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    1. Ekelund, J; Suhonen, J; Jarvelin, MR; Peltonen, L; Lichtermann, D
      No association of the-521 C/T polymorphism in the promoter of DRD4 with novelty seeking

      MOLECULAR PSYCHIATRY
    2. Feng, J; Zheng, J; Gelernter, J; Kranzler, H; Cook, E; Goldman, D; Jones, IR; Craddock, N; Heston, LL; Delisi, L; Peltonen, L; Bennett, WP; Sommer, SS
      An in-frame deletion in the alpha(2C) adrenergic receptor is common in African-Americans

      MOLECULAR PSYCHIATRY
    3. Peltonen, L; Karjalainen, M; Hirvonen, J; Yliruusi, J
      Four sorbitan monoesters: XRDP and DSC studies on bulk material and ellipsometric studies on Langmuir-Blodgett monolayers

      STP PHARMA SCIENCES
    4. Johansson, C; Smedh, C; Partonen, T; Pekkarinen, P; Paunio, T; Ekholm, J; Peltonen, L; Lichtermann, D; Palmgren, J; Adolfsson, R; Schalling, M
      Seasonal affective disorder and serotonin-related polymorphisms

      NEUROBIOLOGY OF DISEASE
    5. Saarela, J; Laine, M; Oinonen, C; von Schantz, C; Jalanko, A; Rouvinen, J; Peltonen, L
      Molecular pathogenesis of a disease: structural consequences of aspartylglucosaminuria mutations

      HUMAN MOLECULAR GENETICS
    6. Ekelund, J; Hovatta, I; Parker, A; Paunio, T; Varilo, T; Martin, R; Suhonen, J; Ellonen, P; Chan, GY; Sinsheimer, JS; Sobel, E; Juvonen, H; Arajarvi, R; Partonen, T; Suvisaari, J; Lonnqvist, J; Meyer, J; Peltonen, L
      Chromosome 1 loci in Finnish schizophrenia families

      HUMAN MOLECULAR GENETICS
    7. Pajukanta, P; Bodnar, JS; Sallinen, R; Chu, M; Airaksinen, T; Xiao, QN; Castellani, LW; Sheth, SS; Wessman, M; Palotie, A; Sinsheimer, JS; Demant, P; Lusis, AJ; Peltonen, L
      Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL

      MAMMALIAN GENOME
    8. Feng, JN; Yan, J; Michaud, S; Craddock, N; Jones, IR; Cook, EH; Goldman, D; Heston, LL; Peltonen, L; Delisi, LE; Sommer, SS
      Scanning of estrogen receptor alpha (ER alpha) and thyroid hormone receptor alpha (TR alpha) genes in patients with psychiatric diseases: Four missense mutations identified in ER alpha gene

      AMERICAN JOURNAL OF MEDICAL GENETICS
    9. Gong, YQ; Slee, RB; Fukai, N; Rawadi, G; Roman-Roman, S; Reginato, AM; Wang, HW; Cundy, T; Glorieux, FH; Lev, D; Zacharin, M; Oexle, K; Marcelino, J; Suwairi, W; Heeger, S; Sabatakos, G; Apte, S; Adkins, WN; Allgrove, J; Arslan-Kirchner, M; Batch, JA; Beighton, P; Black, GCM; Boles, RG; Boon, LM; Borrone, C; Brunner, HG; Carle, GF; Dallapiccola, B; De Paepe, A; Floege, B; Halfhide, ML; Hall, B; Hennekam, RC; Hirose, T; Jans, A; Juppner, H; Kim, CA; Keppler-Noreuil, K; Kohlschuetter, A; LaCombe, D; Lambert, M; Lemyre, E; Letteboer, T; Peltonen, L; Ramesar, RS; Romanengo, M; Somer, H; Steichen-Gersdorf, E; Steinmann, B; Sullivan, B; Superti-Furga, A; Swoboda, W; van den Boogaard, MJ; Van Hul, V; Vikkula, M; Votruba, M; Zabel, B; Garcia, T; Baron, R; Olsen, BR; Warman, ML
      LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development

      CELL
    10. Peltonen, L; McKusick, VA
      Genomics and medicine - Dissecting human disease in the postgenomic era

      SCIENCE
    11. Haravuori, H; Vihola, A; Straub, V; Auranen, M; Richard, I; Marchand, S; Voit, T; Labeit, S; Somer, H; Peltonen, L; Beckmann, JS; Udd, B
      Secondary calpain3 deficiency in 2q-linked muscular dystrophy - Titin is the candidate gene

      NEUROLOGY
    12. Auranen, M; Vanhala, R; Vosman, M; Levander, M; Varilo, T; Hietala, M; Riikonen, R; Peltonen, L; Jarvela, I
      MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features

      NEUROLOGY
    13. Halonen, M; Pelto-Huikko, M; Eskelin, P; Peltonen, L; Ulmanen, I; Kolmer, M
      Subcellular location and expression pattern of autoimmune regulator (Aire), the mouse orthologue for human gene defective in autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED)

      JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY
    14. Peltonen, L; Hirvonen, J; Yliruusi, J
      The behavior of sorbitan surfactants at the water-oil interface: Straight-chained hydrocarbons from pentane to dodecane as an oil phase

      JOURNAL OF COLLOID AND INTERFACE SCIENCE
    15. Peltonen, L; Hirvonen, J; Yliruusi, J
      The effect of temperature on sorbitan surfactant monolayers

      JOURNAL OF COLLOID AND INTERFACE SCIENCE
    16. Lichtermann, D; Ekelund, J; Peltonen, L; Jarvelin, MR
      Genetic architecture of temperament

      AMERICAN JOURNAL OF PSYCHIATRY
    17. Perola, M; Ohman, M; Hiekkalinna, T; Leppavuori, J; Pajukanta, P; Wessman, M; Koskenvuo, M; Palotie, A; Lange, K; Kaprio, J; Peltonen, L
      Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups

      AMERICAN JOURNAL OF HUMAN GENETICS
    18. Peltonen, L; Palotie, A; Lange, K
      Use of population isolates for mapping complex traits

      NATURE REVIEWS GENETICS
    19. Auranen, M; Nieminen, T; Majuri, S; Vanhala, R; Peltonen, L; Jarvela, I
      Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q,13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families

      MOLECULAR PSYCHIATRY
    20. Peltonen, L; Kontturi, K; Hirvonen, J; Sundholm, G; Yliruusi, J
      The effect of hydroxypropyl methylcellulose, microcrystalline cellulose and lactose on the dissolution kinetics of acetylsalicylic acid: on-line pH-titration

      STP PHARMA SCIENCES
    21. Heinonen, O; Kyttala, A; Lehmus, E; Paunio, T; Peltonen, L; Jalanko, A
      Expression of palmitoyl protein thioesterase in neurons

      MOLECULAR GENETICS AND METABOLISM
    22. Pastinen, T; Raitio, M; Lindroos, K; Tainola, P; Peltonen, L; Syvanen, AC
      A system for specific, high-throughput genotyping by allele-specific primer extension on microarrays

      GENOME RESEARCH
    23. Mustajoki, S; Laine, M; Lahtela, M; Mustajoki, P; Peltonen, L; Kauppinen, R
      Acute intermittent porphyria: Expression of mutant and wild-type porphobilinogen deaminase in COS-1 cells

      MOLECULAR MEDICINE
    24. Paloneva, J; Kestila, M; Wu, J; Salminen, A; Bohling, T; Ruotsalainen, V; Hakola, P; Bakker, ABH; Phillips, JH; Pekkarinen, P; Lanier, LL; Timonen, T; Peltonen, L
      Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts

      NATURE GENETICS
    25. Salonen, T; Jarvela, I; Peltonen, L; Jalanko, A
      Detection of eight novel palmitoyl protein thioesterase (PPT) mutations underlying infantile neuronal ceroid lipofuscinosis (INCL;CLN1)

      HUMAN MUTATION
    26. Varilo, T; Laan, M; Hovatta, I; Wiebe, V; Terwilliger, JD; Peltonen, L
      Linkage disequilibrium in isolated populations: Finland and a young sub-population of Kuusamo

      EUROPEAN JOURNAL OF HUMAN GENETICS
    27. Ekelund, J; Lichtermann, D; Hovatta, L; Ellonen, P; Suvisaari, J; Terwilliger, JD; Juvonen, H; Varilo, T; Arajarvi, R; Kokko-Sahin, ML; Lonnqvist, J; Peltonen, L
      Genome-wide scan for schizophrenia in the Finnish population: evidence fora locus on chromosome 7q22

      HUMAN MOLECULAR GENETICS
    28. Peltonen, L; Savukoski, M; Vesa, J
      Genetics of the neuronal ceroid lipofuscinoses

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    29. Peltonen, L; Arieli, Y; Harjula, R; Pyornila, A; Marder, J
      Local cutaneous water barrier in cold- and heat-acclimated pigeons (Columba livia) in relation to cutaneous water evaporation

      JOURNAL OF MORPHOLOGY
    30. Mikkelsson, J; Perola, M; Wartiovaara, U; Peltonen, L; Palotie, A; Penttila, A; Karhunen, PJ
      Plasminogen activator inhibitor-1 (PAI-1) 4G/5G polymorphism, coronary thrombosis, and myocardial infarction in middle-aged Finnish men who died suddenly

      THROMBOSIS AND HAEMOSTASIS
    31. Perola, M; Kainulainen, K; Pajukanta, P; Terwilliger, JD; Hiekkalinna, T; Ellonen, P; Kaprio, J; Koskenvuo, M; Kontula, K; Peltonen, L
      Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings

      JOURNAL OF HYPERTENSION
    32. Kaukonen, J; Juselius, JK; Tiranti, V; Kyttala, A; Zeviani, M; Comi, GP; Keranen, S; Peltonen, L; Suomalainen, A
      Role of adenine nucleotide translocator 1 in mtDNA maintenance

      SCIENCE
    33. Holmberg, V; Lauronen, L; Autti, T; Santavuori, P; Savukoski, M; Uvebrant, F; Hofman, I; Peltonen, L; Jarvela, I
      Phenotype-genotype correlation in eight patients with Finnish variant lateinfantile NCL (CLN5)

      NEUROLOGY
    34. Heinonen, O; Salonen, T; Jalanko, A; Peltonen, L; Copp, A
      CLN-1 and CLN-5, genes for infantile and variant late infantile neuronal ceroid lipofuscinoses, are expressed in the embryonic human brain

      JOURNAL OF COMPARATIVE NEUROLOGY
    35. Ohman, M; Oksanen, L; Kaprio, J; Koskenvuo, M; Mustajoki, P; Rissanen, A; Salmi, J; Kontula, K; Peltonen, L
      Genome-wide scan of obesity in Finnish sibpairs reveals linkage to chromosome Xq24

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    36. Lindqvist, AK; Lahdetie, J; Tienari, PJ; Wikstrom, J; Palo, J; Allen, M; Peltonen, L; Gyllensten, U
      Mapping of the HLA class II susceptibility haplotype for multiple sclerosis in Finland

      HEREDITAS
    37. Ekelund, J; Lichtermann, D; Peltonen, L
      The dopamine D-4 receptor gene and novelty seeking - Dr. Ekelund and colleagues reply

      AMERICAN JOURNAL OF PSYCHIATRY
    38. Pajukanta, P; Cargill, M; Viitanen, L; Nuotio, I; Kareinen, A; Perola, M; Terwilliger, JD; Kempas, E; Day, M; Lilja, H; Rioux, JD; Brettin, T; Viikari, JSA; Ronnemaa, T; Laakso, M; Lander, ES; Peltonen, L
      Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland

      AMERICAN JOURNAL OF HUMAN GENETICS
    39. Aula, N; Salomaki, P; Timonen, R; Verheijen, F; Mancini, G; Mansson, JE; Aula, P; Peltonen, L
      The spectrum of SLC17A5-gene mutations resulting in free sialic acid-storage diseases indicates some genotype-phenotype correlation

      AMERICAN JOURNAL OF HUMAN GENETICS
    40. Virolainen, E; Wessman, M; Hovatta, I; Niemi, KM; Ignatius, J; Kere, J; Peltonen, L; Palotie, A
      Assignment of a novel locus for autosomal recessive congenital ichthyosis chromosome 19p13.1-p13.2

      AMERICAN JOURNAL OF HUMAN GENETICS
    41. Bjorses, P; Halonen, M; Palvimo, JJ; Kolmer, M; Aaltonen, J; Ellonen, P; Perheentupa, J; Ulmanen, I; Peltonen, L
      Mutations in the AIRE gene: Effects on subcellular location and transactivation function of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy protein

      AMERICAN JOURNAL OF HUMAN GENETICS
    42. Peltonen, L
      Positional cloning of disease genes: Advantages of genetic isolates

      HUMAN HEREDITY
    43. Uusitalo, A; Tenhunen, K; Heinonen, O; Hiltunen, JO; Saarma, M; Haltia, M; Jalanko, A; Peltonen, L
      Toward understanding the neuronal pathogenesis of aspartylglucosaminuria: Expression of aspartylglucosaminidase in brain during development

      MOLECULAR GENETICS AND METABOLISM
    44. Klockars, T; Savukoski, M; Isosomppi, J; Peltonen, L
      Positional cloning of the CLN5 gene defective in the Finnish variant of the LINCL

      MOLECULAR GENETICS AND METABOLISM
    45. Paavola, P; Avela, K; Horelli-Kuitunen, N; Barlund, M; Kallioniemi, A; Idanheimo, N; Kyttala, M; de la Chapelle, A; Palotie, A; Lehesjoki, AE; Peltonen, L
      High-resolution physical and genetic mapping of the critical region for Meckel syndrome and Mulibrey Nanism on chromosome 17q22-q23

      GENOME RESEARCH
    46. Horelli-Kuitunen, N; Aaltonen, J; Yaspo, ML; Eeva, M; Wessman, M; Peltonen, L; Palotie, A
      Mapping ESTs by fiber-FISH

      GENOME RESEARCH
    47. Verheijen, FW; Verbeek, E; Aula, N; Beerens, CEMT; Havelaar, AC; Joosse, M; Peltonen, L; Aula, P; Galjaard, H; van der Spek, PJ; Mancini, GMS
      A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases

      NATURE GENETICS
    48. Ohman, M; Oksanen, L; Kainulainen, K; Janne, OA; Kaprio, J; Koskenvuo, M; Mustajoki, P; Kontula, K; Peltonen, L
      Testing of human homologues of murine obesity genes as candidate regions in Finnish obese sib pairs

      EUROPEAN JOURNAL OF HUMAN GENETICS
    49. Bjorses, P; Pelto-Huikko, M; Kaukonen, J; Aaltonen, J; Peltonen, L; Ulmanen, I
      Localization of the APECED protein in distinct nuclear structures

      HUMAN MOLECULAR GENETICS
    50. Peltonen, L; Jalanko, A; Varilo, T
      Molecular genetics of the Finnish disease heritage

      HUMAN MOLECULAR GENETICS
    51. Aouizerat, BE; Allayee, H; Bodnar, J; Krass, KL; Peltonen, L; de Bruin, TWA; Rotter, JI; Lusis, AJ
      Novel genes for familial combined hyperlipidemia

      CURRENT OPINION IN LIPIDOLOGY
    52. Santavuori, P; Gottlob, I; Haltia, M; Rapola, J; Lake, BD; Tyynela, J; Peltonen, L
      Infantile and other types of NCL with GROD

      NEURONAL CEROID LIPOFUSCINOSES (BATTEN DISEASE)
    53. Santavuori, P; Rapola, J; Haltia, M; Tyynela, J; Peltonen, L; Mole, SE
      Finnish variant late infantile NCL

      NEURONAL CEROID LIPOFUSCINOSES (BATTEN DISEASE)
    54. Gecz, J; Barnett, S; Liu, JJ; Hollway, G; Donnelly, A; Eyre, H; Eshkevari, HS; Baltazar, R; Grunn, A; Nagaraja, R; Gilliam, C; Peltonen, L; Sutherland, GR; Baron, M; Mulley, JC
      Characterization of the human glutamate receptor subunit 3 gene (GRIA3), acandidate for bipolar disorder and nonspecific X-linked mental retardation

      GENOMICS
    55. Paavola, P; Horelli-Kuitunen, N; Palotie, A; Peltonen, L
      Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome gene

      GENOMICS
    56. Klockars, T; Holmberg, V; Savukoski, M; Lander, ES; Peltonen, L
      Transcript identification on the CLN5 region on chromosome 13q22

      HUMAN GENETICS
    57. Laine, M; Richter, J; Fahlman, C; Rapola, J; Renlund, M; Peltonen, L; Karlsson, S; Jalanko, A
      Correction of peripheral lysosomal accumulation in mice with aspartylglucosaminuria by bone marrow transplantation

      EXPERIMENTAL HEMATOLOGY
    58. Kainulainen, K; Perola, M; Terwilliger, J; Kaprio, J; Koskenvuo, M; Syvanen, AC; Vartiainen, E; Peltonen, L; Kontula, K
      Evidence for involvement of the type 1 angiotensin II receptor locus in essential hypertension

      HYPERTENSION
    59. Isosomppi, J; Heinonen, O; Hiltunen, JO; Greene, NDE; Vesa, J; Uusitalo, A; Mitchison, HM; Saarma, M; Jalanko, A; Peltonen, L
      Developmental expression of palmitoyl protein thioesterase in normal mice

      DEVELOPMENTAL BRAIN RESEARCH
    60. Souery, D; Lipp, O; Rivelli, SK; Massat, I; Serretti, A; Cavallini, C; Ackenheil, M; Adolfsson, R; Aschauer, H; Blackwood, D; Dam, H; Dikeos, D; Fuchshuber, S; Heiden, M; Jakovljevic, M; Kaneva, R; Kessing, L; Lerer, B; Lonnqvist, J; Mellerup, T; Milanova, V; Muir, W; Nylander, PO; Oruc, L; Papadimitriou, GN; Pekkarinen, P; Peltonen, L; Pull, C; Raeymaekers, P; Shapira, B; Smeraldi, E; Staner, L; Stefanis, C; Verga, M; Verheyen, G; Macciardi, F; Van Broeckhoven, C; Mendlewicz, J
      Tyrosine hydroxylase polymorphism and phenotypic heterogeneity in bipolar affective disorder: A multicenter association study

      AMERICAN JOURNAL OF MEDICAL GENETICS
    61. Wartiovaara, U; Perola, M; Mikkola, H; Totterman, K; Savolainen, V; Penttila, A; Grant, PJ; Tikkanen, MJ; Vartiainen, E; Karhunen, PJ; Peltonen, L; Palotie, A
      Association of FXIII Val34Leu with decreased risk of myocardial infarctionin Finnish males

      ATHEROSCLEROSIS
    62. Kangas, H; Ulmanen, I; Paunio, T; Kwiatkowski, DJ; Lehtovirta, M; Jalanko, A; Peltonen, L
      Functional consequences of amyloidosis mutation for gelsolin polypeptide -analysis of gelsolin-actin interaction and gelsolin processing in gelsolinknock-out fibroblasts

      FEBS LETTERS
    63. Ekelund, J; Lichtermann, D; Jarvelin, MR; Peltonen, L
      Association between novelty seeking and the type 4 dopamine receptor gene in a large Finnish cohort sample

      AMERICAN JOURNAL OF PSYCHIATRY
    64. Leppavuori, J; Kujala, U; Kinnunen, J; Kaprio, J; Nissila, M; Heliovaara, M; Klinger, N; Partanen, J; Terwilliger, JD; Peltonen, L
      Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis: Evidence for a locus on 2q

      AMERICAN JOURNAL OF HUMAN GENETICS
    65. Visapaa, I; Salonen, R; Varilo, T; Paavola, P; Peltonen, L
      Assignment of the locus for hydrolethalus syndrome to a highly restricted region on 11q23-25

      AMERICAN JOURNAL OF HUMAN GENETICS
    66. Hovatta, I; Varilo, T; Suvisaari, J; Terwilliger, JD; Ollikainen, V; Arajarvi, R; Juvonen, H; Kokko-Sahin, ML; Vaisanen, L; Mannila, H; Lonnqvist, J; Peltonen, L
      A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci

      AMERICAN JOURNAL OF HUMAN GENETICS
    67. Kaukonen, J; Zeviani, M; Comi, GP; Piscaglia, MG; Peltonen, L; Suomalainen, A
      A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegia

      AMERICAN JOURNAL OF HUMAN GENETICS
    68. Pajukanta, P; Terwilliger, JD; Perola, M; Hiekkalinna, T; Nuotio, I; Ellonen, P; Parkkonen, M; Hartiala, J; Ylitalo, K; Pihlajamaki, J; Porkka, K; Laakso, M; Viikari, J; Ehnholm, C; Taskinen, MR; Peltonen, L
      Genomewide scan for familial combined hyperlipidemia genes in Finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels

      AMERICAN JOURNAL OF HUMAN GENETICS
    69. Rantamaki, T; Kaitila, I; Syvanen, AC; Lukka, M; Peltonen, L
      Recurrence of Marfan syndrome as a result of parental germ-line mosaicism for an FBN1 mutation

      AMERICAN JOURNAL OF HUMAN GENETICS
    70. HOVATTA I; LICHTERMANN D; JUVONEN H; SUVISAARI J; TERWILLIGER JD; ARAJARVI R; KOKKOSAHIN ML; EKELUND J; LONNQVIST J; PELTONEN L
      LINKAGE ANALYSIS OF PUTATIVE SCHIZOPHRENIA GENE CANDIDATE REGIONS ON CHROMOSOMES 3P, 5Q, 6P, 8P, 20P AND 22Q IN A POPULATION-BASED SAMPLED FINNISH FAMILY SET

      Molecular psychiatry
    71. KESTILA M; LENKKERI U; MANNIKKO M; LAMERDIN J; MCCREADY P; PUTAALA H; RUOTSALAINEN V; MORITA T; NISSINEN M; HERVA R; KASHTAN CE; PELTONEN L; HOLMBERG C; OLSEN A; TRYGGVASON K
      POSITIONALLY CLONED GENE FOR A NOVEL GLOMERULAR PROTEIN - NEPHRIN - IS MUTATED IN CONGENITAL NEPHROTIC SYNDROME

      MOLECULAR CELL
    72. TAHVANAINEN E; PAJUKANTA P; PORKKA K; NIEMINEN S; IKAVALKO L; NUOTIO I; TASKINEN MR; PELTONEN L; EHNHOLM C
      HAPLOTYPES OF THE APOA-I C-III/A-IV GENE-CLUSTER AND FAMILIAL COMBINED HYPERLIPIDEMIA/

      Arteriosclerosis, thrombosis, and vascular biology
    73. SAVUKOSKI M; KLOCKARS T; HOLMBERG V; SANTAVUORI P; LANDER ES; PELTONEN L
      CLN5, A NOVEL GENE ENCODING A PUTATIVE TRANSMEMBRANE PROTEIN MUTATED IN FINNISH VARIANT LATE INFANTILE NEURONAL CEROID-LIPOFUSCINOSIS

      Nature genetics
    74. PAJUKANTA P; NUOTIO I; TERWILLIGER JD; PORKKA KVK; YLITALO K; PIHLAJAMAKI J; SUOMALAINEN AJ; SYVANEN AC; LEHTIMAKI T; VIIKARI JSA; LAAKSO M; TASKINEN MR; EHNHOLM C; PELTONEN L
      LINKAGE OF FAMILIAL COMBINED HYPERLIPIDEMIA TO CHROMOSOME 1Q21-Q23

      Nature genetics
    75. KARTTUNEN L; UKKONEN T; KAINULAINEN K; SYVANEN AC; PELTONEN L
      2 NOVEL FIBRILLIN-1 MUTATIONS RESULTING IN PREMATURE TERMINATION CODONS BUT IN DIFFERENT MUTANT TRANSCRIPT LEVELS AND CLINICAL PHENOTYPES

      Human mutation
    76. SALONEN T; HELLSTEN E; HORELLIKUITUNEN N; PELTONEN L; JALANKO A
      MOUSE PALMITOYL PROTEIN THIOESTERASE - GENE STRUCTURE AND EXPRESSION OF CDNA

      PCR methods and applications
    77. AVELA K; PAAVOLA P; HORELLIKUITUNEN N; BARLUND M; KALLIONIEMI A; DELACHAPELLE A; PALOTIE A; LEHESJOKI AE; PELTONEN L
      CONSTRUCTION OF A PHYSICAL MAP IN THE MECKEL-SYNDROME AND MULIBREY NANISM CRITICAL REGION ON CHROMOSOME 17Q22

      European journal of human genetics
    78. PELTOLA M; KYTTALA A; HEINONEN O; RAPOLA J; PAUNIO T; REVAH F; PELTONEN L; JALANKO A
      ADENOVIRUS-MEDIATED GENE-TRANSFER RESULTS IN DECREASED LYSOSOMAL STORAGE IN BRAIN AND TOTAL CORRECTION IN LIVER OF ASPARTYLGLUCOSAMINURIA (AGU) MOUSE

      Gene therapy
    79. PASTINEN T; PEROLA M; NIINI P; TERWILLIGER J; SALOMAA V; VARTIAINEN E; PELTONEN L; SYVANEN AC
      ARRAY-BASED MULTIPLEX ANALYSIS OF CANDIDATE GENES REVEALS 2 INDEPENDENT AND ADDITIVE GENETIC RISK-FACTORS FOR MYOCARDIAL-INFARCTION IN THE FINNISH POPULATION

      Human molecular genetics (Print)
    80. LIBERT F; COCHAUX P; BECKMAN G; SAMSON M; AKSENOVA M; CAO A; CZEIZEL A; CLAUSTRES M; DELARUA C; FERRARI M; FERREC C; GLOVER G; GRINDE B; GURAN S; KUCINSKAS V; LAVINHA J; MERCIER B; OGUR G; PELTONEN L; ROSATELLI C; SCHWARTZ M; SPITSYN V; TIMAR L; BECKMAN L; PARMENTIER M; VASSART G
      THE DELTA-CCR5 MUTATION CONFERRING PROTECTION AGAINST HIV-1 IN CAUCASIAN POPULATIONS HAS A SINGLE AND RECENT ORIGIN IN NORTHEASTERN EUROPE

      Human molecular genetics
    81. JALANKO A; TENHUNEN K; MCKINNEY CE; LAMARCA ME; RAPOLA J; AUTTI T; JOENSUU R; MANNINEN T; SIPILA I; IKONEN S; RIEKKINEN P; GINNS EI; PELTONEN L
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 05/06/20 alle ore 22:19:23