Zobrazeno 1 - 2
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pro vyhledávání: '"Angela S. Zhu"'
Publikováno v:
Otolaryngology Case Reports, Vol 30, Iss , Pp 100573- (2024)
Barakat syndrome is a rare autosomal dominant disease caused by haplo-insufficiency of transcription factor GATA3 on chromosome 10p14. It is characterized by a triad of hypoparathyroidism, sensorineural hearing loss, and renal disease with high pheno
Externí odkaz:
https://doaj.org/article/5647203eda90455899e90aa912ce709a
Autor:
Harshpreet Chandok, Isabel Rodriguez, Kalyan Banda, Yuan Yuan, Francesca Menghi, George Somlo, Susan E. Yost, Robert Straub, Lacey E. Dobrolecki, Pooja Kumar, Michael T. Lewis, Elizabeth M. Swisher, Marc R. Radke, Edison T. Liu, Angela S. Zhu
SUMMARYLoss of homologous recombination repair (HRR) via germline and somaticBRCA1orBRCA2gene mutations and viaBRCA1promoter methylation has been associated with better response to platinum agents and PARP inhibitors, in both triple negative breast c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d5ca9146807ab4b8b60c3b9a9e7f7c0
https://doi.org/10.1101/2021.08.19.456799
https://doi.org/10.1101/2021.08.19.456799
