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Results: 1-25 | 26-35 |
Results: 26-35/35
Single-nucleotide polymorphisms may cause erroneous results in primer-introduced restriction enzyme analyses: a case of molecular misdiagnosis of homozygous vs heterozygous familial hypercholesterolemia
Authors: Vuorio, AF Paulin, L Saltevo, J Kontula, K
Citation: Af. Vuorio et al., Single-nucleotide polymorphisms may cause erroneous results in primer-introduced restriction enzyme analyses: a case of molecular misdiagnosis of homozygous vs heterozygous familial hypercholesterolemia, MOL CELL PR, 13(6), 1999, pp. 421-424
Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects
Authors: Swan, H Viitasalo, M Piippo, K Laitinen, P Kontula, K Toivonen, L
Citation: H. Swan et al., Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects, J AM COL C, 34(3), 1999, pp. 823-829
Angiotensinogen gene M235T polymorphism predicts left ventricular hypertrophy in endurance athletes
Authors: Karjalainen, J Kujala, UM Stolt, A Mantysaari, M Viitasalo, M Kainulainen, K Kontula, K
Citation: J. Karjalainen et al., Angiotensinogen gene M235T polymorphism predicts left ventricular hypertrophy in endurance athletes, J AM COL C, 34(2), 1999, pp. 494-499
Post mortem molecularly defined familial hypercholesterolemia and sudden cardiac death of young men
Authors: Vuorio, AF Kontula, K Turtola, H Sajantila, A
Citation: Af. Vuorio et al., Post mortem molecularly defined familial hypercholesterolemia and sudden cardiac death of young men, FOREN SCI I, 106(2), 1999, pp. 87-92
Genetic association of alpha(2)-macroglobulin with Alzheimer's disease in a Finnish elderly population
Authors: Myllykangas, L Polvikoski, T Sulkava, R Verkkoniemi, A Crook, R Tienari, PJ Pusa, AK Niinisto, L O'Brien, P Kontula, K Hardy, J Haltia, M Perez-Tur, J
Citation: L. Myllykangas et al., Genetic association of alpha(2)-macroglobulin with Alzheimer's disease in a Finnish elderly population, ANN NEUROL, 46(3), 1999, pp. 382-390
Evidence for involvement of the type 1 angiotensin II receptor locus in essential hypertension
Authors: Kainulainen, K Perola, M Terwilliger, J Kaprio, J Koskenvuo, M Syvanen, AC Vartiainen, E Peltonen, L Kontula, K
Citation: K. Kainulainen et al., Evidence for involvement of the type 1 angiotensin II receptor locus in essential hypertension, HYPERTENSIO, 33(3), 1999, pp. 844-849
Association of seropositivity for Chlamydia pneumoniae and coronary arterydisease in heterozygous' familial hypercholesterolaemia
Authors: Kontula, K Vuorio, A Turtola, H Saikku, P
Citation: K. Kontula et al., Association of seropositivity for Chlamydia pneumoniae and coronary arterydisease in heterozygous' familial hypercholesterolaemia, LANCET, 354(9172), 1999, pp. 46-47
Arg506Gln factor V mutation and Val34Leu factor XIII polymorphism in Finnish patients with inflammatory bowel disease
Authors: Helio, T Wartiovaara, U Halme, L Turunen, UM Mikkola, H Palotie, A Farkkila, M Kontula, K
Citation: T. Helio et al., Arg506Gln factor V mutation and Val34Leu factor XIII polymorphism in Finnish patients with inflammatory bowel disease, SC J GASTR, 34(2), 1999, pp. 170-174
Increased risk of acute myocardial infarction in carriers of the hemochromatosis gene Cys282Tyr mutation - A prospective cohort study in men in eastern Finland
Authors: Tuomainen, TP Kontula, K Nyyssonen, K Lakka, TA Helio, T Salonen, JT
Citation: Tp. Tuomainen et al., Increased risk of acute myocardial infarction in carriers of the hemochromatosis gene Cys282Tyr mutation - A prospective cohort study in men in eastern Finland, CIRCULATION, 100(12), 1999, pp. 1274-1279
Functional analysis of the C(-188)A polymorphism of the human leptin promoter
Authors: Oksanen, L Palvimo, JJ Janne, OA Kontula, K
Citation: L. Oksanen et al., Functional analysis of the C(-188)A polymorphism of the human leptin promoter, HUM GENET, 103(4), 1998, pp. 527-528
Risultati: 1-25 | 26-35 |