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There are 15834 results for: content related to: Low SPINK5 expression in chronic rhinosinusitis

  1. Hint for association of single nucleotide polymorphisms and haplotype in SPINK5 gene with atopic dermatitis in Koreans

    Experimental Dermatology

    Volume 19, Issue 12, December 2010, Pages: 1048–1053, Jung-Hyun Namkung, Jong-Eun Lee, Eugene Kim, Ji-Yeon Byun, Sook Kim, Eun-Soon Shin, Eun-Young Cho and Jun-Mo Yang

    Version of Record online : 19 NOV 2010, DOI: 10.1111/j.1600-0625.2010.01142.x

  2. Association of SPINK5 gene polymorphisms with atopic dermatitis in Northeast China

    Journal of the European Academy of Dermatology and Venereology

    Volume 26, Issue 5, May 2012, Pages: 572–577, L.P. Zhao, Z. Di, L. Zhang, L. Wang, L. Ma, Y. Lv, Y. Hong, H. Wei, H.D. Chen and X.H. Gao

    Version of Record online : 18 MAY 2011, DOI: 10.1111/j.1468-3083.2011.04120.x

  3. Analysis of complement receptor Type 1 expression on red blood cells in negative phenotypes of the Knops blood group system, according to CR1 gene allotype polymorphisms

    Transfusion

    Volume 50, Issue 7, July 2010, Pages: 1435–1443, Bach-Nga Pham, Aymric Kisserli, Béatrice Donvito, Valérie Duret, Brigitte Reveil, Thierry Tabary, Pierre-Yves Le Pennec, Thierry Peyrard, Philippe Rouger and Jacques H.M. Cohen

    Version of Record online : 19 FEB 2010, DOI: 10.1111/j.1537-2995.2010.02599.x

  4. Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome

    Clinical Genetics

    Volume 70, Issue 3, September 2006, Pages: 214–227, G Millat, P Chevalier, L Restier-Miron, A Da Costa, P Bouvagnet, B Kugener, L Fayol, C Gonzàlez Armengod, B Oddou, V Chanavat, E Froidefond, R Perraudin, R Rousson and C Rodriguez-Lafrasse

    Version of Record online : 10 AUG 2006, DOI: 10.1111/j.1399-0004.2006.00671.x

  5. You have full text access to this OnlineOpen article
    Whole genome sequencing shows sleeping sickness relapse is due to parasite regrowth and not reinfection

    Evolutionary Applications

    Volume 9, Issue 2, February 2016, Pages: 381–393, Joshua B. Richardson, Benjamin Evans, Patient P. Pyana, Nick Van Reet, Mark Sistrom, Philippe Büscher, Serap Aksoy and Adalgisa Caccone

    Version of Record online : 9 JAN 2016, DOI: 10.1111/eva.12338

  6. Prenatal diagnosis of a lethal form of Netherton syndrome by SPINK5 mutation analysis

    Prenatal Diagnosis

    Volume 22, Issue 2, February 2002, Pages: 121–126, E. Bitoun, C. Bodemer, J. Amiel, Y. de Prost, C. Stoll, P. Calvas and A. Hovnanian

    Version of Record online : 14 FEB 2002, DOI: 10.1002/pd.247

  7. You have full text access to this OnlineOpen article
    Who's behind that mask and cape? The Asian leopard cat's Agouti (ASIP) allele likely affects coat colour phenotype in the Bengal cat breed

    Animal Genetics

    Volume 45, Issue 6, December 2014, Pages: 893–897, L. C. Gershony, M. C. T. Penedo, B. W. Davis, W. J. Murphy, C. R. Helps and L. A. Lyons

    Version of Record online : 20 AUG 2014, DOI: 10.1111/age.12206

  8. Effects of polymorphisms of the SLCO2B1 transporter gene on the pharmacokinetics of montelukast in humans

    The Journal of Clinical Pharmacology

    Volume 53, Issue 11, November 2013, Pages: 1186–1193, Kyoung-Ah Kim, Hye-Mi Lee, Hyun-Jin Joo, In-Bae Park and Ji-Young Park

    Version of Record online : 23 AUG 2013, DOI: 10.1002/jcph.144

  9. You have free access to this content
    Homozygosity at the MTL locus in clinical strains of Candida albicans: karyotypic rearrangements and tetraploid formation

    Molecular Microbiology

    Volume 52, Issue 5, June 2004, Pages: 1451–1462, Melanie Legrand, Paul Lephart, Anja Forche, Frank-Michael C. Mueller, T. Walsh, P.T. Magee and Beatrice B. Magee

    Version of Record online : 22 APR 2004, DOI: 10.1111/j.1365-2958.2004.04068.x

  10. Netherton Syndrome

    Harper's Textbook of Pediatric Dermatology, Volume 1, 2, Third Edition

    Wei-Li Di, John Harper, Pages: 124.1–124.10, 2011

    Published Online : 24 MAY 2011, DOI: 10.1002/9781444345384.ch124

  11. A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in Morocco

    Clinical Genetics

    Volume 62, Issue 4, October 2002, Pages: 334–339, A Belmouden, R Melki, M Hamdani, K Zaghloul, A Amraoui, S Nadifi, O Akhayat and H-J Garchon

    Version of Record online : 8 OCT 2002, DOI: 10.1034/j.1399-0004.2002.620415.x

  12. Polymorphisms in inflammation genes, tobacco smoke and furred pets and wheeze in children

    Pediatric Allergy and Immunology

    Volume 20, Issue 7, November 2009, Pages: 614–623, Mette Sørensen, Leila Allermann, Ulla Vogel, Paal Skytt Andersen, Cathrine Jespersgaard, Steffen Loft and Ole Raaschou-Nielsen

    Version of Record online : 6 AUG 2009, DOI: 10.1111/j.1399-3038.2009.00855.x

  13. Variation in genes involved in the immune response and prostate cancer risk in the placebo arm of the Prostate Cancer Prevention Trial

    The Prostate

    Volume 75, Issue 13, September 15, 2015, Pages: 1403–1418, Danyelle A. Winchester, Cathee Till, Phyllis J. Goodman, Catherine M. Tangen, Regina M. Santella, Teresa L. Johnson-Pais, Robin J. Leach, Jianfeng Xu, S. Lilly Zheng, Ian M. Thompson, M. Scott Lucia, Scott M. Lippmann, Howard L. Parnes, Paul J. Dluzniewski, William B. Isaacs, Angelo M. De Marzo, Charles G. Drake and Elizabeth A. Platz

    Version of Record online : 5 JUN 2015, DOI: 10.1002/pros.23021

  14. Differential modification of genetic susceptibility to childhood eczema by two probiotics

    Clinical & Experimental Allergy

    Volume 44, Issue 10, October 2014, Pages: 1255–1265, A. R. Morgan, D. Y. Han, K. Wickens, C. Barthow, E. A. Mitchell, T. V. Stanley, J. Dekker, J. Crane and L. R. Ferguson

    Version of Record online : 22 SEP 2014, DOI: 10.1111/cea.12394

  15. Potassium channels involved in human sperm volume regulation—quantitative studies at the protein and mRNA levels

    Molecular Reproduction and Development

    Volume 75, Issue 4, April 2008, Pages: 659–668, C.H. Yeung and T.G. Cooper

    Version of Record online : 21 DEC 2007, DOI: 10.1002/mrd.20812

  16. Characterization of impurities in sisomicin and netilmicin by liquid chromatography/mass spectrometry

    Rapid Communications in Mass Spectrometry

    Volume 22, Issue 22, 30 November 2008, Pages: 3455–3471, Bo Li, Ann Van Schepdael, Jos Hoogmartens and Erwin Adams

    Version of Record online : 13 OCT 2008, DOI: 10.1002/rcm.3748

  17. A heterozygous null mutation combined with the G1258A polymorphism of SPINK5 causes impaired LEKTI function and abnormal expression of skin barrier proteins

    British Journal of Dermatology

    Volume 161, Issue 2, August 2009, Pages: 404–412, W-L. Di, R.C. Hennekam, R.E. Callard and J.I. Harper

    Version of Record online : 12 MAY 2009, DOI: 10.1111/j.1365-2133.2009.09231.x

  18. Distinct SPINK5 and IL-31 polymorphisms are associated with atopic eczema and non-atopic hand dermatitis in Taiwanese nursing population

    Experimental Dermatology

    Volume 20, Issue 12, December 2011, Pages: 975–979, Cheng-Che E. Lan, Hung-Pin Tu, Ching-Shuang Wu, Ying-Chin Ko, Hsin-Su Yu, Yi-Wei Lu, Wan-Chen Li, Yin-Chun Chen and Gwo-Shing Chen

    Version of Record online : 20 OCT 2011, DOI: 10.1111/j.1600-0625.2011.01374.x

  19. ‘Immunogenetics of Aging’: report on the activities of the 15th International HLA and Immunogenetics Working Group and 15th International HLA and Immunogenetics Workshop

    Tissue Antigens

    Volume 77, Issue 3, March 2011, Pages: 187–192, E. Naumova, M. Ivanova, G. Pawelec, I. Constantinescu, K. Bogunia-Kubik, A. Lange, F. Qguz, M. Carin, C. Franceschi, C. Caruso and D. Middleton

    Version of Record online : 8 FEB 2011, DOI: 10.1111/j.1399-0039.2010.01603.x

  20. You have free access to this content
    Molecular basis of severe factor XI deficiency in seven families from the west of France. Seven novel mutations, including an ancient Q88X mutation

    Journal of Thrombosis and Haemostasis

    Volume 2, Issue 1, January 2004, Pages: 71–76, F. Quélin, M. Trossaërt, M. Sigaud, P. D. E. Mazancourt and E. Fressinaud

    Version of Record online : 9 JAN 2004, DOI: 10.1111/j.1538-7836.2004.00554.x