Christine Skerka
Researcher Next ID · RN-043456
Researcher · Immunology and Microbiology
Redwood City, Mexico
- Works count
- 653
- Citation count
- 15,565
- H-index
- 71
- i10-index
- 167
Research interests
Publications
ApoE attenuates unresolvable inflammation by complex formation with activated C1q
Nature Medicine · 2019 · https://doi.org/10.1038/s41591-018-0336-8
Atypical aHUS: State of the art
Molecular Immunology · 2015 · https://doi.org/10.1016/j.molimm.2015.03.246
Complement factor H related proteins (CFHRs)
Molecular Immunology · 2013 · https://doi.org/10.1016/j.molimm.2013.06.001
Complement factor H binds malondialdehyde epitopes and protects from oxidative stress
Nature · 2011 · https://doi.org/10.1038/nature10449
An imbalance of human complement regulatory proteins CFHR1, CFHR3 and factor H influences risk for age-related macular degeneration (AMD)
Human Molecular Genetics · 2010 · https://doi.org/10.1093/hmg/ddq399
Complement regulators and inhibitory proteins
Nature reviews. Immunology · 2009 · https://doi.org/10.1038/nri2620
The yeast Candida albicans evades human complement attack by secretion of aspartic proteases
Molecular Immunology · 2009 · https://doi.org/10.1016/j.molimm.2009.08.019
Factor H–related protein 1 (CFHR-1) inhibits complement C5 convertase activity and terminal complex formation
Blood · 2009 · https://doi.org/10.1182/blood-2009-02-205641
Deletion of Complement Factor H–Related Genes CFHR1 and CFHR3 Is Associated with Atypical Hemolytic Uremic Syndrome
PLoS Genetics · 2007 · https://doi.org/10.1371/journal.pgen.0030041
Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency
Blood · 2007 · https://doi.org/10.1182/blood-2007-09-109876
Anti–factor H autoantibodies block C-terminal recognition function of factor H in hemolytic uremic syndrome
Blood · 2007 · https://doi.org/10.1182/blood-2007-02-071472
Defective complement control of Factor H (Y402H) and FHL-1 in age-related macular degeneration
Molecular Immunology · 2007 · https://doi.org/10.1016/j.molimm.2007.02.012
Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II)
Kidney International · 2006 · https://doi.org/10.1038/sj.ki.5000269
Complement and diseases: Defective alternative pathway control results in kidney and eye diseases
Molecular Immunology · 2005 · https://doi.org/10.1016/j.molimm.2005.06.015
Complement Resistance of Borrelia burgdorferi Correlates with the Expression of BbCRASP-1, a Novel Linear Plasmid-encoded Surface Protein That Interacts with Human Factor H and FHL-1 and Is Unrelated to Erp Proteins
Journal of Biological Chemistry · 2004 · https://doi.org/10.1074/jbc.m308343200
Factor H family proteins: on complement, microbes and human diseases
Biochemical Society Transactions · 2002 · https://doi.org/10.1042/bst0300971
Immune evasion ofBorrelia burgdorferi by acquisition of human complement regulators FHL-1/reconectin and Factor H
European Journal of Immunology · 2001 · https://doi.org/10.1002/1521-4141(200106)31:6<1674::aid-immu1674>3.0.co;2-2
The Molecular Basis of Familial Hemolytic Uremic Syndrome
Journal of the American Society of Nephrology · 2001 · https://doi.org/10.1681/asn.v122297
Further Characterization of Complement Regulator-Acquiring Surface Proteins ofBorrelia burgdorferi
Infection and Immunity · 2001 · https://doi.org/10.1128/iai.69.12.7800-7809.2001
Mapping of the complement regulatory domains in the human factor H-like protein 1 and in factor H1
The Journal of Immunology · 1995 · https://doi.org/10.4049/jimmunol.155.12.5663
Current projects
No projects listed.