Kainulainen K - Search Results

1

Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings.

Perola M, Kainulainen K, Pajukanta P, Terwilliger JD, Hiekkalinna T, Ellonen P, Kaprio J, Koskenvuo M, Kontula K, Peltonen L. Perola M, et al. Among authors: kainulainen k. J Hypertens. 2000 Nov;18(11):1579-85. doi: 10.1097/00004872-200018110-00008. J Hypertens. 2000. PMID: 11081770

2

Evidence for involvement of the type 1 angiotensin II receptor locus in essential hypertension.

Kainulainen K, Perola M, Terwilliger J, Kaprio J, Koskenvuo M, Syvänen AC, Vartiainen E, Peltonen L, Kontula K. Kainulainen K, et al. Hypertension. 1999 Mar;33(3):844-9. doi: 10.1161/01.hyp.33.3.844. Hypertension. 1999. PMID: 10082497

3

Angiotensin converting enzyme gene insertion/deletion polymorphism, angiotensinogen gene polymorphisms, family history of hypertension, and childhood blood pressure.

Taittonen L, Uhari M, Kontula K, Kainulainen K, Miettinen H, Turtinen J, Nuutinen M. Taittonen L, et al. Among authors: kainulainen k. Am J Hypertens. 1999 Sep;12(9 Pt 1):858-66. doi: 10.1016/s0895-7061(99)00060-6. Am J Hypertens. 1999. PMID: 10509542

4

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.

5

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.

6

Markers for the gene ob and serum leptin levels in human morbid obesity.

Oksanen L, Ohman M, Heiman M, Kainulainen K, Kaprio J, Mustajoki P, Koivisto V, Koskenvuo M, Jänne OA, Peltonen L, Kontula K. Oksanen L, et al. Among authors: kainulainen k. Hum Genet. 1997 May;99(5):559-64. doi: 10.1007/s004390050406. Hum Genet. 1997. PMID: 9150718

7

Testing of human homologues of murine obesity genes as candidate regions in Finnish obese sib pairs.

Ohman M, Oksanen L, Kainulainen K, Jänne OA, Kaprio J, Koskenvuo M, Mustajoki P, Kontula K, Peltonen L. Ohman M, et al. Among authors: kainulainen k. Eur J Hum Genet. 1999 Feb-Mar;7(2):117-24. doi: 10.1038/sj.ejhg.5200256. Eur J Hum Genet. 1999. PMID: 10196693

8

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

9

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.

10

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.

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