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1-18 of 18
Keywords: Complement
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Journal Articles
Subject Area:
Genetics
Journal:
Human Heredity
Hum Hered (1995) 45 (4): 215–218.
Published Online: 03 September 2008
.... Complement Group-specific component Ulcerative colitis C3 Original Paper Hum Hered 1995;45:215-218 A. Archimandritis P. Koumentakos M. Domara N. Scandalis A. Fertakis SUDPehnecypitsviaioeornrtlmso,igLteyyna,iotkGfooaAfnsPttGhraoetehennnose,tlreoGarglorielcHoegocyespital, CKeoymWploermdsent Group...
Journal Articles
Subject Area:
Genetics
Hiroaki Nishimukai, Ikuro Maruyama, Satoshi Takenaga, Hajime Kitamura, Kenji Mizutani, Takaaki Shinomiya
Journal:
Human Heredity
Hum Hered (1990) 40 (1): 58–60.
Published Online: 02 September 2008
...Hiroaki Nishimukai; Ikuro Maruyama; Satoshi Takenaga; Hajime Kitamura; Kenji Mizutani; Takaaki Shinomiya A new slow-moving variant of the complement factor B, named BF S075, was found in a Japanese patient with cerebral thrombosis and urticaria. The variant was inherited in a codominant manner...
Journal Articles
Subject Area:
Genetics
Journal:
Human Heredity
Hum Hered (1993) 43 (1): 66–68.
Published Online: 02 September 2008
... to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Haptoglobin Complement C3 Colon cancer Short Communication Hum Hcred 1993;43:66-68 A. Archimandritis G. Theodoropoulos M . Tryphonos A. Germenis M. Tjivras A. Kalos...
Journal Articles
Subject Area:
Genetics
Journal:
Human Heredity
Hum Hered (1990) 40 (5): 272–277.
Published Online: 02 September 2008
... of the disease. Statistically significant associations were found in the complement systems C3 and C4A. The C3F variant was significantly increased in all FAP patients with a relative risk (RR) of 2.0, more pronounced in female patients (RR = 2.6) and patients with an early onset of the disease (RR = 4.5...
Journal Articles
Subject Area:
Genetics
Journal:
Human Heredity
Hum Hered (1987) 37 (3): 196–197.
Published Online: 02 September 2008
.... C3 Complement Isoelectric focusing Hum. Hered. 37: 196-197(1987) © 1987 S. Kargcr AG. Basel 0001 -5652/87/0373-0196 $ 2.75/0 Method for the Typing of the C3 Polymorphism in Stored Sera by Means of Isoelectric Focusing G. Beckman. C. Sikstrom Department of Medical Genetics, University of UmeA...
Journal Articles
Subject Area:
Genetics
Hiroaki Nishimukai, Isao Nakanishi, Yoshihiro Takeuchi, Ryota Sumiyoshi, Kenji Mizutani, Nobutoshi Iida, Takaaki Shinomiya
Journal:
Human Heredity
Hum Hered (1989) 39 (3): 150–155.
Published Online: 02 September 2008
...(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Complement C6 C7 Chronic glomerulonephritis IgA nephropathy Idiopathic membranous nephropathy Minimal-change...
Journal Articles
Subject Area:
Genetics
Journal:
Human Heredity
Hum Hered (1988) 38 (4): 246–250.
Published Online: 02 September 2008
... Medicine. School of Medicine, Ehime University, Ehime; hDepartment of Immunology, The Center for Adult Diseases, Osaka; c Department of Forensic Medicine, Medical College of Oita, Oita, Japan Key Words. Complement C 7 silent allele C6-C7 association Genetic polymorphism Abstract. Three Japanese...
Journal Articles
Subject Area:
Genetics
Journal:
Human Heredity
Hum Hered (1988) 38 (1): 44–47.
Published Online: 02 September 2008
... increase of complement C4 deficiency was found among the SLE patients. The relative risks for AQO and BQ0 homozygosity were 7.2 and 4.1, respectively. Simultaneous occurrence of AQO and BQ0 was found in three patients with a calculated relative risk of about 65. A significant increase of the haptoglobin...
Journal Articles
Subject Area:
Genetics
Journal:
Human Heredity
Hum Hered (1989) 39 (6): 327–332.
Published Online: 02 September 2008
...Robert J. Wyatt; Can Wang; Edmund C. Hudson; MacNeely Jones; Patricia W. Noah; William Rosenberg Phenotype frequencies for the complement proteins C4A, C4B, Bf (factor B) and C3 were performed for 49 Caucasian patients with psoriasis. The C4*A6 allele was present in 26.6% of the patients...
Journal Articles
Subject Area:
Genetics
Journal:
Human Heredity
Hum Hered (1991) 41 (2): 129–133.
Published Online: 02 September 2008
... where only the former 2 are present commonly. This complement system can be a useful genetic marker for anthropological studies. 2 9 2008 © 1991 S. Karger AG, Basel 1991 Copyright / Drug Dosage / Disclaimer Copyright: All rights reserved. No part of this publication may be translated...
Journal Articles
Subject Area:
Genetics
Journal:
Human Heredity
Hum Hered (1992) 42 (3): 168–171.
Published Online: 02 September 2008
..., instructions or products referred to in the content or advertisements. Haptoglobin Group specific component Complement Gastric carcinoma C3 Original Paper Hum Hcrcd 1992;42:168-171 G. Theodoropoulos A. Archimandritis A. Germenis N. Malamas M. Tjivras A. Fertakis Department of Pathologic Physiology...
Journal Articles
Subject Area:
Genetics
Journal:
Human Heredity
Hum Hered (1992) 42 (3): 198–200.
Published Online: 02 September 2008
..., University of Athens, Greece Key Words Complement Group specific component Peptic ulcer Duodenal ulcer C3 Gastric ulcer Abstract The phenotypes and gene frequencies of two serum protein systems (GC, C3) were studied in 238 consecutive patients with peptic ulcer from all over Greece. 173 patients had duodenal...
Journal Articles
Subject Area:
Genetics
Journal:
Human Heredity
Hum Hered (1986) 36 (4): 261–262.
Published Online: 02 September 2008
...L.J. York; W.H. Marshall; S.N. Huang An allele of the seventh complement component, C7*2, which is very rare in Europeans, has been found at balanced polymorphic frequency (0.15) in Chinese. This marker may be useful for anthropological studies. 2 9 2008 © 1986 S. Karger AG, Basel 1986...
Journal Articles
Subject Area:
Genetics
Journal:
Human Heredity
Hum Hered (1985) 35 (4): 255–258.
Published Online: 02 September 2008
...C. Rudduck; L. Beckman; G. Franzén; L. Lindström C3 and C6 complement types were studied in schizophrenic patients and controls. The distributions of the three common C3 types (F, FS and S) among the patients was significantly different from that in the controls (p& <0.005) and the frequency...
Journal Articles
Subject Area:
Genetics
Journal:
Human Heredity
Hum Hered (1992) 42 (3): 162–167.
Published Online: 02 September 2008
...L. Fañanás; P. Moral; M.A. Panadero; J. Bertranpetit Polymorphic variants of C3, BF and C6 complement factors have been investigated in schizophrenic patients subdivided according to the existence or not of a family history of both schizophrenia and other psychiatric disorders. To analyze...
Journal Articles
Subject Area:
Genetics
Kenji Mizutani, Hiroaki Nishimukai, Takumi Yasugi, Kanji Iwahashi, Kengo Tsunekawa, Takaaki Shinomiya
Journal:
Human Heredity
Hum Hered (1991) 41 (4): 270–275.
Published Online: 02 September 2008
...Kenji Mizutani; Hiroaki Nishimukai; Takumi Yasugi; Kanji Iwahashi; Kengo Tsunekawa; Takaaki Shinomiya The polymorphisms of the B subunit of coagulation factor XIII (F13B), plasminogen (PLG), complement C6, C7, factor B (BF) and factor I (IF) were studied among 21 unrelated Japanese patients...
Journal Articles
Subject Area:
Genetics
Journal:
Human Heredity
Hum Hered (1980) 30 (3): 149–154.
Published Online: 29 August 2008
...: 149-154 (1980) Partial Lipodystrophy and Familial C3 Deficiency R. H. McLean and D. Hoefnagel Depariment of Pediatrics, The University of Connecticut Health Center, Farmington, Conn., and Department of Maternal and Child Health, Dartmouth Medical School, Hanover, N.H. Key Words. Complement Partial...
Journal Articles
Subject Area:
Genetics
Journal:
Human Heredity
Hum Hered (1975) 25 (5): 393–397.
Published Online: 28 August 2008
...J.L. MacDonald The C’3 polymorphism of human complement was investigated in a sample of 268 unrelated individuals in North-East England. The two common genes were comparable in frequency with other European populations investigated so far. Two individuals were found to have rare variant C’3 types...