| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/(SICI)1096-911X(199611)27:5<445::AID-MPO10>3.0.CO;2-9 |
| P698 | PubMed publication ID | 8827072 |
| P2093 | author name string | Kreidberg JA | |
| P2860 | cites work | Requirement for Lim1 in head-organizer function | Q24312737 |
| Human platelet-derived growth factor A chain is transcriptionally repressed by the Wilms tumor suppressor WT1 | Q24337538 | ||
| Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus | Q28236741 | ||
| A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease | Q28239519 | ||
| Essential role of stromal mesenchyme in kidney morphogenesis revealed by targeted disruption of Winged Helix transcription factor BF-2 | Q28504535 | ||
| A requirement for bone morphogenetic protein-7 during development of the mammalian kidney and eye | Q28508005 | ||
| Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4 | Q28508296 | ||
| WT-1 is required for early kidney development | Q28512266 | ||
| Deficient outgrowth of the ureteric bud underlies the renal agenesis phenotype in mice manifesting the limb deformity (ld) mutation | Q28513203 | ||
| Bcl-2-deficient mice demonstrate fulminant lymphoid apoptosis, polycystic kidneys, and hypopigmented hair | Q28586758 | ||
| Targeted disruption of Bcl-2 alpha beta in mice: occurrence of gray hair, polycystic kidney disease, and lymphocytopenia | Q28591736 | ||
| An inherited limb deformity created by insertional mutagenesis in a transgenic mouse | Q28592717 | ||
| Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret | Q29620364 | ||
| Mice deficient for PDGF B show renal, cardiovascular, and hematological abnormalities | Q33491173 | ||
| Abnormal kidney development and hematological disorders in PDGF beta-receptor mutant mice. | Q33491174 | ||
| Germ-line transmission of genes introduced into cultured pluripotential cells by retroviral vector | Q34189858 | ||
| Expression patterns of the murine LIM class homeobox gene lim1 in the developing brain and excretory system. | Q34322302 | ||
| Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice. | Q34341740 | ||
| Formins: phosphoprotein isoforms encoded by the mouse limb deformity locus | Q36363617 | ||
| Pax-2 is a DNA-binding protein expressed in embryonic kidney and Wilms tumor | Q36826291 | ||
| Nephrogenic rests, nephroblastomatosis, and the pathogenesis of Wilms' tumor | Q37874427 | ||
| Binding of the Wilms' tumor locus zinc finger protein to the EGR-1 consensus sequence | Q38338176 | ||
| The new mouse genetics: altering the genome by gene targeting | Q38646807 | ||
| Renal Anemia in Polycystic Kidney Disease Mouse | Q39101310 | ||
| The genetics of Wilms' tumor--a case of disrupted development | Q40614052 | ||
| Polycystic kidney disease: primary extracellular matrix abnormality or defective cellular differentiation? | Q40876083 | ||
| N-myc proto-oncogene expression during organogenesis in the developing mouse as revealed by in situ hybridization | Q41558787 | ||
| Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome | Q41660674 | ||
| Transcriptional repression mediated by the WT1 Wilms tumor gene product | Q41661461 | ||
| Contrasting expression patterns of three members of the myc family of protooncogenes in the developing and adult mouse kidney | Q42004438 | ||
| Are morphogenetic tissue interactions mediated by transmissible signal substances or through cell contacts? | Q44340477 | ||
| Nephrogenic Rests in Wilms Tumor Patients with the Drash Syndrome | Q46664411 | ||
| WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour | Q48206248 | ||
| Embryonic lethality in mice homozygous for a targeted disruption of the N-myc gene | Q48400477 | ||
| Deregulation of Pax-2 expression in transgenic mice generates severe kidney abnormalities. | Q52226238 | ||
| Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development | Q52231802 | ||
| Mice with a null mutation of the TGF alpha gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation. | Q52517769 | ||
| TGF alpha deficiency results in hair follicle and eye abnormalities in targeted and waved-1 mice. | Q52517773 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| The Mouse Congenital Polycystic Kidney (cpk) Locus Maps within 1.3 cM of the Chromosome 12 Marker D12Nyu2 | Q57000868 | ||
| Evidence that WT1 mutations in Denys — Drash syndrome patients may act in a dominant-negative fashion | Q59662118 | ||
| Repression of the insulin-like growth factor II gene by the Wilms tumor suppressor WT1 | Q67493857 | ||
| Loss of N-myc function results in embryonic lethality and failure of the epithelial component of the embryo to develop | Q67599796 | ||
| Characterization of the Upper Urinary Tract Anatomy in the Danforth Spontaneous Murine Mutation | Q68227549 | ||
| A null c-myc mutation causes lethality before 10.5 days of gestation in homozygotes and reduced fertility in heterozygous female mice | Q70624275 | ||
| Renal and biliary abnormalities in a new murine model of autosomal recessive polycystic kidney disease | Q70667759 | ||
| Juvenile cystic kidneys (jck): a new mouse mutation which causes polycystic kidneys | Q70758568 | ||
| BMP-7 is an inducer of nephrogenesis, and is also required for eye development and skeletal patterning | Q71817916 | ||
| Denys-Drash syndrome: relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1 | Q72577728 | ||
| Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms' tumour | Q72751031 | ||
| Inductive epitheliomesenchymal interaction in cultured organ rudiments of the mouse | Q73225452 | ||
| P433 | issue | 5 | |
| P921 | main subject | gene targeting | Q211083 |
| P304 | page(s) | 445-452 | |
| P577 | publication date | 1996-11-01 | |
| P1433 | published in | Pediatric Blood & Cancer | Q15754342 |
| P1476 | title | Gene targeting in kidney development | |
| P478 | volume | 27 |
| Q35124266 | Deficiency of the planar cell polarity protein Vangl2 in podocytes affects glomerular morphogenesis and increases susceptibility to injury. |
| Q33744636 | Embryonic renal epithelia: induction, nephrogenesis, and cell differentiation |
| Q28365766 | Failure of ureteric bud invasion: a new model of renal agenesis in mice |
| Q24322628 | Loss-of-function mutations in the LIM-homeodomain gene, LMX1B, in nail-patella syndrome |
| Q34031394 | Principles of Wilms' tumor biology |
| Q77378783 | Renal dysplasia: the risks and consequences of leaving dysplastic tissue in situ |
| Q33379641 | Simulations of a specific inhibitor of the dishevelled PDZ domain |
| Q33888488 | Soluble dominant-negative receptor uncovers essential roles for fibroblast growth factors in multi-organ induction and patterning |
| Q40529835 | Transcriptional activation of c-myc proto-oncogene by WT1 protein |
| Q63199214 | Wilms Tumor Gene Immunoreactivity in Primary Serous Carcinomas of the Fallopian Tube, Ovary, Endometrium, and Peritoneum |
| Q33727614 | Wilms' tumor and related abnormalities in the fetus and newborn |
| Q39979771 | Wilms' tumor protein (-KTS) modulates renin gene transcription. |
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