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Age and Ageing|March 1, 2022
Assessment of coding-based frailty algorithms for long-term outcome prediction among older people in community settings: a cohort study from the Shizuoka Kokuho DatabaseShiori Nishimura, Hiraku Kumamaru, Satoshi Shoji, et al.
Microscopy and Microanalysis : the Official Journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada|January 21, 2003
The pros and cons of apoptosis assays for use in the study of cells, tissues, and organsMichiko Watanabe, Midori Hitomi, Kathy van der Wee, et al.
American Journal of Physiology. Heart and Circulatory Physiology|March 5, 2026
Folic acid prevents functional and structural heart defects induced by prenatal ethanol exposureStephanie M Ford, Cameron J Pedersen, Matthew R Ford, et al.
The Journal of Clinical Endocrinology and Metabolism|September 30, 2016
A Variant in the BACH2 Gene Is Associated With Susceptibility to Autoimmune Addison's Disease in HumansAgnieszka Pazderska, Bergithe E Oftedal, Catherine M Napier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2012
Regions of homozygosity identified by SNP microarray analysis aid in the diagnosis of autosomal recessive disease and incidentally detect parental blood relationshipsKristen Lipscomb Sund, Sarah L Zimmerman, Cameron Thomas, et al.
Epilepsia|November 26, 2003
An Xp; Yq translocation causing a novel contiguous gene syndrome in brothers with generalized epilepsy, ichthyosis, and attention deficitsMichael J Doherty, Ian A Glass, Craig L Bennett, et al.
The EMBO Journal|October 13, 2007
Cited2, a coactivator of HNF4alpha, is essential for liver developmentXiaoling Qu, Eric Lam, Yong-Qiu Doughman, et al.
The Journal of Clinical Endocrinology and Metabolism|October 24, 2009
Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibilityAnna L Mitchell, Heather J Cordell, Rachel Soemedi, et al.
The FEBS Journal|July 13, 2005
A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeastEmma L Blakely, Anna L Mitchell, Nicholas Fisher, et al.
The Journal of Clinical Endocrinology and Metabolism|July 7, 2012
Adrenal steroidogenesis after B lymphocyte depletion therapy in new-onset Addison's diseaseSimon H S Pearce, Anna L Mitchell, Stuart Bennett, et al.
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