Results 181 to 190 of about 124,379,666 (230)

DNA Hypomethylation Is Not Cell Intrinsically Toxic to Polycomb Repressive Complex 2 Deficient Malignant Peripheral Nerve Sheath Tumors. [PDF]

Genes Chromosomes Cancer
Stahl MR, Stehn CM, Seeman ZJ, Faulk C, Largaespada DA.   +4 more
europepmc   +1 more source

Ossification of Mandibular Central Giant Cell Granuloma (CGCG) in Neurofibromatosis Type 1 Patients. [PDF]

Cancer Diagn Progn
Friedrich RE, Kohlrusch FK, Hagel C, Gosau M.   +3 more
europepmc   +1 more source

Molecular Advances in Juvenile Myelomonocytic Leukemia and Associated RASopathy. [PDF]

Cancers (Basel)
Monika F, Abu Mehsen S, Zhang L.
europepmc   +1 more source

Immune landscape characterization of neurofibromas with atypical features in Neurofibromatosis1 reveals PD-1 and the Tim-3/Galectin-9 pathway as potential therapeutic targets. [PDF]

Acta Neuropathol Commun
Brunet A, Coulpier F, Onfroy A, Sako N, Radomska KJ, Aftimos V, Lacroix L, Briand-Suleau A, Maille P, Hermeziu O, Laurendeau I, Pasmant E, Wolkenstein P, Topilko P, Ortonne N.   +14 more
europepmc   +1 more source

Genetic insights into autism spectrum disorder with intellectual disability: a regional population-based study from Northwest China. [PDF]

Front Pediatr
Dai Y, Yao R, Du T, Wang X, Dou N, Zhang F, Liu L.   +6 more
europepmc   +1 more source

High Allelic Heterogeneity in Kazakhstani Patients with Neurofibromatosis Type 1: Results from the First Molecular Study. [PDF]

Genes (Basel)
Idrissova Z, Rakhimbekova F, Orazgaliyeva M, Zhaksybek M, Kovaleva K, Abdikerim S, Ormankyzy A, Vasiluev P.   +7 more
europepmc   +1 more source

Colon cancer in a patient with a mosaic monoallelic germline pathogenic <i>NF1</i> gene variant. [PDF]

Explor Neurosci
Alsabagh F, Chaaban KM, Girardo M, Harahsheh E, Asif MB, Babovic-Vuksanovic D, Sonbol MB, Osundiji MA.   +7 more
europepmc   +1 more source

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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