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Links from Nucleotide

Items: 4

1.
Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF
Athar Khalil, Samer Bou Karroum, Rana Barake, Gabriel Dunya, Samer Abou-Rizk, Amina Kamar, Georges Nemer, Marc Bassim
BMC Med Genet. 2020; 21: 1. Published online 2020 Jan 2. doi: 10.1186/s12881-019-0942-4
PMCID:
PMC6941291
AbstractArticlePDF–1.2M
2.
Mitf-Mdel, a novel melanocyte/melanoma-specific isoform of microphthalmia-associated transcription factor-M, as a candidate biomarker for melanoma
Yixiang Wang, Soroosh Radfar, Suhu Liu, Adam I Riker, Hung T Khong
BMC Med. 2010; 8: 14. Published online 2010 Feb 17. doi: 10.1186/1741-7015-8-14
PMCID:
PMC2839965
AbstractArticlePDF–1.7M
3.
Modeling Retinitis Pigmentosa: Retinal Organoids Generated From the iPSCs of a Patient With the USH2A Mutation Show Early Developmental Abnormalities
Yonglong Guo, Peiyuan Wang, Jacey Hongjie Ma, Zekai Cui, Quan Yu, Shiwei Liu, Yunxia Xue, Deliang Zhu, Jixing Cao, Zhijie Li, Shibo Tang, Jiansu Chen
Front Cell Neurosci. 2019; 13: 361. Published online 2019 Aug 7. doi: 10.3389/fncel.2019.00361
PMCID:
PMC6709881
AbstractArticlePDF–8.0M
4.
DNA Methylation Levels of Melanoma Risk Genes Are Associated with Clinical Characteristics of Melanoma Patients
Érica S. S. de Araújo, Dimitrius T. Pramio, André Y. Kashiwabara, Paula C. Pennacchi, Silvya S. Maria-Engler, Maria I. Achatz, Antonio H. J. F. M. Campos, João P. Duprat, Carla Rosenberg, Dirce M. Carraro, Ana C. V. Krepischi
Biomed Res Int. 2015; 2015: 376423. Published online 2015 Apr 12. doi: 10.1155/2015/376423
PMCID:
PMC4461735
AbstractArticlePDF–539K

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