| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/S11255-014-0784-0 |
| P698 | PubMed publication ID | 25201458 |
| P50 | author | Gavino Faa | Q53513900 |
| Daniela Fanni | Q59679234 | ||
| P2093 | author name string | Clara Gerosa | |
| Giovanni Ottonello | |||
| Vassilios Fanos | |||
| Melania Puddu | |||
| Cristina Loddo | |||
| P2860 | cites work | NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway | Q24293498 |
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| Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations | Q24313346 | ||
| Mutations in the human Jagged1 gene are responsible for Alagille syndrome | Q24314702 | ||
| Repression of Pax-2 by WT1 during normal kidney development | Q24314726 | ||
| Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1 | Q24314766 | ||
| Molecular analysis of SALL1 mutations in Townes-Brocks syndrome | Q24540095 | ||
| Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus | Q28236741 | ||
| Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping | Q28236877 | ||
| Is methylation the key to CD10 loss? | Q28269462 | ||
| Essential roles of Sall1 in kidney development | Q28276723 | ||
| Sprouty1 is a critical regulator of GDNF/RET-mediated kidney induction | Q28508136 | ||
| Wnt9b signaling regulates planar cell polarity and kidney tubule morphogenesis | Q28510389 | ||
| Role of fibroblast growth factor receptors 1 and 2 in the metanephric mesenchyme | Q28511352 | ||
| Maternal diet programs embryonic kidney gene expression | Q28568400 | ||
| Effects of dexamethasone exposure on rat metanephric development: in vitro and in vivo studies | Q28573286 | ||
| Inactivation of FGF8 in early mesoderm reveals an essential role in kidney development | Q28585034 | ||
| Six2 is required for suppression of nephrogenesis and progenitor renewal in the developing kidney | Q28586205 | ||
| PAX2 is reactivated in urinary tract obstruction and partially protects collecting duct cells from programmed cell death | Q28588102 | ||
| Pax 2/8-regulated Gata 3 expression is necessary for morphogenesis and guidance of the nephric duct in the developing kidney | Q28588295 | ||
| Six2 defines and regulates a multipotent self-renewing nephron progenitor population throughout mammalian kidney development | Q28592487 | ||
| PAX2 mutations in oligomeganephronia. | Q31903380 | ||
| Kidney development in the absence of Gdnf and Spry1 requires Fgf10. | Q33525015 | ||
| The contribution of Notch1 to nephron segmentation in the developing kidney is revealed in a sensitized Notch2 background and can be augmented by reducing Mint dosage. | Q33615861 | ||
| Actin depolymerizing factors cofilin1 and destrin are required for ureteric bud branching morphogenesis. | Q33741934 | ||
| Features of Alagille syndrome in 92 patients: frequency and relation to prognosis | Q33853650 | ||
| The candidate Wilms' tumour gene is involved in genitourinary development | Q34189819 | ||
| Morphogenesis and molecular mechanisms involved in human kidney development. | Q34207078 | ||
| Hereditary syndrome of imperforate anus with hand, foot, and ear anomalies | Q34227070 | ||
| GONADOBLASTOMA ASSOCIATED WITH PURE GONADAL DYSGENESIS IN MONOZYGOUS TWINS. | Q34256931 | ||
| Basic fibroblast growth factor can mediate the early inductive events in renal development | Q34359827 | ||
| Donor splice-site mutations in WT1 are responsible for Frasier syndrome | Q34449327 | ||
| The dysregulated podocyte phenotype: a novel concept in the pathogenesis of collapsing idiopathic focal segmental glomerulosclerosis and HIV-associated nephropathy | Q34756388 | ||
| Transcriptional regulation of podocyte disease | Q35987628 | ||
| Renal failure and hypertension in Alagille syndrome with a novel JAG1 mutation | Q36192207 | ||
| Multicystic dysplastic kidney and variable phenotype in a family with a novel deletion mutation of PAX2. | Q36210080 | ||
| A high-resolution anatomical ontology of the developing murine genitourinary tract. | Q36225377 | ||
| Matrix metalloproteinases MMP2 and MMP9 are produced in early stages of kidney morphogenesis but only MMP9 is required for renal organogenesis in vitro | Q36254654 | ||
| The renin-angiotensin system in the development of the congenital anomalies of the kidney and urinary tract | Q36443280 | ||
| Developmental biology of the human kidney | Q37039209 | ||
| Bone morphogenetic protein 4 regulates the budding site and elongation of the mouse ureter | Q37176177 | ||
| Factors influencing mammalian kidney development: implications for health in adult life. | Q37220034 | ||
| Fate mapping using Cited1-CreERT2 mice demonstrates that the cap mesenchyme contains self-renewing progenitor cells and gives rise exclusively to nephronic epithelia. | Q37235452 | ||
| A new role for the renin-angiotensin system in the development of the ureteric bud and renal collecting system | Q37277838 | ||
| odd skipped related1 reveals a novel role for endoderm in regulating kidney versus vascular cell fate | Q37342893 | ||
| High-resolution gene expression analysis of the developing mouse kidney defines novel cellular compartments within the nephron progenitor population | Q37356678 | ||
| MMP9 limits apoptosis and stimulates branching morphogenesis during kidney development | Q37367724 | ||
| Cell and molecular biology of kidney development | Q37555042 | ||
| WT1 and kidney progenitor cells | Q37795569 | ||
| Adverse consequences of accelerated neonatal growth: cardiovascular and renal issues | Q37799566 | ||
| Semaphorins in kidney development and disease: modulators of ureteric bud branching, vascular morphogenesis, and podocyte-endothelial crosstalk | Q37845241 | ||
| "Physiological" renal regenerating medicine in VLBW preterm infants: could a dream come true? | Q38046917 | ||
| Chronic renal failure and XY gonadal dysgenesis: "Frasier" syndrome--a commentary on reported cases | Q39602598 | ||
| The many faces of RET dysfunction in kidney | Q39694457 | ||
| Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases | Q39801627 | ||
| The major podocyte protein nephrin is transcriptionally activated by the Wilms' tumor suppressor WT1. | Q40484861 | ||
| Real-time analysis of ureteric bud branching morphogenesis in vitro | Q40503619 | ||
| WT1 regulates the expression of the major glomerular podocyte membrane protein Podocalyxin | Q40767021 | ||
| Wnt-4 is a mesenchymal signal for epithelial transformation of metanephric mesenchyme in the developing kidney | Q41006079 | ||
| Beta-catenin is necessary to keep cells of ureteric bud/Wolffian duct epithelium in a precursor state | Q41291637 | ||
| Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome | Q41660674 | ||
| Semaphorin3a regulates endothelial cell number and podocyte differentiation during glomerular development | Q42644799 | ||
| Identification of multipotent progenitors in the embryonic mouse kidney by a novel colony-forming assay. | Q42807539 | ||
| Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population | Q45149880 | ||
| Cyclooxygenase-2 in rat nephron development | Q50111225 | ||
| Townes-Brocks syndrome in an infant with translocation t (5;16). | Q50533093 | ||
| An immunohistochemical study of developing glomeruli in human fetal kidneys. | Q51604360 | ||
| Renal hypoplasia without optic coloboma associated with PAX2 gene deletion | Q61409831 | ||
| Role of the Angiotensin Type 2 Receptor Gene in Congenital Anomalies of the Kidney and Urinary Tract, CAKUT, of Mice and Men | Q63951732 | ||
| Antenatal diagnosis of congenital abnormalities in the urinary tract. Results from the Northern Region Fetal Abnormality Survey | Q67968900 | ||
| Nephropathy-gonadal dysgenesis, type 2: renal failure in three siblings with XY dysgenesis in one | Q69048272 | ||
| A syndrome of chronic renal failure and XY gonadal dysgenesis in young phenotypic females without genital ambiguity | Q69903006 | ||
| Histological features of glomerular immaturity in infants and small children with normal or altered tubular function | Q70807110 | ||
| BMP-7 is an inducer of nephrogenesis, and is also required for eye development and skeletal patterning | Q71817916 | ||
| Use of antibodies to RCC and CD10 in the differential diagnosis of renal neoplasms | Q73461795 | ||
| Histomorphometric analysis of postnatal glomerulogenesis in extremely preterm infants | Q80343146 | ||
| Histochemical and immunohistochemical study of the glomerular development in human fetuses | Q81568859 | ||
| MUC1 in mesenchymal-to-epithelial transition during human nephrogenesis: changing the fate of renal progenitor/stem cells? | Q85033239 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 109-116 | |
| P577 | publication date | 2014-09-09 | |
| P1433 | published in | International Urology and Nephrology | Q15763616 |
| P1476 | title | From ureteric bud to the first glomeruli: genes, mediators, kidney alterations | |
| P478 | volume | 47 |
| Q38723460 | Assessment of kidney function in preterm infants: lifelong implications |
| Q64072894 | Preterm birth and risk of chronic kidney disease from childhood into mid-adulthood: national cohort study |
| Q52941787 | Reading First Coordinates from the Nephrogenic Zone in Human Fetal Kidney. |
| Q27003302 | When morphogenetic proteins encounter special extracellular matrix and cell-cell connections at the interface of the renal stem/progenitor cell niche |
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