A conditional Spink5 knock-out mouse model of Netherton syndrome

被引：0
|
作者：
Wang, Y. [1 ]
Petrova, E. [1 ]
Izabelle, C. [1 ]
Leturcq, F. [1 ]
des Claustres, M. Bonnet [1 ]
Hovnanian, A. [1 ]
机构：
[1] INSERM, Imagine Inst, UMR1163, Paris, France
来源：
JOURNAL OF INVESTIGATIVE DERMATOLOGY | 2018年 / 138卷 / 09期
关键词：
D O I：
10.1016/j.jid.2018.06.076
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
LB1542
引用
收藏
页码：B13 / B13
页数：1
相关论文
共 50 条
  • [1] Comparative analyses of Netherton syndrome patients and Spink5 conditional knock-out mice uncover disease-relevant pathways
    Petrova, Evgeniya
    Lopez-Gay, Jesus Maria
    Fahrner, Matthias
    Leturcq, Florent
    de Villartay, Jean-Pierre
    Barbieux, Claire
    Gonschorek, Patrick
    Tsoi, Lam C.
    Gudjonsson, Johann E.
    Schilling, Oliver
    Hovnanian, Alain
    COMMUNICATIONS BIOLOGY, 2024, 7 (01)
  • [2] Comparative analyses of Netherton syndrome patients and Spink5 conditional knock-out mice uncover disease-relevant pathways
    Evgeniya Petrova
    Jesús María López-Gay
    Matthias Fahrner
    Florent Leturcq
    Jean-Pierre de Villartay
    Claire Barbieux
    Patrick Gonschorek
    Lam C. Tsoi
    Johann E. Gudjonsson
    Oliver Schilling
    Alain Hovnanian
    Communications Biology, 7
  • [3] Molecular signatures of skin barrier defect and inflammation in Netherton syndrome uncovered by comparing patients to viable Spink5 knock-out mice
    Petrova, E.
    Orts, J. M. Lopez-Gay
    Fahrner, M.
    Leturcq, F.
    Villartay, J-Pd
    Barbieux, C.
    Tsoi, L.
    Gudjonsson, J.
    Schilling, O.
    Hovnanian, A.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2023, 143 (11) : S352 - S352
  • [4] A viable mouse model for Netherton syndrome based on mosaic inactivation of the Spink5 gene
    Kasparek, Petr
    Ileninova, Zuzana
    Haneckova, Radka
    Kanchev, Ivan
    Jenickova, Irena
    Sedlacek, Radislav
    BIOLOGICAL CHEMISTRY, 2016, 397 (12) : 1287 - 1292
  • [5] A case of Netherton syndrome with mutation in SPINK5 and FLG
    Shi, Zhen-rui
    Xu, Min
    Tan, Guo-zhen
    Wang, Liangchun
    Guo, Qing
    Tang, Zeng-qi
    EUROPEAN JOURNAL OF DERMATOLOGY, 2017, 27 (05) : 536 - 537
  • [6] A case of Netherton syndrome with mutation in SPINK5 and FLG
    Zhen-rui Shi
    Min Xu
    Guo-zhen Tan
    Liangchun Wang
    Qing Guo
    Zeng-qi Tang
    European Journal of Dermatology, 2017, 27 : 536 - 537
  • [7] The role of SPINK5 mutation distribution in phenotypes of Netherton syndrome
    Xu, Min
    Shi, Yujie
    Lin, Li
    Wang, Liang
    Zhu, Xianzhong
    Xiong, Jinglin
    Yin, Jiawen
    Qi, Qing
    Yang, Wenlin
    FRONTIERS IN GENETICS, 2025, 16
  • [8] Development of a Netherton Syndrome model based on targeted deletion of SPINK5 in human keratinocytes
    Galvez Cortes, V.
    Bonafont Arago, J.
    Mencia, A.
    Carretero, M.
    Chacon Solano, E.
    Murillas Angoiti, R.
    Vicente, A.
    Di, W.
    Larcher, F.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2019, 139 (09) : S267 - S267
  • [9] A New SPINK5 Mutation in a Patient with Netherton Syndrome: A Case Report
    Alpigiani, Maria G.
    Salvati, Pietro
    Schiaffino, Maria Cristina
    Occella, Corrado
    Castiglia, Daniela
    Covaciu, Claudia
    Lorini, Renata
    PEDIATRIC DERMATOLOGY, 2012, 29 (04) : 521 - 522
  • [10] Characterization and expression analysis of the Spink5 gene, the mouse ortholog of the defective gene in Netherton syndrome
    Galliano, MF
    Roccasecca, RM
    Descargues, P
    Micheloni, A
    Levy, E
    Zambruno, G
    D'Alessio, M
    Hovnanian, A
    GENOMICS, 2005, 85 (04) : 483 - 492
12345