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Genetic backgrounds and modifier genes of NTD mouse models: An opportunity for …

Leduc(RY),Singh(P),McDermid(HE) Birth Defects Res 2017-00-30

...Cecr2, which is studied using both a hypomorphic and a presumptive null mutation on two different backgrounds: one susce...

A mutation in the tuft mouse disrupts TET1 activity and alters the expression o…

Fong(KS),Hufnagel(RB),Khadka(VS),Corley(MJ),… Dis Model Mech 2016-00-01

...Cecr2, Epha7 and Grhl2 were significantly reduced in some embryos presenting neural tube closure defects, whereas one or...

Gene-by-environment interactions involving maternal exposures with orofacial cl…

Erdogan-Yildirim(Z),Carlson(JC),Mukhopadhyay… medRxiv 2024-12-17

...CECR2 - a chromatin remodeling protein required for neural tube closure-and FURIN, a critical protease during early embr...

Ten genes associated with MGMT promoter methylation predict the prognosis of pa…

Zhang(Y),Zhu(J) Oncol Rep 2019-02-00

...CECR2, histone acetyl‑lysine reader, endosulfine α, G‑patch domain‑containing 8, KIAA1109, MGMT, protocadherin β 13, sel...

Synergistic ligand anchoring and electronic modulation in CeMIL-101-NH₂ boostin…

Chen(J),Wang(L),Huang(X),Wang(J),Meng(H),Gao… J Colloid Interface Sci 2026-04-00

...CeCr2-SBU-NH2 clusters compared to Ni10/Cr-SBU-BDC clusters. Finally, the catalyst maintains high activity and structura...

Weighted gene co-expression network analysis and whole genome sequencing identi…

Abudereheman(M),Lian(Z),Ainitu(B) Front Oncol 2024-00-00

...CECR2, and LAMA3) were confirmed in a Venn diagram of the 278 hub genes and the mutated genes from WES. KEGG analysis re...

The HARE-HTH and associated domains: novel modules in the coordination of epige…

Aravind(L),Iyer(LM) Cell Cycle 2012-01-01

...CECR2 and NURF1. Based on the crystal structure of Ioc3, we establish that these motifs in conjunction with the DDT moti...

Novel complex integrating mitochondria and the microtubular cytoskeleton with c…

Liu(L),Amy(V),Liu(G),McKeehan(WL) In Vitro Cell Dev Biol Anim 2002-00-00

...CECR2), ubiquitously expressed transcript (UXT), and chromosome 19 open reading frames 5 (C19ORF5) but still of unknown ...

Clinical and molecular cytogenetic findings of cat eye syndrome and a 2-year-ol…

Xu(L),Cheng(X),Tang(L),Min(S),Wu(J),Zhu(H),L… BMC Pediatr 2024-10-14

...CECR2, SLC25A18, ATP6V1E1, and BCL2L13 are strong candidate genes for causing the main CES phenotype. The ear anomalies ...

The interaction of HT-2 toxin and Akt1 on gene expression regulation in Kashin-…

Liao(X),Yang(X),Jia(X),Zhang(Q),Naren(G),Zha… Toxicon 2025-09-00

...CECR2, TMOD1, ZNF704 and RHOBTB1 were identified as hub genes; in the module most associated with HT-2-siAkt1, the hub g...

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