Cargando…

Commentary: Identification of Mutation Regions on NF1 Responsible for High- and Low-Risk Development of Optic Pathway Glioma in Neurofibromatosis Type I

Detalles Bibliográficos
Autores principales:	Anastasaki, Corina, Gao, Feng, Gutmann, David H.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2019
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6405421/ https://www.ncbi.nlm.nih.gov/pubmed/30881378 http://dx.doi.org/10.3389/fgene.2019.00115

Ejemplares similares

Identification of Mutation Regions on NF1 Responsible for High- and Low-Risk Development of Optic Pathway Glioma in Neurofibromatosis Type I
por: Xu, Min, et al.
Publicado: (2018)

Children with 5′-end NF1 gene mutations are more likely to have glioma
por: Anastasaki, Corina, et al.
Publicado: (2017)

RAS and beyond: the many faces of the neurofibromatosis type 1 protein
por: Anastasaki, Corina, et al.
Publicado: (2022)

Mice with missense and nonsense NF1 mutations display divergent phenotypes compared with human neurofibromatosis type I
por: Li, Kairong, et al.
Publicado: (2016)

Independent NF1 mutations underlie café-au-lait macule development in a woman with segmental NF1
por: Freret, Morgan E., et al.
Publicado: (2018)

Updated nomenclature for human and mouse neurofibromatosis type 1 genes
por: Anastasaki, Corina, et al.
Publicado: (2017)

LGG-01. NF1 MUTATION DRIVES NEURONAL ACTIVITY-DEPENDENT OPTIC GLIOMA INITIATION
por: Pan, Yuan, et al.
Publicado: (2021)

Neurofibromatosis Type 1-Associated Optic Pathway Gliomas: Current Challenges and Future Prospects
por: Tang, Yunshuo, et al.
Publicado: (2023)

SCN5A Nonsense Mutation and NF1 Frameshift Mutation in a Family With Brugada Syndrome and Neurofibromatosis
por: Micaglio, Emanuele, et al.
Publicado: (2019)

The cell of origin dictates the temporal course of neurofibromatosis-1 (Nf1) low-grade glioma formation
por: Solga, Anne C, et al.
Publicado: (2017)

Challenges in Drug Discovery for Neurofibromatosis Type 1-Associated Low-Grade Glioma
por: Ricker, Cora A., et al.
Publicado: (2016)

Two Novel NF1 Pathogenic Variants Causing the Creation of a New Splice Site in Patients With Neurofibromatosis Type I
por: Setrajcic Dragos, Vita, et al.
Publicado: (2019)

Human iPSC-Derived Neurons and Cerebral Organoids Establish Differential Effects of Germline NF1 Gene Mutations
por: Anastasaki, Corina, et al.
Publicado: (2020)

Clinical characteristics and in silico analysis of congenital pseudarthrosis of the tibia combined with neurofibromatosis type 1 caused by a novel NF1 mutation
por: Xu, Jingfang, et al.
Publicado: (2022)

KIR2DL5 mutation and loss underlies sporadic dermal neurofibroma pathogenesis and growth
por: Anastasaki, Corina, et al.
Publicado: (2017)

Familial Lipomas Without Classic Neurofibromatosis-1 Caused by a Missense Germline NF1 Mutation
por: Ramirez, Erika, et al.
Publicado: (2021)

Midkine activation of CD8(+) T cells establishes a neuron–immune–cancer axis responsible for low-grade glioma growth
por: Guo, Xiaofan, et al.
Publicado: (2020)

Neuronal hyperexcitability drives central and peripheral nervous system tumor progression in models of neurofibromatosis-1
por: Anastasaki, Corina, et al.
Publicado: (2022)

MRI Screening for Optic Gliomas in Neurofibromatosis Type 1
por: Millichap, J. Gordon
Publicado: (2015)

Non-optic glioma in adults and children with neurofibromatosis 1
por: Sellmer, Laura, et al.
Publicado: (2017)

LGG-50. Human induced pluripotent stem cell engineering establishes a humanized mouse platform for pediatric low-grade glioma modeling
por: Anastasaki, Corina, et al.
Publicado: (2022)

Optic Pathway Glioma in Children with Neurofibromatosis Type 1: A Multidisciplinary Entity, Posing Dilemmas in Diagnosis and Management Multidisciplinary Management of Optic Pathway Glioma in Children with Neurofibromatosis Type 1
por: Lohkamp, Laura-Nanna, et al.
Publicado: (2022)

Molecular Diagnosis of Neurofibromatosis by Multigene Panel Testing
por: Zhang, Zeng-Yun-Ou, et al.
Publicado: (2021)

Optic glioma and precocious puberty in a girl with neurofibromatosis type 1 carrying an R681X mutation of NF1: case report and review of the literature
por: Kocova, Mirjana, et al.
Publicado: (2015)

Homonymous Retinal Ganglion Cell Layer Atrophy With Asymptomatic Optic Tract Glioma in Neurofibromatosis Type I
por: Momen, Amirah I., et al.
Publicado: (2020)

Current update on the visual outcome of optic pathway glioma associated with neurofibromatosis type-1
por: Zeid, Janice Lasky
Publicado: (2022)

NFB-17. "Optic Pathway findings in children with Neurofibromatosis type-1 (NF-1)
por: Roka, Kleoniki, et al.
Publicado: (2022)

BIOL-16. OBESOGENIC DIET EXPOSURE INCREASES NF1-OPTIC PATHWAY GLIOMA FORMATION IN PART THROUGH EFFECTS ON THE CELL OF ORIGIN
por: Chan, Ambrose, et al.
Publicado: (2023)

Neurofibromatosis Type 1: A Novel NF1 Mutation Associated with Mitochondrial Complex I Deficiency
por: Domingues, Sara, et al.
Publicado: (2014)

Estrogen activation of microglia underlies the sexually dimorphic differences in Nf1 optic glioma–induced retinal pathology
por: Toonen, Joseph A., et al.
Publicado: (2017)

A case of neurofibromatosis 1 presenting with optic pathway glioma with an early onset and an aggressive course
por: Ganesh, Suma, et al.
Publicado: (2008)

Optic pathway glioma and the sex association in neurofibromatosis type 1: a single-center study
por: Henning, Anne Munk, et al.
Publicado: (2021)

Mutation-Directed Therapeutics for Neurofibromatosis Type I
por: Leier, Andre, et al.
Publicado: (2020)

The Spectrum of NF1 Mutations in Korean Patients with Neurofibromatosis Type 1
por: Jeong, Seon-Yong, et al.
Publicado: (2006)

Optic Nerve Glioma in Neurofibromatosis: Radiological Clues to Diagnosis in a Young Child
por: Patel, Harsh, et al.
Publicado: (2021)

NFB-02. Maternal high-fat diet exposure increases the proliferation and glial differentiation of the cells of origin for NF1-optic glioma
por: Zhang, Kailong, et al.
Publicado: (2022)

Mutation and Copy Number Alterations Analysis of KIF23 in Glioma
por: Zhao, Zheng, et al.
Publicado: (2021)

Identification of Low-Confidence Regions in the Pig Reference Genome (Sscrofa10.2)
por: Warr, Amanda, et al.
Publicado: (2015)

Somatic neurofibromatosis type 1 (NF1) inactivation characterizes NF1-associated pilocytic astrocytoma
por: Gutmann, David H., et al.
Publicado: (2013)

Identification of two novel frame shift mutations of the NF1 gene in Korean patients with neurofibromatosis type 1.
por: Park, K. C., et al.
Publicado: (2000)

Cannot write session to /tmp/vufind_sessions/sess_gl3v6l84jpbtg99qipoeaemeof