Literature DB >> 26420579

Mutation in MMP2 gene may result in scleroderma-like skin thickening.

B Bader-Meunier1, L Bonafé2, S Fraitag3, S Breton3, C Bodemer1, G Baujat1.   

Abstract

Entities:  

Keywords:  Fibroblasts; Gene Polymorphism; Systemic Sclerosis

Mesh：

Substances：

Year:  2015        PMID： 26420579     DOI： 10.1136/annrheumdis-2015-208182

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN： 0003-4967            Impact factor:   19.103


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  4 in total

1.  A novel mutation in the matrix metallopeptidase 2 coding gene associated with intrafamilial variability of multicentric osteolysis, nodulosis, and arthropathy.

Authors:  Liisa Kröger; Tuija Löppönen; Leena Ala-Kokko; Heikki Kröger; Hanna-Mari Jauhonen; Kaisa Lehti; Jarmo Jääskeläinen
Journal:  Mol Genet Genomic Med       Date:  2019-07-03       Impact factor: 2.183

Review 2.  Monogenic Immune Diseases Provide Insights Into the Mechanisms and Treatment of Chronic Graft-Versus-Host Disease.

Authors:  Jacob Rozmus
Journal:  Front Immunol       Date:  2021-02-04       Impact factor: 7.561

3.  Multicentric Osteolysis, Nodulosis, and Arthropathy in two unrelated children with matrix metalloproteinase 2 variants: Genetic-skeletal correlations.

Authors:  Hanan Elsebaie; Mohamed Abdelhafiz Mansour; Solaf M Elsayed; Shady Mahmoud; Tamer A El-Sobky
Journal:  Bone Rep       Date:  2021-07-10

4.  A case of Myhre syndrome mimicking juvenile scleroderma.

Authors:  Barbara Jensen; Rebecca James; Ying Hong; Ebun Omoyinmi; Clarissa Pilkington; Neil J Sebire; Kevin J Howell; Paul A Brogan; Despina Eleftheriou
Journal:  Pediatr Rheumatol Online J       Date:  2020-09-11       Impact factor: 3.413
  4 in total

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