U.S. flag

An official website of the United States government

Display Settings:

Format
Sort by

Send to:

Choose Destination

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
ArticlePDF–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
ArticlePDF–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
ArticlePDF–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
ArticlePDF–539K

Display Settings:

Format
Sort by

Send to:

Choose Destination

Supplemental Content

Filter your results:

Find related data

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
You are here: NCBI > Literature > PubMed Central (PMC)
Support Center