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Tropical Gastroenterology : Official Journal of the Digestive Diseases Foundation|November 1, 2008
Clinical relevance of HBV DNA load in patients with chronic hepatitis B infectionK Madan, Y Batra, J K Jha, et al.
Oncology|July 31, 2009
Clinical profile, etiology and therapeutic outcome in 324 hepatocellular carcinoma patients at a tertiary care center in IndiaShashi B Paul, Sreenivasa Baba Chalamalasetty, Sreenivas Vishnubhatla, et al.
American Journal of Physiology. Endocrinology and Metabolism|March 6, 2025
Plasma complement system markers and their association with cardiometabolic risk factors: an ethnic comparison of White European and Black African menReuben M Reed, Wioleta M Zelek, B Paul Morgan, et al.
Arthritis and Rheumatism|July 13, 2004
Dissection of class III major histocompatibility complex haplotypes associated with rheumatoid arthritisJulia L Newton, Sinéad M J Harney, Andrew E Timms, et al.
Arthritis Care & Research|January 11, 2012
Is there a higher genetic load of susceptibility loci in familial ankylosing spondylitis?Reeti Joshi, John D Reveille, Matthew A Brown, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|February 10, 2018
Measurement of soluble CD59 in CSF in demyelinating disease: Evidence for an intrathecal source of soluble CD59Wioleta M Zelek, Lewis M Watkins, Owain W Howell, et al.
FEBS Letters|May 19, 2004
Monoglucosylated glycans in the secreted human complement component C3: implications for protein biosynthesis and structureM D Max Crispin, Gayle E Ritchie, Alison J Critchley, et al.
Molecular Neurodegeneration|April 7, 2016
Inhibition of the classical pathway of the complement cascade prevents early dendritic and synaptic degeneration in glaucomaPete A Williams, James R Tribble, Keating W Pepper, et al.
Kidney International|August 3, 2012
Sensitive and specific assays for C3 nephritic factors clarify mechanisms underlying complement dysregulationDanielle Paixão-Cavalcante, Margarita López-Trascasa, Lillemor Skattum, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|December 28, 2020
Functional Genomic Analysis of a RUNX3 Polymorphism Associated With Ankylosing SpondylitisMatteo Vecellio, Liye Chen, Carla J Cohen, et al.
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