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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Bibliografske podrobnosti
izdano v: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.
Format: Artigo
Jezik:Inglês
Izdano: American Society for Clinical Investigation 2018
Teme:
Technical Advance
Online dostop: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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