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1.
Allele-specific activation, enzyme kinetics, and inhibitor sensitivities of EGFR exon 19 deletion mutations in lung cancer.
Proc Natl Acad Sci U S A
; 119(30): e2206588119, 2022 07 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-35867821
2.
Wnt/ß-catenin signaling in the development and therapeutic resistance of non-small cell lung cancer.
J Transl Med
; 22(1): 565, 2024 Jun 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-38872189
3.
Integration of machine learning to identify diagnostic genes in leukocytes for acute myocardial infarction patients.
J Transl Med
; 21(1): 761, 2023 10 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-37891664
4.
Mechanisms of receptor tyrosine kinase activation in cancer.
Mol Cancer
; 17(1): 58, 2018 02 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-29455648
5.
Structure-Guided Strategies of Targeted Therapies for Patients with EGFR-Mutant Non-Small Cell Lung Cancer.
Biomolecules
; 13(2)2023 01 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-36830579
6.
Verbena Attenuates Adriamycin-Induced Renal Tubular Injury via Inhibition of ROS-ERK1/2-NLRP3 Signal Pathway.
Evid Based Complement Alternat Med
; 2022: 7760945, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36212965
7.
Erratum: Epigenomic characterization of a p53-regulated 3p22.2 tumor suppressor that inhibits STAT3 phosphorylation via protein docking and is frequently methylated in esophageal and other carcinomas: Erratum.
Theranostics
; 12(4): 1736-1737, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35198069
8.
A novel mutation within the 2B rod domain of keratin 9 in a Chinese pedigree with epidermolytic palmoplantar keratoderma combined with knuckle pads and camptodactyly.
Eur J Dermatol
; 21(5): 675-9, 2011.
Artículo
en Inglés
| MEDLINE | ID: mdl-21715251
9.
Structure-function analysis of oncogenic EGFR Kinase Domain Duplication reveals insights into activation and a potential approach for therapeutic targeting.
Nat Commun
; 12(1): 1382, 2021 03 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-33654076
10.
On-target Resistance to the Mutant-Selective EGFR Inhibitor Osimertinib Can Develop in an Allele-Specific Manner Dependent on the Original EGFR-Activating Mutation.
Clin Cancer Res
; 25(11): 3341-3351, 2019 06 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30796031
11.
Tumor suppressive BTB/POZ zinc-finger protein ZBTB28 inhibits oncogenic BCL6/ZBTB27 signaling to maintain p53 transcription in multiple carcinogenesis.
Theranostics
; 9(26): 8182-8195, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31754389
12.
MiR-148b-3p inhibits renal carcinoma cell growth and pro-angiogenic phenotype of endothelial cell potentially by modulating FGF2.
Biomed Pharmacother
; 107: 359-367, 2018 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-30099339
13.
Epigenomic characterization of a p53-regulated 3p22.2 tumor suppressor that inhibits STAT3 phosphorylation via protein docking and is frequently methylated in esophageal and other carcinomas.
Theranostics
; 8(1): 61-77, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-29290793
14.
Genetic diagnosis of a Chinese multiple endocrine neoplasia type 2A family through whole genome sequencing.
J Biosci
; 42(2): 209-218, 2017 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-28569245
15.
Dickkopf-related protein 2 induces G0/G1 arrest and apoptosis through suppressing Wnt/ß-catenin signaling and is frequently methylated in breast cancer.
Oncotarget
; 8(24): 39443-39459, 2017 Jun 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-28467796
16.
The epigenetic modifier CHD5 functions as a novel tumor suppressor for renal cell carcinoma and is predominantly inactivated by promoter CpG methylation.
Oncotarget
; 7(16): 21618-30, 2016 Apr 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-26943038
17.
Epigenetic inactivation of the CpG demethylase TET1 as a DNA methylation feedback loop in human cancers.
Sci Rep
; 6: 26591, 2016 05 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-27225590
18.
A Small Indel Mutant Mouse Model of Epidermolytic Palmoplantar Keratoderma and Its Application to Mutant-specific shRNA Therapy.
Mol Ther Nucleic Acids
; 5: e299, 2016 Mar 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-27003758
19.
A novel CRX mutation by whole-exome sequencing in an autosomal dominant cone-rod dystrophy pedigree.
Int J Ophthalmol
; 8(6): 1112-7, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26682157
20.
Characterization of the nasopharyngeal carcinoma methylome identifies aberrant disruption of key signaling pathways and methylated tumor suppressor genes.
Epigenomics
; 7(2): 155-73, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-25479246