Results 181 to 190 of about 23,942 (228)

Selumetinib Treatment in a Neurofibromatosis Type 1 Child With Second Hit Mutation on the NF1 Gene. [PDF]

Int J Dev Neurosci
Su S, Bai Y, Lu Y, Ren Y, Zhang W, Wang G, Ma K, Zhang H.   +7 more
europepmc   +1 more source

Multifocal Breast Cancer With Discordant Molecular Profiles in a Patient With NF1 and MUTYH Germline Variants: A Case Report. [PDF]

Cureus
Su L, Lu AY, Narasimhamurthy M.
europepmc   +1 more source

Gene Expression, Pathway Analysis, and Drug Discovery of Neurofibromatosis 2 Vestibular Schwannomas

Translation: The University of Toledo Journal of Medical Sciences
Mark Houdi, Hunter Eby, Ali Imami
openaire   +2 more sources

Pharmacogenomic Synthetic Lethal Screens Reveal Hidden Vulnerabilities and New Therapeutic Approaches for Treatment of NF1-Associated Tumors. [PDF]

Mol Cancer Ther
Williams KB, Larsson AT, Keller BJ, Chaney KE, Williams RL, Bhunia MM, Draper GM, Jubenville TA, Hudson WA, Georg GI, Moertel CL, Ratner N, Largaespada DA.   +12 more
europepmc   +1 more source

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
europepmc   +1 more source

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

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
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
europepmc   +1 more source