scholarly article | Q13442814 |
P356 | DOI | 10.1007/978-3-319-51436-9_9 |
P8608 | Fatcat ID | release_rx36ga3sird6jb6hic2otzey5y |
P698 | PubMed publication ID | 28409348 |
P50 | author | Kieran M Short | Q55711086 |
P2093 | author name string | Ian M Smyth | |
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SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes | Q24292967 | ||
SIX2 and BMP4 mutations associate with anomalous kidney development | Q24318341 | ||
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family | Q24318377 | ||
Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humans | Q24321323 | ||
SLIT2-mediated ROBO2 signaling restricts kidney induction to a single site | Q24338774 | ||
3 dimensional modelling of early human brain development using optical projection tomography | Q24802592 | ||
Organ In Vitro Culture: What Have We Learned about Early Kidney Development? | Q26822965 | ||
Localized Smooth Muscle Differentiation Is Essential for Epithelial Bifurcation during Branching Morphogenesis of the Mammalian Lung | Q27314520 | ||
Altered ureteric branching morphogenesis and nephron endowment in offspring of diabetic and insulin-treated pregnancy | Q27335350 | ||
Ret and Etv4 Promote Directed Movements of Progenitor Cells during Renal Branching Morphogenesis | Q27345189 | ||
The origin of the mammalian kidney: implications for recreating the kidney in vitro | Q28080749 | ||
Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs | Q28245837 | ||
Mutations in GRIP1 cause Fraser syndrome | Q28264673 | ||
Neonatal vascularization and oxygen tension regulate appropriate perinatal renal medulla/papilla maturation | Q28272436 | ||
Regulation of ureteric bud branching morphogenesis by sulfated proteoglycans in the developing kidney | Q28582695 | ||
Six2 is required for suppression of nephrogenesis and progenitor renewal in the developing kidney | Q28586205 | ||
Hox11 paralogous genes are essential for metanephric kidney induction | Q28587041 | ||
Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia | Q28587212 | ||
Six2 defines and regulates a multipotent self-renewing nephron progenitor population throughout mammalian kidney development | Q28592487 | ||
Cited1 and Cited2 are differentially expressed in the developing kidney but are not required for nephrogenesis | Q28593339 | ||
The branching programme of mouse lung development | Q28750946 | ||
Watersheds in digital spaces: an efficient algorithm based on immersion simulations | Q29013909 | ||
Optical projection tomography as a tool for 3D microscopy and gene expression studies | Q29617950 | ||
Luminal mitosis drives epithelial cell dispersal within the branching ureteric bud | Q30409579 | ||
Three-dimensional imaging reveals ureteric and mesenchymal defects in Fgfr2-mutant kidneys | Q30492344 | ||
Invasion of distal nephron precursors associates with tubular interconnection during nephrogenesis. | Q30525293 | ||
Actin depolymerizing factors cofilin1 and destrin are required for ureteric bud branching morphogenesis. | Q33741934 | ||
Prenatal exposure to alcohol reduces nephron number and raises blood pressure in progeny. | Q34023916 | ||
Fras1 deficiency results in cryptophthalmos, renal agenesis and blebbed phenotype in mice | Q34199876 | ||
Cellular and physical mechanisms of branching morphogenesis | Q34341494 | ||
Glomerular number and size in autopsy kidneys: the relationship to birth weight | Q34533810 | ||
Intergenerational programming of impaired nephrogenesis and hypertension in rats following maternal protein restriction during pregnancy | Q34823400 | ||
FGF9 and FGF20 maintain the stemness of nephron progenitors in mice and man. | Q36036048 | ||
Developmental Programming of Branching Morphogenesis in the Kidney | Q36104860 | ||
Branching morphogenesis independent of mesenchymal-epithelial contact in the developing kidney | Q36394811 | ||
Renal hypodysplasia associates with a WNT4 variant that causes aberrant canonical WNT signaling | Q36719225 | ||
Fate mapping using Cited1-CreERT2 mice demonstrates that the cap mesenchyme contains self-renewing progenitor cells and gives rise exclusively to nephronic epithelia. | Q37235452 | ||
Glial cell line-derived neurotrophic factor activates the receptor tyrosine kinase RET and promotes kidney morphogenesis | Q37289586 | ||
Ret-dependent cell rearrangements in the Wolffian duct epithelium initiate ureteric bud morphogenesis. | Q37388146 | ||
Extracellular matrix and cytoskeletal dynamics during branching morphogenesis. | Q38011553 | ||
Effect of fetal and child health on kidney development and long-term risk of hypertension and kidney disease | Q38111135 | ||
Concise review: can the intrinsic power of branching morphogenesis be used for engineering epithelial tissues and organs? | Q38160017 | ||
The receptor tyrosine kinase regulator Sprouty1 is a target of the tumor suppressor WT1 and important for kidney development | Q38352220 | ||
ROBO2 restricts the nephrogenic field and regulates Wolffian duct-nephrogenic cord separation | Q38859639 | ||
Renal aplasia in humans is associated with RET mutations | Q39141569 | ||
Branching morphogenesis of the ureteric epithelium during kidney development is coordinated by the opposing functions of GDNF and Sprouty1. | Q40223314 | ||
The role of GDNF/Ret signaling in ureteric bud cell fate and branching morphogenesis. | Q40476726 | ||
Real-time analysis of ureteric bud branching morphogenesis in vitro | Q40503619 | ||
Wnt11 and Ret/Gdnf pathways cooperate in regulating ureteric branching during metanephric kidney development. | Q40642802 | ||
GDNF signalling through the Ret receptor tyrosine kinase | Q41190484 | ||
FREM1 mutations cause bifid nose, renal agenesis, and anorectal malformations syndrome | Q41834808 | ||
Involvement of laminin binding integrins and laminin-5 in branching morphogenesis of the ureteric bud during kidney development | Q43849604 | ||
Comparing and distinguishing the structure of biological branching | Q44317003 | ||
Tomographic quantification of branching morphogenesis and renal development. | Q45344463 | ||
Spatial mapping and quantification of developmental branching morphogenesis. | Q46238561 | ||
Global quantification of tissue dynamics in the developing mouse kidney | Q46360772 | ||
Developmental plasticity and regenerative capacity in the renal ureteric bud/collecting duct system | Q47613569 | ||
An integrated pipeline for the multidimensional analysis of branching morphogenesis. | Q50622854 | ||
Cell and fibronectin dynamics during branching morphogenesis. | Q50720691 | ||
Morphometric index of the developing murine kidney | Q50792365 | ||
Nephron formation adopts a novel spatial topology at cessation of nephrogenesis. | Q51852105 | ||
Analysis of early nephron patterning reveals a role for distal RV proliferation in fusion to the ureteric tip via a cap mesenchyme-derived connecting segment. | Q51933152 | ||
Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2(1Neu) +/- mutant mice. | Q52172685 | ||
HIF1A signaling selectively supports proliferation of breast cancer in the brain | Q56883100 | ||
Morphogenetic Interaction between Embryonic Mouse Tissues separated by a Membrane Filter | Q59064712 | ||
De Novo Uroplakin IIIa Heterozygous Mutations Cause Human Renal Adysplasia Leading to Severe Kidney Failure | Q59382431 | ||
Normal Lactational Environment Restores Nephron Endowment and Prevents Hypertension after Placental Restriction in the Rat | Q59709759 | ||
Inductive epitheliomesenchymal interaction in cultured organ rudiments of the mouse | Q73225452 | ||
Trans-filter induction of tubules in mouse metanephrogenic mesenchyme | Q74019292 | ||
Mild vitamin A deficiency leads to inborn nephron deficit in the rat | Q77650600 | ||
Cell contact in relation to embryonic induction | Q78858372 | ||
Genetic disorders of human congenital anomalies of the kidney and urinary tract (CAKUT) | Q79105221 | ||
Prenatal detection of congenital renal malformations by fetal ultrasonographic examination: an analysis of 709,030 births in 12 European countries | Q80959159 | ||
P921 | main subject | morphogenesis | Q815547 |
P304 | page(s) | 233-256 | |
P577 | publication date | 2017-01-01 | |
P1433 | published in | Results and problems in cell differentiation | Q26842363 |
P1476 | title | Imaging, Analysing and Interpreting Branching Morphogenesis in the Developing Kidney | |
P478 | volume | 60 |
Q47827883 | A Whole Brain Staining, Embedding, and Clearing Pipeline for Adult Zebrafish to Visualize Cell Proliferation and Morphology in 3-Dimensions. |
Q47174465 | Concepts for a therapeutic prolongation of nephrogenesis in preterm and low-birth-weight babies must correspond to structural-functional properties in the nephrogenic zone |
Q52941787 | Reading First Coordinates from the Nephrogenic Zone in Human Fetal Kidney. |
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