Vorinostat, a histone deacetylase inhibitor, as a potential novel treatment for psoriasis von Samuelov, Liat, Bochner, Ron, Magal, Lee, Malovitski, Kiril, Sagiv, Nadav, Nousbeck, Janna, Keren, Aviad, Fuchs‐Telem, Dana, Sarig, Ofer, Gilhar, Amos, Sprecher, Eli

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Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-Methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and leigh-Like Syndrom... von Sarig, Ofer, Goldsher, Dorit, Nousbeck, Janna, Fuchs-Telem, Dana, Cohen-Katsenelson, Ksenya, Iancu, Theodore C., Manov, Irena, Saada, Ann, Sprecher, Eli, Mandel, Hanna

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Familial Pityriasis Rubra Pilaris Is Caused by Mutations in CARD14 von Fuchs-Telem, Dana, Sarig, Ofer, van Steensel, Maurice A.M., Isakov, Ofer, Israeli, Shirli, Nousbeck, Janna, Richard, Katharina, Winnepenninckx, Veronique, Vernooij, Marigje, Shomron, Noam, Uitto, Jouni, Fleckman, Philip, Richard, Gabriele, Sprecher, Eli

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The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12 von Goldsmith, Tomer, Fuchs-Telem, Dana, Israeli, Shirli, Sarig, Ofer, Padalon-Brauch, Gilly, Bergman, Reuven, Indelman, Margarita, Sprecher, Eli, Nousbeck, Janna

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A Mutation in LIPN, Encoding Epidermal Lipase N, Causes a Late-Onset Form of Autosomal-Recessive Congenital Ichthyosis von Israeli, Shirli, Khamaysi, Ziyad, Fuchs-Telem, Dana, Nousbeck, Janna, Bergman, Reuven, Sarig, Ofer, Sprecher, Eli

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A Mutation in a Skin-Specific Isoform of SMARCAD1 Causes Autosomal-Dominant Adermatoglyphia von Nousbeck, Janna, Burger, Bettina, Fuchs-Telem, Dana, Pavlovsky, Mor, Fenig, Shlomit, Sarig, Ofer, Itin, Peter, Sprecher, Eli

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Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Syndrome Is Caused by a POC1A Mutation von Sarig, Ofer, Nahum, Sagi, Rapaport, Debora, Ishida-Yamamoto, Akemi, Fuchs-Telem, Dana, Qiaoli, Li, Cohen-Katsenelson, Ksenya, Spiegel, Ronen, Nousbeck, Janna, Israeli, Shirli, Borochowitz, Zvi-Uri, Padalon-Brauch, Gilly, Uitto, Jouni, Horowitz, Mia, Shalev, Stavit, Sprecher, Eli

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RBM28, a protein deficient in ANE syndrome, regulates hair follicle growth via miR-203 and p63 von Warshauer, Emily, Samuelov, Liat, Sarig, Ofer, Vodo, Dan, Bindereif, Albrecht, Kanaan, Moien, Gat, Uri, Fuchs-Telem, Dana, Shomron, Noam, Farberov, Luba, Pasmanik-Chor, Metsada, Nardini, Gil, Winkler, Eyal, Meilik, Benjamin, Petit, Isabelle, Aberdam, Daniel, Paus, Ralf, Sprecher, Eli, Nousbeck, Janna

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Infantile Mitochondrial Hepatopathy Is a Cardinal Feature of MEGDEL Syndrome (3-Methylglutaconic Aciduria Type IV With Sensorineural Deafness, Encephalopathy and Leigh-Like Syndrom... von Sarig, O, Goldsher, D, Nousbeck, J, Fuchs-Telem, D, Cohen-Katsenelson, K, Iancu, T C, Manov, I, Saada, A, Sprecher, E, Mandel, H

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RIN2 Deficiency Results in Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis: MACS Syndrome von Basel-Vanagaite, Lina, Sarig, Ofer, Hershkovitz, Dov, Fuchs-Telem, Dana, Rapaport, Debora, Gat, Andrea, Isman, Gila, Shirazi, Idit, Shohat, Mordechai, Enk, Claes D., Birk, Efrat, Kohlhase, Jürgen, Matysiak-Scholze, Uta, Maya, Idit, Knopf, Carlos, Peffekoven, Anette, Hennies, Hans-Christian, Bergman, Reuven, Horowitz, Mia, Ishida-Yamamoto, Akemi, Sprecher, Eli

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Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3 von Eytan, Ori, Fuchs-Telem, Dana, Mevorach, Baruch, Indelman, Margarita, Bergman, Reuven, Sarig, Ofer, Goldberg, Ilan, Adir, Noam, Sprecher, Eli

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Placenta-derived PLX-PAD mesenchymal-like stromal cells are efficacious in rescuing blood flow in hind limb ischemia mouse model by a dose- and site-dependent mechanism of action von Zahavi-Goldstein, Efrat, Blumenfeld, Michal, Fuchs-Telem, Dana, Pinzur, Lena, Rubin, Shy, Aberman, Zami, Sher, Noa, Ofir, Racheli

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Human Placental-Derived Adherent Stromal Cells Co-Induced with TNF-α and IFN-γ Inhibit Triple-Negative Breast Cancer in Nude Mouse Xenograft Models von Allen, Hoshea, Shraga-Heled, Niva, Blumenfeld, Michal, Dego-Ashto, Tamar, Fuchs-Telem, Dana, Gilert, Ariel, Aberman, Zami, Ofir, Racheli

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Analysis of CARD14 Polymorphisms in Pityriasis Rubra Pilaris: Activation of NF-κB von Li, Qiaoli, Jin Chung, Hye, Ross, Nicholas, Keller, Matthew, Andrews, Jonathan, Kingman, Joshua, Sarig, Ofer, Fuchs-Telem, Dana, Sprecher, Eli, Uitto, Jouni

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Cole Disease Results from Mutations in ENPP1 von Eytan, Ori, Morice-Picard, Fanny, Sarig, Ofer, Ezzedine, Khaled, Isakov, Ofer, Li, Qiaoli, Ishida-Yamamoto, Akemi, Shomron, Noam, Goldsmith, Tomer, Fuchs-Telem, Dana, Adir, Noam, Uitto, Jouni, Orlow, Seth J., Taieb, Alain, Sprecher, Eli

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Intramuscular Administration of Placenta-Derived Stromal Cells Enhances Survival of Rhesus Macaque Monkeys Exposed to Total Body Irradiation von Sher, Noa, Prezma, Tal, Fuchs-Telem, Dana, Shraga- Heled, Niva, Authier, Simon, Chang, Polly, Ascah, Alexis, Bakke, James, Gahagen, Janet, Ofir, Racheli

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Semidominant Inheritance in Epidermolytic Ichthyosis von Nousbeck, Janna, Padalon-Brauch, Gilly, Fuchs-Telem, Dana, Israeli, Shirli, Sarig, Ofer, Sheffer, Ruth, Sprecher, Eli

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Analysis of CARD14 Polymorphisms in Pityriasis Rubra Pilaris: Activation of NF-[kappa]B von Li, Qiaoli, Jin Chung, Hye, Ross, Nicholas, Keller, Matthew, Andrews, Jonathan, Kingman, Joshua, Sarig, Ofer, Fuchs-telem, Dana, Sprecher, Eli, Uitto, Jouni

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Inflammatory peeling skin syndrome caused a novel mutation in CDSN von Telem, Dana Fuchs, Israeli, Shirli, Sarig, Ofer, Sprecher, Eli

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RBM 28, a protein deficient in ANE syndrome, regulates hair follicle growth via miR‐203 and p63 von Warshauer, Emily, Samuelov, Liat, Sarig, Ofer, Vodo, Dan, Bindereif, Albrecht, Kanaan, Moien, Gat, Uri, Fuchs‐Telem, Dana, Shomron, Noam, Farberov, Luba, Pasmanik‐Chor, Metsada, Nardini, Gil, Winkler, Eyal, Meilik, Benjamin, Petit, Isabelle, Aberdam, Daniel, Paus, Ralf, Sprecher, Eli, Nousbeck, Janna

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