X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (252) 252
membranoproliferative glomerulonephritis (222) 222
index medicus (175) 175
urology & nephrology (144) 144
dense deposit disease (124) 124
hemolytic-uremic syndrome (106) 106
male (102) 102
complement (98) 98
glomerulonephritis (93) 93
female (92) 92
glomerulonephritis, membranoproliferative - immunology (84) 84
alternative pathway (81) 81
immunology (74) 74
glomerulonephritis, membranoproliferative - pathology (66) 66
animals (65) 65
adult (63) 63
nephrology (63) 63
adolescent (60) 60
child (57) 57
c3 glomerulopathy (55) 55
complement factor h - genetics (54) 54
biopsy (52) 52
glomerulonephritis, membranoproliferative - genetics (52) 52
eculizumab (48) 48
medicine & public health (48) 48
middle aged (48) 48
complement factor-h (42) 42
pediatrics (41) 41
glomerulonephritis type-ii (39) 39
mutation (39) 39
complement activation (37) 37
c3 nephritic factor (36) 36
dense-deposit disease (36) 36
macular degeneration (36) 36
disease (35) 35
c3 glomerulonephritis (34) 34
research (34) 34
glomerulonephritis, membranoproliferative - drug therapy (33) 33
kidney - pathology (33) 33
risk factors (33) 33
factor h (32) 32
factor-h (32) 32
glomerulonephritis, membranoproliferative - diagnosis (32) 32
complement c3 - metabolism (31) 31
activation (30) 30
kidney transplantation (30) 30
mice (29) 29
young adult (29) 29
kidney diseases (28) 28
nephritic factor (28) 28
glomerulonephritis, membranoproliferative - therapy (27) 27
complement c3 - analysis (26) 26
complement system proteins - immunology (26) 26
treatment outcome (26) 26
autoantibodies (25) 25
diagnosis (25) 25
kidney glomerulus - pathology (25) 25
mutations (25) 25
aged (24) 24
complement c3 - immunology (24) 24
monoclonal gammopathy (24) 24
biochemistry & molecular biology (23) 23
complement factor h (23) 23
glomerulonephritis - immunology (23) 23
glomerulopathy (23) 23
pathology (23) 23
glomerulonephritis, membranoproliferative - blood (22) 22
mesangiocapillary glomerulonephritis (22) 22
mpgn (22) 22
retrospective studies (22) 22
care and treatment (21) 21
child, preschool (21) 21
complement factor h - deficiency (21) 21
complement factor h - metabolism (21) 21
glomerulonephritis, membranoproliferative - etiology (21) 21
kidney glomerulus - immunology (21) 21
transplantation (21) 21
complement c3 nephritic factor - analysis (20) 20
complement pathway, alternative (20) 20
glomerulonephritis, membranoproliferative - complications (20) 20
health aspects (20) 20
kidneys (20) 20
atypical hemolytic uremic syndrome (19) 19
glomerulonephritis - pathology (19) 19
hemolytic-uremic syndrome - genetics (19) 19
proteinuria (19) 19
article (18) 18
autoimmunity (18) 18
membrane cofactor protein (18) 18
recurrence (18) 18
renal-transplantation (18) 18
analysis (17) 17
autoantibodies - immunology (17) 17
deficiency (17) 17
genetic predisposition to disease (17) 17
nephrotic syndrome (17) 17
proteins (17) 17
time factors (17) 17
antibodies, monoclonal, humanized - therapeutic use (16) 16
children (16) 16
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Kidney International, ISSN 0085-2538, 07/2006, Volume 70, Issue 1, pp. 42 - 50
Journal Article
Kidney International, ISSN 0085-2538, 08/2012, Volume 82, Issue 4, pp. 454 - 464
Dense deposit disease and glomerulonephritis with isolated C3 deposits are glomerulopathies characterized by deposits of C3 within or along the glomerular... 
complement | glomerulonephritis | clinical immunology | membranoproliferative glomerulonephritis (MPGN) | LONG-TERM | HEMOLYTIC-UREMIC SYNDROME | MESANGIOCAPILLARY GLOMERULONEPHRITIS | GLOMERULONEPHRITIS TYPE-II | MACULAR DEGENERATION | FACTOR-H DEFICIENCY | GLOMERULAR-FILTRATION-RATE | UROLOGY & NEPHROLOGY | MUTATIONS | MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS | MEMBRANE COFACTOR PROTEIN | Humans | Child, Preschool | Male | Complement System Proteins - metabolism | Young Adult | Time Factors | DNA Mutational Analysis | Renal Insufficiency - immunology | Child | Glomerulonephritis, Membranoproliferative - pathology | Genetic Predisposition to Disease | Risk Assessment | Complement C3 - metabolism | Gene Frequency | Risk Factors | Glomerulonephritis - genetics | Glomerulonephritis - immunology | Glomerulonephritis - mortality | Biomarkers - blood | Kidney Glomerulus - pathology | Disease Progression | Glomerulonephritis, Membranoproliferative - genetics | Glomerulonephritis, Membranoproliferative - immunology | Phenotype | Complement Factor H - metabolism | Glomerulonephritis, Membranoproliferative - mortality | Glomerulonephritis - pathology | Adolescent | Age of Onset | Membrane Cofactor Protein - genetics | Kidney Glomerulus - immunology | Mutation | Complement Factor I - metabolism | Haplotypes | Complement C3 Nephritic Factor - genetics | Glomerulonephritis - therapy | Infant | Case-Control Studies | Adult | Complement System Proteins - genetics | Female | Membrane Cofactor Protein - metabolism | Complement Pathway, Alternative - genetics | France | Renal Insufficiency - genetics | Kaplan-Meier Estimate | Complement Factor I - genetics | Treatment Outcome | Chi-Square Distribution | Glomerulonephritis, Membranoproliferative - therapy | Biopsy | Complement C3 Nephritic Factor - metabolism | Complement Factor H - genetics
Journal Article
Molecular Immunology, ISSN 0161-5890, 03/2016, Volume 71, pp. 131 - 142
Journal Article
Kidney International, ISSN 0085-2538, 08/2012, Volume 82, Issue 4, pp. 465 - 473
C3 glomerulonephritis (C3GN) is a recently described disorder that typically results from abnormalities in the alternative pathway (AP) of complement. Here, we... 
C3GN | proteomics | C3 glomerulopathy | MPGN | alternative pathway of complement | C3 glomerulonephritis | MACULAR DEGENERATION | CLASSIFICATION | RISK | PROTEIN 5 | DENSE DEPOSIT DISEASE | ALTERNATIVE PATHWAY | UROLOGY & NEPHROLOGY | MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS | Complement C3 - analysis | Predictive Value of Tests | Recurrence | Follow-Up Studies | Humans | Middle Aged | Complement System Proteins - immunology | Laser Capture Microdissection | Molecular Sequence Data | Male | Glomerulonephritis, Membranoproliferative - complications | Complement System Proteins - analysis | Young Adult | Time Factors | DNA Mutational Analysis | Mass Spectrometry | Adult | Autoantibodies - analysis | Complement System Proteins - genetics | Female | Complement Pathway, Alternative - genetics | Proteomics - methods | Child | Amino Acid Sequence | Glomerulonephritis, Membranoproliferative - pathology | Genetic Predisposition to Disease | Proteinuria - immunology | Treatment Outcome | Complement C3 Nephritic Factor - analysis | Hematuria - immunology | Kidney Transplantation | Minnesota | Kidney Glomerulus - pathology | Glomerulonephritis, Membranoproliferative - therapy | Glomerulonephritis, Membranoproliferative - genetics | Glomerulonephritis, Membranoproliferative - immunology | Biopsy | Adolescent | Aged | Kidney Glomerulus - immunology | Mutation | Complement Factor H - genetics
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 1/2007, Volume 22, Issue 1, pp. 2 - 9
Journal Article
Journal Article
Journal Article
Molecular Immunology, ISSN 0161-5890, 2006, Volume 43, Issue 1, pp. 97 - 106
The complement system is a central part of innate immunity and in its normal setting aimed to recognize and eliminate microbes. For elimination toxic... 
Factor H | Alternative pathway control | Membranoproliferative glomerulonephritis (MPGN) | Hemolytic uremic syndrome (HUS) | Age-related macular degeneration (ARMD) | Innate immunity | Complement | Pattern recognition | ACTIVATION | HEMOLYTIC-UREMIC SYNDROME | PROTEIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLOMERULONEPHRITIS TYPE-II | MACULAR DEGENERATION | IMMUNOLOGY | factor H | membranoproliferative glomerulonephritis (MPGN) | TRANSPLANTATION | FACTOR-H DEFICIENCY | innate immunity | GENE | age-related macular degeneration (ARMD) | MUTATIONS | complement | alternative pathway control | MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS | hemolytic uremic syndrome (HUS) | pattern recognition | Glomerulonephritis, Membranoproliferative - pathology | Hemolytic-Uremic Syndrome - metabolism | Complement C3 Convertase, Alternative Pathway - metabolism | Humans | Complement Factor H - deficiency | Mice, Knockout | Hemolytic-Uremic Syndrome - pathology | Glomerulonephritis, Membranoproliferative - genetics | Hemolytic-Uremic Syndrome - genetics | Macular Degeneration - metabolism | Animals | Complement Factor H - metabolism | Macular Degeneration - genetics | Swine | Mice | Complement Pathway, Alternative - genetics | Mutation | Complement Factor H - genetics | Complement C3 Convertase, Alternative Pathway - deficiency | Complement C3 Convertase, Alternative Pathway - genetics | Glomerulonephritis, Membranoproliferative - metabolism | Disease Models, Animal | Macular Degeneration - pathology | Macular degeneration | Genetic research
Journal Article