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    1. Kallinen, J; Marin, K; Heinonen, S; Mannermaa, A; Palotie, A; Ryynanen, M
      Wide scope prenatal diagnosis at Kuopio University Hospital 1997-1998: integration of gene tests and fetal karyotyping

      BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY
    2. Kallela, M; Wessman, M; Havanka, H; Palotie, A; Farkkila, M
      Familial migraine with and without aura: clinical characteristics and co-occurrence

      EUROPEAN JOURNAL OF NEUROLOGY
    3. Sallinen, R; Latvanlehto, A; Kvist, AP; Rehn, M; Eerola, I; Chu, ML; Bonaldo, P; Saitta, B; Bressan, GM; Pihlajaniemi, T; Vuorio, E; Palotie, A; Wessman, M; Horelli-Kuitunen, N
      Physical mapping of mouse collagen genes on Chromosome 10 by high-resolution FISH

      MAMMALIAN GENOME
    4. 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
    5. Rajantie, I; Ekman, N; Iljin, K; Arighi, E; Gunji, Y; Kaukonen, J; Palotie, A; Dewerchin, M; Carmeliet, P; Alitalo, K
      Bmx tyrosine kinase has a redundant function downstream of angiopoietin and vascular endothelial growth factor receptors in arterial endothelium

      MOLECULAR AND CELLULAR BIOLOGY
    6. Kallinen, J; Heinonen, S; Palotie, A; Mannermaa, A; Ryynanen, M
      Antenatal gene tests in low-risk pregnancies: molecular screening for aspartylglucosaminuria (AGU) and infantile neuronal ceroid lipofuscinosis (INCL) in Finland

      PRENATAL DIAGNOSIS
    7. Stenman, J; Hedstrom, J; Grenman, R; Leivo, I; Finne, P; Palotie, A; Orpana, A
      Relative levels of SCCA2 and SCCA1 mRNA in primary tumors predicts recurrent disease in squamous cell cancer of the head and neck

      INTERNATIONAL JOURNAL OF CANCER
    8. 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
    9. Peltonen, L; Palotie, A; Lange, K
      Use of population isolates for mapping complex traits

      NATURE REVIEWS GENETICS
    10. De Baere, E; Fukushima, Y; Small, K; Udar, N; Van Camp, G; Verhoeven, K; Palotie, A; De Paepe, A; Messiaen, L
      Identification of BPESC1, a novel gene disrupted by a balanced chromosomaltranslocation, t(3;4)(q23;p15.2), in a patient with BPES

      GENOMICS
    11. Wartiovaara, U; Mikkola, H; Szoke, G; Haramura, G; Karpati, L; Balogh, I; Lassila, R; Muszbek, L; Palotie, A
      Effect of Va134Leu polymorphism on the activation of the coagulation factor XIII-A

      THROMBOSIS AND HAEMOSTASIS
    12. 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
    13. Kuittinen, T; Eggert, A; Lindholm, P; Horelli-Kuitunen, N; Palotie, A; Maris, JM; Saarma, M
      A novel human processed gene, DAD-R, maps to 12p12 and is expressed in several organs

      FEBS LETTERS
    14. 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
    15. Philibert, RA; King, BH; Winfield, S; Cook, EH; Lee, YH; Stubblefield, B; Damschroder-Williams, P; Dea, C; Palotie, A; Tengstrom, C; Martin, BM; Ginns, EI
      Association of an X-chromosome dodecamer insertional variant allele with mental retardation (vol 3, pg 303, 1998)

      MOLECULAR PSYCHIATRY
    16. 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
    17. Horelli-Kuitunen, N; Aaltonen, J; Yaspo, ML; Eeva, M; Wessman, M; Peltonen, L; Palotie, A
      Mapping ESTs by fiber-FISH

      GENOME RESEARCH
    18. Stenman, J; Finne, P; Stahls, A; Grenman, R; Stenman, UH; Palotie, A; Orpana, A
      Accurate determination of relative messenger RNA levels by RT-PCR

      NATURE BIOTECHNOLOGY
    19. Kaukonen, J; Savolainen, ER; Palotie, A
      Human Emt tyrosine kinase is specifically expressed both in mature T-lymphocytes and T-cell associated hematopoietic malignancies

      LEUKEMIA & LYMPHOMA
    20. Laiho, E; Niemi, KM; Ignatius, J; Kere, J; Palotie, A; Saarialho-Kere, U
      Clinical and morphological correlations for transglutaminase 1 gene mutations in autosomal recessive congenital ichthyosis

      EUROPEAN JOURNAL OF HUMAN GENETICS
    21. Kvist, AP; Latvanlehto, A; Sund, M; Horelli-Kuitunen, N; Rehn, M; Palotie, A; Beier, D; Pihlajaniemi, T
      Complete exon-intron organization and chromosomal location of the gene formouse type XIII collagen (col13a1) and comparison with its human homologue

      MATRIX BIOLOGY
    22. 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
    23. Kallela, M; Wessman, M; Farkkila, M; Palotie, A; Koskenvuo, M; Honkasalo, ML; Kaprio, J
      Clinical characteristics of migraine in a population-based twin sample: similarities and differences between migraine with and without aura

      CEPHALALGIA
    24. Sallinen, R; Kuang, W; Engvall, E; Palotie, A; Wessman, M; Horelli-Kuitunen, N
      Assignment of laminin alpha 2-chain gene (Lama2) to mouse chromosome 10A4-B1 by fluorescence in situ hybridization

      CYTOGENETICS AND CELL GENETICS
    25. Horelli-Kuitunen, N; Gahmberg, N; Eeva, M; Palotie, A; Jarvela, I
      Interstitial deletion of bands 11q21 -> 22.3 in a three-year-old girl defined using fluorescence in situ hybridization on metaphase chromosomes

      AMERICAN JOURNAL OF MEDICAL GENETICS
    26. Helio, T; Wartiovaara, U; Halme, L; Turunen, UM; Mikkola, H; Palotie, A; Farkkila, M; Kontula, K
      Arg506Gln factor V mutation and Val34Leu factor XIII polymorphism in Finnish patients with inflammatory bowel disease

      SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
    27. 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
    28. Kallela, M; Wessman, M; Farkkila, M; Palotie, A; Koskenvuo, M; Honkasalo, ML; Kaprio, J
      Clinical characteristics of migraine concordant monozygotic twin pairs

      ACTA NEUROLOGICA SCANDINAVICA
    29. PHILIBERT RA; KING BH; WINFIELD S; COOK EH; LEE YH; STUBBLEFIELD B; DAMSCHRODERWILLIAMS P; DEA C; PALOTIE A; TENGSTROM C; MARTIN BM; GINNS EI
      ASSOCIATION OF AN X-CHROMOSOME DODECAMER INSERTIONAL VARIANT ALLELE WITH MENTAL-RETARDATION

      Molecular psychiatry
    30. PHILIBERT RA; HORELLIKUITUNEN N; ROBB AS; LEE YH; LONG RT; DAMSCHRODERWILLIAMS P; MARTIN BM; BRENNAN MB; PALOTIE A; GINNS EI
      THE CHARACTERIZATION AND SEQUENCE-ANALYSIS OF 30 CTG-REPEAT CONTAINING GENOMIC COSMID CLONES

      European journal of human genetics
    31. 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
    32. WARTIOVAARA U; SALVEN P; MIKKOLA H; LASSILA R; KAUKONEN J; JOUKOV V; ORPANA A; RISTIMAKI A; HEIKINHEIMO M; JOENSUU H; ALITALO K; PALOTIE A
      PERIPHERAL-BLOOD PLATELETS EXPRESS VEGF-C AND VEGF WHICH ARE RELEASEDDURING PLATELET ACTIVATION

      Thrombosis and haemostasis
    33. BONO P; SALMI M; SMITH DJ; LEPPANEN I; HORELLIKUITUNEN N; PALOTIE A; JALKANEN S
      ISOLATION, STRUCTURAL CHARACTERIZATION, AND CHROMOSOMAL MAPPING OF THE MOUSE VASCULAR ADHESION PROTEIN-1 GENE AND PROMOTER

      The Journal of immunology (1950)
    34. WARTIOVAARA U; PEROLA M; MIKKOLA H; TOTTERMAN K; SAVOLAINEN V; PENTTILA A; GRANT PJ; TIKKANEN M; VARTIAINEN E; KARHUNEN P; PELTONEN L; PALOTIE A
      ASSOCIATION OF FXIIIV34L WITH LOWER INCIDENCE OF MYOCARDIAL-INFARCTION IN FINNISH MALES WITH CORONARY-ARTERY DISEASE

      British Journal of Haematology
    35. VISAPAA I; FELLMAN V; VARILO T; PALOTIE A; RAIVIO KO; PELTONEN L
      ASSIGNMENT OF THE LOCUS FOR A NEW LETHAL NEONATAL METABOLIC SYNDROME TO 2Q33-37

      American journal of human genetics
    36. MAKELABENGS P; JARVINEN N; VUOPALA K; SUOMALAINEN A; IGNATIUS J; SIPILA M; HERVA R; PALOTIE A; PELTONEN L
      ASSIGNMENT OF THE DISEASE LOCUS FOR LETHAL CONGENITAL CONTRACTURE SYNDROME TO A RESTRICTED REGION OF CHROMOSOME 9Q34, BY GENOME SCAN USING 5 AFFECTED INDIVIDUALS

      American journal of human genetics
    37. TYNI T; RAPOLA J; PAETAU A; PALOTIE A; PIHKO H
      PATHOLOGY OF LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY CAUSED BY THE G1528C MUTATION

      PEDIATRIC PATHOLOGY & LABORATORY MEDICINE
    38. AALTONEN J; BJORSES P; PERHEENTUPA J; HORELLIKUITUNEN N; PALOTIE A; PELTONEN L; LEE YS; FRANCIS F; HENNIG S; THIEL C; LEHRACH H; YASPO ML
      AN AUTOIMMUNE-DISEASE, APECED, CAUSED BY MUTATIONS IN A NOVEL GENE FEATURING 2 PHD-TYPE ZINC-FINGER DOMAINS

      Nature genetics
    39. AALTONEN J; HORELLIKUITUNEN N; FAN JB; BJORSES P; PERHEENTUPA J; MYERS R; PALOTIE A; PELTONEN L
      HIGH-RESOLUTION PHYSICAL AND TRANSCRIPTIONAL MAPPING OF THE AUTOIMMUNE POLYENDOCRINOPATHY-CANDIDIASIS-ECTODERMAL DYSTROPHY LOCUS ON CHROMOSOME 21Q22.3 FISH

      PCR methods and applications
    40. SUVANTO P; WARTIOVAARA K; LINDAHL M; ARUMAE U; MOSHNYAKOV M; HORELLIKUITUNEN N; AIRAKSINEN MS; PALOTIE A; SARIOLA H; SAARMA M
      CLONING, MESSENGER-RNA DISTRIBUTION AND CHROMOSOMAL LOCALIZATION OF THE GENE FOR GLIAL-CELL LINE-DERIVED NEUROTROPHIC FACTOR-RECEPTOR-BETA,A HOMOLOG TO GDNFR-ALPHA

      Human molecular genetics
    41. HORELLIKUITUNEN N; KVIST AP; HELAAKOSKI T; KIVIRIKKO K; PIHLAJANIEMI T; PALOTIE A
      THE ORDER AND TRANSCRIPTIONAL ORIENTATION OF THE HUMAN COL13A1 AND P4HA GENES ON CHROMOSOME-10 LONG ARM DETERMINED BY HIGH-RESOLUTION FISH

      Genomics
    42. HELANDER HM; KOIVURANTA KT; HORELLIKUITUNEN N; PALVIMO JJ; PALOTIE A; HILTUNEN JK
      MOLECULAR-CLONING AND CHARACTERIZATION OF THE HUMAN MITOCHONDRIAL 2,4-DIENOYL-COA REDUCTASE GENE (DECR)

      Genomics
    43. KLOCKARS T; ISOSOMPPI J; LAAN M; KAKKO N; PALOTIE A; PELTONEN L
      THE VISUAL ASSIGNMENT OF GENES BY FIBER-FISH - BTF3 PROTEIN HOMOLOG GENE (BTF3) AND A NOVEL PSEUDOGENE OF HUMAN RNA HELICASE-A (DDX9P) ON 13Q22 (VOL 44, PG 355, 1997)

      Genomics
    44. HAGG PM; HORELLIKUITUNEN N; EKLUND L; PALOTIE A; PIHLAJANIEMI T
      CLONING OF MOUSE TYPE-XV COLLAGEN SEQUENCES AND MAPPING OF THE CORRESPONDING GENE TO 4B1-3 - COMPARISON OF MOUSE AND HUMAN ALPHA-1(XV) COLLAGEN SEQUENCES INDICATES DIVERGENCE IN THE NUMBER OF SMALL COLLAGENOUSDOMAINS

      Genomics
    45. KLOCKARS T; ISOSOMPPI J; LAAN M; KAKKO N; PALOTIE A; PELTONEN L
      THE VISUAL ASSIGNMENT OF GENES BY FIBER-FISH - BTF3 PROTEIN HOMOLOG GENE (BTF3) AND A NOVEL PSEUDOGENE OF HUMAN RNA HELICASE A (DDX9P) ON 13Q22

      Genomics
    46. KOIVUNEN P; HORELLIKUITUNEN N; HELAAKOSKI T; KARVONEN P; JAAKKOLA M; PALOTIE A; KIVIRIKKO KI
      STRUCTURES OF THE HUMAN GENE FOR THE PROTEIN DISULFIDE ISOMERASE-RELATED POLYPEPTIDE ERP60 AND A PROCESSED GENE AND ASSIGNMENT OF THESE GENES TO 15Q15 AND 1Q21

      Genomics
    47. KAUKONEN J; ALANENKURKI L; JALKANEN M; PALOTIE A
      THE MAPPING AND VISUAL ORDERING OF THE HUMAN SYNDECAN-1 AND N-MYC GENES NEAR THE TELOMERIC REGION OF CHROMOSOME 2P

      Human genetics
    48. LAUTEALA T; HORELLIKUITUNEN N; CLOSS E; SAVONTAUS ML; LUKKARINEN M; SIMELL O; CUNNINGHAM J; PALOTIE A; AULA P
      HUMAN CATIONIC AMINO-ACID TRANSPORTER GENE HCAT-2 IS ASSIGNED TO 8P22BUT IS NOT THE CAUSATIVE GENE IN LYSINURIC PROTEIN INTOLERANCE

      Human genetics
    49. MIKKOLA H; MUSZBEK L; HARAMURA G; HAMALAINEN E; JALANKO A; PALOTIE A
      MOLECULAR MECHANISMS OF MUTATIONS IN FACTOR-XIII A-SUBUNIT DEFICIENCY- IN-VITRO EXPRESSION IN COS-CELLS DEMONSTRATES INTRACELLULAR DEGRADATION OF THE MUTANT PROTEINS

      Thrombosis and haemostasis
    50. SITBON G; HURTIG M; PALOTIE A; LONNGREN J; SYVANEN AC
      A COLORIMETRIC MINISEQUENCING ASSAY FOR THE MUTATION IN CODON-506 OF THE COAGULATION-FACTOR-V GENE

      Thrombosis and haemostasis
    51. SINISALO J; AALTO T; PALOTIE A; SYRJALA M
      LOW-FREQUENCY OF FV R506G MUTATION IN A FINNISH VENOUS THROMBOSIS POPULATION

      Thrombosis and haemostasis
    52. MIKKOLA H; YEE V; SEITZ R; MUSZBEK L; CAPEL P; FONDU P; ABGRALL J; BEURRIER P; CARON C; CHABOCHE C; NIEWENHUIS H; LOPACIUK S; TUSELL J; TENGBJORN L; DEMOERLOOSE P; GIANGRANDE P; JONES P; WATSON H; SYRJALA M; PALOTIE A
      MOLECULAR-GENETICS OF FXIII DEFICIENCY IN EUROPE

      Thrombosis and haemostasis
    53. WARTIOVAARA U; JOUKOV V; MIKKOLA H; ALITALO K; PALOTIE A
      VASCULAR ENDOTHELIAL GROWTH-FACTOR-C (VEGF-C) IS EXPRESSED IN THROMBOCYTES

      Thrombosis and haemostasis
    54. TYNI T; RAPOLA J; PALOTIE A; PIHKO H
      HYPOPARATHYROIDISM IN A PATIENT WITH LONG-CHAIN 3-HYDROXYACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY CAUSED BY THE G1528C MUTATION

      The Journal of pediatrics
    55. TYNI T; PALOTIE A; VIINIKKA L; VALANNE L; SALO MK; VONDOBELN U; JACKSON S; WANDERS R; VENIZELOS N; PIHKO H
      LONG-CHAIN 3-HYDROXYACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY WITH THEG1528C MUTATION - CLINICAL PRESENTATION OF 13 PATIENTS

      The Journal of pediatrics
    56. CHILOV D; KUKK E; TAIRA S; JELTSCH M; KAUKONEN J; PALOTIE A; JOUKOV V; ALITALO K
      GENOMIC ORGANIZATION OF HUMAN AND MOUSE GENES FOR VASCULAR ENDOTHELIAL GROWTH-FACTOR-C

      The Journal of biological chemistry
    57. HELIO T; FARKKILA M; HALME L; TURUNEN U; PALOTIE A; KONTULA K
      ARG506GLN FACTOR-V MUTATION IN PATIENTS WITH ULCERATIVE-COLITIS AND CROHNS-DISEASE

      Gut
    58. KUKK E; WARTIOVAARA U; GUNJI Y; KAUKONEN J; BUHRING HJ; RAPPOLD I; MATIKAINEN MT; VIHKO P; PARTANEN J; PALOTIE A; ALITALO K; ALITALO R
      ANALYSIS OF TIE RECEPTOR TYROSINE KINASE IN HEMATOPOIETIC PROGENITOR AND LEUKEMIA-CELLS

      British Journal of Haematology
    59. ALITALO K; JUSSILA L; THOMASCRUSELLS J; DEWAAL R; SALVEN P; WARTIOVAARA U; PALOTIE A; MATIKAINEN MT; ALITALO R
      LYMPHATIC ENDOTHELIAL STAINING BY ANTIBODIES AGAINST VASCULAR ENDOTHELIAL GROWTH-FACTOR RECEPTOR-3

      Blood
    60. MIKKOLA H; YEE V; SEITZ R; INBAL A; MUSZBEK L; LOPACIUK S; SCHILLING F; PALOTIE A; GIANGRANDE P; JONES P; WATSON H; TENGBJORN L; TUSELL J; DEMOERLOOSE P; NIEWENHUIS K; ABGRALL J; BEURRIER P; CARON C; CHABOCHE C; CAPEL P; FONDU P; EBERL W; WENZEL E
      MOLECULAR-GENETICS OF FACTOR-XIII DEFICIENCY IN EUROPE

      Blood
    61. WARTIOVAARA U; PEROLA M; MIKKOLA H; TOTTERMAN K; SAVOLAINEN V; KARHUNEN P; GRANT P; PELTONEN L; PALOTIE A; HEIKINHEIMO M
      ASSOCIATION OF FXIIII VAL34LEU WITH LOWER INCIDENCE OF MYOCARDIAL-INFARCTION IN FINNISH PATIENTS WITH CORONARY HEART-DISEASE

      Blood
    62. MIKKOLA H; MUSZBEK L; LAIHO E; SYRJALA M; HAMALAINEN E; HARAMURA G; SALMI T; PELTONEN L; PALOTIE A
      MOLECULAR MECHANISM OF A MILD PHENOTYPE IN COAGULATION-FACTOR-XIII (FXIII) DEFICIENCY - A SPLICING MUTATION PERMITTING PARTIAL CORRECT SPLICING OF FXIII A-SUBUNIT MESSENGER-RNA

      Blood
    63. MAKELABENGS P; JARVINEN N; VUOPALA K; SUOMALAINEN A; PALOTIE A; PELTONEN L
      THE ASSIGNMENT OF THE LETHAL CONGENITAL CONTRACTURE SYNDROME (LCCS) LOCUS TO CHROMOSOME 9Q33-34

      American journal of human genetics
    64. HORELLIKUITUNEN N; AALTONEN J; YASPO ML; BJORSES P; PELTONEN L; PALOTIE A
      EST MAPPING USING FIBER-FISH

      American journal of human genetics
    65. LAIHO E; IGNATIUS J; MIKKOLA H; YEE VC; TELLER DC; NIEMI KM; SAARIALHOKERE U; KERE J; PALOTIE A
      TRANSGLUTAMINASE-1 MUTATIONS IN AUTOSOMAL RECESSIVE CONGENITAL ICHTHYOSIS - PRIVATE AND RECURRENT MUTATIONS IN AN ISOLATED POPULATION

      American journal of human genetics
    66. LAAN M; ISOSOMPPI J; KLOCKARS T; PELTONEN L; PALOTIE A
      UTILIZATION OF FISH IN POSITIONAL CLONING - AN EXAMPLE ON 13Q22

      PCR methods and applications
    67. HEISKANEN M; KALLIONIEMI O; PALOTIE A
      FIBER-FISH - EXPERIENCES AND A REFINED PROTOCOL

      GENETIC ANALYSIS-BIOMOLECULAR ENGINEERING
    68. KLOCKARS T; SAVUKOSKI M; ISOSOMPPI J; LAAN M; JARVELA I; PETRUKHIN K; PALOTIE A; PELTONEN L
      EFFICIENT CONSTRUCTION OF A PHYSICAL MAP BY FIBER-FISH OF THE CLN5 REGION - REFINED ASSIGNMENT AND LONG-RANGE CONTIG COVERING THE CRITICAL REGION ON 13Q22

      Genomics
    69. PALOTIE A; HEISKANEN M; LAAN M; HORELLIKUITUNEN N
      HIGH-RESOLUTION FLUORESCENCE IN-SITU HYBRIDIZATION - A NEW APPROACH IN GENOME MAPPING

      Annals of medicine
    70. HEISKANEN M; PELTONEN L; PALOTIE A
      VISUAL MAPPING BY HIGH-RESOLUTION FISH

      Trends in genetics
    71. NISHIO H; HEISKANEN M; PALOTIE A; BELANGER L; DUGAICZYK A
      TANDEM ARRANGEMENT OF THE HUMAN SERUM-ALBUMIN MULTIGENE FAMILY IN THESUB-CENTROMERIC REGION OF 4Q - EVOLUTION AND CHROMOSOMAL DIRECTION OFTRANSCRIPTION

      Journal of Molecular Biology
    72. HIETALA M; AULA P; SYVANEN AC; ISONIEMI A; PELTONEN L; PALOTIE A
      DNA-BASED CARRIER SCREENING IN PRIMARY HEALTH-CARE - SCREENING FOR ASPARTYLGLUCOSAMINURIA MUTATIONS IN MATERNITY HEALTH OFFICES

      Clinical chemistry
    73. PAAVONEN K; HORELLIKUITUNEN N; CHILOV D; KUKK E; PENNANEN S; KALLIONIEMI OP; PAJUSOLA K; OLOFSSON B; ERIKSSON U; JOUKOV V; PALOTIE A; ALITALO K
      NOVEL HUMAN VASCULAR ENDOTHELIAL GROWTH-FACTOR GENES VEGF-B AND VEGF-C LOCALIZE TO CHROMOSOMES 11Q13 AND 4Q34, RESPECTIVELY

      Circulation
    74. KAUKONEN J; LAHTINEN I; LAINE S; ALITALO K; PALOTIE A
      BMX TYROSINE KINASE GENE IS EXPRESSED IN GRANULOCYTES AND MYELOID LEUKEMIAS

      British Journal of Haematology
    75. KAUKONEN J; ALITALO K; PALOTIE A
      NONRECEPTOR PROTEIN-TYROSINE KINASES OF BTK-SUBFAMILY ARE WIDELY EXPRESSED IN HEMATOPOIETIC PRECURSORS, SHOWING TRACES OF LINEAGE SPECIFICITY AT LATER STAGES OF DIFFERENTIATION

      Blood
    76. WARTIOVAARA U; JOUKOV V; MIKKOLA H; ALITALO K; PALOTIE A
      VASCULAR ENDOTHELIAL GROWTH-FACTOR-C (VEGF-C) IS EXPRESSED IN THROMBOCYTES

      Blood
    77. MIKKOLA H; YEE VC; MUSZBEK L; SEITZ R; SALMI T; JALANKO A; PELTONEN L; PALOTIE A
      MOLECULAR-BASIS OF COAGULATION-FACTOR-XIII DEFICIENCY

      Blood
    78. MIKKOLA H; YEE VC; SYRJALA M; SEITZ R; EGBRING R; PETRINI P; LJUNG R; INGERSLEV J; TELLER DC; PELTONEN L; PALOTIE A
      4 NOVEL MUTATIONS IN DEFICIENCY OF COAGULATION-FACTOR-XIII - CONSEQUENCES TO EXPRESSION AND STRUCTURE OF THE A-SUBUNIT

      Blood
    79. ILMONEN M; HELIO T; BUTLER R; PALOTIE A; PIETINEN P; HUTTUNEN JK; TIKKANEN MJ
      2 NEW IMMUNOGENETIC POLYMORPHISMS OF THE APO-B GENE AND THEIR EFFECT ON SERUM-LIPID LEVELS AND RESPONSES TO CHANGES IN DIETARY-FAT INTAKE

      Arteriosclerosis, thrombosis, and vascular biology
    80. VISAKORPI T; HYYTINEN E; KOIVISTO P; TANNER M; KEINANEN R; PALMBERG C; PALOTIE A; TAMMELA T; ISOLA J; KALLIONIEMI OP
      IN-VIVO AMPLIFICATION OF THE ANDROGEN RECEPTOR GENE AND PROGRESSION OF HUMAN PROSTATE-CANCER

      Nature genetics
    81. LAAN M; KALLIONIEMI OP; HELLSTEN E; ALITALO K; PELTONEN L; PALOTIE A
      MECHANICALLY STRETCHED CHROMOSOMES AS TARGETS FOR HIGH-RESOLUTION FISH MAPPING

      PCR methods and applications
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      THE REARRANGED L-MYC FUSION GENE (RLF) ENCODES A ZN-15 RELATED ZINC-FINGER PROTEIN

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      MOLECULAR-CLONING, CHROMOSOMAL ASSIGNMENT, AND EXPRESSION OF THE MOUSE ASPARTYLGLUCOSAMINIDASE GENE

      Genomics
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      VISUAL MAPPING BY FIBER-FISH

      Genomics
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      HEAD-TO-TAIL ORGANIZATION OF THE HUMAN COL6A1 AND COL6A2 GENES BY FIBER-FISH

      Genomics
    86. HELLSTEN E; VESA J; HEISKANEN M; MAKELA TP; JARVELA I; COWELL JK; MEAD S; ALITALO K; PALOTIE A; PELTONEN L
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      Genomics
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      SOLID-PHASE MINISEQUENCING CONFIRMED BY FISH ANALYSIS IN DETERMINATION OF GENE COPY NUMBER

      Human genetics
    88. SYRJALA M; TATLISUMAK T; LINDSBERG P; PALOTIE A; KASTE M
      FV ARG-506-GLN MUTATION IN ISCHEMIC STROKE

      Thrombosis and haemostasis
    89. MIKKOLA H; YEE V; SYRJALA M; SEITZ R; EGBRING R; LJUNGA R; PETRINI P; INGERSLEV I; TELLER D; PELTONEN L; PALOTIE A
      MOLECULAR DEFECTS IN FACTOR-XIII DEFICIENCY - CONSEQUENCES TO EXPRESSION AND STRUCTURE OF THE A-SUBUNIT

      Thrombosis and haemostasis
    90. RYTKONEN EMK; HALILA R; LAAN M; SAKSELA M; KALLIONIEMI OP; PALOTIE A; RAIVIO KO
      THE HUMAN GENE FOR XANTHINE DEHYDROGENASE (XDH) IS LOCALIZED ON CHROMOSOME BAND 2P22

      Cytogenetics and cell genetics
    91. LOUKOVAARA M; CARSON M; PALOTIE A; ADLERCREUTZ H
      REGULATION OF SEX HORMONE-BINDING GLOBULIN PRODUCTION BY ISOFLAVONOIDS AND PATTERNS OF ISOFLAVONOID CONJUGATION IN HEPG2 CELL-CULTURES

      Steroids
    92. SAINIO M; STRACHAN T; BLOMSTEDT G; SALONEN O; SETALA K; PALOTIE A; PALO J; PYYKKO I; PELTONEN L; JAASKELAINEN J
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      Neurology
    93. ANTTILA P; IHALAINEN J; SALO A; HEISKANEN M; JUVONEN E; PALOTIE A
      IDIOPATHIC MACROCYTIC ANEMIA IN THE AGED - MOLECULAR AND CYTOGENETIC FINDINGS

      British Journal of Haematology
    94. MIKKOLA H; YEE V; MUSZBEK L; SYRJALA M; SEITZ R; EGBRING R; LJUNG R; PETRINI P; INGERSLEV J; TELLER D; JALANKO A; PELTONEN L; PALOTIE A
      MOLECULAR DEFECTS IN COAGULATION-FACTOR-XIII DEFICIENCY

      Blood
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      APPLICATION OF HIGH-RESOLUTION FISH TECHNIQUES IN POSITIONAL CLONING

      American journal of human genetics
    96. HIETALA M; HAKONEN A; ARO AR; LONNQVIST J; NIEMELA P; PALOTIE A; PELTONEN L; AULA P
      CARRIER SCREENING FOR ASPARTYLGLUCOSAMINURIA IN FINLAND - A PILOT-STUDY AMONG PREGNANT-WOMEN

      American journal of human genetics
    97. ILMONEN M; HELIO T; EBELING T; PYORALA K; UUSITUPA M; PALOTIE A; TIKKANEN MJ
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      Human mutation
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      A NOVEL METHOD TO QUANTITATE METHYLATION OF SPECIFIC GENOMIC REGIONS

      PCR methods and applications
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      CALCITONIN-GENE METHYLATION IN CHRONIC MYELOPROLIFERATIVE DISORDERS

      Leukemia
    100. HEISKANEN M; KARHU R; HELLSTEN E; PELTONEN L; KALLIONIEMI OP; PALOTIE A
      HIGH-RESOLUTION MAPPING USING FLUORESCENCE IN-SITU HYBRIDIZATION TO EXTENDED DNA FIBERS PREPARED FROM AGAROSE-EMBEDDED CELLS

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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 31/05/20 alle ore 00:59:36