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The Journal of Biological Chemistry|September 13, 2008
Complement factor H binds to denatured rather than to native pentameric C-reactive proteinSvetlana Hakobyan, Claire L Harris, Carmen W van den Berg, et al.
Annals of the Rheumatic Diseases|October 27, 2009
The chromosome 16q region associated with ankylosing spondylitis includes the candidate gene tumour necrosis factor receptor type 1-associated death domain (TRADD)Jennifer J Pointon, David Harvey, Tugce Karaderi, et al.
Cancers|July 2, 2021
Development of EndoScreen Chip, a Microfluidic Pre-Endoscopy Triage Test for Esophageal AdenocarcinomaJulie A Webster, Alain Wuethrich, Karthik B Shanmugasundaram, et al.
RSC Advances|May 2, 2022
The effects of microstructure, Nb content and secondary Ruddlesden-Popper phase on thermoelectric properties in perovskite CaMn1- Nb O3 (x = 0-0.10) thin filmsE Ekström, A le Febvrier, F Bourgeois, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 12, 2010
Complement component c1q mediates mitochondria-driven oxidative stress in neonatal hypoxic-ischemic brain injuryVadim S Ten, Jun Yao, Veniamin Ratner, et al.
The Journal of Clinical Investigation|September 21, 2010
Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulationRubén Martínez-Barricarte, Meike Heurich, Francisco Valdes-Cañedo, et al.
American Journal of Physiology. Renal Physiology|March 17, 2023
Tacrolimus induces fibroblast-to-myofibroblast transition via a TGF-β-dependent mechanism to contribute to renal fibrosisAdaku C Ume, Tara Y Wenegieme, Jennae N Shelby, et al.
American Journal of Human Genetics|September 26, 2002
Autosomal dominant familial calcium pyrophosphate dihydrate deposition disease is caused by mutation in the transmembrane protein ANKHCharlene J Williams, Yun Zhang, Andrew Timms, et al.
Bone|January 2, 2016
Deletion of the membrane complement inhibitor CD59a drives age and gender-dependent alterations to bone phenotype in miceAnja C Bloom, Fraser L Collins, Rob J Van't Hof, et al.
Molecular Immunology|January 31, 2016
Genetic analysis and functional characterization of novel mutations in a series of patients with atypical hemolytic uremic syndromeNóra Szarvas, Ágnes Szilágyi, Dorottya Csuka, et al.
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