Early Components of the Complement Classical Activation Pathway in Human Systemic Autoimmune Diseases (Q26766486)

1

0 references

Yee Ling Wu

2

0 references

Yan Yang

3

0 references

Charles H Spencer

4

0 references

Georges Hauptmann

5

0 references

Lee A Hebert

6

0 references

John P Atkinson

7

0 references

C Yung Yu

8

0 references

language of work or name

English

0 references

publication date

2016

0 references

published in

Frontiers in Immunology

1 reference

Structural basis for activation of the complement system by component C4 cleavage

volume

7

0 references

page(s)

36

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Finding the missing heritability of complex diseases

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Type II human complement C2 deficiency. Allele-specific amino acid substitutions (Ser189 --> Phe; Gly444 --> Arg) cause impaired C2 secretion

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Assignment of the complement serine protease genes C1r and C1s to chromosome 12 region 12p13

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Human genes for complement components C1r and C1s in a close tail-to-tail arrangement

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Structural basis of the polymorphism of human complement components C4A and C4B: gene size, reactivity and antigenicity.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Substitution of a single amino acid (aspartic acid for histidine) converts the functional activity of human complement C4B to C4A

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Structural Basis for the Function of Complement Component C4 within the Classical and Lectin Pathways of Complement

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Genetic heterogeneity in human disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

The properdin system and immunity. I. Demonstration and isolation of a new serum protein, properdin, and its role in immune phenomena

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Diversity in intrinsic strengths of the human complement system: serum C4 protein concentrations correlate with C4 gene size and polygenic variations, hemolytic activities, and body mass index

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Identification of a selective nonpeptide antagonist of the anaphylatoxin C3a receptor that demonstrates antiinflammatory activity in animal models

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Complement. Second of two parts

7 April 2017

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Complement. First of two parts

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

The molecular basis for the difference in immune hemolysis activity of the Chido and Rodgers isotypes of human complement component C4

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

A molecular map of the human major histocompatibility complex class III region linking complement genes C4, C2 and factor B

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

A comparison of the properties of two classes, C4A and C4B, of the human complement component C4

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

The complete exon-intron structure of a human complement component C4A gene. DNA sequences, polymorphism, and linkage to the 21-hydroxylase gene

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Type I human complement C2 deficiency. A 28-base pair gene deletion causes skipping of exon 6 during RNA splicing

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Complement: a key system for immune surveillance and homeostasis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Effects of Complement C4 Gene Copy Number Variations, Size Dichotomy, and C4A Deficiency on Genetic Risk and Clinical Presentation of Systemic Lupus Erythematosus in East Asian Populations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Detection of alloantibody-mediated complement activation: A diagnostic advance in monitoring kidney transplant rejection?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Clinical presentation of human C1q deficiency: How much of a lupus?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Cell-bound complement activation products in systemic lupus erythematosus: comparison with anti-double-stranded DNA and standard complement measurements

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Anti-C1q antibodies in systemic lupus erythematosus

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Autoantibodies to complement components in C3 glomerulopathy and atypical hemolytic uremic syndrome.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Anti-factor H autoantibodies assay

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

The identification of a novel splicing mutation in C1qB in a Japanese family with C1q deficiency: a case report.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Genome-wide association study of dermatomyositis reveals genetic overlap with other autoimmune disorders

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Soluble CR1 therapy improves complement regulation in C3 glomerulopathy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Anti-C1q autoantibodies, novel tests, and clinical consequences

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Monitoring and modeling treatment of atypical hemolytic uremic syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Autoantibody stabilization of the classical pathway C3 convertase leading to C3 deficiency and Neisserial sepsis: C4 nephritic factor revisited

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Complement in the immunopathogenesis of rheumatic disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Identification of novel coding mutation in C1qA gene in an African-American pedigree with lupus and C1q deficiency

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Genetically determined partial complement C4 deficiency states are not independent risk factors for SLE in UK and Spanish populations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Increased frequency of complement C4B deficiency in rheumatoid arthritis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Association between copy number variation of complement component C4 and Graves' disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Molecular basis of hereditary C1q deficiency--revisited: identification of several novel disease-causing mutations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Cutaneous manifestations of complement deficiencies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

The complex nature of serum C3 and C4 as biomarkers of lupus renal flare.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Hereditary C1q deficiency: a new family with C1qA deficiency.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Cell-bound complement biomarkers for systemic lupus erythematosus: from benchtop to bedside

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Molecular basis of complete complement C4 deficiency in two North-African families with systemic lupus erythematosus

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Great genotypic and phenotypic diversities associated with copy-number variations of complement C4 and RP-C4-CYP21-TNX (RCCX) modules: a comparison of Asian-Indian and European American populations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

The role of complement in the antiphospholipid syndrome-associated pathology

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European A

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Excessive complement activation is associated with placental injury in patients with antiphospholipid antibodies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Activated complement components and complement activator molecules on the surface of cell-derived microparticles in patients with rheumatoid arthritis and healthy individuals

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Cell-bound complement activation products (CB-CAPs) as a source of lupus biomarkers.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Immunogenetic risk and protective factors for the idiopathic inflammatory myopathies: distinct HLA-A, -B, -Cw, -DRB1, and -DQA1 allelic profiles distinguish European American patients with different myositis autoantibodies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Lymphoma and other malignancies in primary Sjögren's syndrome: a cohort study on cancer incidence and lymphoma predictors

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

The extracellular matrix and inflammation: fibromodulin activates the classical pathway of complement by directly binding C1q.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Sex, MHC and complement C4 in autoimmune diseases

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Restoration of C1q levels by bone marrow transplantation attenuates autoimmune disease associated with C1q deficiency in mice

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

A protective role for innate immunity in systemic lupus erythematosus

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Complement C4d in graft capillaries -- the missing link in the recognition of humoral alloreactivity

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Genetic sophistication of human complement components C4A and C4B and RP-C4-CYP21-TNX (RCCX) modules in the major histocompatibility complex

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Determining the one, two, three, or four long and short loci of human complement C4 in a major histocompatibility complex haplotype encoding C4A or C4B proteins

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Complement and systemic lupus erythematosus

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Long-term risk of mortality and lymphoproliferative disease and predictive classification of primary Sjögren's syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Continual low-level activation of the classical complement pathway

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Systemic lupus erythematosus, complement deficiency, and apoptosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

The role of complement in B cell activation and tolerance.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Genomics of the major histocompatibility complex: haplotypes, duplication, retroviruses and disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Modular variations of the human major histocompatibility complex class III genes for serine/threonine kinase RP, complement component C4, steroid 21-hydroxylase CYP21, and tenascin TNX (the RCCX module). A mechanism for gene deletions and disease as

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Selective complement C1s deficiency caused by homozygous four-base deletion in the C1s gene.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Characterization of non-expressed C4 genes in a case of complete C4 deficiency: identification of a novel point mutation leading to a premature stop codon

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Molecular basis of a new type of C1q-deficiency associated with a non-functional low molecular weight (LMW) C1q: parallels and differences to other known genetic C1q-defects

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Complement in acute and chronic arthritides: assessment of C3c, C9, and protectin (CD59) in synovial membrane

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Homozygous hereditary C1q deficiency and systemic lupus erythematosus. A new family and the molecular basis of C1q deficiency in three families

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Hereditary C1q deficiency and systemic lupus erythematosus.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

The dichotomous size variation of human complement C4 genes is mediated by a novel family of endogenous retroviruses, which also establishes species-specific genomic patterns among Old World primates

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Inherited structural polymorphism of the fourth component of human complement

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Deficiency of C1r in human serum. Effects on the structure and function of macromolecular C1.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

C1r deficiency: an inborn error associated with cutaneous and renal disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Formation of a hemolytically active cellular intermediate by the interaction between properdin factors B and D and the activated third component of complement

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Lupus diseases associated with hereditary and acquired deficiencies of complement

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Reflection of disease activity in rheumatoid arthritis by indices of activation of the classical complement pathway

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

A structural model for the location of the Rodgers and the Chido antigenic determinants and their correlation with the human complement component C4A/C4B isotypes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

The relationship of complement-mediated microvasculopathy to the histologic features and clinical duration of disease in dermatomyositis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Acquired C1 inhibitor deficiency associated with systemic lupus erythematosus affecting the central nervous system

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Circulating and intra-articular immune complexes in patients with rheumatoid arthritis. Correlation of 125I-Clq binding activity with clinical and biological features of the disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Intra-articular and circulating immune complexes and antiglobulins (IgG and IgM) in rheumatoid arthritis; correlation with clinical features

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Chido and Rodgers blood groups are distinct antigenic components of human complement C4.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

IFN-gamma up-regulates expression of the complement components C3 and C4 by stabilization of mRNA.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Identification of a novel non-coding mutation in C1qB in a Dutch child with C1q deficiency associated with recurrent infections.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Generation of a recombinant, membrane-targeted form of the complement regulator CD59: activity in vitro and in vivo.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Reference typing report for complement component C4.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Multiple identification of a particular type of hereditary C1q deficiency in the Turkish population: review of the cases and additional genetic and functional analysis

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Acquired C1 inhibitor deficiency revealing systemic lupus erythematosus

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Linkage of Chido and HL-A.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

An IgG autoantibody which inactivates C1-inhibitor

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Phenotyping of human complement component C4, a class-III HLA antigen

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Terminal complement complexes and C1/C1 inhibitor complexes in rheumatoid arthritis and other arthritic conditions

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Hereditary complement (C2) deficiency with dermatomyositis

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Rga (Rodgers) and the HLA region: linkage and associations

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

A case of selective Clq deficiency

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Relative resistance of the F-42-stabilized classical pathway C3 convertase to inactivation by C4-binding protein.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Mannan-binding lectin-associated serine protease (MASP)-1 is crucial for lectin pathway activation in human serum, whereas neither MASP-1 nor MASP-3 is required for alternative pathway function.

31 May 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Three distinct profiles of serum complement C4 proteins in pediatric systemic lupus erythematosus (SLE) patients: tight associations of complement C4 and C3 protein levels in SLE but not in healthy subjects.

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Clinical presentations and molecular basis of complement C1r deficiency in a male African-American patient with systemic lupus erythematosus.

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Interaction of human C1q with IgG and IgM: revisited

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Molecular, genetic and epidemiologic studies on selective complete C1q deficiency in Turkey

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Hereditary C1q deficiency and secondary Sjögren's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Functional complement C1q abnormality leads to impaired immune complexes and apoptotic cell clearance

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Molecular basis of a selective C1s deficiency associated with early onset multiple autoimmune diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

The reaction mechanism of the internal thioester in the human complement component C4.

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Complete complement components C4A and C4B deficiencies in human kidney diseases and systemic lupus erythematosus.

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

High C4 gene copy numbers protects against Vogt-Koyanagi-Harada syndrome in Chinese Han.

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Confirmation of C4 gene copy number variation and the association with systemic lupus erythematosus in Chinese Han population.

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Deletion variants of RABGAP1L, 10q21.3, and C4 are associated with the risk of systemic lupus erythematosus in Korean women

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Molecular interactions between MASP-2, C4, and C2 and their activation fragments leading to complement activation via the lectin pathway.

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Molecular heterogeneity in deficiency of complement protein C2 type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Systemic and local anti-C5 therapy reduces the disease severity in experimental autoimmune uveoretinitis.

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Successful cure of C1q deficiency in human subjects treated with hematopoietic stem cell transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Inflammatory Muscle Diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Case records of the Massachusetts General Hospital. Case 18-2014. A 32-Year-old man with a rash, myalgia, and weakness.

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Immunogenetic studies of juvenile dermatomyositis: HLA-DR antigen frequencies.

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Complement inhibitor C4b-binding protein in primary Sjögren's syndrome and its association with other disease markers.

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish family

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

SLE with C1q deficiency treated with fresh frozen plasma: a 10-year experience

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Reconstitution of the Complement Function in C1q-Deficient (C1qa-/-) Mice with Wild-Type Bone Marrow Cells

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Complement activation in patients with isolated antiphospholipid antibodies or primary antiphospholipid syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Hypocomplementaemia as an immunological marker of morbidity and mortality in patients with primary Sjogren's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Anti-cyclic citrullinated peptide antibodies from rheumatoid arthritis patients activate complement via both the classical and alternative pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Hyper IgM syndrome and complement Clq deficiency in an individual with systemic lupus erythematosus-like disease

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Homozygosity for a novel mutation in the C1q C chain gene in a Turkish family with hereditary C1q deficiency.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

Deficiency of human complement protein C4 due to identical frameshift mutations in the C4A and C4B genes.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

A novel type II complement C2 deficiency allele in an African-American family

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4753731

The binding site for C1q on IgG

28 November 2018

1 reference

https://api.crossref.org/works/10.3389%2FFIMMU.2016.00036

Molecular basis of human complement C1s deficiency

21 January 2018

1 reference

12 December 2020

Complement activation in patients with primary antiphospholipid syndrome

1 reference

12 December 2020

Characterization of a non-functional form of Clq found in patients with a genetically linked deficiency of Clq activity

1 reference

12 December 2020

Vascular Deposits of Immunoglobulin and Complement in Idiopathic Inflammatory Myopathy

1 reference

12 December 2020

Complementemia and obstetric outcome in pregnancy with antiphospholipid syndrome

1 reference

12 December 2020

Comparison of the suppressive effects of soluble CR1 and C5a receptor antagonist in acute arthritis induced in rats by blocking of CD59

1 reference

12 December 2020

Reticulocytes bearing C4d as biomarkers of disease activity for systemic lupus erythematosus

1 reference

12 December 2020

Complement in disseminated (systemic) lupus erythematosus

1 reference

12 December 2020

Platelet C4d is highly specific for systemic lupus erythematosus

1 reference

12 December 2020

The molecular basis of complete complement C4A and C4B deficiencies in a systemic lupus erythematosus patient with homozygous C4A and C4B mutant genes

1 reference

12 December 2020

Development of systemic lupus erythematosus in a patient with selective complete C1q deficiency

1 reference

12 December 2020

A homozygous point mutation results in a stop codon in the C1q B-chain of a C1q-deficient individual

1 reference

12 December 2020

HLA haplotypes with C4B5; evidence for further allelic heterogeneity

1 reference

12 December 2020

Microvascular deposition of complement membrane attack complex in dermatomyositis

1 reference

12 December 2020

Experimental arthritis: Targeted anti-C5 drug neutralizes complement in the joint

1 reference

12 December 2020

Lupus-erythematosus-like syndrome with a familial defect of complement

1 reference

12 December 2020

Vascular deposition of complement-split products in kidney allografts with cell-mediated rejection

1 reference

12 December 2020

The mannan-binding lectin (MBL) pathway of complement activation: biochemistry, biology and clinical implications

1 reference

12 December 2020

Serum complement component levels in human glomerulonephritis

1 reference

12 December 2020

Measurement of erythrocyte C4d and complement receptor 1 in systemic lupus erythematosus

1 reference

12 December 2020

Analysis of human C4A and C4B binding to an immune complex in serum

1 reference

12 December 2020

C1q deficiency in an Inuit family: Identification of a new class of C1q disease-causing mutations

1 reference

12 December 2020

Systemic lupus erythematosus with C1q deficiency

1 reference

12 December 2020

A critical role for complement in maintenance of self-tolerance

1 reference

12 December 2020

Genetic analysis of complement C1s deficiency associated with systemic lupus erythematosus highlights alternative splicing of normal C1s gene

1 reference

12 December 2020

Membrane Attack Complex Deposits in Cutaneous Lesions of Dermatomyositis

1 reference

12 December 2020

C1-inhibitor autoantibodies in SLE

1 reference

12 December 2020

PCR-RFLP genotyping of C1q mutations and single nucleotide polymorphisms in Malaysian patients with systemic lupus erythematosus

1 reference

12 December 2020

Existence of Different but Overlapping IgG- and IgM-Binding Sites on the Globular Domain of Human C1q†

1 reference

12 December 2020

The globular heads of C1q specifically recognize surface blebs of apoptotic vascular endothelial cells

1 reference

12 December 2020

Complement C1q and C8 deficiency in an individual with recurrent bacterial meningitis and adult-onset systemic lupus erythematosus-like illness

1 reference

12 December 2020

Microvascular changes in early and advanced dermatomyositis: a quantitative study

1 reference

12 December 2020

Structural and functional studies in C1q deficiency

1 reference

12 December 2020

Clinical and immunological studies in a case of selective complete C1q deficiency

1 reference

12 December 2020

Successful plasma infusion treatment of a patient with C2 deficiency and systemic lupus erythematosus: clinical experience over forty-five months

1 reference

12 December 2020

Homozygous deficiency of C4 in a child with a lupus erythematosus syndrome

1 reference

12 December 2020

Autoantibodies to the collagen-like region of C1q are strongly associated with classical pathway-mediated hypocomplementemia in systemic lupus erythematosus

1 reference

12 December 2020

Unique phenotypes of C1s deficiency and abnormality caused by two compound heterozygosities in a Japanese family

1 reference

12 December 2020

DNA analysis in a MHC heterozygous patient with complete C4 deficiency--homozygosity for C4 gene deletion and C4 pseudogene

1 reference

12 December 2020

Hot-stop PCR: a simple and general assay for linear quantitation of allele ratios

1 reference

12 December 2020

Complement activation in patients with rheumatoid arthritis mediated in part by C-reactive protein

1 reference

12 December 2020

In vitro stimulation of C1s proteolytic activities by C1s-presenting autoantibodies from patients with systemic lupus erythematosus

1 reference

12 December 2020

Identifiers

DOI

10.3389/FIMMU.2016.00036

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

235208

OpenCitations bibliographic resource ID

235208

1 reference