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■ Search Result - Abbreviation : EPHA2

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Abbreviation: EPHA2
Appearance Frequency: 49 time(s)
Long forms: 10

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
EPH receptor A2
(18 times)
Neoplasms
(4 times)
HCC (2 times)
ACTN1 (1 time)
AMPK (1 time)
2006 Downstream target genes of the neuropeptide S-NPSR1 pathway.
ephrin type-A receptor 2
(10 times)
Neoplasms
(3 times)
CRC (1 time)
CRPC (1 time)
EFNA5 (1 time)
2012 Oncogene-specific activation of tyrosine kinase networks during prostate cancer progression.
ephreceptor tyrosinekinase-type A2
(5 times)
Ophthalmology
(2 times)
ARC (3 times)
CI (1 time)
OGG1 (1 time)
2011 Association of EPHA2 polymorphisms and age-related cortical cataract in a Han Chinese population.
Erythropoietin-producing hepatocellular receptor A2
(5 times)
Neoplasms
(3 times)
AEs (1 time)
ANXA2 (1 time)
DLT (1 time)
2019 Deregulation of miR-520d-3p promotes hepatocellular carcinoma development via lncRNA MIAT regulation and EPHA2 signaling activation.
ephrin-A receptor 2
(4 times)
Cell Death
(1 time)
BRAFi (1 time)
ESCC (1 time)
MPM (1 time)
2015 Phosphotyrosine profiling identifies ephrin receptor A2 as a potential therapeutic target in esophageal squamous-cell carcinoma.
Eph-receptor type-A2
(3 times)
Molecular Biology
(2 times)
ECM (1 time)
HLE (1 time)
LOD (1 time)
2008 The EPHA2 gene is associated with cataracts linked to chromosome 1p.
EPHA2 gene
(1 time)
Medicine
(1 time)
SNVs (1 time)
UV (1 time)
VAFs (1 time)
2017 Germ-line and somatic EPHA2 coding variants in lens aging and cataract.
Epha2-null
(1 time)
Cell Biology
(1 time)
EFNA5 (1 time)
2018 Epha2 and Efna5 participate in lens cell pattern-formation.
ephrin receptor kinase 2
(1 time)
Medicine
(1 time)
AV (1 time)
CXCR2 (1 time)
FOXC1 (1 time)
2019 MicroRNA-regulated pathways of flow-stimulated angiogenesis and vascular remodeling in vivo.
10  Ephrin receptor subfamily 2
(1 time)
Clinical Laboratory Techniques
(1 time)
ADCC (1 time)
CRYBA4 (1 time)
MYH9 (1 time)
2019 Novel mutations associated with autosomal-dominant congenital cataract identified in Chinese families.