Works by Sarig, Ofer

Results: 47
    1
    2
    3
    4
    5
    6
    7

    RBM28, a protein deficient in ANE syndrome, regulates hair follicle growth via miR-203 and p63.

    Published in:
    Experimental Dermatology, 2015, v. 24, n. 8, p. 618, doi. 10.1111/exd.12737
    By:
    • 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
    Publication type:
    Article
    8
    9
    10
    11
    12
    13
    14
    15
    16
    17

    Ustekinumab therapy for Netherton syndrome.

    Published in:
    Journal of Dermatology (John Wiley & Sons, Inc.), 2023, v. 50, n. 4, p. 494, doi. 10.1111/1346-8138.16645
    By:
    • Samuelov, Liat;
    • Shehadeh, Waseem;
    • Sarig, Ofer;
    • Gat, Andrea;
    • Matz, Hagit;
    • Sprecher, Eli
    Publication type:
    Article
    18
    19

    Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa.

    Published in:
    Pediatric Dermatology, 2023, v. 40, n. 6, p. 1021, doi. 10.1111/pde.15440
    By:
    • Bergson, Shir;
    • Daniely, Daniel;
    • Bomze, David;
    • Mohamad, Janan;
    • Malovitski, Kiril;
    • Meijers, Odile;
    • Briskin, Valeria;
    • Bihari, Ofer;
    • Malchin, Natalia;
    • Israeli, Shirli;
    • Mashiah, Jacob;
    • Falik‐Zaccai, Tzipora;
    • Avitan‐Hersh, Emily;
    • Eskin‐Schwartz, Marina;
    • Allon‐Shalev, Stavit;
    • Sarig, Ofer;
    • Sprecher, Eli;
    • Samuelov, Liat
    Publication type:
    Article
    20

    Woolly hair in tricho‐dento‐osseous syndrome.

    Published in:
    Pediatric Dermatology, 2023, v. 40, n. 6, p. 1094, doi. 10.1111/pde.15309
    By:
    • Perandones‐González, Héctor;
    • Rusiñol‐Batlle, Lluis;
    • Bosquez, David;
    • Brunet‐Llobet, Lluis;
    • Ivars, Marta;
    • Yubero, Délia;
    • Sarig, Ofer;
    • Malki, Liron;
    • Peled, Alon;
    • Sprecher, Eli;
    • Baselga, Eulalia
    Publication type:
    Article
    21
    22
    23
    24
    25
    26

    Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis.

    Published in:
    PLoS Genetics, 2016, v. 12, n. 10, p. 1, doi. 10.1371/journal.pgen.1006369
    By:
    • Peled, Alon;
    • Sarig, Ofer;
    • Samuelov, Liat;
    • Bertolini, Marta;
    • Ziv, Limor;
    • Weissglas-Volkov, Daphna;
    • Eskin-Schwartz, Marina;
    • Adase, Christopher A.;
    • Malchin, Natalia;
    • Bochner, Ron;
    • Fainberg, Gilad;
    • Goldberg, Ilan;
    • Sugawara, Koji;
    • Baniel, Avital;
    • Tsuruta, Daisuke;
    • Luxenburg, Chen;
    • Adir, Noam;
    • Duverger, Olivier;
    • Morasso, Maria;
    • Shalev, Stavit
    Publication type:
    Article
    27
    28
    29
    30
    31

    Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene.

    Published in:
    PLoS Genetics, 2016, v. 12, n. 5, p. 1, doi. 10.1371/journal.pgen.1006008
    By:
    • Vodo, Dan;
    • Sarig, Ofer;
    • Geller, Shamir;
    • Ben-Asher, Edna;
    • Olender, Tsviya;
    • Bochner, Ron;
    • Goldberg, Ilan;
    • Nosgorodsky, Judith;
    • Alkelai, Anna;
    • Tatarskyy, Pavel;
    • Peled, Alon;
    • Baum, Sharon;
    • Barzilai, Aviv;
    • Ibrahim, Saleh M.;
    • Zillikens, Detlef;
    • Lancet, Doron;
    • Sprecher, Eli
    Publication type:
    Article
    32

    Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-Methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and leigh-Like Syndrome) caused by novel mutations in SERAC1.

    Published in:
    American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 9, p. 2204, doi. 10.1002/ajmg.a.36059
    By:
    • Sarig, Ofer;
    • Goldsher, Dorit;
    • Nousbeck, Janna;
    • Fuchs ‐ Telem, Dana;
    • CohEN ‐ KatsENelson, KsENya;
    • Iancu, Theodore C.;
    • Manov, IrENa;
    • Saada, Ann;
    • Sprecher, Eli;
    • Mandel, Hanna
    Publication type:
    Article
    33
    34

    A Mutation in TP63 Causing a Mild Ectodermal Dysplasia Phenotype.

    Published in:
    Journal of Investigative Dermatology, 2014, v. 134, n. 8, p. 2277, doi. 10.1038/jid.2014.159
    By:
    • Goldsmith, Tomer;
    • Eytan, Ori;
    • Magal, Lee;
    • Solomon, Michal;
    • Israeli, Shirli;
    • Warshauer, Emily;
    • Grafi-Cohen, Meital;
    • Aberdam, Daniel;
    • van Bokhoven, Hans;
    • Zhou, Huiqing;
    • Sarig, Ofer;
    • Sprecher, Eli;
    • Nousbeck, Janna
    Publication type:
    Article
    35
    36

    Semidominant Inheritance in Epidermolytic Ichthyosis.

    Published in:
    Journal of Investigative Dermatology, 2013, v. 133, n. 11, p. 2626, doi. 10.1038/jid.2013.193
    By:
    • Nousbeck, Janna;
    • Padalon-Brauch, Gilly;
    • Fuchs-Telem, Dana;
    • Israeli, Shirli;
    • Sarig, Ofer;
    • Sheffer, Ruth;
    • Sprecher, Eli
    Publication type:
    Article
    37

    Digenic Inheritance in Epidermolysis Bullosa Simplex.

    Published in:
    Journal of Investigative Dermatology, 2012, v. 132, n. 12, p. 2852, doi. 10.1038/jid.2012.229
    By:
    • Padalon-Brauch, Gilly;
    • Amitai, Dani Ben;
    • Vodo, Dan;
    • Harel, Avikam;
    • Sarig, Ofer;
    • Sprecher, Eli;
    • Mashiah, Jacob
    Publication type:
    Article
    38

    Population-Specific Association between a Polymorphic Variant in ST18, Encoding a Pro-Apoptotic Molecule, and Pemphigus Vulgaris.

    Published in:
    Journal of Investigative Dermatology, 2012, v. 132, n. 7, p. 1798, doi. 10.1038/jid.2012.46
    By:
    • Sarig, Ofer;
    • Bercovici, Sivan;
    • Zoller, Lilach;
    • Goldberg, Ilan;
    • Indelman, Margarita;
    • Nahum, Sagi;
    • Israeli, Shirli;
    • Sagiv, Nadav;
    • Martinez de Morentin, Helena;
    • Katz, Oren;
    • Baum, Sharon;
    • Barzilai, Aviv;
    • Trau, Henri;
    • Murrell, Dedee F;
    • Bergman, Reuven;
    • Hertl, Michael;
    • Rosenberg, Shai;
    • Nöthen, Markus M;
    • Skorecki, Karl;
    • Schmidt, Enno
    Publication type:
    Article
    39

    IGFBP7 as a Potential Therapeutic Target in Psoriasis.

    Published in:
    2011
    By:
    • Nousbeck, Janna;
    • Ishida-Yamamoto, A.;
    • Bidder, Miri;
    • Fuchs, Dana;
    • Eckl, Katja;
    • Hennies, Hans Christian;
    • Sagiv, Nadav;
    • Gat, Andrea;
    • Gini, Meri;
    • Filip, Irina;
    • Matz, Hagit;
    • Goldberg, Ilan;
    • Enk, Claes D.;
    • Sarig, Ofer;
    • Meilik, Benny;
    • Aberdam, Daniel;
    • Gilhar, Amos;
    • Sprecher, Eli
    Publication type:
    Letter
    40
    41
    42
    43

    Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting.

    Published in:
    Nature Genetics, 2013, v. 45, n. 10, p. 1244, doi. 10.1038/ng.2739
    By:
    • Samuelov, Liat;
    • Sarig, Ofer;
    • Harmon, Robert M;
    • Rapaport, Debora;
    • Ishida-Yamamoto, Akemi;
    • Isakov, Ofer;
    • Koetsier, Jennifer L;
    • Gat, Andrea;
    • Goldberg, Ilan;
    • Bergman, Reuven;
    • Spiegel, Ronen;
    • Eytan, Ori;
    • Geller, Shamir;
    • Peleg, Sarit;
    • Shomron, Noam;
    • Goh, Christabelle S M;
    • Wilson, Neil J;
    • Smith, Frances J D;
    • Pohler, Elizabeth;
    • Simpson, Michael A
    Publication type:
    Article
    44
    45
    46
    47