WP1066 induces cell death in a schwannomatosis patient–derived schwannoma cell line

Schwannomatosis is a rare genetic disorder that predisposes individuals to development of multiple schwannomas mainly in spinal and peripheral nerves and to debilitating chronic pain often unrelated to any schwannoma. Pathogenic variants of two genes, SMARCB1 and LZTR1, are causal in familial cases....

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Detalles Bibliográficos
Autores principales: Allaf, Abdulrahman, Victoria, Berta, Rosario, Rosa, Misztal, Carly, Humayun Gultekin, Sakir, Dinh, Christine T., Fernandez-Valle, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2022
Materias:
Research Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9235848/
https://www.ncbi.nlm.nih.gov/pubmed/35732500
http://dx.doi.org/10.1101/mcs.a006178

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9235848/
https://www.ncbi.nlm.nih.gov/pubmed/35732500
http://dx.doi.org/10.1101/mcs.a006178

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