J. Lugassy

Naegeli-franceschetti-jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations in Krt14

J. Lugassy, P. Itin, A. Ishida-Yamamoto, 2022 .

Modulation of TCR responsiveness by the Grb2-family adaptor, Gads.

J. Lugassy, H. Urlaub, Dvora Beach, 2015, Cellular signalling.

Rapid detection of homozygous mutations in congenital recessive ichthyosis

J. Lugassy, H. Hennies, M. Indelman, 2008, Archives of Dermatological Research.

Galli–Galli disease is an acantholytic variant of Dowling–Degos disease

J. Lugassy, M. Indelman, R. Bergman, 2007, The British journal of dermatology.

Novel mutations in DSG1 causing striate palmoplantar keratoderma

J. Lugassy, R. Bergman, E. Sprecher, 2009, Clinical and experimental dermatology.

The Enzymatic Activity of Lysyl Oxidas-like-2 (LOXL2) Is Not Required for LOXL2-induced Inhibition of Keratinocyte Differentiation*

J. Lugassy, G. Neufeld, O. Kessler, 2011, The Journal of Biological Chemistry.

KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndrome.

J. Lugassy, P. Itin, D. Bercovich, 2008, The Journal of investigative dermatology.

The Enzymatic Activity of Lysyl Oxidas-like-2 (LOXL2) Is Not Required for LOXL2-induced Inhibition of Keratinocyte Differentiation*

J. Lugassy, G. Neufeld, V. Smith, 2011, The Journal of Biological Chemistry.