Hans Geir Eiken

Ontology type: schema:Person     

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Hans Geir



Publications in SciGraph latest 50 shown

  • 2020-10-02 Seasonal dynamics of lotic bacterial communities assessed by 16S rRNA gene amplicon deep sequencing in SCIENTIFIC REPORTS
  • 2020-01-17 Genome- and transcriptome-derived microsatellite loci in lumpfish Cyclopterus lumpus: molecular tools for aquaculture, conservation and fisheries management in SCIENTIFIC REPORTS
  • 2019-12-19 Faecal pollution affects abundance and diversity of aquatic microbial community in anthropo-zoogenically influenced lotic ecosystems in SCIENTIFIC REPORTS
  • 2017-05-08 Helminths of brown bears (Ursus arctos) in the Kola Peninsula in PARASITOLOGY RESEARCH
  • 2012-04-18 Identification and evaluation of novel di- and tetranucleotide microsatellite markers from the brown bear (Ursus arctos) in CONSERVATION GENETICS RESOURCES
  • 2012-01-17 Connectivity and population subdivision at the fringe of a large brown bear (Ursus arctos) population in North Western Europe in CONSERVATION GENETICS
  • 2009-12-08 Inverse correlation between PDGFC expression and lymphocyte infiltration in human papillary thyroid carcinomas in BMC CANCER
  • 2003-12-11 Evaluation of five different cDNA labeling methods for microarrays using spike controls in BMC BIOTECHNOLOGY
  • 2001-08 Monocyte chemoattractant protein-1 enhances and interleukin-10 suppresses the production of inflammatory cytokines in adult rat cardiomyocytes in BASIC RESEARCH IN CARDIOLOGY
  • 2000-11-16 Enhanced detection of mutations in BRCA1 exon 11 using restriction endonuclease fingerprinting-single-strand conformation polymorphism in JOURNAL OF MOLECULAR MEDICINE
  • 2000-03-12 Screening for BRCA1 gene mutations by capillary electrophoretic REF-SSCP in BREAST CANCER RESEARCH
  • 1997-10 Pituitary dwarfism in the R271W Pit-1 gene mutation in EUROPEAN JOURNAL OF PEDIATRICS
  • 1997-07 Phenylketonuria and the peoples of Northern Ireland in HUMAN GENETICS
  • 1996-07 Phenylketonuria genotypes correlated to metabolic phenotype groups in Norway in EUROPEAN JOURNAL OF PEDIATRICS
  • 1996-07 The Ca2+-sensing receptor gene (PCAR1) mutation T151M in isolated autosomal dominant hypoparathyroidism in HUMAN GENETICS
  • 1996-02 Mutations in the iduronate-2-sulfatase gene in five Norwegians with Hunter syndrome in HUMAN GENETICS
  • 1996 Relative Frequency, Heterogeneity and Geographic Clustering of PKU Mutations in Norway in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1995-02 The PKU mutation S349P causes complete loss of catalytic activity in the recombinant phenylalanine hydroxylase enzyme in HUMAN GENETICS
  • 1994-02 394delTT: a Nordic cystic fibrosis mutation in HUMAN GENETICS
  • 1993-09 The phenylketonuria G272X haplotype 7 mutation in European populations in HUMAN GENETICS
  • 1993 Expression of Wild Type and Mutant Forms of Human Phenylalanine Hydroxylase in E. Coli in CHEMISTRY AND BIOLOGY OF PTERIDINES AND FOLATES
  • 1992-03 PKU mutations R408Q and F299C in Norway: Haplotype associations, geographic distributions and phenotype characteristics in HUMAN GENETICS
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