A porcine model of neurofibromatosis type 1 that mimics the human disease

Loss of the NF1 tumor suppressor gene causes the autosomal dominant condition, neurofibromatosis type 1 (NF1). Children and adults with NF1 suffer from pathologies including benign and malignant tumors to cognitive deficits, seizures, growth abnormalities, and peripheral neuropathies. NF1 encodes ne...

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Detalhes bibliográficos
Publicado no:JCI Insight
Main Authors: White, Katherine A., Swier, Vicki J., Cain, Jacob T., Kohlmeyer, Jordan L., Meyerholz, David K., Tanas, Munir R., Uthoff, Johanna, Hammond, Emily, Li, Hua, Rohret, Frank A., Goeken, Adam, Chan, Chun-Hung, Leidinger, Mariah R., Umesalma, Shaikamjad, Wallace, Margaret R., Dodd, Rebecca D., Panzer, Karin, Tang, Amy H., Darbro, Benjamin W., Moutal, Aubin, Cai, Song, Li, Wennan, Bellampalli, Shreya S., Khanna, Rajesh, Rogers, Christopher S., Sieren, Jessica C., Quelle, Dawn E., Weimer, Jill M.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2018
Assuntos:
Technical Advance
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6124439/
https://ncbi.nlm.nih.gov/pubmed/29925695
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/jci.insight.120402
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