1. Krüppel-like Factor-9 and Krüppel-like Factor-13: Highly Related, Multi-Functional, Transcriptional Repressors and Activators of Oncogenesis
   Frank A. Simmen et al, 2023, Cancers CrossRef
2. Genetic Risk Score Constructed from Polymorphisms in the VEGFA, TBX5, and SMAD7 Genes Provides Novel Insights into the Molecular Mechanisms of the Tetralogy of Fallot and Ventricular Septal Defect (Case-Control Study from the Pakistani Population)
   Sana Ashiq et al, 2023, The American Journal of Cardiology CrossRef
3. SMAD4 loss-of-function mutation predisposes to congenital heart disease
   Yin Wang et al, 2023, European Journal of Medical Genetics CrossRef
4. Somatic GATA4 mutation contributes to tetralogy of Fallot
   Pradhan Abhinav et al, 2024, Experimental and Therapeutic Medicine CrossRef
5. The Involvement of Krüppel-like Factors in Cardiovascular Diseases
   Michelle G. Santoyo-Suarez et al, 2023, Life CrossRef
6. Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease
   Hong-Yu Shi et al, 2022, Diagnostics CrossRef
7. Discovery of GJC1 (Cx45) as a New Gene Underlying Congenital Heart Disease and Arrhythmias
   Yan-Jie Li et al, 2023, Biology CrossRef
8. Is the Cis-Element CACCC-Box a Master Regulatory Element during Cardiovascular Disease? A Bioinformatics Approach from the Perspective of the Krüppel-like Family of Transcription Factors
   Juan Andrés García-Loredo et al, 2024, Life CrossRef
9. The kruppel-like factor (KLF) family, diseases, and physiological events
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10. A Comprehensive Review of Management Strategies for Bicuspid Aortic Valve (BAV): Exploring Epidemiology, Aetiology, Aortopathy, and Interventions in Light of Recent Guidelines
    Halil Ibrahim Bulut et al, 2023, Journal of Cardiovascular Development and Disease CrossRef
11. KLF13 promotes VSMCs phenotypic dedifferentiation by directly binding to the SM22α promoter
    Xiaofan Yuan et al, 2024, Journal of Cellular Physiology CrossRef