CARD14-associated papulosquamous eruption: A spectrum including features of psoriasis and pityriasis rubra pilaris von Craiglow, Brittany G., Boyden, Lynn M., Hu, Ronghua, Virtanen, Marie, Su, John, Rodriguez, Gabriela, McCarthy, Catherine, Luna, Paula, Larralde, Margarita, Humphrey, Stephen, Holland, Kristen E., Hogeling, Marcia, Hidalgo-Matlock, Benjamin, Ferrari, Bruno, Fernandez-Faith, Esteban, Drolet, Beth, Cordoro, Kelly M., Bowcock, Anne M., Antaya, Richard J., Ashack, Kurt, Ashack, Richard J., Lifton, Richard P., Milstone, Leonard M., Paller, Amy S., Choate, Keith A.

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Recessive Mutations in AP1B1 Cause Ichthyosis, Deafness, and Photophobia von Boyden, Lynn M., Atzmony, Lihi, Hamilton, Claire, Zhou, Jing, Lim, Young H., Hu, Ronghua, Pappas, John, Rabin, Rachel, Ekstien, Joseph, Hirsch, Yoel, Prendiville, Julie, Lifton, Richard P., Ferguson, Shawn, Choate, Keith A.

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High Bone Density Due to a Mutation in LDL-Receptor–Related Protein 5 von Boyden, Lynn M, Mao, Junhao, Belsky, Joseph, Mitzner, Lyle, Farhi, Anita, Mitnick, Mary A, Wu, Dianqing, Insogna, Karl, Lifton, Richard P

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Skint-1 is a highly specific, unique selecting component for epidermal T cells von Barbee, Susannah D, Woodward, Martin J, Turchinovich, Gleb, Mention, Jean-Jacques, Lewis, Julia M, Boyden, Lynn M, Lifton, Richard P, Tigelaar, Robert, Hayday, Adrian C

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Mutations in ASPRV1 Cause Dominantly Inherited Ichthyosis von Boyden, Lynn M., Zhou, Jing, Hu, Ronghua, Zaki, Theodore, Loring, Erin, Scott, Jared, Traupe, Heiko, Paller, Amy S., Lifton, Richard P., Choate, Keith A.

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Mutations in KDSR Cause Recessive Progressive Symmetric Erythrokeratoderma von Boyden, Lynn M., Vincent, Nicholas G., Zhou, Jing, Hu, Ronghua, Craiglow, Brittany G., Bayliss, Susan J., Rosman, Ilana S., Lucky, Anne W., Diaz, Luis A., Goldsmith, Lowell A., Paller, Amy S., Lifton, Richard P., Baserga, Susan J., Choate, Keith A.

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Skint1 , the prototype of a newly identified immunoglobulin superfamily gene cluster, positively selects epidermal γδ T cells von Lifton, Richard P, Boyden, Lynn M, Lewis, Julia M, Barbee, Susannah D, Bas, Anna, Girardi, Michael, Hayday, Adrian C, Tigelaar, Robert E

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The Genomic and Phenotypic Landscape of Ichthyosis: An Analysis of 1000 Kindreds von Sun, Qisi, Burgren, Nareh M, Cheraghlou, Shayan, Paller, Amy S, Larralde, Margarita, Bercovitch, Lionel, Levinsohn, Jonathan, Ren, Ivy, Hu, Rong Hua, Zhou, Jing, Zaki, Theodore, Fan, Ryan, Tian, Charlie, Saraceni, Corey, Nelson-Williams, Carol J, Loring, Erin, Craiglow, Brittany G, Milstone, Leonard M, Lifton, Richard P, Boyden, Lynn M, Choate, Keith A

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Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia von Boyden, Lynn M., Craiglow, Brittany G., Zhou, Jing, Hu, Ronghua, Loring, Erin C., Morel, Kimberly D., Lauren, Christine T., Lifton, Richard P., Bilguvar, Kaya, Paller, Amy S., Choate, Keith A.

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The Molecular Revolution in Cutaneous Biology: Identification of Skin Disease Genes von Boyden, Lynn M., Choate, Keith A.

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Mutations in PERP Cause Dominant and Recessive Keratoderma von Duchatelet, Sabine, Boyden, Lynn M., Ishida-Yamamoto, Akemi, Zhou, Jing, Guibbal, Laure, Hu, Ronghua, Lim, Young H., Bole-Feysot, Christine, Nitschké, Patrick, Santos-Simarro, Fernando, de Lucas, Raul, Milstone, Leonard M., Gildenstern, Vanessa, Helfrich, Yolanda R., Attardi, Laura D., Lifton, Richard P., Choate, Keith A., Hovnanian, Alain

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Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation von Vahidnezhad, Hassan, Youssefian, Leila, Saeidian, Amir Hossein, Boyden, Lynn M, Touati, Andrew, Harvey, Nailah, Naji, Mahtab, Zabihi, Masoud, Barzegar, Mohammadreza, Sotoudeh, Soheila, Liu, Lu, Guy, Alyson, Kariminejad, Ariana, Zeinali, Sirous, Choate, Keith A, McGrath, John A., Uitto, Jouni

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Whole-Exome Sequencing Reveals Somatic Mutations in HRAS and KRAS, which Cause Nevus Sebaceus von Levinsohn, Jonathan L., Tian, Li C., Boyden, Lynn M., McNiff, Jennifer M., Narayan, Deepak, Loring, Erin S., Yun, Duri, Sugarman, Jeffrey L., Overton, John D., Mane, Shrikant M., Lifton, Richard P., Paller, Amy S., Wagner, Annette M., Antaya, Richard J., Choate, Keith A.

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Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities von Boyden, Lynn M., Choi, Murim, Choate, Keith A., Nelson-Williams, Carol J., Farhi, Anita, Toka, Hakan R., Tikhonova, Irina R., Bjornson, Robert, Mane, Shrikant M., Colussi, Giacomo, Lebel, Marcel, Gordon, Richard D., Semmekrot, Ben A., Poujol, Alain, Välimäki, Matti J., De Ferrari, Maria E., Sanjad, Sami A., Gutkin, Michael, Karet, Fiona E., Tucci, Joseph R., Stockigt, Jim R., Keppler-Noreuil, Kim M., Porter, Craig C., Anand, Sudhir K., Whiteford, Margo L., Davis, Ira D., Dewar, Stephanie B., Bettinelli, Alberto, Fadrowski, Jeffrey J., Belsha, Craig W., Hunley, Tracy E., Nelson, Raoul D., Trachtman, Howard, Cole, Trevor R. P., Pinsk, Maury, Bockenhauer, Detlef, Shenoy, Mohan, Vaidyanathan, Priya, Foreman, John W., Rasoulpour, Majid, Thameem, Farook, Al-Shahrouri, Hania Z., Radhakrishnan, Jai, Gharavi, Ali G., Goilav, Beatrice, Lifton, Richard P.

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Dominant de novo DSP mutations cause erythrokeratodermia-cardiomyopathy syndrome von Boyden, Lynn M, Kam, Chen Y, Hernández-Martín, Angela, Zhou, Jing, Craiglow, Brittany G, Sidbury, Robert, Mathes, Erin F, Maguiness, Sheilagh M, Crumrine, Debra A, Williams, Mary L, Hu, Ronghua, Lifton, Richard P, Elias, Peter M, Green, Kathleen J, Choate, Keith A

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Expanding the Genotypic Spectrum of Bathing Suit Ichthyosis von Marukian, Nareh V, Hu, Rong-Hua, Craiglow, Brittany G, Milstone, Leonard M, Zhou, Jing, Theos, Amy, Kaymakcalan, Hande, Akkaya, Deniz A, Uitto, Jouni J, Vahidnezhad, Hassan, Youssefian, Leila, Bayliss, Susan J, Paller, Amy S, Boyden, Lynn M, Choate, Keith A

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Capillary Malformation-Arteriovenous Malformation Syndrome: Review of the Literature, Proposed Diagnostic Criteria, and Recommendations for Management von Orme, Charisse M., Boyden, Lynn M., Choate, Keith A., Antaya, Richard J., King, Brett A.

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Capillary malformation–arteriovenous malformation syndrome: Identification of a family with a novel mutation von Boyden, Lynn M., PhD, Orme, Charisse M., MD, PhD, Antaya, Richard J., MD, Choate, Keith A., MD, PhD, King, Brett A., MD, PhD

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High-Bone-Mass Disease and LRP5 von Whyte, Michael P, Reinus, William H, Mumm, Steven

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Focal Palmoplantar Keratoderma and Gingival Keratosis Caused by a KRT16 Mutation von Zaki, Theodore D, Boyden, Lynn M, Mathes, Erin, Hu, Rong-Hua, Zhou, Jing, Loring, Erin, North, Jeffrey, Oza, Vikash, Choate, Keith A

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