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Parental age and risk of genetic syndromes predisposing to nervous system tumor…

Adel Fahmideh(M),Tettamanti(G),Lavebratt(C),… Clin Epidemiol 2018-00-00

...NF1 and NF2 genes in spermatozoa of older fathers.

Novel therapeutic targets in salivary duct carcinoma uncovered by comprehensive…

Gargano(SM),Senarathne(W),Feldman(R),Florent… Cancer Med 2019-00-00

...NF1 (n = 5 each); KMT2C (MLL3) and PTEN (n = 3 each); BRAF (p.V600E), KDM5C and NOTCH1 (n = 2 each). Androgen receptor w...

Pathogenic Epigenetic Consequences of Genetic Alterations in IDH-Wild-Type Diff…

Ohka(F),Shinjo(K),Deguchi(S),Matsui(Y),Okuno… Cancer Res 2019-10-01

...NF1 and spontaneously develops tumors highly comparable with human IDH-wild-type DAG without characteristic molecular fe...

Melanocytic Skin Neoplasms: What Lesson From Genomic Aberrations?

Urso(C) Am J Dermatopathol 2019-09-00

...NF1 mutations, and ALK, ROS1, NTRK1, RET, MET, BRAF, NTRK3, and PRKCA fusions. Melanomas also showed a variable number o...

Homogeneously staining region (hsr) on chromosome 11 is highly specific for KMT…

Sakhdari(A),Tang(Z),Ok(CY),Bueso-Ramos(CE),M… Cancer Genet 2019-00-00

...NF1 (n = 4), and TET2 (n = 3). Thirty (83%) patients died over a median follow-up of 7.6 months (range, 0.4-33.4). In su...

Histopathological Types, Clinical Presentation, Imaging Studies, Treatment Stra…

Iglesias(P) J Clin Med 2025-06-26

...NF1, TSC1) and suggest a shared histogenesis. Copy number imbalances correlate with reduced progression-free survival in...

Social support moderates quality of life outcomes during a mind-body interventi…

Brewer(JR),Hooker(JE),Kanaya(M),LaCamera(DE)… J Neurooncol 2025-10-00

...NF1, NF2-related schwannomatosis, and other forms) are incurable genetic disorders linked to poor quality of life (QoL)....

Recurrent SMARCB1 Inactivation in Epithelioid Malignant Peripheral Nerve Sheath…

Schaefer(IM),Dong(F),Garcia(EP),Fletcher(CDM… Am J Surg Pathol 2019-00-00

...NF1 and NF2 mutations. No cases had SUZ12 or EED mutations. In summary, we identified recurrent SMARCB1 alterations in E...

A clinico-genomic analysis of soft tissue sarcoma patients reveals CDKN2A delet…

Bui(NQ),Przybyl(J),Trabucco(SE),Frampton(G),… Clin Sarcoma Res 2019-00-00

...NF1 (11%), and ATRX (11%). When all genomic alterations were tested for prognostic significance in the specific Stanford...

Mutational Profile in Vulvar, Vaginal, and Urethral Melanomas: Review of 37 Cas…

Zarei(S),Voss(JS),Jin(L),Jenkins(SM),Bryce(A… Int J Gynecol Pathol 2020-11-00

...NF1 (19%). Overall 66% (21/32) of cases showed a pathogenic alteration in at least one of the MAPK pathway genes. No sta...

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