Results 151 to 160 of about 24,332 (187)

Glial-to-mesenchymal transition of tumor Schwann cells drives the genetic burden in MPNSTs from neurofibromatosis type 1 mouse model. [PDF]

Sci Adv
Radomska KJ, Onfroy A, Lecerf L, Job B, Beaude A, Sanz LS, El Jalkh T, Thieffry D, Charnay P, Wolkenstein P, Ortonne N, Coulpier F, Topilko P.   +12 more
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Single-cell transcriptomic profiling of malignant peripheral nerve sheath tumors. [PDF]

Neurooncol Adv
Gui C, Bunda S, Li M, Singh O, Zadeh G, Suppiah S.   +5 more
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Schwannomatosis tumor modeling: progress and prospects for translational research. [PDF]

J Biol Eng
Madison MS, Xu H, Gonzalez-Vargas Y, Yonk MG, Thompson CM, Haney H, Babbitt D, Du Y, Hirbe AC, Boulis NM, Bai RY, Lei K.   +11 more
europepmc   +1 more source

Editorial: Advances in systems neurogenetics. [PDF]

Front Neurosci
Carney P, Zhang B.
europepmc   +1 more source

Refined genotype-phenotype correlations in neurofibromatosis type 1 patients with <i>NF1</i> point variants. [PDF]

J Med Genet
Pacot L, Blok M, Vidaud D, Fertitta L, Laurendeau I, Coustier A, Maillard T, Barbance C, Hadjadj D, Ye M, Lallemand D, Ferkal S, Funalot B, Lunati-Rozie A, Hebrard B, Bhouri R, Spruijt L, Bessis D, Geneviève D, Vernimmen V, Broen MPG, Sigaudy S, Odent S, Damaj L, Quélin C, Pasquier L, Layet V, Gilbert-Dussardier B, Nicolas G, Guerrot AM, Leheup B, Bursztejn AC, Petit F, Boute-Bénéjean O, Capri Y, Guimier A, Lyonnet S, Baujat G, Bourrat E, Isidor B, Nizon M, Barbarot S, Toutain A, Blesson S, Van-Gils J, Morice-Picard F, Audebert-Bellanger S, Mazereeuw-Hautier J, Ziegler A, Alembik Y, Piard J, Brischoux-Boucher E, Guerrini-Rousseau L, Morera J, Paquis-Flucklinger V, Delobel B, Alessandri JL, Parfait B, NF-France network, Wolkenstein P, Pasmant E.   +60 more
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"To have children or not?" Between desire, responsibility, luck, and guilt: reproductive decision-making in individuals with neurofibromatosis type 1. [PDF]

Orphanet J Rare Dis
Kowal K, Domaradzki J.
europepmc   +1 more source

Neurofibromatosis type 1: From gene to population and cancer

, 2018
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The Neurofibromatosis Type 1 Gene

Annual Review of Neuroscience, 1993
Sometimes referred to as peripheral neurofibromatosis or von Reck­ linghausen disease, neurofibromatosis 1 (NFl) is one of the most common medical conditions inherited in human populations. NFl , inherited as an autosomal dominant, affects approximately 1 in 3500 individuals world­ wide with no apparent ethnic predilection.
D, Viskochil, R, White, R, Cawthon
openaire   +3 more sources

Neurofibromatosis type 1 gene mutations in neuroblastoma

Nature Genetics, 1993
The introduction of human chromosome 17 suppresses the tumourigenicity of a neuroblastoma cell line in the absence of any effects on in vitro growth and the neurofibromatosis type 1 (NF1) gene may be responsible. Here we report that 4 out of 10 human neuroblastoma lines express little or no neurofibromin and that two of these lines show evidence of NF1
I, The, A E, Murthy, G E, Hannigan, L B, Jacoby, A G, Menon, J F, Gusella, A, Bernards   +6 more
openaire   +2 more sources