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Page 1
Cutaneous and Developmental Effects of CARD14 Overexpression in Zebrafish.
Baniel A, Ziv L, Ben-Moshe Z, Sarig O, Mohamad J, Peled A, Rechavi G, Gothilf Y, Sprecher E. Baniel A, et al. Among authors: mohamad j. Biomedicines. 2022 Dec 8;10(12):3192. doi: 10.3390/biomedicines10123192. Biomedicines. 2022. PMID: 36551948 Free PMC article.
Loss-of-Function Mutations in SERPINB8 Linked to Exfoliative Ichthyosis with Impaired Mechanical Stability of Intercellular Adhesions.
Pigors M, Sarig O, Heinz L, Plagnol V, Fischer J, Mohamad J, Malchin N, Rajpopat S, Kharfi M, Lestringant GG, Sprecher E, Kelsell DP, Blaydon DC. Pigors M, et al. Among authors: mohamad j. Am J Hum Genet. 2016 Aug 4;99(2):430-6. doi: 10.1016/j.ajhg.2016.06.004. Epub 2016 Jul 28. Am J Hum Genet. 2016. PMID: 27476651 Free PMC article.
ARCI7 Revisited and Repositioned.
Mohamad J, Malchin N, Shalev S, Sarig O, Sprecher E. Mohamad J, et al. J Invest Dermatol. 2017 Apr;137(4):970-972. doi: 10.1016/j.jid.2016.12.008. Epub 2016 Dec 21. J Invest Dermatol. 2017. PMID: 28011144 Free article. No abstract available.
Punctate palmoplantar keratoderma: an unusual mutation causing an unusual phenotype.
Vodo D, Sarig O, Jeddah D, Malchin N, Eskin-Schwarz M, Mohamad J, Rabinowitz T, Goldberg I, Shomron N, Khamaysi Z, Bergman R, Sprecher E. Vodo D, et al. Among authors: mohamad j. Br J Dermatol. 2018 Jun;178(6):1455-1457. doi: 10.1111/bjd.16502. Epub 2018 Apr 16. Br J Dermatol. 2018. PMID: 29494755 No abstract available.
SAM syndrome is characterized by extensive phenotypic heterogeneity.
Taiber S, Samuelov L, Mohamad J, Barak EC, Sarig O, Shalev SA, Lestringant G, Sprecher E. Taiber S, et al. Among authors: mohamad j. Exp Dermatol. 2018 Jul;27(7):787-790. doi: 10.1111/exd.13551. Exp Dermatol. 2018. PMID: 29604126 Review.
Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type A.
Mohamad J, Sarig O, Godsel LM, Peled A, Malchin N, Bochner R, Vodo D, Rabinowitz T, Pavlovsky M, Taiber S, Fried M, Eskin-Schwartz M, Assi S, Shomron N, Uitto J, Koetsier JL, Bergman R, Green KJ, Sprecher E. Mohamad J, et al. J Invest Dermatol. 2018 Aug;138(8):1736-1743. doi: 10.1016/j.jid.2018.04.032. Epub 2018 Jun 27. J Invest Dermatol. 2018. PMID: 29758285 Free PMC article.
Loss-of-function mutations in caspase recruitment domain-containing protein 14 (CARD14) are associated with a severe variant of atopic dermatitis.
Peled A, Sarig O, Sun G, Samuelov L, Ma CA, Zhang Y, Dimaggio T, Nelson CG, Stone KD, Freeman AF, Malki L, Vidal LS, Chamarthy LM, Briskin V, Mohamad J, Pavlovsky M, Walter JE, Milner JD, Sprecher E. Peled A, et al. Among authors: mohamad j. J Allergy Clin Immunol. 2019 Jan;143(1):173-181.e10. doi: 10.1016/j.jaci.2018.09.002. Epub 2018 Sep 21. J Allergy Clin Immunol. 2019. PMID: 30248356 Clinical Trial.
PLACK syndrome shows remarkable phenotypic homogeneity.
Mohamad J, Samuelov L, Ben-Amitai D, Malchin N, Sarig O, Sprecher E. Mohamad J, et al. Clin Exp Dermatol. 2019 Jul;44(5):580-583. doi: 10.1111/ced.13887. Epub 2019 Jan 17. Clin Exp Dermatol. 2019. PMID: 30656735 No abstract available.
Variant PADI3 in Central Centrifugal Cicatricial Alopecia.
Malki L, Sarig O, Romano MT, Méchin MC, Peled A, Pavlovsky M, Warshauer E, Samuelov L, Uwakwe L, Briskin V, Mohamad J, Gat A, Isakov O, Rabinowitz T, Shomron N, Adir N, Simon M, McMichael A, Dlova NC, Betz RC, Sprecher E. Malki L, et al. Among authors: mohamad j. N Engl J Med. 2019 Feb 28;380(9):833-841. doi: 10.1056/NEJMoa1816614. Epub 2019 Feb 13. N Engl J Med. 2019. PMID: 30763140
70 results