High-Intensity Cycling Sprint Performance in Recreationally Active Adults: A Systematic Review and Meta-AnalysisRachel Tan, Jordan K Cass, Isabella G Lincoln, et al.
Cytogenetic and Genome Research|April 18, 2009
A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technologyB A Talseth-Palmer, N A Bowden, C Meldrum, et al.
Immunity|June 1, 1996
DNAM-1, a novel adhesion molecule involved in the cytolytic function of T lymphocytesA Shibuya, D Campbell, C Hannum, et al.
Health Technology Assessment (Winchester, England)|January 1, 1997
Neonatal screening for inborn errors of metabolism: cost, yield and outcomeR J Pollitt, A Green, C J McCabe, et al.
Quality & Safety in Health Care|June 1, 2010
Assessing quality of care from hospital case notes: comparison of reliability of two methodsA Hutchinson, J E Coster, K L Cooper, et al.
Neurobiology of Aging|January 4, 2011
Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK seriesDaniel McNaughton, William Knight, Rita Guerreiro, et al.
British Journal of Clinical Pharmacology|June 5, 2013
A novel assay to measure B cell responses to keyhole limpet haemocyanin vaccination in healthy volunteers and subjects with systemic lupus erythematosusJohn Ferbas, Shelley S Belouski, Michelle Horner, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 5, 2014
Activating mutations in STIM1 and ORAI1 cause overlapping syndromes of tubular myopathy and congenital miosisVasyl Nesin, Graham Wiley, Maria Kousi, et al.
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