Search Results - "Miettinen, Raija" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland

Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland

by JÄÄSKELÄINEN, Pertti, KUUSISTO, Johanna, MIETTINEN, Raija, KÄRKKÄINEN, Päivi, KÄRKKÄINEN, Satu, HEIKKINEN, Sami, PELTOLA, Paula, PIHLAJAMÄKI, Jussi, VAUHKONEN, Ilkka, LAAKSO, Markku
Published in Journal of molecular medicine (Berlin, Germany) (01.07.2002)

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New Amino Acid Substitutions in the IRS-2 Gene in Finnish and Chinese Subjects With Late-Onset Type 2 Diabetes

New Amino Acid Substitutions in the IRS-2 Gene in Finnish and Chinese Subjects With Late-Onset Type 2 Diabetes

by Wang, Hua, Rissanen, Johanna, Miettinen, Raija, Kärkkäinen, Päivi, Kekäläinen, Päivi, Kuusisto, Johanna, Mykkänen, Leena, Karhapää, Pauli, Laakso, Markku
Published in Diabetes (New York, N.Y.) (01.08.2001)

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Promoter Polymorphisms −359T/C and −303A/G of the Catalytic Subunit p110β Gene of Human Phosphatidylinositol 3-Kinase Are Not Associated With Insulin Secretion or Insulin Sensitivity in Finnish Subjects

Promoter Polymorphisms −359T/C and −303A/G of the Catalytic Subunit p110β Gene of Human Phosphatidylinositol 3-Kinase Are Not Associated With Insulin Secretion or Insulin Sensitivity in Finnish Subjects

by Kossila, Maija, Pihlajamaki, Jussi, Karkkainen, Paivi, Miettinen, Raija, Kekalainen, Paivi, Vauhkonen, Ilkka, Yla-Herttuala, Seppo, Laakso, Markku
Published in Diabetes care (01.01.2003)

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Mitral valve prolapse and mitral regurgitation are common in patients with polycystic kidney disease type 1

Mitral valve prolapse and mitral regurgitation are common in patients with polycystic kidney disease type 1

by Lumiaho, A, Ikäheimo, R, Miettinen, R, Niemitukia, L, Laitinen, T, Rantala, A, Lampainen, E, Laakso, M, Hartikainen, J
Published in American journal of kidney diseases (01.12.2001)

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A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy

A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy

by Kärkkäinen, Satu, Heliö, Tiina, Miettinen, Raija, Tuomainen, Petri, Peltola, Paula, Rummukainen, Juha, Ylitalo, Kari, Kaartinen, Maija, Kuusisto, Johanna, Toivonen, Lauri, Nieminen, Markku S, Laakso, Markku, Peuhkurinen, Keijo
Published in European heart journal (01.05.2004)

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Genetics of hypertrophic cardiomyopathy in eastern Finland: few founder mutations with benign or intermediary phenotypes

Genetics of hypertrophic cardiomyopathy in eastern Finland: few founder mutations with benign or intermediary phenotypes

by Jääskeläinen, Pertti, Miettinen, Raija, Kärkkäinen, Päivi, Toivonen, Lauri, Laakso, Markku, Kuusisto, Johanna
Published in Annals of medicine (Helsinki) (2004)

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Genetics and phenotypic characteristics of autosomal dominant polycystic kidney disease in Finns

Genetics and phenotypic characteristics of autosomal dominant polycystic kidney disease in Finns

by PELTOLA, Paula, LUMIAHO, Anne, MIETTINEN, Raija, PIHLAJAMÄKI, Jussi, SANDFORD, Richard, LAAKSO, Markku
Published in Journal of molecular medicine (Berlin, Germany) (01.08.2005)

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Two novel mutations in the β-myosin heavy chain gene associated with dilated cardiomyopathy

Two novel mutations in the β-myosin heavy chain gene associated with dilated cardiomyopathy

by Kärkkäinen, Satu, Heliö, Tiina, Jääskeläinen, Pertti, Miettinen, Raija, Tuomainen, Petri, Ylitalo, Kari, Kaartinen, Maija, Reissell, Eeva, Toivonen, Lauri, Nieminen, Markku S., Kuusisto, Johanna, Laakso, Markku, Peuhkurinen, Keijo
Published in European journal of heart failure (01.12.2004)

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No variants in the cardiac actin gene in Finnish patients with dilated or hypertrophic cardiomyopathy

No variants in the cardiac actin gene in Finnish patients with dilated or hypertrophic cardiomyopathy

by Kärkkäinen, Satu, Peuhkurinen, Keijo, Jääskeläinen, Pertti, Miettinen, Raija, Kärkkäinen, Päivi, Kuusisto, Johanna, Laakso, Markku
Published in The American heart journal (01.06.2002)

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Insulin resistance is related to left ventricular hypertrophy in patients with polycystic kidney disease type 1

Insulin resistance is related to left ventricular hypertrophy in patients with polycystic kidney disease type 1

by Lumiaho, Anne, Pihlajamäki, Jussi, Hartikainen, Juha, Ikäheimo, Risto, Miettinen, Raija, Niemitukia, Lea, Lampainen, Erkki, Laakso, Markku
Published in American journal of kidney diseases (01.06.2003)

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Promoter polymorphisms -359T/C and -303A/G of the catalytic subunit p110(beta) gene of human phosphatidylinositol 3-kinase are not associated with insulin secretion or insulin sensitivity in Finnish subjects

Promoter polymorphisms -359T/C and -303A/G of the catalytic subunit p110(beta) gene of human phosphatidylinositol 3-kinase are not associated with insulin secretion or insulin sensitivity in Finnish subjects

by Kossila, Maija, Pihlajamaki, Jussi, Karkkainen, Paivi, Miettinen, Raija
Published in Diabetes care (01.01.2003)

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A novel mutation, Arg71Thr, in the δ-sarcoglycan gene is associated with dilated cardiomyopathy

A novel mutation, Arg71Thr, in the δ-sarcoglycan gene is associated with dilated cardiomyopathy

by KÄRKKÄINEN, Satu, MIETTINEN, Raija, LAAKSO, Markku, PEUHKURINEN, Keijo, TUOMAINEN, Petri, KÄRKKÄINEN, Päivi, HELIÖ, Tiina, REISSELL, Eeva, KAARTINEN, Maija, TOIVONEN, Lauri, NIEMINEN, Markku S, KUUSISTO, Johanna
Published in Journal of molecular medicine (Berlin, Germany) (01.12.2003)

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The Pro12Ala substitution in the peroxisome proliferator activated receptor gamma 2 is associated with an insulin-sensitive phenotype in families with familial combined hyperlipidemia and in nondiabetic elderly subjects with dyslipidemia

The Pro12Ala substitution in the peroxisome proliferator activated receptor gamma 2 is associated with an insulin-sensitive phenotype in families with familial combined hyperlipidemia and in nondiabetic elderly subjects with dyslipidemia

by Pihlajamäki, Jussi, Miettinen, Raija, Valve, Raisa, Karjalainen, Leena, Mykkänen, Leena, Kuusisto, Johanna, Deeb, Samir, Auwerx, Johan, Laakso, Markku
Published in Atherosclerosis (01.08.2000)

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Apolipoprotein E gene promoter (-219G/T) polymorphism is associated with premature coronary heart disease

Apolipoprotein E gene promoter (-219G/T) polymorphism is associated with premature coronary heart disease

by VIITANEN, Laura, PIHLAJAMÄKI, Jussi, MIETTINEN, Raija, KÄRKKÄINEN, Päivi, VAUHKONEN, Ilkka, HALONEN, Pirjo, KAREINEN, Anu, LEHTO, Seppo, LAAKSO, Markku
Published in Journal of molecular medicine (Berlin, Germany) (01.12.2001)

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The cardiac β-myosin heavy chain gene is not the predominant gene for hypertrophic cardiomyopathy in the Finnish population

The cardiac β-myosin heavy chain gene is not the predominant gene for hypertrophic cardiomyopathy in the Finnish population

by Jääskeläinen, Pertti, Soranta, Marja, Miettinen, Raija, Saarinen, Laura, Pihlajamäki, Jussi, Silvennoinen, Karoliina, Tikanoja, Tero, Laakso, Markku, Kuusisto, Johanna
Published in Journal of the American College of Cardiology (15.11.1998)

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Variants in the hepatocyte nuclear factor-1(alpha) and -4(alpha) genes in Finnish and Chinese subjects with late-onset type 2 diabetes

Variants in the hepatocyte nuclear factor-1(alpha) and -4(alpha) genes in Finnish and Chinese subjects with late-onset type 2 diabetes

by Rissanen, Johanna, Wang, Hua, Miettinen, Raija, Karkkainen, Paivi
Published in Diabetes care (01.10.2000)

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No variants in the cardiac actin gene in Finnish patients with dilated or hypertrophic cardiomyopathy

No variants in the cardiac actin gene in Finnish patients with dilated or hypertrophic cardiomyopathy

by Kärkkäinen, Satu, Peuhkurinen, Keijo, Jääskeläinen, Pertti, Miettinen, Raija, Kärkkäinen, Päivi, Kuusisto, Johanna, Laakso, Markku
Published in The American heart journal (01.06.2002)

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Promoter polymorphisms -359T/C and -303A/G of the catalytic subunit p110beta gene of human phosphatidylinositol 3-kinase are not associated with insulin secretion or insulin sensitivity in finnish subjects

Promoter polymorphisms -359T/C and -303A/G of the catalytic subunit p110beta gene of human phosphatidylinositol 3-kinase are not associated with insulin secretion or insulin sensitivity in finnish subjects

by Kossila, Maija, Pihlajamäki, Jussi, Kärkkäinen, Päivi, Miettinen, Raija, Kekäläinen, Päivi, Vauhkonen, Ilkka, Ylä-Herttuala, Seppo, Laakso, Markku
Published in Diabetes care (01.01.2003)

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Variants in the hepatocyte nuclear factor-1α and -4α genes in Finnish and Chinese subjects with late-onset type 2 diabetes

Variants in the hepatocyte nuclear factor-1α and -4α genes in Finnish and Chinese subjects with late-onset type 2 diabetes

by RISSANEN, Johanna, HUA WANG, LAAKSO, Markku, MIETTINEN, Raija, KARKKAINEN, Paivi, KEKÄLÄINEN, Päivi, MYKKÄNEN, Leena, KUUSISTO, Johanna, KARHAPÄÄ, Pauli, NISKANEN, Leo, UUSITUPA, Matti
Published in Diabetes care (01.10.2000)

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Promoter polymorphisms -359T/C and -303A/G of the catalytic subunit p110β gene of human phospatidylinositol 3-kinase are not associated with insulin secretion or insulin sensitivity in Finnish subjects

Promoter polymorphisms -359T/C and -303A/G of the catalytic subunit p110β gene of human phospatidylinositol 3-kinase are not associated with insulin secretion or insulin sensitivity in Finnish subjects

by KOSSILA, Maija, PIHLAJAMÄKI, Jussi, KÄRKKÄINEN, Päivi, MIETTINEN, Raija, KEKÄLÄINEN, Päivi, VAUHKONEN, Ilkka, YLÄ-HERTTUALA, Seppo, LAAKSO, Markku
Published in Diabetes care (2003)

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