Literature DB >> 27028151

Novel TGFBI mutation p.(Leu558Arg) in a lattice corneal dystrophy patient.

Lubica Dudakova1, Michalis Palos2, Katerina Jirsova1, Pavlina Skalicka2, Pavel Dundr3, Petra Liskova1,2.   

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Year:  2016        PMID： 27028151     DOI： 10.3109/13816810.2015.1126615

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN： 1381-6810            Impact factor:   1.803


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  3 in total

1.  Transforming growth factor β induced mutation-associated phenotype in a Chinese family exhibiting lattice corneal dystrophy.

Authors:  Chao Qu; Man Yu; Xiaoxin Guo; Jing Li; Xiaoqi Liu; Yi Shi; Bo Gong
Journal:  Biomed Rep       Date:  2017-08-30

2.  A pathogenic variant in the transforming growth factor beta I (TGFBI) in four Iranian extended families segregating granular corneal dystrophy type II: A literature review.

Authors:  Aliasgar Mohammadi; Azam Ahmadi Shadmehri; Mahnaz Taghavi; Gholamhossein Yaghoobi; Mohammad Reza Pourreza; Mohammad Amin Tabatabaiefar
Journal:  Iran J Basic Med Sci       Date:  2020-08       Impact factor: 2.699

3.  TGF-β1 enhanced myocardial differentiation through inhibition of the Wnt/β-catenin pathway with rat BMSCs.

Authors:  Yang Lv; Xiu-Juan Li; Hai-Ping Wang; Bo Liu; Wei Chen; Lei Zhang
Journal:  Iran J Basic Med Sci       Date:  2020-08       Impact factor: 2.699
  3 in total

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