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Nkx2 6
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Curated Studies
Most Correlated Studies
L1000 CMAP - Hepatocellular carcinoma Hep G2 cells with shRNA-mediated gene knockdown (1 of 2)
Lung cancer NCI-H3255 and HCC4019 cells depleted of TITF1
Identification of Novel Cardiac Genes through Differentiation of Mouse ESCs
Atria from P1 C57BL-6 with atrial NKX2-5 knockouts
Embryonic hearts with hypomorphic NKX2-5 mutations
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Literature
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NKX2-6 related congenital heart disease: Biallelic homeodomain-disrupting variants and truncus arter…
NKX2-6 mutation predisposes to familial atrial fibrillation.
Conotruncal malformations and absent thymus due to a deleterious NKX2-6 mutation.
Prevalence and spectrum of Nkx2.6 mutations in patients with congenital heart disease.
A novel NKX2.6 mutation associated with congenital ventricular septal defect.
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Hydroxychloroquin (HCQ) in chILD of Genetic Defect
Hydroxychloroquine in Children's Interstitial Lung Diseases With Genetic Causes
Hydroxychloroquin (HCQ) in Pediatric Interstitial Lung Disease (ILD)
Genetic Causes and Clinical Features of Childhood Interstitial Lung Diseases in China
Utilization of Confocal Microscopy During Cardiac Surgery
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