Molecular basis of hereditary C1q deficiency--revisited: identification of several novel disease-causing mutations.
about
Early Components of the Complement Classical Activation Pathway in Human Systemic Autoimmune DiseasesComplement System Part II: Role in ImmunityAnti-C1q antibodies in systemic lupus erythematosus.Anti-C1q antibodies as a follow-up marker in SLE patientsMolecular characterization of the complement C1q, C2 and C4 genes in Brazilian patients with juvenile systemic lupus erythematosusBiomarkers for kidney involvement in pediatric lupus.Evasion and interactions of the humoral innate immune response in pathogen invasion, autoimmune disease, and cancerIdentification of novel coding mutation in C1qA gene in an African-American pedigree with lupus and C1q deficiencyRare variants, autoimmune disease, and arthritisThe identification of a novel splicing mutation in C1qB in a Japanese family with C1q deficiency: a case report.Chromatin landscapes and genetic risk in systemic lupus.Newborn screening for primary immunodeficiencies: beyond SCID and XLA.Bioinformatics analysis reveals transcriptome and microRNA signatures and drug repositioning targets for IBD and other autoimmune diseases.The complement system in systemic lupus erythematosus: an update.Progress with the use of monoclonal antibodies for the treatment of systemic lupus erythematosus.Newly Described Autoinflammatory Diseases in Pediatric Dermatology.Complement in removal of the dead - balancing inflammation.C1q as an autocrine and paracrine regulator of cellular functions.C1q rs292001 polymorphism and C1q antibodies in juvenile lupus and their relation to lupus nephritis.C1q Deficiency and Neuropsychiatric Systemic Lupus Erythematosus"Association of rs172378 C1q gene cluster polymorphism with lupus nephritis in Bulgarian patients".Association of rs172378 C1q gene cluster polymorphism with lupus nephritis in Bulgarian patients.MafB is a critical regulator of complement component C1q.Early Complement Component Deficiency in a Single-Centre Cohort of Pediatric Onset Lupus.Systemic lupus erythematosus with C1q deficiency: treatment with fresh frozen plasma.Is the A-Chain the Engine That Drives the Diversity of C1q Functions? Revisiting Its Unique Structure.Systemic lupus erythematosus due to C1q deficiency with progressive encephalopathy, intracranial calcification and acquired moyamoya cerebral vasculopathy.Anti-Double-Stranded DNA Isotypes and Anti-C1q Antibody Improve the Diagnostic Specificity of Systemic Lupus Erythematosus
P2860
Q26766486-D23D2CB4-1EE5-4802-97C9-2A9BED5B6FBAQ28263460-4BC2DA9F-0677-46C8-A5FF-4B175FCA3ADAQ34717540-116C5647-7A6A-482D-9FCC-6EA755762BDCQ35448756-2EA24BD6-2C69-4ABA-B750-C3582BD0EC3CQ35666548-D33E4282-FCC9-4D56-9CAF-3FF90CB69FA3Q35810911-AF8811A8-AE93-472F-BAF4-DDB161009236Q36090335-6A0CE7AB-456D-4BCE-B61C-7B73DD7B06FFQ36430216-5513643B-56DD-4E21-A855-FF4EC94F23D4Q37012282-83ACB9EA-17CA-4D9B-B29A-00F018F3E1DDQ37418321-EB0A9D76-E72C-4FE5-B5EE-25CF2F312BB5Q37466284-5C8B2770-0299-43A5-A5A3-D0D6C47CC117Q37974987-83C558D7-AD76-427F-8478-42154B856867Q38001400-E0B57F4C-CF0D-4D35-87D0-923471FC2AB1Q38213193-BEA506A7-3BEA-4BD6-B517-31295766BC1EQ38389307-D6981D95-F521-4DEE-8D79-A365DF5A54ABQ38971704-73049B8E-1902-47D4-99DE-1236AACB6075Q38991044-0E8419B0-7F7B-4211-B024-B9AFE0F88A87Q39028351-730A23A6-6A16-47FF-BDD1-FA7EBC4C9E23Q39272808-E32AC5E5-AD62-4F1B-BEC1-09511B49AC95Q39906091-54F52168-FDE6-492E-9C7A-9ACFD1CC2CCAQ43926615-BA11B691-4301-48C3-87AC-C8DF40D09920Q43926821-DC48B0CB-341F-4095-9339-B737117FEA1CQ47105666-6650D007-0673-485C-85DF-4C38DC0F94F9Q47965723-111E77E2-8297-45F1-BCC3-C062BA4D7196Q48347745-29C0B1CB-547D-4F1F-8137-4DA355A3C90AQ49829223-9D0E23F0-651B-4908-AC4F-7F67B5848543Q51013012-89E46B39-C768-4971-A670-FEB211BE14EFQ58549171-900797C2-93D0-4300-8362-555BA09FBB41
P2860
Molecular basis of hereditary C1q deficiency--revisited: identification of several novel disease-causing mutations.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 09 June 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Molecular basis of hereditary ...... vel disease-causing mutations.
@en
Molecular basis of hereditary ...... vel disease-causing mutations.
@nl
type
label
Molecular basis of hereditary ...... vel disease-causing mutations.
@en
Molecular basis of hereditary ...... vel disease-causing mutations.
@nl
prefLabel
Molecular basis of hereditary ...... vel disease-causing mutations.
@en
Molecular basis of hereditary ...... vel disease-causing mutations.
@nl
P2093
P2860
P356
P1433
P1476
Molecular basis of hereditary ...... vel disease-causing mutations.
@en
P2093
B Schiller
L Schejbel
L Truedsson
S Hagelberg
P2860
P2888
P304
P356
10.1038/GENE.2011.39
P50
P577
2011-06-09T00:00:00Z