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PLoS ONE, ISSN 1932-6203, 11/2013, Volume 8, Issue 11, p. e81341
There is increasing evidence that complement may play a role in bone development. Our previous studies demonstrated that the key complement receptor C5aR was... 
OSTEOCLASTOGENESIS | ACTIVATION | C1S | MULTIDISCIPLINARY SCIENCES | OSSIFICATION CENTER | OSTEOBLASTS | MECHANISMS | GENERATION | BONE | DIFFERENTIATION | EXPRESSION | Bony Callus - immunology | Elasticity | Male | Bony Callus - pathology | Femur - diagnostic imaging | Complement C3a - genetics | X-Ray Microtomography | Fractures, Bone - genetics | Bony Callus - diagnostic imaging | Gene Deletion | Gene Expression - immunology | Fractures, Bone - diagnostic imaging | Complement C5a - deficiency | Femur - injuries | Fractures, Bone - immunology | Complement C3a - deficiency | Hardness | Interleukin-6 - secretion | Fracture Healing - immunology | Complement Activation - genetics | Biomechanical Phenomena | Animals | Interleukin-6 - biosynthesis | Complement C5a - genetics | Mice | Complement C3a - immunology | Complement C5a - immunology | Fracture Healing - genetics | Fractures | Research | Femur | Callus | Osteotomy | Complement component C5a | Complement | Proteins | Biomedical materials | Immunology | Computed tomography | Rodents | Tomography | Biocompatibility | Stiffness | Repair | Immune system | Cytokines | Chondroblasts | Plastic surgery | Bone healing | Trauma | Biomechanics | Studies | Complement activation | Complement component C5 | Complement component C3 | Sepsis | Healing | Regulation | Clinical medicine | Bone | Laboratory animals | Biological Sciences | Naturvetenskap | Biomedical Sciences | Biokemi och molekylärbiologi | Biologiska vetenskaper | Biochemistry and Molecular Biology | Natural Sciences | Biomedicinsk vetenskap
Journal Article
GENES AND IMMUNITY, ISSN 1466-4879, 02/2019, Volume 20, Issue 2, pp. 121 - 130
C1s deficiency is strongly associated with the development of human systemic lupus erythematosus (SLE); however, the mechanisms by which C1s deficiency... 
C1S DEFICIENCY | ICGN | DENDRITIC CELLS | GENES | DISEASE | MOUSE | GENETICS & HEREDITY | MICE | IMMUNOLOGY | MOLECULAR-BASIS | ANTI-C1Q AUTOANTIBODIES | COMPLEMENT COMPONENTS | Glomerulonephritis | Genetic aspects | Rats as laboratory animals | Systemic lupus erythematosus | Research
Journal Article
Biochemical Journal, ISSN 0264-6021, 11/2010, Volume 431, Issue 3, pp. 363 - 371
IRIDA (iron-refractory iron-deficiency anaemia) is a rare autosomal-recessive disorder hallmarked by hypochromic microcytic anaemia, low transferrin saturation... 
Iron-refractory iron-deficiency anaemia (IRIDA) | Transmembrane protease serine 6 (TMPRSS6) | Hepcidin | Matriptase-2 | Haemojuvelin | hepcidin | BIOCHEMISTRY & MOLECULAR BIOLOGY | IRON-DEFICIENCY ANEMIA | MECHANISMS | MATRIPTASE-2 TMPRSS6 | IDENTIFICATION | iron-refractory iron deficiency anaemia (IRIDA) | transmembrane protease serine 6 (TMPRSS6) | METABOLISM | haemojuvelin | TRANSMEMBRANE SERINE-PROTEASE | MALABSORPTION | matriptase-2 | EXPRESSION | Humans | GPI-Linked Proteins | Child, Preschool | Molecular Sequence Data | Male | Phylogeny | Anemia, Iron-Deficiency - enzymology | Anemia, Iron-Deficiency - urine | Hepcidins | Base Sequence | Serine Endopeptidases - genetics | Female | Membrane Proteins - metabolism | Antimicrobial Cationic Peptides - genetics | Child | Protein Structure, Tertiary | Amino Acid Sequence | Antimicrobial Cationic Peptides - urine | Membrane Proteins - genetics | Anemia, Iron-Deficiency - etiology | RNA, Messenger - genetics | Gene Expression Regulation | Models, Molecular | Serine Endopeptidases - chemistry | Sequence Alignment | Animals | Membrane Proteins - chemistry | Pedigree | Cell Line, Tumor | Protein Binding | Anemia, Iron-Deficiency - genetics | Serine Endopeptidases - metabolism | Enzyme Activation | Mutation | TTSP, type II transmembrane serine protease | cdTMPRSS6, catalytic domain of TMPRSS6 | CUB domain, complement factor C1s | PIC, phosphoinositidase C | HJV, haemojuvelin | DMEM, Dulbecco's modified Eagle's medium | SLC11A2, solute carrier family 11, member 2 | qRT-PCR, quantitative real-time PCR | BMP, bone morphogenetic protein | TMPRSS6, transmembrane protease serine 6 | ALAS2, aminolevulinate δ synthase 2 | GAPDH, glyceraldehyde-3-phosphate dehydrogenase | EGFP, enhanced green fluorescent protein | SEA domain, sea urchin sperm protein, enteropeptidase and agrin domain | FBS, fetal bovine serum | ORF, open reading frame | LDLR domain, low-density-lipoprotein receptor class A domain | iron-refractory irondeficiency anaemia (IRIDA) | SELDI–TOF, surface-enhanced laser-desorption ionization–time-of-flight | C1r, urchin embryonic growth factor and BMP domain | CMV, cytomegalovirus | IRIDA, iron-refractory iron-deficiency anaemia | SLC25A28, solute carrier family 25, member 28
Journal Article
The Journal of Immunology, ISSN 0022-1767, 02/2009, Volume 182, Issue 3, pp. 1681 - 1688
Journal Article
ANNALS OF INTERNAL MEDICINE, ISSN 0003-4819, 11/2000, Volume 133, Issue 10, pp. 837 - 837
Journal Article
Annals of internal medicine, ISSN 0003-4819, 2000, Volume 133, Issue 10, pp. 838 - 839
Journal Article
Journal Article
Annals of internal medicine, ISSN 0003-4819, 2000, Volume 133, Issue 10, pp. 837 - 839
Journal Article
Journal Article