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Items: 4

1.

Genetic Therapies for Hearing Loss: Accomplishments and Remaining Challenges.

Taiber S, Avraham KB.

Neurosci Lett. 2019 Nov 20;713:134527. doi: 10.1016/j.neulet.2019.134527. Epub 2019 Oct 3. Review.

PMID:
31586696
2.

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.

J Invest Dermatol. 2018 Aug;138(8):1736-1743. doi: 10.1016/j.jid.2018.04.032. Epub 2018 Jun 27.

3.

SAM syndrome is characterized by extensive phenotypic heterogeneity.

Taiber S, Samuelov L, Mohamad J, Barak EC, Sarig O, Shalev SA, Lestringant G, Sprecher E.

Exp Dermatol. 2018 Jul;27(7):787-790. doi: 10.1111/exd.13551. Review.

PMID:
29604126
4.

Engineering of a red-light-activated human cAMP/cGMP-specific phosphodiesterase.

Gasser C, Taiber S, Yeh CM, Wittig CH, Hegemann P, Ryu S, Wunder F, Möglich A.

Proc Natl Acad Sci U S A. 2014 Jun 17;111(24):8803-8. doi: 10.1073/pnas.1321600111. Epub 2014 Jun 2.

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