HomeLiterature Search
Popular searches
Integrating Histologic and Genomic Characteristics to Predict Tumor Mutation Bu…

Qiu(Y),Liu(L),Yang(H),Chen(H),Deng(Q),Xiao(D… Front Oncol 2020-00-00

...NF1, KMT2D, and GRIN2A. No significant correlations were found between TMB and age, neuro-invasion (p = 0.125), and tumo...

Prevalence of Germline Pathogenic and Likely Pathogenic Variants in Patients Wi…

Yao K(KA),Clifford(J),Li(S),LaDuca(H),Hulick… JNCI Cancer Spectr 2020-12-00

...NF1) was compared between women with a primary breast cancer (PBC) and SBC who underwent multigene panel testing at a si...

Genetic Analysis and Clinical Characteristics of Hereditary Pheochromocytoma an…

Choi(H),Kim(KJ),Hong(N),Shin(S),Choi(JR),Kan… Endocrinol Metab (Seoul) 2020-00-00

...NF1, MAX, SDHA, and SDHD). We report the expected prevalence of germline mutations in Korean PPGL patients. NGS is a use...

Extra-central nervous system metastasis from high-grade glioma: a single-instit…

Faraj(CA),McCutcheon(IE),Gubbiotti(MA),Perni… J Neurooncol 2025-05-00

...NF1, TERT promoter, and BRAF V600E mutations. Median OS from HGG diagnosis was 23.4 months, and median OS following ECM ...

Multi-gene panel sequencing reveals the relationship between driver gene mutati…

Li(J),Li(X),Guo(H),Zhou(S),Ding(H),Li(B),Li(… Discov Oncol 2025-03-07

...NF1 (p < 0.01), KRAS (p < 0.01), and TP53 (p < 0.001) were significantly associated with gender. This work revealed the ...

Neuropsychological profile in Italian children with neurofibromatosis type 1 (N…

Parmeggiani(A),Boiani(F),Capponi(S),Duca(M),… Eur J Paediatr Neurol 2018-09-00

Neurofibromatosis type 1 is a genetic disorder associated with cognitive deficits, learning disabilities and behavioral ...

Resolving the phylogenetic origin of glioblastoma via multifocal genomic analys…

Brastianos(PK),Nayyar(N),Rosebrock(D),Leshch… NPJ Precis Oncol 2017-00-00

...NF1(n = 3), TP53(n = 4) and EGFR(n = 5). However, by phylogenetic analysis, there were no protein-coding mutations as re...

Analysis of Gene Expression Variance in Schizophrenia Using Structural Equation…

Igolkina(AA),Armoskus(C),Newman(JRB),Evgrafo… Front Mol Neurosci 2018-00-00

...NF1, and KRAS and SOS1 in the MAPK pathway; between PSPH and SHMT2 in serine biosynthesis; between AKT3 and TSC2 in the ...

Targetable Alterations in Adult Patients With Soft-Tissue Sarcomas: Insights fo…

Lucchesi(C),Khalifa(E),Laizet(Y),Soubeyran(I… JAMA Oncol 2018-00-01

...NF1, CDKN2B, KMT2D, GLI1, ATM, TERT, PI3KCA, NOTCH1, MAP2K4, ERBB4, ARID1A, TSC2, and TNFAIP3. At least 1 targetable GA ...

Dynamic Monitoring of Circulating Tumor DNA to Predict the Risk of Non In Situ …

Guo(G),Zhang(Z),Zhang(J),Wang(D),Xu(S),Wu(S)… Cancer Med 2025-03-00

...NF1) were most common in patients with situ recurrent GBM, while mutations in the MUC family and TP53 pathway (MUC16, CH...

Previous 856 857 858 859 860 861 862 863 864 Next Vol. 860 / of 901 页

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com