Pages that link to "Q24307999"
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The following pages link to Mutations in NOTCH1 cause aortic valve disease (Q24307999):
Displaying 50 items.
- bicuspid aortic valve (Q860167) (← links)
- Notch receptor 1 (Q4044985) (← links)
- Hairy/enhancer-of-split related with YRPW motif 2 (Q21985972) (← links)
- Hairy/enhancer-of-split related with YRPW motif protein 1 (Q21985973) (← links)
- Notch 1 (Q21986193) (← links)
- Transcription factor genes Smad4 and Gata4 cooperatively regulate cardiac valve development. [corrected] (Q24293493) (← links)
- NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway (Q24293498) (← links)
- Hesr1 and Hesr2 regulate atrioventricular boundary formation in the developing heart through the repression of Tbx2 (Q24294772) (← links)
- Identification of de novo mutations and rare variants in hypoplastic left heart syndrome (Q24298680) (← links)
- Notch signaling is essential for ventricular chamber development (Q24299001) (← links)
- Integration of a Notch-dependent mesenchymal gene program and Bmp2-driven cell invasiveness regulates murine cardiac valve formation. (Q24301606) (← links)
- Structural basis for cooperativity in recruitment of MAML coactivators to Notch transcription complexes (Q24307538) (← links)
- Haploinsufficiency of TAB2 causes congenital heart defects in humans (Q24314581) (← links)
- Faulty initiation of proteoglycan synthesis causes cardiac and joint defects (Q24314605) (← links)
- Slug is a direct Notch target required for initiation of cardiac cushion cellularization (Q24318449) (← links)
- Association of common variants in the human eyes shut ortholog (EYS) with statin-induced myopathy: evidence for additional functions of EYS (Q24320093) (← links)
- Novel NOTCH1 mutations in patients with bicuspid aortic valve disease and thoracic aortic aneurysms (Q24323103) (← links)
- Increased dietary intake of vitamin A promotes aortic valve calcification in vivo (Q24630155) (← links)
- Direct inhibition of the NOTCH transcription factor complex (Q24634015) (← links)
- Modeling congenital disease and inborn errors of development in Drosophila melanogaster (Q26765017) (← links)
- Drosophila tools and assays for the study of human diseases (Q26765022) (← links)
- Genetic testing in congenital heart disease: A clinical approach (Q26765163) (← links)
- Large animal models of cardiovascular disease (Q26766350) (← links)
- Calcific aortic valve disease: is it another face of atherosclerosis? (Q26782519) (← links)
- Bioengineering and Stem Cell Technology in the Treatment of Congenital Heart Disease (Q26799556) (← links)
- Calcification in Aortic Stenosis: The Skeleton Key (Q26801389) (← links)
- Coordinating tissue interactions: Notch signaling in cardiac development and disease (Q26822995) (← links)
- Regulatory circuits controlling vascular cell calcification (Q26825788) (← links)
- Genetics of thoracic aortic aneurysm: at the crossroad of transforming growth factor-β signaling and vascular smooth muscle cell contractility (Q26828019) (← links)
- Endocardial and epicardial epithelial to mesenchymal transitions in heart development and disease (Q26830155) (← links)
- Impact of notch signaling on inflammatory responses in cardiovascular disorders (Q26851816) (← links)
- Congenital heart disease: emerging themes linking genetics and development (Q26859219) (← links)
- Genetics of congenital heart disease: the glass half empty (Q26862793) (← links)
- Epithelial-mesenchymal transitions: insights from development (Q26868634) (← links)
- Fibrocalcific aortic valve disease: opportunity to understand disease mechanisms using mouse models (Q26994661) (← links)
- Of mice and men: molecular genetics of congenital heart disease (Q26995476) (← links)
- Genetic basis of familial valvular heart disease (Q27004837) (← links)
- Role of Notch signaling in the mammalian heart (Q27006155) (← links)
- Conserved transcriptional regulatory mechanisms in aortic valve development and disease (Q27014023) (← links)
- Genetics of valvular heart disease (Q27014805) (← links)
- In vitro models of aortic valve calcification: solidifying a system (Q27022156) (← links)
- Molecular and cellular aspects of calcific aortic valve disease (Q27026105) (← links)
- Differentiation defect in neural crest-derived smooth muscle cells in patients with aortopathy associated with bicuspid aortic valves (Q27311656) (← links)
- Excessive nitrite affects zebrafish valvulogenesis through yielding too much NO signaling (Q27313670) (← links)
- Physiological notch signaling maintains bone homeostasis via RBPjk and Hey upstream of NFATc1 (Q27334560) (← links)
- RAM-induced Allostery Facilitates Assembly of a Notch Pathway Active Transcription Complex (Q27650201) (← links)
- The impact of mechanical forces in heart morphogenesis (Q27692679) (← links)
- Bicuspid Aortic Valve: a Review with Recommendations for Genetic Counseling (Q28080091) (← links)
- Functional Analysis of Two Novel Mutations in TWIST1 Protein Motifs Found in Ventricular Septal Defect Patients (Q28115006) (← links)
- Notch3 is necessary for neuronal differentiation and maturation in the adult spinal cord (Q28246800) (← links)