Pages that link to "Q30549880"
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The following pages link to Calcineurin is required in urinary tract mesenchyme for the development of the pyeloureteral peristaltic machinery. (Q30549880):
Displaying 50 items.
- Discs-large homolog 1 regulates smooth muscle orientation in the mouse ureter (Q24676483) (← links)
- Anatomy and Physiology of the Urinary Tract: Relation to Host Defense and Microbial Infection (Q26782602) (← links)
- Lower urinary tract development and disease (Q27000375) (← links)
- Congenital urinary tract obstruction: the long view (Q27009005) (← links)
- Development of the kidney medulla (Q27015938) (← links)
- Fstl1 antagonizes BMP signaling and regulates ureter development (Q27308086) (← links)
- Association between congenital defects in papillary outgrowth and functional obstruction in Crim1 mutant mice (Q28264027) (← links)
- Neonatal vascularization and oxygen tension regulate appropriate perinatal renal medulla/papilla maturation (Q28272436) (← links)
- Development and differentiation of the ureteric bud into the ureter in the absence of a kidney collecting system (Q28507290) (← links)
- Tbx18 regulates the development of the ureteral mesenchyme (Q28586369) (← links)
- Hydroureternephrosis due to loss of Sox9-regulated smooth muscle cell differentiation of the ureteric mesenchyme (Q28587480) (← links)
- A Wnt7b-dependent pathway regulates the orientation of epithelial cell division and establishes the cortico-medullary axis of the mammalian kidney (Q28587526) (← links)
- Systems biology combining human- and animal-data miRNA and mRNA data identifies new targets in ureteropelvic junction obstruction (Q30253062) (← links)
- Angiotensin II regulates growth of the developing papillas ex vivo (Q30419466) (← links)
- Inducible nitric oxide synthase modulates hydronephrosis following partial or complete unilateral ureteral obstruction in the neonatal mouse (Q30433591) (← links)
- Glomerulotubular disconnection in neonatal mice after relief of partial ureteral obstruction (Q30444355) (← links)
- Mechanisms of renal injury and progression of renal disease in congenital obstructive nephropathy (Q30449258) (← links)
- Wnt signaling and renal medulla formation (Q30453346) (← links)
- Heart-specific deletion of CnB1 reveals multiple mechanisms whereby calcineurin regulates cardiac growth and function (Q30493276) (← links)
- GLI3 repressor controls functional development of the mouse ureter (Q30498339) (← links)
- The pelvis-kidney junction contains HCN3, a hyperpolarization-activated cation channel that triggers ureter peristalsis (Q30583731) (← links)
- Non-invasive markers of ureteropelvic junction obstruction (Q33294284) (← links)
- p53 regulates metanephric development (Q33561738) (← links)
- Cre/lox recombination in the lower urinary tract (Q33763688) (← links)
- The role of calcium/calmodulin-activated calcineurin in rapid and slow endocytosis at central synapses (Q34196522) (← links)
- Activation of NFAT signaling in podocytes causes glomerulosclerosis (Q34455455) (← links)
- NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21. (Q34504363) (← links)
- Congenital progressive hydronephrosis (cph) is caused by an S256L mutation in aquaporin-2 that affects its phosphorylation and apical membrane accumulation (Q34598401) (← links)
- Adam10 mediates the choice between principal cells and intercalated cells in the kidney. (Q34787740) (← links)
- LEF1 identifies androgen-independent epithelium in the developing prostate (Q35001290) (← links)
- Calcineurin A-alpha but not A-beta is required for normal kidney development and function (Q35103375) (← links)
- Smad4 regulates ureteral smooth muscle cell differentiation during mouse embryogenesis (Q35225701) (← links)
- Molecular anatomy of the kidney: what have we learned from gene expression and functional genomics? (Q35294012) (← links)
- Urothelial Defects from Targeted Inactivation of Exocyst Sec10 in Mice Cause Ureteropelvic Junction Obstructions (Q35653795) (← links)
- Antagonism of BMP4 signaling disrupts smooth muscle investment of the ureter and ureteropelvic junction (Q35754460) (← links)
- Absence of canonical Smad signaling in ureteral and bladder mesenchyme causes ureteropelvic junction obstruction (Q35853268) (← links)
- Transcriptional dysregulation in the ureteric bud causes multicystic dysplastic kidney by branching morphogenesis defect (Q35857109) (← links)
- Disruption of glomerular basement membrane charge through podocyte-specific mutation of agrin does not alter glomerular permselectivity (Q35928165) (← links)
- Renal defects associated with improper polarization of the CRB and DLG polarity complexes in MALS-3 knockout mice (Q36119534) (← links)
- Vesicoureteric reflux and renal malformations: a developmental problem (Q36376471) (← links)
- Going in circles: conserved mechanisms control radial patterning in the urinary and digestive tracts (Q36411148) (← links)
- An emerging role for calcineurin Aalpha in the development and function of the kidney (Q36417660) (← links)
- Down syndrome critical region-1 is a transcriptional target of nuclear factor of activated T cells-c1 within the endocardium during heart development (Q36631526) (← links)
- Uroplakins: new molecular players in the biology of urinary tract malformations. (Q36689787) (← links)
- Pathophysiology and treatment of ureteropelvic junction obstruction (Q36736484) (← links)
- Scaffolding proteins DLG1 and CASK cooperate to maintain the nephron progenitor population during kidney development (Q36977379) (← links)
- Ablation of developing podocytes disrupts cellular interactions and nephrogenesis both inside and outside the glomerulus (Q37018408) (← links)
- Plumbing the depths of urinary tract obstruction by using murine models (Q37137183) (← links)
- Activation of NFAT signaling establishes a tumorigenic microenvironment through cell autonomous and non-cell autonomous mechanisms (Q37164683) (← links)
- Fibroproliferative response to urothelial failure obliterates the ureter lumen in a mouse model of prenatal congenital obstructive nephropathy (Q37166604) (← links)