Kainulainen K - Search Results

1

Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome.

Kainulainen K, Karttunen L, Puhakka L, Sakai L, Peltonen L. Kainulainen K, et al. Nat Genet. 1994 Jan;6(1):64-9. doi: 10.1038/ng0194-64. Nat Genet. 1994. PMID: 8136837

2

Two mutations in Marfan syndrome resulting in truncated fibrillin polypeptides.

Kainulainen K, Sakai LY, Child A, Pope FM, Puhakka L, Ryhänen L, Palotie A, Kaitila I, Peltonen L. Kainulainen K, et al. Proc Natl Acad Sci U S A. 1992 Jul 1;89(13):5917-21. doi: 10.1073/pnas.89.13.5917. Proc Natl Acad Sci U S A. 1992. PMID: 1631074 Free PMC article.

3

Elucidation of the gene defect in Marfan syndrome. Success by two complementary research strategies.

Peltonen L, Kainulainen K. Peltonen L, et al. Among authors: kainulainen k. FEBS Lett. 1992 Jul 27;307(1):116-21. doi: 10.1016/0014-5793(92)80913-2. FEBS Lett. 1992. PMID: 1639186 Free article. Review.

4

Marfan gene discovered.

Kainulainen K, Peltonen L. Kainulainen K, et al. Ann Med. 1991 Oct;23(4):395-6. doi: 10.3109/07853899109148080. Ann Med. 1991. PMID: 1930934 Free article. No abstract available.

5

Marfan syndrome: exclusion of genetic linkage to five genes coding for connective tissue components in the long arm of chromosome 2.

Kainulainen K, Savolainen A, Palotie A, Kaitila I, Rosenbloom J, Peltonen L. Kainulainen K, et al. Hum Genet. 1990 Feb;84(3):233-6. doi: 10.1007/BF00200565. Hum Genet. 1990. PMID: 1968032

6

Location on chromosome 15 of the gene defect causing Marfan syndrome.

Kainulainen K, Pulkkinen L, Savolainen A, Kaitila I, Peltonen L. Kainulainen K, et al. N Engl J Med. 1990 Oct 4;323(14):935-9. doi: 10.1056/NEJM199010043231402. N Engl J Med. 1990. PMID: 2402262 Free article.

7

DNA diagnostics of the Marfan syndrome: application of amplifiable polymorphic markers.

Rantamäki T, Lönnqvist L, Karttunen L, Kainulainen K, Peltonen L. Rantamäki T, et al. Among authors: kainulainen k. Eur J Hum Genet. 1994;2(1):66-75. doi: 10.1159/000472343. Eur J Hum Genet. 1994. PMID: 8044654

8

A novel mutation of the fibrillin gene causing ectopia lentis.

Lönnqvist L, Child A, Kainulainen K, Davidson R, Puhakka L, Peltonen L. Lönnqvist L, et al. Among authors: kainulainen k. Genomics. 1994 Feb;19(3):573-6. doi: 10.1006/geno.1994.1110. Genomics. 1994. PMID: 8188302

9

Two novel fibrillin-1 mutations resulting in premature termination codons but in different mutant transcript levels and clinical phenotypes.

Karttunen L, Ukkonen T, Kainulainen K, Syvänen AC, Peltonen L. Karttunen L, et al. Among authors: kainulainen k. Hum Mutat. 1998;Suppl 1:S34-7. doi: 10.1002/humu.1380110112. Hum Mutat. 1998. PMID: 9452033 No abstract available.

10

Two polymorphisms for the human elastin gene.

Kainulainen K, Rosenbloom J, Peltonen L. Kainulainen K, et al. Nucleic Acids Res. 1990 May 25;18(10):3114. doi: 10.1093/nar/18.10.3114-a. Nucleic Acids Res. 1990. PMID: 1971944 Free PMC article.

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