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Laforin, the most common protein mutated in Lafora disease, regulates autophagy

Human molecular genetics, 2010-07, Vol.19 (14), p.2867-2876

2010

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C3 glomerulopathy-associated CFHR1 mutation alters FHR oligomerization and complement regulation

The Journal of clinical investigation, 2013-06, Vol.123 (6), p.2434-2446

2013

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Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains

The Journal of experimental medicine, 2007-06, Vol.204 (6), p.1249-1256

2007

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Complement Factor H Is Expressed in Adipose Tissue in Association With Insulin Resistance

Diabetes (New York, N.Y.), 2010-01, Vol.59 (1), p.200-209

2010

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The disease-protective complement factor H allotypic variant Ile62 shows increased binding affinity for C3b and enhanced cofactor activity

Human molecular genetics, 2009-09, Vol.18 (18), p.3452-3461

2009

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Combined Complement Gene Mutations in Atypical Hemolytic Uremic Syndrome Influence Clinical Phenotype

Journal of the American Society of Nephrology, 2013-03, Vol.24 (3), p.475-486

2013

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Intracellular Complement Activation Sustains T Cell Homeostasis and Mediates Effector Differentiation

Immunity (Cambridge, Mass.), 2013-12, Vol.39 (6), p.1143-1157

2013

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Sensitive and specific assays for C3 nephritic factors clarify mechanisms underlying complement dysregulation

Kidney international, 2012-11, Vol.82 (10), p.1084-1092

2012

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Regulation of glycogen synthesis by the laforin–malin complex is modulated by the AMP-activated protein kinase pathway

Human molecular genetics, 2008-03, Vol.17 (5), p.667-678

2008

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C3 glomerulopathy - understanding a rare complement-driven renal disease

Nature reviews. Nephrology, 2019-03, Vol.15 (3), p.129-143

2019

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The complotype: dictating risk for inflammation and infection

Trends in immunology, 2012-10, Vol.33 (10), p.513-521

2012

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Laforin and Malin Deletions in Mice Produce Similar Neurologic Impairments

Journal of neuropathology and experimental neurology, 2012-05, Vol.71 (5), p.413-421

2012

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C4BP(β-)-mediated immunomodulation attenuates inflammation in DSS-induced murine colitis and in myeloid cells from IBD patients

Pharmacological research, 2023-11, Vol.197, p.106948-106948, Article 106948

2023

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Absence of CD59 in Guinea Pigs: Analysis of the Cavia porcellus Genome Suggests the Evolution of a CD59 Pseudogene

The Journal of immunology (1950), 2018-01, Vol.200 (1), p.327-335

2018

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Interaction of Shiga toxin 2 with complement regulators of the factor H protein family

Molecular immunology, 2014-03, Vol.58 (1), p.77-84

2014

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FHR-1 Binds to C-Reactive Protein and Enhances Rather than Inhibits Complement Activation

The Journal of immunology (1950), 2017-07, Vol.199 (1), p.292-303

2017

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Substitutions at position 263 within the von Willebrand factor type A domain determine the functionality of complement C2 protein

Frontiers in immunology, 2022-12, Vol.13, p.1061696-1061696

2022

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Antibody directs properdin-dependent activation of the complement alternative pathway in a mouse model of abdominal aortic aneurysm

Proceedings of the National Academy of Sciences - PNAS, 2012-02, Vol.109 (7), p.E415-E422

2012

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Complement Factor H Binds to Denatured Rather than to Native Pentameric C-reactive Protein

The Journal of biological chemistry, 2008-11, Vol.283 (45), p.30451-30460

2008

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Interaction between Complement Regulators and Streptococcus pyogenes: Binding of C4b-Binding Protein and Factor H/Factor H-Like Protein 1 to M18 Strains Involves Two Different Cell Surface Molecules

The Journal of immunology (1950), 2004-12, Vol.173 (11), p.6899-6904

2004

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New approaches to the treatment of dense deposit disease

Journal of the American Society of Nephrology, 2007-09, Vol.18 (9), p.2447-2456

2007

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Coexistence of Closed and Open Conformations of Complement Factor B in the Alternative Pathway C3bB(Mg2+) Proconvertase

The Journal of immunology (1950), 2009-12, Vol.183 (11), p.7347-7351

2009

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A retrospective study of pregnancy-associated atypical hemolytic uremic syndrome

Kidney international, 2018-02, Vol.93 (2), p.450-459

2018

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Mutations in Proteins of the Alternative Pathway of Complement and the Pathogenesis of Atypical Hemolytic Uremic Syndrome

American journal of kidney diseases, 2008-07, Vol.52 (1), p.171-180

2008

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Laforin, the most common protein mutated in Lafora disease, regulates autophagy

C3 glomerulopathy-associated CFHR1 mutation alters FHR oligomerization and complement regulation

Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains

Complement Factor H Is Expressed in Adipose Tissue in Association With Insulin Resistance

The disease-protective complement factor H allotypic variant Ile62 shows increased binding affinity for C3b and enhanced cofactor activity

Combined Complement Gene Mutations in Atypical Hemolytic Uremic Syndrome Influence Clinical Phenotype

Intracellular Complement Activation Sustains T Cell Homeostasis and Mediates Effector Differentiation

Sensitive and specific assays for C3 nephritic factors clarify mechanisms underlying complement dysregulation

Regulation of glycogen synthesis by the laforin–malin complex is modulated by the AMP-activated protein kinase pathway

C3 glomerulopathy - understanding a rare complement-driven renal disease

The complotype: dictating risk for inflammation and infection

Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis

Laforin and Malin Deletions in Mice Produce Similar Neurologic Impairments

C4BP(β-)-mediated immunomodulation attenuates inflammation in DSS-induced murine colitis and in myeloid cells from IBD patients

Absence of CD59 in Guinea Pigs: Analysis of the Cavia porcellus Genome Suggests the Evolution of a CD59 Pseudogene

Interaction of Shiga toxin 2 with complement regulators of the factor H protein family

FHR-1 Binds to C-Reactive Protein and Enhances Rather than Inhibits Complement Activation

Substitutions at position 263 within the von Willebrand factor type A domain determine the functionality of complement C2 protein

Antibody directs properdin-dependent activation of the complement alternative pathway in a mouse model of abdominal aortic aneurysm

Complement Factor H Binds to Denatured Rather than to Native Pentameric C-reactive Protein

Interaction between Complement Regulators and Streptococcus pyogenes: Binding of C4b-Binding Protein and Factor H/Factor H-Like Protein 1 to M18 Strains Involves Two Different Cell Surface Molecules

New approaches to the treatment of dense deposit disease

Coexistence of Closed and Open Conformations of Complement Factor B in the Alternative Pathway C3bB(Mg2+) Proconvertase

A retrospective study of pregnancy-associated atypical hemolytic uremic syndrome

Mutations in Proteins of the Alternative Pathway of Complement and the Pathogenesis of Atypical Hemolytic Uremic Syndrome

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