The Immunomodulatory Properties of β-2,6 Fructans: A Comprehensive Review von Young, Ian D, Latousakis, Dimitrios, Juge, Nathalie

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Mucosal or systemic microbiota exposures shape the B cell repertoire von Li, Hai, Limenitakis, Julien P., Greiff, Victor, Yilmaz, Bahtiyar, Schären, Olivier, Urbaniak, Camilla, Zünd, Mirjam, Lawson, Melissa A. E., Young, Ian D., Rupp, Sandra, Heikenwälder, Mathias, McCoy, Kathy D., Hapfelmeier, Siegfried, Ganal-Vonarburg, Stephanie C., Macpherson, Andrew J.

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Lipopolysaccharide associated with β-2,6 fructan mediates TLR4-dependent immunomodulatory activity in vitro von Young, Ian D., Nepogodiev, Sergey A., Black, Ian M., Le Gall, Gwenaelle, Wittmann, Alexandra, Latousakis, Dimitrios, Visnapuu, Triinu, Azadi, Parastoo, Field, Robert A., Juge, Nathalie, Kawasaki, Norihito

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Mutations in Two Nonhomologous Genes in a Head-to-Head Configuration Cause Ellis-van Creveld Syndrome von Ruiz-Perez, Victor L., Stuart Tompson, W.J., Helen Blair, J., Espinoza-Valdez, Cecilia, Lapunzina, Pablo, Silva, Elias O., Hamel, Ben, Gibbs, John L., Young, Ian D., Wright, Michael J., Goodship, Judith A.

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Effect of purification of galactooligosaccharides derived from lactulose with Saccharomyces cerevisiae on their capacity to bind immune cell receptor Dectin-2 von Young, Ian D., Montilla, Antonia, Olano, Agustín, Wittmann, Alexandra, Kawasaki, Norihito, Villamiel, Mar

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Inactivating Mutation in the Human Parathyroid Hormone Receptor Type 1 Gene in Blomstrand Chondrodysplasia von Karaplis, Andrew C, He, Bin, Nguyen, M. T. Audrey, Young, Ian D, Semeraro, David, Ozawa, Hidehiro, Amizuka, Norio

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Lactobacillus reuteri Surface Mucus Adhesins Upregulate Inflammatory Responses Through Interactions With Innate C-Type Lectin Receptors von Bene, Krisztián P, Kavanaugh, Devon W, Leclaire, Charlotte, Gunning, Allan P, MacKenzie, Donald A, Wittmann, Alexandra, Young, Ian D, Kawasaki, Norihito, Rajnavolgyi, Eva, Juge, Nathalie

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Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene von Foster, Jamie W., Dominguez-Steglich, Marina A., Guioli, Silvana, Kwok, Cheni, Weller, Polly A., Stevanović, Milena, Weissenbach, Jean, Mansour, Sahar, Young, Ian D., Goodfellow, Peter N., Brook, J. David, Schafer, Alan J.

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Lipopolysaccharide associated with β-2,6 fructan mediates TLR4-dependent immunomodulatory activity in vitro von Young, Ian D., Nepogodiev, Sergey A., Black, Ian M., Le Gall, Gwenaelle, Wittmann, Alexandra, Latousakis, Dimitrios, Visnapuu, Triinu, Azadi, Parastoo, Field, Robert A., Juge, Nathalie, Kawasaki, Norihito

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Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family von Yi Li, Quan, Newbury-Ecob, Ruth A., Terrett, Jonathan A., Wilson, David I., Curtis, Andrew R.J., Ho Yi, Cheong, Gebuhr, Tom, Bullen, Philip J., Robson, Stephen C., Strachan, Tom, Bonnet, Damien, Lyonnet, Stanislas, Young, Ian D., Raeburn, J. Alexander, Buckler, Alan J., Law, David J., Brook, J. David

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Microcephalic osteodysplastic primordial short stature type II with café-au-lait spots and moyamoya disease: Another patient von Young, Ian D., Barrow, Margaret, Hall, Christine M.

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Clinical and genetic heterogeneity in Desbuquois dysplasia von Faivre, Laurence, Le Merrer, Martine, Zerres, Klaus, Hariz, Mongi Ben, Scheffer, Déborah, Young, Ian D., Maroteaux, Pierre, Munnich, Arnold, Cormier-Daire, Valérie

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The Mutational Spectrum of the Sonic Hedgehog Gene in Holoprosencephaly: SHH Mutations Cause a Significant Proportion of Autosomal Dominant Holoprosencephaly von Nanni, Luisa, Ming, Jeffrey E., Bocian, Maureen, Steinhaus, Kathryn, Bianchi, Diana W., de Die-Smulders, Christine, Giannotti, Aldo, Imaizumi, Kiyoshi, Jones, Kenneth L., Del Campo, Miguel, Martin, Rick A., Meinecke, Peter, Pierpont, Mary Ella M., Robin, Nathaniel H., Young, Ian D., Roessler, Erich, Muenke, Maximilian

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Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family von Yi Li, Quan, Newbury-Ecob, Ruth A., Terrett, Jonathan A., Wilson, David I., Curtis, Andrew R.J., Ho Yi, Cheong, Gebuhr, Tom, Bullen, Philip J., Robson, Stephen C., Strachan, Tom, Bonnet, Damien, Lyonnet, Stanislas, Young, Ian D., Raeburn, J. Alexander, Buckler, Alan J., Law, David J., Brook, J. David

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Eric Lander, David Page, Aravinda Chakravarti (eds): Annual review of genomics and human genetics, volume 5. Annual Reviews, Palo Alto, 2004 (ISBN 0-8243-3705-0), hardcover von Young, Ian D

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Eric Lander, David Page, Richard Lifton (eds): Annual review of genomics and human genetics (volume 4): Annual Reviews, Palo Alto, California, 2003 (ISBN 0-8243-3704-2) hardcover,... von Young, Ian D

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Eric Lander, David Page, Richard Lifton (eds): Annual review of genomics and human genetics (volume 4) von Young, Ian D.

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A Posteriori Dietary Patterns Are Related to Risk of Type 2 Diabetes: Findings from a Systematic Review and Meta-Analysis von McEvoy, Claire T., PhD, RD, Cardwell, Christopher R., PhD, Woodside, Jayne V., PhD, Young, Ian S., MD, MB, BCh, FRCP, Hunter, Steven J., MD, MB, BCh, FRCP, McKinley, Michelle C., PhD

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Oxidative-Nitrosative Stress and Systemic Vascular Function in Highlanders With and Without Exaggerated Hypoxemia von Bailey, Damian M., PhD, Rimoldi, Stefano F., MD, Rexhaj, Emrush, MD, Pratali, Lorenza, MD, PhD, Salinas Salmòn, Carlos, MD, Villena, Mercedes, MD, McEneny, Jane, PhD, Young, Ian S., MD, Nicod, Pascal, MD, Allemann, Yves, MD, Scherrer, Urs, MD, Sartori, Claudio, MD

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The Role of SOX9 in Autosomal Sex Reversal and Campomelic Dysplasia [and Discussion] von Schafer, Alan J., Dominguez-Steglich, Marina A., Guioli, Silvana, Kwok, Cheni, Weller, Polly A., Stevanovic, Milena, Weissenbach, Jean, Mansour, Sahar, Young, Ian D., Goodfellow, Peter N., Brook, J. David, Foster, Jamie W., Burgoyne, P., Graves, J. A. M.

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