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Simvastatin for cognitive deficits and behavioural problems in patients with ne…

van der Vaart(Thijs),Plasschaert(Ellen),Riet… Lancet Neurol 2014-01-16

Neurofibromatosis type 1 is a common genetic disorder characterised by neurocutaneous manifestations and cognitive and b...

Polymorphism in genes of growth hormone receptor (GHR) and insulin-like growth …

Maj(A),Snochowski(M),Siadkowska(E),Rowinska(… Neuro Endocrinol Lett 2008-12-00

...NF1 transcription factor binding site. Also, the ghr genotype appeared to significantly influence the igf1 gene expressi...

An integrative characterization of recurrent molecular aberrations in glioblast…

Sintupisut(Nardnisa),Liu(Pei-Ling),Yeang(Che… Nucleic Acids Res 2013-12-30

...NF1 mutations-passed the majority of the validation tests. Furthermore, several modules associated with less well-report...

Somatic variants in diverse genes leads to a spectrum of focal cortical malform…

Lai(D),Gade(M),Yang(E),Koh(HY),Lu(J),Walley(… Brain 2022-00-27

...NF1 and NIPBL, genes previously associated with neurodevelopmental disorders. No rare pathogenic or likely pathogenic so...

The clinical significance of adenomatous polyposis coli (APC) and catenin Beta …

Karachaliou(GS),Alkallas(R),Carroll(SB),Care… BMC Cancer 2022-01-05

...NF1, RAC1, and PTEN genes were seen in the mut compared with wt patients from the 3-melanoma institution cohort. Analysi...

Extrauterine RAD51B -Rearranged Soft Tissue Tumors : A Clinicopathologic and Mo…

Zhu(P),Yin(X),Huang(D),Lao(IW),Yu(L),Bai(Q),… Am J Surg Pathol 2026-02-01

...NF1 genes, liked to high-grade morphology and aggressive behavior. DNA methylation profiling demonstrated that RAD51B -r...

Comprehensive Genomic Profiling Facilitates Implementation of the National Comp…

Suh(James H),Johnson(Adrienne),Albacker(Lee)… Oncologist 0000-00-00

...NF1 (13%), MYC (9.8%), RICTOR (6.4%), PIK3CA (5.4%), CDK4 (4.3%), CCND1 (4.0%), BRCA2 (2.5%), NRAS (2.3%), BRCA1 (1.7%),...

Flared inflammatory episode transforms advanced myelodysplastic syndrome into a…

Ju(B),Xiu(NN),Xu(J),Yang(XD),Sun(XY),Zhao(XC) World J Clin Cases 2023-06-16

...NF1 in molecular analysis. Initially, neutropenia was the predominant hematological abnormality, with mild anemia and th...

Establishment of a Novel IDH1 wild type Glioblastoma Cell Line, SHG142, and Its…

Gao(H),Wang(H),Yao(L),Zhao(G),Tang(L),Zhang(… Front Biosci (Landmark Ed) 2026-03-26

...NF1 and supported lineage continuity from P2 to P50 through shared SNVs and conserved driver events. CD133+ SHG142 GSCs ...

Personalized medicine in triple-negative breast cancer: combining neoantigen va…

Martinez-Enriquez(LC),Bernal-Estévez(DA),Alz… Front Oncol None

...NF1 (p.Phe1593SerfsTer31), and PIK3CA (p.Glu542Lys), all supported by OncoKB level-1 evidence. This case highlights the ...

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