Transglutaminase 1 Replacement Therapy Successfully Mitigates the Autosomal Recessive Congenital Ichthyosis Phenotype in Full-Thickness Skin Disease Equivalents

Roswitha Plank; Guy Yealland; Enrico Miceli; Dulce Lima Cunha; Patrick Graff; Sari Thomforde; Robert Gruber; Verena Moosbrugger-Martinz; Katja Eckl; Marcelo Calderón; Hans Christian Hennies; Sarah Hedtrich

doi:10.1016/j.jid.2018.11.002

Transglutaminase 1 Replacement Therapy Successfully Mitigates the Autosomal Recessive Congenital Ichthyosis Phenotype in Full-Thickness Skin Disease Equivalents

Roswitha Plank, Guy Yealland, Enrico Miceli, Dulce Lima Cunha, Patrick Graff, Sari Thomforde, Robert Gruber, Verena Moosbrugger-Martinz, Katja Eckl, Marcelo Calderón, Hans Christian Hennies, Sarah Hedtrich

Research output: Contribution to journal › Letter › peer-review

19 Citations (Scopus)

Original language	English
Pages (from-to)	1191-1195
Number of pages	5
Journal	Journal of Investigative Dermatology
Volume	139
Issue number	5
Early online date	15 Nov 2018
DOIs	https://doi.org/10.1016/j.jid.2018.11.002
Publication status	Published - 1 May 2019

Access to Document

10.1016/j.jid.2018.11.002Licence: Unspecified

JID-2018-0139-Letter_091118_SupplementAccepted author manuscript, 8.78 MBLicence: Unspecified

Cite this

Plank, R., Yealland, G., Miceli, E., Lima Cunha, D., Graff, P., Thomforde, S., Gruber, R., Moosbrugger-Martinz, V., Eckl, K., Calderón, M., Hennies, H. C., & Hedtrich, S. (2019). Transglutaminase 1 Replacement Therapy Successfully Mitigates the Autosomal Recessive Congenital Ichthyosis Phenotype in Full-Thickness Skin Disease Equivalents. Journal of Investigative Dermatology, 139(5), 1191-1195. https://doi.org/10.1016/j.jid.2018.11.002

@article{a2cadb67b016488e84543100c059c545,

title = "Transglutaminase 1 Replacement Therapy Successfully Mitigates the Autosomal Recessive Congenital Ichthyosis Phenotype in Full-Thickness Skin Disease Equivalents",

author = "Roswitha Plank and Guy Yealland and Enrico Miceli and {Lima Cunha}, Dulce and Patrick Graff and Sari Thomforde and Robert Gruber and Verena Moosbrugger-Martinz and Katja Eckl and Marcelo Calder{\'o}n and Hennies, {Hans Christian} and Sarah Hedtrich",

year = "2019",

month = may,

day = "1",

doi = "10.1016/j.jid.2018.11.002",

language = "English",

volume = "139",

pages = "1191--1195",

journal = "Journal of Investigative Dermatology",

issn = "0022-202X",

publisher = "Nature Publishing Group",

number = "5",

}

Plank, R, Yealland, G, Miceli, E, Lima Cunha, D, Graff, P, Thomforde, S, Gruber, R, Moosbrugger-Martinz, V, Eckl, K, Calderón, M, Hennies, HC & Hedtrich, S 2019, 'Transglutaminase 1 Replacement Therapy Successfully Mitigates the Autosomal Recessive Congenital Ichthyosis Phenotype in Full-Thickness Skin Disease Equivalents', Journal of Investigative Dermatology, vol. 139, no. 5, pp. 1191-1195. https://doi.org/10.1016/j.jid.2018.11.002

TY - JOUR

T1 - Transglutaminase 1 Replacement Therapy Successfully Mitigates the Autosomal Recessive Congenital Ichthyosis Phenotype in Full-Thickness Skin Disease Equivalents

AU - Plank, Roswitha

AU - Yealland, Guy

AU - Miceli, Enrico

AU - Lima Cunha, Dulce

AU - Graff, Patrick

AU - Thomforde, Sari

AU - Gruber, Robert

AU - Moosbrugger-Martinz, Verena

AU - Eckl, Katja

AU - Calderón, Marcelo

AU - Hennies, Hans Christian

AU - Hedtrich, Sarah

PY - 2019/5/1

Y1 - 2019/5/1

UR - http://www.scopus.com/inward/record.url?scp=85060760191&partnerID=8YFLogxK

U2 - 10.1016/j.jid.2018.11.002

DO - 10.1016/j.jid.2018.11.002

M3 - Letter

C2 - 30448383

VL - 139

SP - 1191

EP - 1195

JO - Journal of Investigative Dermatology

JF - Journal of Investigative Dermatology

SN - 0022-202X

IS - 5

ER -

Transglutaminase 1 Replacement Therapy Successfully Mitigates the Autosomal Recessive Congenital Ichthyosis Phenotype in Full-Thickness Skin Disease Equivalents

Access to Document

Other files and links

Hans Hennies

Cite this

Transglutaminase 1 Replacement Therapy Successfully Mitigates the Autosomal Recessive Congenital Ichthyosis Phenotype in Full-Thickness Skin Disease Equivalents

Access to Document

Other files and links

Profiles

Hans Hennies

Cite this