Genetic variation of the Toll-like receptors in a Swedish allergic rhinitis case population von Henmyr, V, Carlberg, D, Manderstedt, E, Lind-Halldén, C, Säll, T, Cardell, L O, Halldén, C

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Characterization of genetic variation in TLR8 in relation to allergic rhinitis von Henmyr, V., Lind‐Halldén, C., Carlberg, D., Halldén, C., Melén, E., Wickman, M., Bergström, A., Säll, T., Cardell, L. O.

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Origin of Swedish hemophilia A mutations von HALLDÉN, C., NILSSON, D., SÄLL, T., LIND‐HALLDÉN, C., LIDÉN, A. C., LJUNG, R.

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Origin of Swedish hemophilia B mutations von Halldén, C., Mårtensson, A., Nilsson, D., Säll, T., Lind‐Halldén, C., Lidén, A. C., Ljung, R.

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Mutation analysis of Swedish haemophilia B families - high frequency of unique mutations von Mårtensson, A., Letelier, A., Halldén, C., Ljung, R.

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Replication of genomewide associations with allergic sensitization and allergic rhinitis von Nilsson, D., Henmyr, V., Halldén, C., Säll, T., Kull, I., Wickman, M., Melén, E., Cardell, L. O.

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Origin of mutation in sporadic cases of severe haemophilia A in Sweden von Mårtensson, A., Ivarsson, S., Letelier, A., Manderstedt, E., Halldén, C., Ljung, R.

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The evolutionary history of the common chloroplast genome of Arabidopsis thaliana and A. suecica von JAKOBSSON, M., SÄLL, T., LIND‐HALLDÉN, C., HALLDÉN, C.

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CLC- a novel susceptibility gene for allergic rhinitis von Bryborn, M, Halldén, C, Säll, T, Cardell, L.O

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Chloroplast DNA indicates a single origin of the allotetraploid Arabidopsis suecica von Säll, T., Jakobsson, M., Lind‐Halldén, C., Halldén, C.

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Characterization of genetic variation in TLR 8 in relation to allergic rhinitis von Henmyr, V., Lind‐Halldén, C., Carlberg, D., Halldén, C., Melén, E., Wickman, M., Bergström, A., Säll, T., Cardell, L. O.

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Detection of F8 int22h inversions using digital droplet PCR and mile‐post assays von Manderstedt, Eric, Lind‐Halldén, Christina, Ljung, Rolf, Astermark, Jan, Halldén, Christer

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Effect of androgen deprivation therapy on the expression of prostate cancer biomarkers MSMB and MSMB-binding protein CRISP3 von Dahlman, A, Edsjö, A, Halldén, C, Persson, J L, Fine, S W, Lilja, H, Gerald, W, Bjartell, A

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Small and large PROS1 deletions but no other types of rearrangements detected in patients with protein S deficiency von LIND-HALLDEN, Christina, DAHLEN, Anna, HILLARP, Andreas, ZÖLLER, Bengt, DAHLBÄCK, Björn, HALLDEN, Christer

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Chronic Rhinosinusitis Patients Show Accumulation of Genetic Variants in PARS2 von Henmyr, Viktor, Lind-Halldén, Christina, Halldén, Christer, Säll, Torbjörn, Carlberg, Daniel, Bachert, Claus, Cardell, Lars-Olaf

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Important research questions in allergy and related diseases: 3-chronic rhinosinusitis and nasal polyposis - a GALEN study von Bachert, C, Van Bruaene, N, Toskala, E, Zhang, N, Olze, H, Scadding, G, Van Drunen, C M, Mullol, J, Cardell, L, Gevaert, P, Van Zele, T, Claeys, S, Halldén, C, Kostamo, K, Foerster, U, Kowalski, M, Bieniek, K, Olszewska-Ziaber, A, Nizankowska-Mogilnicka, E, Szczeklik, A, Swierczynska, M, Arcimowicz, M, Lund, V, Fokkens, W, Zuberbier, T, Akdis, C, Canonica, G, Van Cauwenberge, P, Burney, P, Bousquet, J

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Co‐segregation of the PROS1 locus and protein S deficiency in families having no detectable mutations in PROS1 von Lanke, E., Johansson, A. M., Hillarp, A., Lethagen, S., Zöller, B., Dahlbäck, B., Halldén, C.

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Investigation of disease-associated factors in haemophilia A patients without detectable mutations von HALLDÉN, C., KNOBE, K. E., SJÖRIN, E., NILSSON, D., LJUNG, R.

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Competition as a source of errors in RAPD analysis von Hallden, C, Hansen, M, Nilsson, N.O, Hjerdin, A, Saell, T. (Hilleshoeg AB, Landskrona (Sweden))

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Primer Mixtures in RAPD Analysis von Saell, T, Lind-Hallden, C, Hallden, C

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