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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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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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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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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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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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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Phenotypic spectrum of autosomal recessive congenital ichthyosis due to PNPLA1 mutation von Boyden, L.M., Craiglow, B.G., Hu, R.H., Zhou, J., Browning, J., Eichenfield, L., Lim, Y.L., Luu, M., Randolph, L.M., Ginarte, M., Fachal, L., Rodriguez‐Pazos, L., Vega, A., Kramer, D., Yosipovitch, G., Vahidnezhad, H., Youssefian, L., Uitto, J., Lifton, R.P., Paller, A.S., Milstone, L.M., Choate, K.A.

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Dihedral ψ Angle Dependence of the Amide III Vibration:  A Uniquely Sensitive UV Resonance Raman Secondary Structural Probe von Asher, Sanford A, Ianoul, Anatoli, Mix, Guido, Boyden, Mary N, Karnoup, Anton, Diem, Max, Schweitzer-Stenner, Reinhard

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Implant Standardization for Hemiarthroplasty: Implementation of a Pricing Matrix System at a Level II Community Based Trauma System von Althausen, Peter L., MD, MBA, Lu, Minggen, PhD, Thomas, Kenneth C., MD, Shannon, Steven F., BS, Biagi, Brian N., BS, Boyden, Eric M., MD

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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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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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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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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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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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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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Spain: The Centre of the World, 1519-1682 von Boyden, James M.

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

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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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