111 related articles for article (PubMed ID: 8865989)
21. C8A and C8B polymorphisms in Norwegians and Norwegian lapps.
Rogde S; Teisberg P; Olaisen B
Hum Hered; 1989; 39(2):81-8. PubMed ID: 2759635
[TBL] [Abstract][Full Text] [Related]
22. Genetic control of the eighth component of complement.
Raum D; Spence MA; Balavitch D; Tideman S; Merritt AD; Taggart RT; Petersen BH; Day NK; Alper CA
J Clin Invest; 1979 Sep; 64(3):858-65. PubMed ID: 468996
[TBL] [Abstract][Full Text] [Related]
23. Isolation, characterization, and chromosomal mapping of the human insulin promoter factor 1 (IPF-1) gene.
Inoue H; Riggs AC; Tanizawa Y; Ueda K; Kuwano A; Liu L; Donis-Keller H; Permutt MA
Diabetes; 1996 Jun; 45(6):789-94. PubMed ID: 8635654
[TBL] [Abstract][Full Text] [Related]
24. A novel human odorant-binding protein gene family resulting from genomic duplicons at 9q34: differential expression in the oral and genital spheres.
Lacazette E; Gachon AM; Pitiot G
Hum Mol Genet; 2000 Jan; 9(2):289-301. PubMed ID: 10607840
[TBL] [Abstract][Full Text] [Related]
25. Construction of a GT polymorphism map of human 9q.
Kwiatkowski DJ; Henske EP; Weimer K; Ozelius L; Gusella JF; Haines J
Genomics; 1992 Feb; 12(2):229-40. PubMed ID: 1339384
[TBL] [Abstract][Full Text] [Related]
26. Linkage analysis of the human dopamine beta-hydroxylase gene.
Perry SE; Summar ML; Phillips JA; Robertson D
Genomics; 1991 Jun; 10(2):493-5. PubMed ID: 2071155
[TBL] [Abstract][Full Text] [Related]
27. The eighth component of human complement: evidence that it is an oligomeric serum protein assembled from products of three different genes.
Ng SC; Rao AG; Howard OM; Sodetz JM
Biochemistry; 1987 Aug; 26(17):5229-33. PubMed ID: 3676249
[TBL] [Abstract][Full Text] [Related]
28. [Detecting the DNA polymorphism of human complement component C8A by PCR-SSCP analysis].
Yang ZH; Zhang L; Zhou B; Wang C; Jia J
Sichuan Da Xue Xue Bao Yi Xue Ban; 2006 May; 37(3):471-3. PubMed ID: 16761437
[TBL] [Abstract][Full Text] [Related]
29. Gamma subunit of complement component 8 is a neuroinflammation inhibitor.
Kim JH; Afridi R; Han J; Jung HG; Kim SC; Hwang EM; Shim HS; Ryu H; Choe Y; Hoe HS; Suk K
Brain; 2021 Mar; 144(2):528-552. PubMed ID: 33382892
[TBL] [Abstract][Full Text] [Related]
30. Large linkage analysis in 100 families with autosomal recessive spinal muscular atrophy (SMA) and 11 CEPH families using 15 polymorphic loci in the region 5q11.2-q13.3.
Wirth B; Pick E; Leutner A; Dadze A; Voosen B; Knapp M; Piechaczek-Wappenschmidt B; Rudnik-Schöneborn S; Schönling J; Cox S
Genomics; 1994 Mar; 20(1):84-93. PubMed ID: 7912691
[TBL] [Abstract][Full Text] [Related]
31. Human C81 (alpha-gamma) polymorphism: detection in the alpha-gamma subunit on SDS-PAGE, formal genetics and linkage relationship.
Rittner C; Hargesheimer W; Stradmann B; Bertrams J; Baur MP; Petersen BH
Am J Hum Genet; 1986 Apr; 38(4):482-91. PubMed ID: 3458364
[TBL] [Abstract][Full Text] [Related]
32. Locus D1S21 contains exonic sequence from the C8 beta component of complement.
Power LM; Chua SC; Leibel RL
Mamm Genome; 1994 Feb; 5(2):125-6. PubMed ID: 8180476
[No Abstract] [Full Text] [Related]
33. Genetic aspects of complement component C8 in Norwegian meningococcal disease patients.
Rogde S; Høiby EA; Teisberg P; Olaisen B
Scand J Infect Dis; 1990; 22(6):673-9. PubMed ID: 2284574
[TBL] [Abstract][Full Text] [Related]
34. Gene responsible for deficient activity of the beta subunit of C8, the eighth component of complement, is located on mouse chromosome 4.
Tanaka S; Suzuki T; Sakaizumi M; Harada Y; Matsushima Y; Miyashita N; Fukumori Y; Inai S; Moriwaki K; Yonekawa H
Immunogenetics; 1991; 33(1):18-23. PubMed ID: 1995474
[TBL] [Abstract][Full Text] [Related]
35. Identification of clusters of biallelic polymorphic sequence-tagged sites (pSTSs) that generate highly informative and automatable markers for genetic linkage mapping.
Nickerson DA; Whitehurst C; Boysen C; Charmley P; Kaiser R; Hood L
Genomics; 1992 Feb; 12(2):377-87. PubMed ID: 1531472
[TBL] [Abstract][Full Text] [Related]
36. Fucosyltransferase genes are dispersed in the genome: FUT7 is located on 9q34.3 distal to D9S1830.
Reguigne-Arnould I; Wolfe J; Hornigold N; Fauré S; Mollicone R; Oriol R; Coullin P
C R Acad Sci III; 1996 Sep; 319(9):783-8. PubMed ID: 8952881
[TBL] [Abstract][Full Text] [Related]
37. Identification of a human LMX1 (LMX1.1)-related gene, LMX1.2: tissue-specific expression and linkage mapping on chromosome 9.
Iannotti CA; Inoue H; Bernal E; Aoki M; Liu L; Donis-Keller H; German MS; Permutt MA
Genomics; 1997 Dec; 46(3):520-4. PubMed ID: 9441763
[TBL] [Abstract][Full Text] [Related]
38. Comparative mapping of 50 human chromosome 9 loci in the laboratory mouse.
Pilz A; Woodward K; Povey S; Abbott C
Genomics; 1995 Jan; 25(1):139-49. PubMed ID: 7774911
[TBL] [Abstract][Full Text] [Related]
39. Molecular evolution of epididymal lipocalin genes localized on mouse chromosome 2.
Suzuki K; Lareyre JJ; Sánchez D; Gutierrez G; Araki Y; Matusik RJ; Orgebin-Crist MC
Gene; 2004 Sep; 339():49-59. PubMed ID: 15363845
[TBL] [Abstract][Full Text] [Related]
40. Linkage map of human chromosome 9 microsatellite polymorphisms.
Wilkie PJ; Krizman DB; Weber JL
Genomics; 1992 Mar; 12(3):607-9. PubMed ID: 1559711
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
