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JCI Insight|March 26, 2020
Aberrant cell migration contributes to defective airway epithelial repair in childhood wheezeThomas Iosifidis, Erika N Sutanto, Alysia G Buckley, et al.Blood|September 5, 2009
The role and regulation of friend of GATA-1 (FOG-1) during blood development in the zebrafishJulio D Amigo, Gabriele E Ackermann, John J Cope, et al.Journal of Medical Genetics|April 17, 2008
Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the -2578AA genotypeD Lambrechts, K Poesen, R Fernández-Santiago, et al.Heliyon|February 6, 2024
Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosisCalum Harvey, Marcel Weinreich, James A K Lee, et al.The Journal of Biological Chemistry|February 11, 2014
Iron regulatory protein-1 protects against mitoferrin-1-deficient porphyriaJacky Chung, Sheila A Anderson, Babette Gwynn, et al.Journal of the American Academy of Dermatology|February 28, 2004
A systemic type I 5 alpha-reductase inhibitor is ineffective in the treatment of acne vulgarisJames Leyden, Wilma Bergfeld, Lynn Drake, et al.ESMO Open|September 21, 2018
Somatic cancer genetics in the UK: real-world data from phase I of the Cancer Research UK Stratified Medicine ProgrammeColin R Lindsay, Emily C Shaw, Fiona Blackhall, et al.Journal of Medical Genetics|September 25, 2008
20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficitsS R Lalani, J V Thakuria, G F Cox, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|December 22, 2011
The frequency of CSF oligoclonal banding in multiple sclerosis increases with latitudeJ Lechner-Scott, B Spencer, T de Malmanche, et al.Cell Reports|March 7, 2025
ARHGAP12 and ARHGAP29 exert distinct regulatory effects on switching between two cell morphological states through GSK-3 activityVinton W T Cheng, Philippa Vaughn-Beaucaire, Gary C Shaw, et al.Pageof 136