Search Results - "Kärrman, Carina"

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  1. 1

    Pharmacological characterization of AZD5069, a slowly reversible CXC chemokine receptor 2 antagonist by Nicholls, David J, Wiley, Katherine, Dainty, Ian, MacIntosh, Fraser, Phillips, Caroline, Gaw, Alasdair, Mårdh, Carina Kärrman

    “…In normal physiologic responses to injury and infection, inflammatory cells enter tissue and sites of inflammation through a chemotactic process regulated by…”
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    Benchmarking of Human Dose Prediction for Inhaled Medicines from Preclinical In Vivo Data by Ericsson, Therese, Fridén, Markus, Kärrman-Mårdh, Carina, Dainty, Ian, Grime, Ken

    Published in Pharmaceutical research (01-12-2017)
    “…Purpose A scientifically robust prediction of human dose is important in determining whether to progress a candidate drug into clinical development. A…”
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    Targets of Neutrophil Influx and Weaponry: Therapeutic Opportunities for Chronic Obstructive Airway Disease by Thomas, Matthew, Malmgren, Anna, Stenvall, Kristina, Uddin, Mohib, Root, James, Mårdh, Carina Kärrman, Karabelas, Kostas

    Published in Journal of immunology research (01-01-2017)
    “…Neutrophils are important effector cells of antimicrobial immunity in an acute inflammatory response, with a primary role in the clearance of extracellular…”
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    Cloning, characterization and immunolocalization of human ameloblastin by MacDougall, Mary, Simmons, Darrin, Gu, Ting Ting, Forsman-Semb, Kristina, Kärrman Mårdh, Carina, Mesbah, Michael, Forest, Nadine, Krebsbach, Paul H., Yamada, Yoishi, Berdal, Ariane

    Published in European journal of oral sciences (01-08-2000)
    “…Amelogenesis imperfecta is a broad classification of hereditary enamel defects, exhibiting both genetic and clinical diversity. Most amelogenesis imperfecta…”
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  9. 9

    Ameloblastin Gene (AMBN) Maps within the Critical Region for Autosomal Dominant Amelogenesis Imperfecta at Chromosome 4q21 by MacDougall, Mary, DuPont, Barbara R., Simmons, Darrin, Reus, Bonnie, Krebsbach, Paul, Kärrman, Carina, Holmgren, Gösta, Leach, Robin J., Forsman, Kristina

    Published in Genomics (San Diego, Calif.) (01-04-1997)
    “…Amelogenesis imperfecta (AI) is a broad group of hereditary enamel defects that is characterized by a high degree of clinical diversity. Recently, the local…”
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    IL-13 and IL-4, but not IL-5 nor IL-17A, induce hyperresponsiveness in isolated human small airways by Manson, Martijn L., Säfholm, Jesper, James, Anna, Johnsson, Anna-Karin, Bergman, Per, Al-Ameri, Mamdoh, Orre, Ann-Charlotte, Kärrman-Mårdh, Carina, Dahlén, Sven-Erik, Adner, Mikael

    Published in Journal of allergy and clinical immunology (01-03-2020)
    “…Specific inflammatory pathways are indicated to contribute to severe asthma, but their individual involvement in the development of airway hyperresponsiveness…”
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    Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patients by Kärrman Mårdh, Carina, Bäckman, Birgitta, Simmons, Darrin, Golovleva, Irina, Gu, Ting Ting, Holmgren, Gösta, MacDougall, Mary, Forsman-Semb, Kristina

    Published in European journal of oral sciences (01-02-2001)
    “…A gene encoding the enamel protein ameloblastin (AMBN) was recently localized to a region on chromosome 4q21 containing a gene for the inherited enamel defect…”
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    Mapping of the Locus for Autosomal Dominant Amelogenesis Imperfecta (AIH2) to a 4-Mb YAC Contig on Chromosome 4q11–q21 by Kärrman, Carina, Bäckman, Birgitta, Dixon, Michael, Holmgren, Gösta, Forsman, Kristina

    Published in Genomics (San Diego, Calif.) (15-01-1997)
    “…Amelogenesis imperfecta (AI) is a clinically and genetically heterogeneous group of inherited enamel defects. We recently mapped a locus for autosomal dominant…”
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  15. 15

    Genetic heterogeneity of autosomal dominant amelogenesis imperfecta demonstrated by its exclusion from the AIH2 region on human chromosome 4Q by Kärrman, Carina, Bäckman, Birgitta, Holmgren, Gösta, Forsman, Kristina

    Published in Archives of oral biology (01-08-1996)
    “…Amelogenesis imperfecta (AI) is a group of hereditary enamel defects, characterized by large clinical diversity. On the basis of differences in clinical…”
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    Journal Article