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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:JCI Insight
Egile Nagusiak: 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.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Society for Clinical Investigation 2018
Gaiak:
Technical Advance
Sarrera elektronikoa: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
Etiketak: Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!

Antzeko izenburuak