Literature DB >> 24005053

Identifying a hyperkeratosis signature in autosomal recessive congenital ichthyosis: Mdm2 inhibition prevents hyperkeratosis in a rat ARCI model.

Gehad Youssef1, Masahiro Ono2, Stuart J Brown1, Veronica A Kinsler3, Neil J Sebire4, John I Harper1, Ryan F L O'Shaughnessy5.   

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Year:  2013        PMID： 24005053     DOI： 10.1038/jid.2013.374

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN： 0022-202X            Impact factor:   8.551


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  15 in total

1.  Acitretin-related ossification.

Authors:  Maarten J Rood; Sjan P M Lavrijsen; Tom W J Huizinga
Journal:  J Rheumatol       Date:  2007-04       Impact factor: 4.666

2.  Development of ichthyosiform skin compensates for defective permeability barrier function in mice lacking transglutaminase 1.

Authors:  Nobuo Kuramoto; Toshihiro Takizawa; Takami Takizawa; Masato Matsuki; Hiroyuki Morioka; John M Robinson; Kiyofumi Yamanishi
Journal:  J Clin Invest       Date:  2002-01       Impact factor: 14.808

3.  Corrective gene transfer in the human skin disorder lamellar ichthyosis.

Authors:  K A Choate; D A Medalie; J R Morgan; P A Khavari
Journal:  Nat Med       Date:  1996-11       Impact factor: 53.440

4.  Human oncoprotein MDM2 activates the Akt signaling pathway through an interaction with the repressor element-1 silencing transcription factor conferring a survival advantage to cancer cells.

Authors:  S Singh; M Ramamoorthy; C Vaughan; W A Yeudall; S Deb; S Palit Deb
Journal:  Cell Death Differ       Date:  2012-12-14       Impact factor: 15.828

5.  Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1.

Authors:  Florence Jobard; Caroline Lefèvre; Aysen Karaduman; Claudine Blanchet-Bardon; Serap Emre; Jean Weissenbach; Meral Ozgüc; Mark Lathrop; Jean-François Prud'homme; Judith Fischer
Journal:  Hum Mol Genet       Date:  2002-01-01       Impact factor: 6.150

Review 6.  Recent advances in the therapeutic perspectives of Nutlin-3.

Authors:  Paola Secchiero; Raffaella Bosco; Claudio Celeghini; Giorgio Zauli
Journal:  Curr Pharm Des       Date:  2011       Impact factor: 3.116

7.  Nongenotoxic p53 activation protects cells against S-phase-specific chemotherapy.

Authors:  Dominique Kranz; Matthias Dobbelstein
Journal:  Cancer Res       Date:  2006-11-01       Impact factor: 12.701

8.  Autosomal recessive congenital ichthyosis.

Authors:  Judith Fischer
Journal:  J Invest Dermatol       Date:  2009-06       Impact factor: 8.551

9.  Mutations in the gene for transglutaminase 1 in autosomal recessive lamellar ichthyosis.

Authors:  L J Russell; J J DiGiovanna; G R Rogers; P M Steinert; N Hashem; J G Compton; S J Bale
Journal:  Nat Genet       Date:  1995-03       Impact factor: 38.330

10.  Long-term faithful recapitulation of transglutaminase 1-deficient lamellar ichthyosis in a skin-humanized mouse model, and insights from proteomic studies.

Authors:  Karin Aufenvenne; Robert H Rice; Ingrid Hausser; Vinzenz Oji; Hans Christian Hennies; Marcela Del Rio; Heiko Traupe; Fernando Larcher
Journal:  J Invest Dermatol       Date:  2012-03-22       Impact factor: 8.551
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  4 in total

Review 1.  Targeting MDM2 for novel molecular therapy: Beyond oncology.

Authors:  Wei Wang; Jiang-Jiang Qin; Mehrdad Rajaei; Xin Li; Xiaoyi Yu; Courtney Hunt; Ruiwen Zhang
Journal:  Med Res Rev       Date:  2019-10-06       Impact factor: 12.944

2.  Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans.

Authors:  Lisa Heinz; Gwang-Jin Kim; Slaheddine Marrakchi; Julie Christiansen; Hamida Turki; Marc-Alexander Rauschendorf; Mark Lathrop; Ingrid Hausser; Andreas D Zimmer; Judith Fischer
Journal:  Am J Hum Genet       Date:  2017-06-01       Impact factor: 11.025

3.  A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma.

Authors:  V A Kinsler; S Drury; A Khan; R Waelchli; G Rukaite; A Barnicoat; N Lench; J I Harper; R F L O'Shaughnessy
Journal:  Br J Dermatol       Date:  2014-12-09       Impact factor: 9.302

Review 4.  Experimental Models for the Study of Hereditary Cornification Defects.

Authors:  Dragan Copic; Maria Laggner; Polina Kalinina; Katharina Klas; Erwin Tschachler; Michael Mildner
Journal:  Biomedicines       Date:  2021-02-26
  4 in total

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