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Results: 1-25 | 26-34
Results: 1-25/34
MOLECULAR-GENETICS OF THE LONG QT SYNDROME - 2 NOVEL MUTATIONS OF THEKVLQT1 GENE AND PHENOTYPIC-EXPRESSION OF THE MUTANT-GENE IN A LARGE KINDRED
Authors: SAARINEN K SWAN H KAINULAINEN K TOIVONEN L VIITASALO M KONTULA K
Citation: K. Saarinen et al., MOLECULAR-GENETICS OF THE LONG QT SYNDROME - 2 NOVEL MUTATIONS OF THEKVLQT1 GENE AND PHENOTYPIC-EXPRESSION OF THE MUTANT-GENE IN A LARGE KINDRED, Human mutation, 11(2), 1998, pp. 158-165
2 NOVEL FIBRILLIN-1 MUTATIONS RESULTING IN PREMATURE TERMINATION CODONS BUT IN DIFFERENT MUTANT TRANSCRIPT LEVELS AND CLINICAL PHENOTYPES
Authors: KARTTUNEN L UKKONEN T KAINULAINEN K SYVANEN AC PELTONEN L
Citation: L. Karttunen et al., 2 NOVEL FIBRILLIN-1 MUTATIONS RESULTING IN PREMATURE TERMINATION CODONS BUT IN DIFFERENT MUTANT TRANSCRIPT LEVELS AND CLINICAL PHENOTYPES, Human mutation, 1998, pp. 34-37
SUPERSYMMETRIC ELECTROWEAK PHASE-TRANSITION - DIMENSIONAL REDUCTION VERSUS EFFECTIVE POTENTIAL
Authors: CLINE JM KAINULAINEN K
Citation: Jm. Cline et K. Kainulainen, SUPERSYMMETRIC ELECTROWEAK PHASE-TRANSITION - DIMENSIONAL REDUCTION VERSUS EFFECTIVE POTENTIAL, Nuclear physics. B, 510(1-2), 1998, pp. 88-102
STRONGLY FIRST-ORDER ELECTROWEAK PHASE-TRANSITION INDUCED BY PRIMORDIAL HYPERMAGNETIC FIELDS
Authors: ELMFORS P ENQVIST K KAINULAINEN K
Citation: P. Elmfors et al., STRONGLY FIRST-ORDER ELECTROWEAK PHASE-TRANSITION INDUCED BY PRIMORDIAL HYPERMAGNETIC FIELDS, Physics letters. Section B, 440(3-4), 1998, pp. 269-274
SUPERSYMMETRIC ELECTROWEAK BARYOGENESIS IN THE WKB APPROXIMATION
Authors: CLINE JM JOYCE M KAINULAINEN K
Citation: Jm. Cline et al., SUPERSYMMETRIC ELECTROWEAK BARYOGENESIS IN THE WKB APPROXIMATION, Physics letters. Section B, 417(1-2), 1998, pp. 79-86
MODEL-INDEPENDENT PREDICTIONS OF BIG-BANG NUCLEOSYNTHESIS FROM HE-4 AND LI-7 - CONSISTENCY AND IMPLICATIONS
Authors: FIELDS BD KAINULAINEN K OLIVE KA THOMAS D
Citation: Bd. Fields et al., MODEL-INDEPENDENT PREDICTIONS OF BIG-BANG NUCLEOSYNTHESIS FROM HE-4 AND LI-7 - CONSISTENCY AND IMPLICATIONS, New astronomy, 1(1), 1997, pp. 77-96
NUCLEOSYNTHESIS LIMITS ON THE MASS OF LONG-LIVED TAU-NEUTRINOS AND MUON-NEUTRINOS
Authors: FIELDS BD KAINULAINEN K OLIVE KA
Citation: Bd. Fields et al., NUCLEOSYNTHESIS LIMITS ON THE MASS OF LONG-LIVED TAU-NEUTRINOS AND MUON-NEUTRINOS, Astroparticle physics, 6(2), 1997, pp. 169-185
MARKERS FOR THE GENE OB AND SERUM LEPTIN LEVELS IN HUMAN MORBID-OBESITY
Authors: OKSANEN L OHMAN M HEIMAN M KAINULAINEN K KAPRIO J MUSTAJOKI P KOIVISTO V KOSKENVUO M JANNE OA PELTONEN L KONTULA K
Citation: L. Oksanen et al., MARKERS FOR THE GENE OB AND SERUM LEPTIN LEVELS IN HUMAN MORBID-OBESITY, Human genetics, 99(5), 1997, pp. 559-564
NOVEL POLYMORPHISM OF THE HUMAN OB GENE PROMOTER IN LEAN AND MORBIDLYOBESE SUBJECTS
Authors: OKSANEN L KAINULAINEN K HEIMAN M MUSTAJOKI P KAUPPINENMAKELIN R KONTULA K
Citation: L. Oksanen et al., NOVEL POLYMORPHISM OF THE HUMAN OB GENE PROMOTER IN LEAN AND MORBIDLYOBESE SUBJECTS, International journal of obesity, 21(6), 1997, pp. 489-494
CANDIDATE GENES FOR HUMAN OBESITY - ASSOCIATION AND SIB-PAIR STUDY
Authors: OKSANEN L OHMAN M KAINULAINEN K MUSTAJOKI P KAPRIO J HEIMAN M KOIVISTO V KOSKENVUO M JANNE OA PELTONEN L KONTULA K
Citation: L. Oksanen et al., CANDIDATE GENES FOR HUMAN OBESITY - ASSOCIATION AND SIB-PAIR STUDY, Diabetologia, 40, 1997, pp. 705-705
VITAMIN-D-RECEPTOR POLYMORPHISM AND TREATMENT OF PSORIASIS WITH CALCIPOTRIOL
Authors: KONTULA K VALIMAKI S KAINULAINEN K VIITANEN AM KESKIOJA J
Citation: K. Kontula et al., VITAMIN-D-RECEPTOR POLYMORPHISM AND TREATMENT OF PSORIASIS WITH CALCIPOTRIOL, British journal of dermatology, 136(6), 1997, pp. 977-978
DYNAMICS OF 2-HIGGS-DOUBLET CP VIOLATION AND BARYOGENESIS AT THE ELECTROWEAK PHASE-TRANSITION
Authors: CLINE JM KAINULAINEN K VISCHER AP
Citation: Jm. Cline et al., DYNAMICS OF 2-HIGGS-DOUBLET CP VIOLATION AND BARYOGENESIS AT THE ELECTROWEAK PHASE-TRANSITION, Physical review. D. Particles and fields, 54(4), 1996, pp. 2451-2472
SUPERSYMMETRIC ELECTROWEAK PHASE-TRANSITION - BEYOND PERTURBATION-THEORY
Authors: CLINE JM KAINULAINEN K
Citation: Jm. Cline et K. Kainulainen, SUPERSYMMETRIC ELECTROWEAK PHASE-TRANSITION - BEYOND PERTURBATION-THEORY, Nuclear physics. B, 482(1-2), 1996, pp. 73-91
POLYMORPHISM OF THE BETA(3)-ADRENERGIC RECEPTOR GENE IN MORBID-OBESITY
Authors: OKSANEN L MUSTAJOKI P KAPRIO J KAINULAINEN K JANNE O PELTONEN L KONTULA K
Citation: L. Oksanen et al., POLYMORPHISM OF THE BETA(3)-ADRENERGIC RECEPTOR GENE IN MORBID-OBESITY, International journal of obesity, 20(12), 1996, pp. 1055-1061
APOE ALLELES IN ALZHEIMERS-DISEASE AND VASCULAR DEMENTIA IN A POPULATION AGED 85+
Authors: SULKAVA R KAINULAINEN K VERKKONIEMI A NIINISTO L SOBEL E DAVANIPOUR Z POLVIKOSKI T HALTIA M KONTULA K
Citation: R. Sulkava et al., APOE ALLELES IN ALZHEIMERS-DISEASE AND VASCULAR DEMENTIA IN A POPULATION AGED 85+, Neurobiology of aging, 17(3), 1996, pp. 373-376
COMMON POLYMORPHISM OF THE VITAMIN-D-RECEPTOR GENE IS ASSOCIATED WITHVARIATION OF PEAK BONE MASS IN YOUNG FINNS
Authors: VIITANEN AM KARKKAINEN M LAITINEN K LAMBERGALLARDT C KAINULAINEN K RASANEN L VIIKARI J VALIMAKI MJ KONTULA K
Citation: Am. Viitanen et al., COMMON POLYMORPHISM OF THE VITAMIN-D-RECEPTOR GENE IS ASSOCIATED WITHVARIATION OF PEAK BONE MASS IN YOUNG FINNS, Calcified tissue international, 59(4), 1996, pp. 231-234
BOUNDS ON DIRAC NEUTRINO MASSES FROM NUCLEOSYNTHESIS
Authors: DOLGOV AD KAINULAINEN K ROTHSTEIN IZ
Citation: Ad. Dolgov et al., BOUNDS ON DIRAC NEUTRINO MASSES FROM NUCLEOSYNTHESIS, Physical review. D. Particles and fields, 51(8), 1995, pp. 4129-4133
PRIMORDIAL BARYON ASYMMETRY AND SPHALERONS
Authors: KAINULAINEN K
Citation: K. Kainulainen, PRIMORDIAL BARYON ASYMMETRY AND SPHALERONS, Nuclear physics. B, 1995, pp. 291-294
DIFFUSION AND DEBYE-SCREENING NEAR EXPANDING DOMAIN-WALLS
Authors: CLINE JM KAINULAINEN K
Citation: Jm. Cline et K. Kainulainen, DIFFUSION AND DEBYE-SCREENING NEAR EXPANDING DOMAIN-WALLS, Physics letters. Section B, 356(1), 1995, pp. 19-25
LINKAGE OF THE LONG QT SYNDROME TO THE SHORT ARM OF CHROMOSOME-11 - USE OF 5 HIGHLY POLYMORPHIC MARKERS TOWARDS MORE DETAILED LOCALIZATION OF THE MUTANT-GENE
Authors: KAINULAINEN K SWAN H MIETTINEN H VIITASALO M ROVAMO L TOIVONEN L KONTULA K
Citation: K. Kainulainen et al., LINKAGE OF THE LONG QT SYNDROME TO THE SHORT ARM OF CHROMOSOME-11 - USE OF 5 HIGHLY POLYMORPHIC MARKERS TOWARDS MORE DETAILED LOCALIZATION OF THE MUTANT-GENE, Human genetics, 96(4), 1995, pp. 395-400
APOLIPOPROTEIN-E, DEMENTIA, AND CORTICAL DEPOSITION OF BETA-AMYLOID PROTEIN
Authors: POLVIKOSKI T SULKAVA R HALTIA M KAINULAINEN K VUORIO A VERKKONIEMI A NIINISTO L HALONEN P KONTULA K
Citation: T. Polvikoski et al., APOLIPOPROTEIN-E, DEMENTIA, AND CORTICAL DEPOSITION OF BETA-AMYLOID PROTEIN, The New England journal of medicine, 333(19), 1995, pp. 1242-1247
LACK OF ASSOCIATION OF APOLIPOPROTEIN-E ALLELE EPSILON-4 WITH LATE-ONSET ALZHEIMERS-DISEASE AMONG FINNISH CENTENARIANS
Authors: SOBEL E LOUHIJA J SULKAVA R DAVANIPOUR Z KONTULA K MIETTINEN H TIKKANEN M KAINULAINEN K TILVIS R
Citation: E. Sobel et al., LACK OF ASSOCIATION OF APOLIPOPROTEIN-E ALLELE EPSILON-4 WITH LATE-ONSET ALZHEIMERS-DISEASE AMONG FINNISH CENTENARIANS, Neurology, 45(5), 1995, pp. 903-907
PREDISPOSING GENES FOR HYPERTENSION - SIBPAIR ANALYSES OF THE GENES OF RENIN-ANGIOTENSIN-ALDOSTERONE (RAA) SYSTEM
Authors: PEROLA M KAINULAINEN K KAPRIO J KOSKENVUO M PELTONEN L KONTULA K
Citation: M. Perola et al., PREDISPOSING GENES FOR HYPERTENSION - SIBPAIR ANALYSES OF THE GENES OF RENIN-ANGIOTENSIN-ALDOSTERONE (RAA) SYSTEM, American journal of human genetics, 57(4), 1995, pp. 1851-1851
MUTATIONS IN THE FIBRILLIN GENE RESPONSIBLE FOR DOMINANT ECTOPIA LENTIS AND NEONATAL MARFAN-SYNDROME
Authors: KAINULAINEN K KARTTUNEN L PUHAKKA L SAKAI L PELTONEN L
Citation: K. Kainulainen et al., MUTATIONS IN THE FIBRILLIN GENE RESPONSIBLE FOR DOMINANT ECTOPIA LENTIS AND NEONATAL MARFAN-SYNDROME, Nature genetics, 6(1), 1994, pp. 64-69
A NOVEL MUTATION OF THE FIBRILLIN GENE CAUSING ECTOPIA LENTIS
Authors: LONNQVIST L CHILD A KAINULAINEN K DAVIDSON R PUHAKKA L PELTONEN L
Citation: L. Lonnqvist et al., A NOVEL MUTATION OF THE FIBRILLIN GENE CAUSING ECTOPIA LENTIS, Genomics, 19(3), 1994, pp. 573-576
Risultati: 1-25 | 26-34