Literature DB >> 25970271

Correction: A Novel GJA8 Mutation (p.V44A) Causing Autosomal Dominant Congenital Cataract.

Yanan Zhu, Hao Yu, Wei Wang, Xiaohua Gong, Ke Yao.   

Abstract

Entities:  

Year:  2015        PMID: 25970271      PMCID: PMC4430210          DOI: 10.1371/journal.pone.0125949

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


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The legends for Fig 4 and Fig 5 are incorrectly switched. Please see the complete, corrected Fig 4 here.
Fig 4

Statistical analysis of DAPI (A) and PI (B) loading in different solutions.

Data are presented as mean±SDs. There was a significant difference in the percentage of dye-stained cells between the Cx50WILD and Cx50V44A groups in the Ca2+-free environment (P<0.001, marked with ***); there was also a significant difference between the Ca2+-free Cx50WILD and the 1.2 mM Ca2+/300 μM FFA Cx50WILD group (P<0.001, marked with ***).

Fig 5

PI dye uptake in HeLa cells stably transfected with Cx50WILD and Cx50V44A.

The PI dye uptake assay revealed similar results as the DAPI dye uptake assay. The three pictures in the last line show the Cx50 protein, PI-stained nuclei (nucleoli)/cytoplasm, and merged look of the wild-type cells in Ca2+-free HBSS. Scale bar: 20 μm.

Statistical analysis of DAPI (A) and PI (B) loading in different solutions.

Data are presented as mean±SDs. There was a significant difference in the percentage of dye-stained cells between the Cx50WILD and Cx50V44A groups in the Ca2+-free environment (P<0.001, marked with ***); there was also a significant difference between the Ca2+-free Cx50WILD and the 1.2 mM Ca2+/300 μM FFA Cx50WILD group (P<0.001, marked with ***). Please see the complete, corrected Fig 5 here.

PI dye uptake in HeLa cells stably transfected with Cx50WILD and Cx50V44A.

The PI dye uptake assay revealed similar results as the DAPI dye uptake assay. The three pictures in the last line show the Cx50 protein, PI-stained nuclei (nucleoli)/cytoplasm, and merged look of the wild-type cells in Ca2+-free HBSS. Scale bar: 20 μm.
  1 in total

1.  A novel GJA8 mutation (p.V44A) causing autosomal dominant congenital cataract.

Authors:  Yanan Zhu; Hao Yu; Wei Wang; Xiaohua Gong; Ke Yao
Journal:  PLoS One       Date:  2014-12-17       Impact factor: 3.240

  1 in total
  2 in total

1.  Mutation analysis of connexin 50 gene among Iranian families with autosomal dominant cataracts.

Authors:  Masoumeh Mohebi; Saeed Chenari; Abolfazl Akbari; Fariba Ghassemi; Mehran Zarei-Ghanavati; Ghasem Fakhraie; Nahid Babaie; Mansour Heidari
Journal:  Iran J Basic Med Sci       Date:  2017-03       Impact factor: 2.699

Review 2.  Connexinopathies: a structural and functional glimpse.

Authors:  Isaac E García; Pavel Prado; Amaury Pupo; Oscar Jara; Diana Rojas-Gómez; Paula Mujica; Carolina Flores-Muñoz; Jorge González-Casanova; Carolina Soto-Riveros; Bernardo I Pinto; Mauricio A Retamal; Carlos González; Agustín D Martínez
Journal:  BMC Cell Biol       Date:  2016-05-24       Impact factor: 4.241

  2 in total

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