Cellular Basis of Secondary Infections and Impaired Desquamation in Certain Inherited Ichthyoses von Chan, Aegean, Godoy-Gijon, Elena, Nuno-Gonzalez, Almudena, Crumrine, Debra, Hupe, Melanie, Choi, Eung-Ho, Gruber, Robert, Williams, Mary L, Choate, Keith, Fleckman, Philip H, Elias, Peter M

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Cellular Basis of Secondary Infections and Impaired Desquamation in Certain Inherited Ichthyoses von Chan, Aegean, Godoy-Gijon, Elena, Nuno-Gonzalez, Almudena, Crumrine, Debra, Hupe, Melanie, Choi, Eung-Ho, Gruber, Robert, Williams, Mary L, Choate, Keith, Fleckman, Philip H, Elias, Peter M

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A Sensitive Microassay for Prolyl Hydroxylase: Activity in Normal and Psoriatic Skin von Fleckman, Philip H., Jeffrey, John J., Elsen, Arthur Z.

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Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis von McLean, W H Irwin, Palmer, Colin N A, Irvine, Alan D, Terron-Kwiatkowski, Ana, Zhao, Yiwei, Liao, Haihui, Lee, Simon P, Goudie, David R, Sandilands, Aileen, Campbell, Linda E, Smith, Frances J D, O'Regan, Gráinne M, Watson, Rosemarie M, Cecil, Jo E, Bale, Sherri J, Compton, John G, DiGiovanna, John J, Fleckman, Philip, Lewis-Jones, Sue, Arseculeratne, Gehan, Sergeant, Ann, Munro, Colin S, El Houate, Brahim, McElreavey, Ken, Halkjaer, Liselotte B, Bisgaard, Hans, Mukhopadhyay, Somnath

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Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris von McLean, W H Irwin, Smith, Frances J D, Irvine, Alan D, Terron-Kwiatkowski, Ana, Sandilands, Aileen, Campbell, Linda E, Zhao, Yiwei, Liao, Haihui, Evans, Alan T, Goudie, David R, Lewis-Jones, Sue, Arseculeratne, Gehan, Munro, Colin S, Sergeant, Ann, O'Regan, Gráinne, Bale, Sherri J, Compton, John G, DiGiovanna, John J, Presland, Richard B, Fleckman, Philip

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Filaggrin Genotype in Ichthyosis Vulgaris Predicts Abnormalities in Epidermal Structure and Function von Gruber, Robert, Elias, Peter M, Crumrine, Debra, Lin, Tzu-Kai, Brandner, Johanna M, Hachem, Jean-Pierre, Presland, Richard B, Fleckman, Philip, Janecke, Andreas R, Sandilands, Aileen, McLean, W.H. Irwin, Fritsch, Peter O, Mildner, Michael, Tschachler, Erwin, Schmuth, Matthias

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A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming von Irvine, Alan D, Shiohama, Aiko, Sundberg, John P, Presland, Richard B, Kudoh, Jun, Campbell, Linda E, Callanan, John J, Kawasaki, Hiroshi, Shimizu, Nobuyoshi, Mangan, Niamh E, Saunders, Sean P, Fleckman, Philip, Sandilands, Aileen, Kubo, Akiharu, Amagai, Masayuki, McLean, W H Irwin, Fallon, Padraic G, Sasaki, Takashi

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Consensus recommendations for the use of retinoids in ichthyosis and other disorders of cornification in children and adolescents von Zaenglein, Andrea L., Levy, Moise L., Stefanko, Nicole S., Benjamin, Latanya T., Bruckner, Anna L., Choate, Keith, Craiglow, Brittany G., DiGiovanna, John J., Eichenfield, Lawrence F., Elias, Peter, Fleckman, Philip, Lawley, Leslie P., Lewis, Richard A., Lucky, Anne W., Mathes, Erin F., Milstone, Leonard M., Paller, Amy S., Patel, Sonali S., Siegel, Dawn H., Teng, Joyce, Tanumihardjo, Sherry A., Thaxton, Lauren, Williams, Mary L.

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Mutations in ABCA12 Underlie the Severe Congenital Skin Disease Harlequin Ichthyosis von David Kelsell, P., Elizabeth Norgett, E., Unsworth, Harriet, Teh, Muy-Teck, Cullup, Thomas, Mein, Charles A., Patricia Dopping-Hepenstal, J., Beverly Dale, A., Tadini, Gianluca, Fleckman, Philip, Karen Stephens, G., Virginia Sybert, P., Susan Mallory, B., Bernard North, V., David Witt, R., Sprecher, Eli, E. M. Taylor, Aileen, Ilchyshyn, Andrew, Cameron Kennedy, T., Goodyear, Helen, Moss, Celia, Paige, David, John Harper, I., Bryan Young, D., Irene Leigh, M., Robin Eady, A.J., Edel O’Toole, A.

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Clinical and Pathological Features of Pachyonychia Congenita von Leachman, Sancy A., Kaspar, Roger L., Fleckman, Philip, Florell, Scott R., Smith, Frances J.D., McLean, W.H. Irwin, Lunny, Declan P., Milstone, Leonard M., van Steensel, Maurice A.M., Munro, Colin S., O'Toole, Edel A., Celebi, Julide T., Kansky, Aleksej, Lane, EBirgitte

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Executive summary: Consensus recommendations for the use of retinoids in ichthyosis and other disorders of cornification in children and adolescents von Zaenglein, Andrea L., Levy, Moise L., Stefanko, Nicole S., Benjamin, Latanya T., Bruckner, Anna L., Choate, Keith, Craiglow, Brittany G., DiGiovanna, John J., Eichenfield, Lawrence F., Elias, Peter, Fleckman, Philip, Lawley, Leslie P., Lewis, Richard A., Lucky, Anne W., Mathes, Erin F., Milstone, Leonard M., Paller, Amy S., Patel, Sonali S., Siegel, Dawn H., Teng, Joyce, Tanumihardjo, Sherry A., Thaxton, Lauren, Williams, Mary L.

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Tissue response and Msx1 expression after human fetal digit tip amputation in vitro von Allan, Christopher H., Fleckman, Philip, Fernandes, Russell J., Hager, Barbara, James, Jennifer, Wisecarver, Zudtky, Kyle Satterstrom, F., Gutierrez, Alicia, Norman, Anthony, Pirrone, Anna, Underwood, Robert A., Rubin, Brian P., Zhang, Miqin, Ramay, Hassna R., Clark, John M.

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Reduced Stability and Bi-Allelic, Coequal Expression of Profilaggrin mRNA in Keratinocytes Cultured From Subjects With Ichthyosis Vulgaris von Nirunsuksiri, Wilas, Zhang, She-Hui, Fleckman, Philip

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A homozygous frameshift mutation in the murine filaggrin gene facilitates enhanced percutaneous allergen priming von Fallon, Padraic G., Sasaki, Takashi, Sandilands, Aileen, Campbell, Linda E., Saunders, Sean P., Mangan, Niamh E., Callanan, John J., Kawasaki, Hiroshi, Shiohama, Aiko, Kubo, Akiharu, Sundberg, John, Presland, Richard B., Fleckman, Philip, Shimizu, Nobuyoshi, Kudoh, Jun, Irvine, Alan D., Amagai, Masayuki, McLean, W. H. Irwin

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A homozygous frameshift mutation in the mouse Fig gene facilitates enhanced percutaneous allergen priming von FALLON, Padraic G, SASAKI, Takashi, SUNDBERG, John P, PRESLAND, Richard B, FLECKMAN, Philip, SHIMIZU, Nobuyoshi, KUDOH, Jun, IRVINE, Alan D, AMAGAI, Masayuki, MCLEAN, W. H. Irwin, SANDILANDS, Aileen, CAMPBELL, Linda E, SAUNDERS, Sean P, MANGAN, Niamh E, CALLANAN, John J, KAWASAKI, Hiroshi, SHIOHAMA, Aiko, KUBO, Akiharu

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Expression of MSX1 and Keratins 14 and 19 After Human Fetal Digit Tip Amputation in Vitro von Allan, Christopher H., Fleckman, Philip, Gutierrez, Alicia, Caldwell, Trevor, Underwood, Robert

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084Expression of MSX1 and Keratins 14 and 19 After Human Fetal Digit Tip Amputation in Vitro von Allan, Christopher H., Fleckman, Philip, Gutierrez, Alicia, Caldwell, Trevor, Underwood, Robert

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Dermatome setting for autografts to cover INTEGRA von FANG, P, ENGRAV, L. H, WARNER, P, GIBRAN, N. S, HONARI, S, KIRILUK, D. B, COLE, J. K, FLECKMAN, Philip, HEIMBACH, D. M, BAUER, G. J, MATSUMURA, H

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Glycosaminoglycan Synthesis by Human Keratinocytes: Cell Growth and Medium Calcium Effects von Piepkorn, Michael, Fleckman, Philip, Carney, Helen, Linker, Alfred

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The Distinctive Pattern of Proteoglycan and Glycosaminoglycan Free Chain Synthesis by Cultured Human Epidermal Keratinocytes von Carney, Helen, Piepkorn, Michael, Fleckman, Philip, Hovingh, Peter, Linker, Alfred

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