| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1007/S00467-011-1820-2 |
| P698 | PubMed publication ID | 21359618 |
| P2093 | author name string | Ihor V Yosypiv | |
| P2860 | cites work | Developmental roles of the histone lysine demethylases | Q22306162 |
| Angiotensin II increases Pax-2 expression in fetal kidney cells via the AT2 receptor | Q24293720 | ||
| The BRCT-domain containing protein PTIP links PAX2 to a histone H3, lysine 4 methyltransferase complex | Q24296996 | ||
| Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis | Q24317237 | ||
| Shc phosphotyrosine-binding domain dominantly interacts with epidermal growth factor receptors and mediates Ras activation in intact cells | Q24324437 | ||
| SLIT2-mediated ROBO2 signaling restricts kidney induction to a single site | Q24338774 | ||
| Docking protein FRS2 links the protein tyrosine kinase RET and its oncogenic forms with the mitogen-activated protein kinase signaling cascade | Q24550950 | ||
| The many roles of histone deacetylases in development and physiology: implications for disease and therapy | Q24628821 | ||
| GFRalpha1 is an essential receptor component for GDNF in the developing nervous system and kidney | Q24649094 | ||
| Angiotensin-(1-7) is an endogenous ligand for the G protein-coupled receptor Mas | Q24680069 | ||
| The transcriptional coactivators p300 and CBP are histone acetyltransferases | Q27860843 | ||
| The GDNF family: signalling, biological functions and therapeutic value | Q28216478 | ||
| Promotion and attenuation of FGF signaling through the Ras-MAPK pathway | Q28312210 | ||
| Gene targeting in mice reveals a requirement for angiotensin in the development and maintenance of kidney morphology and growth factor regulation | Q28505894 | ||
| Sprouty1 is a critical regulator of GDNF/RET-mediated kidney induction | Q28508136 | ||
| Targeted disruption of mouse EGF receptor: effect of genetic background on mutant phenotype | Q28509173 | ||
| Gata3 acts downstream of beta-catenin signaling to prevent ectopic metanephric kidney induction | Q28579892 | ||
| A Wnt7b-dependent pathway regulates the orientation of epithelial cell division and establishes the cortico-medullary axis of the mammalian kidney | Q28587526 | ||
| Distal ureter morphogenesis depends on epithelial cell remodeling mediated by vitamin A and Ret | Q28587600 | ||
| A role for angiotensin II AT1 receptors in ureteric bud cell branching | Q28587789 | ||
| Regulation of ureteric bud outgrowth by Pax2-dependent activation of the glial derived neurotrophic factor gene | Q28588874 | ||
| Murine forkhead/winged helix genes Foxc1 (Mf1) and Foxc2 (Mfh1) are required for the early organogenesis of the kidney and urinary tract | Q28590442 | ||
| Erk MAP kinase regulates branching morphogenesis in the developing mouse kidney | Q28590780 | ||
| Murine double nullizygotes of the angiotensin type 1A and 1B receptor genes duplicate severe abnormal phenotypes of angiotensinogen nullizygotes | Q28592947 | ||
| Angiotensin induces the urinary peristaltic machinery during the perinatal period | Q28592988 | ||
| Renal agenesis and the absence of enteric neurons in mice lacking GDNF | Q28594756 | ||
| EGF receptor transactivation by G-protein-coupled receptors requires metalloproteinase cleavage of proHB-EGF | Q29619098 | ||
| CBP and p300 are essential for renin cell identity and morphological integrity of the kidney | Q30436207 | ||
| Identity of the renin cell is mediated by cAMP and chromatin remodeling: an in vitro model for studying cell recruitment and plasticity | Q30445131 | ||
| Distribution of renin mRNA and its protein in the developing kidney | Q30460012 | ||
| Angiotensin II regulates nephrogenesis and renal vascular development | Q30464404 | ||
| Differential expression of angiotensin II receptors during early renal morphogenesis | Q30470383 | ||
| Abnormal water metabolism in mice lacking the type 1A receptor for ANG II. | Q31462282 | ||
| Ontogeny of somatic angiotensin-converting enzyme. | Q52217968 | ||
| Expression of murine renin genes during fetal development. | Q52242156 | ||
| Development of glomerular perfusion rate and nephron filtration rate in rats 17-60 days old | Q52312999 | ||
| How descending limb of Henle's loop permeability affects hypertonic urine formation. | Q52759457 | ||
| Mice lacking angiotensin-converting enzyme have low blood pressure, renal pathology, and reduced male fertility. | Q52909701 | ||
| Shc Phosphotyrosine-Binding Domain Dominantly Interacts with Epidermal Growth Factor Receptors and Mediates Ras Activation in Intact Cells | Q56567842 | ||
| Renal agenesis and hypodysplasia in ret-k- mutant mice result from defects in ureteric bud development | Q60418568 | ||
| Inductive interactions between the mesenchyme and the ureteric bud | Q64447212 | ||
| Regulation of luminal alkalinization and acidification in the cortical collecting duct by angiotensin II | Q71597227 | ||
| Nephrogenesis and renovascular development in angiotensinogen-deficient mice | Q71828758 | ||
| In situ hybridization and immunohistochemistry of renal angiotensinogen in neonatal and adult rat kidneys | Q71993004 | ||
| Angiotensin converting enzyme in renal ontogeny: hypothesis for multiple roles | Q72297494 | ||
| Renin-angiotensin system in neonatal rats: induction of a renal abnormality in response to ACE inhibition or angiotensin II antagonism | Q72378607 | ||
| Angiotensin II regulates H(+)-ATPase activity in rat cortical collecting duct | Q72383081 | ||
| Temporal and spatial expression pattern of the angiotensinogen gene in mice and rats | Q73086282 | ||
| Neonatal angiotensin-converting enzyme inhibition in the rat induces persistent abnormalities in renal function and histology | Q73086461 | ||
| Inductive epitheliomesenchymal interaction in cultured organ rudiments of the mouse | Q73225452 | ||
| Vasoconstriction by in situ formed angiotensin II: role of ACE and chymase | Q73482851 | ||
| Effect of maternal iron restriction during pregnancy on renal morphology in the adult rat offspring | Q73619704 | ||
| Growth-dependent induction of angiotensin II type 2 receptor in rat mesangial cells | Q73741462 | ||
| Angiotensin-converting enzyme inhibition decreases growth factor expression in the neonatal rat kidney | Q73848148 | ||
| Real-time PCR quantification of AT1 and AT2 angiotensin receptor mRNA expression in the developing rat kidney | Q73938583 | ||
| Angiotensin type II receptor expression and ureteral budding | Q74591947 | ||
| Apoptosis induced by vitamin A signaling is crucial for connecting the ureters to the bladder | Q81267283 | ||
| Cardiovascular phenotype of mice lacking all three subtypes of angiotensin II receptors | Q81322401 | ||
| Glial-cell-line-derived neurotrophic factor is required for bud initiation from ureteric epithelium | Q41078366 | ||
| Angiotensin II activation of cyclin D1-dependent kinase activity | Q41168284 | ||
| Angiotensin II and prostaglandins in control of vasa recta blood flow | Q41428237 | ||
| Angiotensin II-induced proliferation of cultured murine mesangial cells: inhibitory role of atrial natriuretic peptide | Q41592054 | ||
| Histone deacetylases are critical regulators of the renin-angiotensin system during ureteric bud branching morphogenesis | Q41851966 | ||
| The late intrauterine and postnatal development of human renal glomeruli | Q42228731 | ||
| Angiotensin II-induced activation of c-Ret signaling is critical in ureteric bud branching morphogenesis | Q42910496 | ||
| Critical and distinct roles for key RET tyrosine docking sites in renal development | Q43061478 | ||
| Independent two-photon measurements of albumin GSC give low values | Q43116319 | ||
| Loss of Sprouty1 rescues renal agenesis caused by Ret mutation. | Q43186033 | ||
| Cholesterol depletion inhibits epidermal growth factor receptor transactivation by angiotensin II in vascular smooth muscle cells: role of cholesterol-rich microdomains and focal adhesions in angiotensin II signaling. | Q43755949 | ||
| Targeted proteomic profiling of renal Na(+) transporter and channel abundances in angiotensin II type 1a receptor knockout mice | Q43908220 | ||
| Angiotensin II stimulates basolateral K channels in rat cortical collecting ducts | Q44185756 | ||
| TGF-beta superfamily members modulate growth, branching, shaping, and patterning of the ureteric bud. | Q44738676 | ||
| Embryonic origin and lineage of juxtaglomerular cells | Q44882484 | ||
| Ren1c homozygous null mice are hypotensive and polyuric, but heterozygotes are indistinguishable from wild-type | Q45162612 | ||
| Angiotensin II type 1 receptor-EGF receptor cross-talk regulates ureteric bud branching morphogenesis | Q46958290 | ||
| In vitro branching tubulogenesis: implications for developmental and cystic disorders, nephron number, renal repair, and nephron engineering | Q47906324 | ||
| Morphometric index of the developing murine kidney | Q50792365 | ||
| Postnatal time frame for renal vulnerability to enalapril in rats. | Q51451049 | ||
| Mechanisms of impaired urinary concentrating ability in adult rats treated neonatally with enalapril. | Q51471225 | ||
| Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2(1Neu) +/- mutant mice. | Q52172685 | ||
| The renal lesions that develop in neonatal mice during angiotensin inhibition mimic obstructive nephropathy. | Q52177384 | ||
| Activation of angiotensin-generating systems in the developing rat kidney. | Q52202960 | ||
| Developmental expression of renal angiotensin II receptor genes in the mouse. | Q52211588 | ||
| Renal tubular dysgenesis, a not uncommon autosomal recessive disorder leading to oligohydramnios: Role of the Renin-Angiotensin system | Q33247520 | ||
| Haplotype mapping of a diploid non-meiotic organism using existing and induced aneuploidies | Q33313490 | ||
| Kidney development in the absence of Gdnf and Spry1 requires Fgf10. | Q33525015 | ||
| Reduced growth, abnormal kidney structure, and type 2 (AT2) angiotensin receptor-mediated blood pressure regulation in mice lacking both AT1A and AT1B receptors for angiotensin II. | Q33593068 | ||
| Organotypic specificity of key RET adaptor-docking sites in the pathogenesis of neurocristopathies and renal malformations in mice | Q33685678 | ||
| Angiotensin II AT2 receptor regulates ureteric bud morphogenesis | Q33727770 | ||
| Targeted inactivation of EGF receptor inhibits renal collecting duct development and function. | Q33748529 | ||
| The transcription factors Etv4 and Etv5 mediate formation of the ureteric bud tip domain during kidney development | Q33874543 | ||
| Patterning a complex organ: branching morphogenesis and nephron segmentation in kidney development | Q33904019 | ||
| Role of fibroblast growth factor receptors 1 and 2 in the ureteric bud. | Q34040095 | ||
| The angiotensin II AT2 receptor is an AT1 receptor antagonist. | Q34086986 | ||
| Renal branching morphogenesis: concepts, questions, and recent advances | Q34558288 | ||
| A shifting paradigm: histone deacetylases and transcriptional activation | Q34725666 | ||
| Early expression of all the components of the renin-angiotensin-system in human development | Q35782663 | ||
| Young Scholars Award Lecture: Intratubular angiotensinogen in hypertension and kidney diseases | Q36116868 | ||
| Developmental biology of the human kidney | Q37039209 | ||
| Role of fibroblast growth factor receptor 2 in kidney mesenchyme. | Q37109888 | ||
| Regulation of growth factor signaling by FRS2 family docking/scaffold adaptor proteins | Q37152909 | ||
| Bone morphogenetic protein 4 regulates the budding site and elongation of the mouse ureter | Q37176177 | ||
| Stimulatory and inhibitory signaling molecules that regulate renal branching morphogenesis | Q37350774 | ||
| MMP9 limits apoptosis and stimulates branching morphogenesis during kidney development | Q37367724 | ||
| Deletion of Frs2alpha from the ureteric epithelium causes renal hypoplasia | Q37430764 | ||
| Etv4 and Etv5 are required downstream of GDNF and Ret for kidney branching morphogenesis | Q37455527 | ||
| Molecular mechanisms of the antagonistic action between AT1 and AT2 receptors | Q37477602 | ||
| Genetics of congenital anomalies of the kidney and urinary tract | Q37783542 | ||
| Developmentally regulated conversion of mesenchyme to epithelium | Q38667909 | ||
| Renal aplasia in humans is associated with RET mutations | Q39141569 | ||
| Glomeruli and blood pressure. Less of one, more the other? | Q39554411 | ||
| The many faces of RET dysfunction in kidney | Q39694457 | ||
| Downregulation of Spry-1, an inhibitor of GDNF/Ret, causes angiotensin II-induced ureteric bud branching | Q39957943 | ||
| PTEN modulates GDNF/RET mediated chemotaxis and branching morphogenesis in the developing kidney | Q40125775 | ||
| Branching morphogenesis of the ureteric epithelium during kidney development is coordinated by the opposing functions of GDNF and Sprouty1. | Q40223314 | ||
| Pattern and regulation of cell proliferation during murine ureteric bud development | Q40570569 | ||
| Wnt11 and Ret/Gdnf pathways cooperate in regulating ureteric branching during metanephric kidney development. | Q40642802 | ||
| Ureteric bud outgrowth in response to RET activation is mediated by phosphatidylinositol 3-kinase | Q40750881 | ||
| Ureteric bud derivatives express angiotensinogen and AT1 receptors | Q40800662 | ||
| Signaling complexes and protein-protein interactions involved in the activation of the Ras and phosphatidylinositol 3-kinase pathways by the c-Ret receptor tyrosine kinase. | Q40854118 | ||
| GDNF induces branching and increased cell proliferation in the ureter of the mouse. | Q41070429 | ||
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | morphogenesis | Q815547 |
| P304 | page(s) | 1499-1512 | |
| P577 | publication date | 2011-02-26 | |
| P1433 | published in | Pediatric Nephrology | Q15749796 |
| P1476 | title | Renin-angiotensin system in ureteric bud branching morphogenesis: insights into the mechanisms | |
| P478 | volume | 26 |
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| Q56774769 | Association of angiotensin type 2 receptor gene polymorphisms with ureteropelvic junction obstruction in Brazilian patients |
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