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Systematic screening for genetic polymorphism in human platelet glycoprotein Ibalpha.
Kaski S, Kekomäki R, Partanen J. Kaski S, et al. Among authors: partanen j. Immunogenetics. 1996;44(3):170-6. doi: 10.1007/BF02602582. Immunogenetics. 1996. PMID: 8662083
Major histocompatibility complex located complement C4 and steroid 21-hydroxylase gene rearrangements in couples with recurrent spontaneous abortions.
Laitinen T, Lokki ML, Partanen J, Tulppala M, Ylikorkala O, Koskimies S. Laitinen T, et al. Among authors: partanen j. Eur J Immunogenet. 1992 Dec;19(6):413-8. doi: 10.1111/j.1744-313x.1992.tb00084.x. Eur J Immunogenet. 1992. PMID: 1362078
Determination of deletion sizes in the MHC-linked complement C4 and steroid 21-hydroxylase genes by pulsed-field gel electrophoresis.
Partanen J, Kere J, Wessberg S, Koskimies S. Partanen J, et al. Genomics. 1989 Aug;5(2):345-9. doi: 10.1016/0888-7543(89)90067-0. Genomics. 1989. PMID: 2551816
Restriction fragment analysis of non-deleted complement C4 null genes suggests point mutations in C4A null alleles, but gene conversions in C4B null alleles.
Partanen J, Campbell RD. Partanen J, et al. Immunogenetics. 1989;30(6):520-3. doi: 10.1007/BF02421186. Immunogenetics. 1989. PMID: 2574160 No abstract available.
DNA polymorphism of human HLA-linked complement C4 allotypes, including C4 null alleles, in the Finnish population.
Partanen J, Peltonen L, Koskimies S, Carroll MC. Partanen J, et al. Hum Hered. 1987;37(4):241-9. doi: 10.1159/000153711. Hum Hered. 1987. PMID: 2888726
DNA polymorphism unique for a complotype with deletion of HLA-linked C4B and 21-hydroxylase B genes causing congenital adrenal hyperplasia.
Partanen J, Koskimies S, Sipilä I. Partanen J, et al. Hum Genet. 1988 Apr;78(4):372-3. doi: 10.1007/BF00291739. Hum Genet. 1988. PMID: 2896160
Association between restriction fragment length variants of the complement C4 genes and MHC haplotypes.
Partanen J. Partanen J. J Immunogenet. 1987 Dec;14(6):285-93. doi: 10.1111/j.1744-313x.1987.tb00393.x. J Immunogenet. 1987. PMID: 2903197
Low degree of DNA polymorphism in the HLA-linked lymphotoxin (tumour necrosis factor beta) gene.
Partanen J, Koskimies S. Partanen J, et al. Scand J Immunol. 1988 Sep;28(3):313-6. doi: 10.1111/j.1365-3083.1988.tb01454.x. Scand J Immunol. 1988. PMID: 2904171
Major histocompatibility complex class II and III in Addison's disease. MHC alleles do not predict autoantibody specificity and 21-hydroxylase gene polymorphism has no independent role in disease susceptibility.
Partanen J, Peterson P, Westman P, Aranko S, Krohn K. Partanen J, et al. Hum Immunol. 1994 Oct;41(2):135-40. doi: 10.1016/0198-8859(94)90006-x. Hum Immunol. 1994. PMID: 7860358
HLA-linked heat-shock protein 70 (HSP70-2) gene polymorphism and celiac disease.
Partanen J, Milner C, Campbell RD, Mäki M, Lipsanen V, Koskimies S. Partanen J, et al. Tissue Antigens. 1993 Jan;41(1):15-9. doi: 10.1111/j.1399-0039.1993.tb01971.x. Tissue Antigens. 1993. PMID: 8096093
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