| scholarly article | Q13442814 |
| P2093 | author name string | R Nusse | |
| U Francke | |||
| Y K Wang | |||
| L A Pérez-Jurado | |||
| C H Samos | |||
| R Peoples | |||
| P2860 | cites work | Natural history of Williams syndrome: physical characteristics | Q34406298 |
| Wnt genes | Q34452880 | ||
| The Drosophila EcR gene encodes an ecdysone receptor, a new member of the steroid receptor superfamily | Q34920066 | ||
| Signaling by wingless in Drosophila | Q40564670 | ||
| The genetic basis of patterned baldness in Drosophila | Q40621447 | ||
| Biological activity of soluble wingless protein in cultured Drosophila imaginal disc cells | Q41479991 | ||
| Intercellular signalling in Drosophila segment formation reconstructed in vitro | Q41547862 | ||
| Role of extracellular disulfide-bonded cysteines in the ligand binding function of the beta 2-adrenergic receptor | Q42109345 | ||
| Incidence and spectrum of renal abnormalities in Williams-Beuren syndrome | Q44980072 | ||
| Identification of genes within CpG-enriched DNA from human chromosome 4p16.3. | Q45307223 | ||
| Swaying is a mutant allele of the proto-oncogene Wnt-1 | Q48622186 | ||
| Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome | Q52223418 | ||
| Expression of the proto-oncogene int-1 is restricted to postmeiotic male germ cells and the neural tube of mid-gestational embryos. | Q52255806 | ||
| LIM-kinase deleted in Williams syndrome. | Q55066510 | ||
| Expression of the proto-oncogene int-1 is restricted to specific neural cells in the developing mouse embryo | Q63487544 | ||
| Chromosomal mapping of genes involved in growth control | Q70340861 | ||
| Williams syndrome: autosomal dominant inheritance | Q72646769 | ||
| LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition | Q24309104 | ||
| The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis | Q24321717 | ||
| Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients | Q24336101 | ||
| A simple method for displaying the hydropathic character of a protein | Q26778481 | ||
| A large family of putative transmembrane receptors homologous to the product of the Drosophila tissue polarity gene frizzled | Q28278437 | ||
| A human homologue of the Drosophila polarity gene frizzled has been identified and mapped to 17q21.1 | Q28289254 | ||
| The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain | Q28586297 | ||
| Targeted disruption of the murine int-1 proto-oncogene resulting in severe abnormalities in midbrain and cerebellar development | Q28593581 | ||
| A new member of the frizzled family from Drosophila functions as a Wingless receptor | Q29620189 | ||
| The genetic control of tissue polarity in Drosophila | Q30311367 | ||
| Mapping irradiation hybrids to cosmid and yeast artificial chromosome libraries by direct hybridization of Alu-PCR products | Q33631550 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | nervous system development | Q1345738 |
| Drosophila | Q312154 | ||
| Frizzled class receptor 9 | Q21115915 | ||
| P304 | page(s) | 465-72 | |
| P577 | publication date | 1997-03-01 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23 | |
| P478 | volume | 6 |
| Q42544481 | 2012 William Allan Award: Adventures in cytogenetics |
| Q40094394 | A comparative study of educational provision for children with neurogenetic syndromes: parent and teacher survey |
| Q24301647 | A novel set of Wnt-Frizzled fusion proteins identifies receptor components that activate beta -catenin-dependent signaling |
| Q34146234 | A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23 |
| Q44163889 | ASD, ADHD, mental health conditions and psychopharmacology in neurogenetic syndromes: parent survey |
| Q27304784 | Adaptive Behavior and Development of Infants and Toddlers with Williams Syndrome |
| Q42119593 | Anti-inflammatory activity of Wnt signaling in enteric nervous system: in vitro preliminary evidences in rat primary cultures |
| Q22242621 | Behavioural phenotypes and special educational needs: is aetiology important in the classroom? |
| Q34165885 | Beta-catenin signaling in hepatic development and progenitors: which way does the WNT blow? |
| Q30577163 | Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome |
| Q77803739 | Cellular mechanisms of wingless/Wnt signal transduction |
| Q24531938 | Characterization and gene structure of a novel retinoblastoma-protein-associated protein similar to the transcription regulator TFII-I |
| Q35023630 | Comparative mapping of the region of human chromosome 7 deleted in williams syndrome. |
| Q28587080 | Control of bone formation by the serpentine receptor Frizzled-9 |
| Q40865493 | Cooperative induction of mammary tumorigenesis by TGFalpha and Wnts |
| Q36583742 | DNA methylation and hormone receptor status in breast cancer |
| Q30844917 | Developmental disorders of vision |
| Q24305287 | Differential effects of secreted frizzled-related proteins (sFRPs) on osteoblastic differentiation of mouse mesenchymal cells and apoptosis of osteoblasts |
| Q37351287 | Dynamic expression of secreted Frizzled-related protein 3 (sFRP3) in the developing mouse spinal cord and dorsal root ganglia |
| Q28071320 | Frizzled Receptors in Development and Disease |
| Q27010132 | Frizzled homolog proteins, microRNAs and Wnt signaling in cancer |
| Q29347259 | Frizzled-9 impairs acetylcholine receptor clustering in skeletal muscle cells |
| Q28119021 | Frizzled-9 is activated by Wnt-2 and functions in Wnt/beta -catenin signaling |
| Q35003320 | Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome |
| Q38735394 | Genetic deletion of sonic hedgehog causes hemiagenesis and ectopic development of the thyroid in mouse |
| Q24678653 | Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome |
| Q41757188 | IV. Neuroanatomy of Williams syndrome: a high-resolution MRI study |
| Q42120937 | Injury prevention |
| Q24290958 | Molecular cloning and characterization of MFRP, a novel gene encoding a membrane-type Frizzled-related protein |
| Q22003792 | Molecular cloning of Frizzled-10, a novel member of the Frizzled gene family |
| Q46900906 | Mutation rate in human microsatellites |
| Q30543830 | Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype. |
| Q29616716 | Structural diversity of G protein-coupled receptors and significance for drug discovery |
| Q40975654 | The BCL7 gene family: deletion of BCL7B in Williams syndrome. |
| Q39055176 | The Impact on the Family of Four Neurogenetic Syndromes: A Comparative Study of Parental Views |
| Q22004256 | The murine CYLN2 gene: genomic organization, chromosome localization, and comparison to the human gene that is located within the 7q11.23 Williams syndrome critical region |
| Q42344194 | The work experience of a patient affected by Williams Syndrome: a pilot project at the Bambino Gesù Children's Hospital. |
| Q47938190 | Two novel Xenopus frizzled genes expressed in developing heart and brain |
| Q40212341 | Upregulation of frizzled 9 in astrocytomas. |
| Q52165839 | V. Multi-level analysis of cortical neuroanatomy in Williams syndrome. |
| Q37635264 | WNT/Frizzled signalling: receptor-ligand selectivity with focus on FZD-G protein signalling and its physiological relevance: IUPHAR Review 3 |
| Q33942663 | Williams (Williams Beuren) syndrome: a distinct neurobehavioral disorder |
| Q28187660 | Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23 |
| Q35264833 | Williams syndrome: an update on clinical and molecular aspects |
| Q34388540 | Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes |
| Q35210607 | Williams-Beuren syndrome: a challenge for genotype-phenotype correlations |
| Q33634325 | Williams-Beuren syndrome: an update and review for the primary physician |
| Q90249957 | Wnt Signaling in vascular eye diseases |
| Q34316155 | Wnt signaling and mammary tumorigenesis |
| Q41739278 | Wnt-1 inhibits nerve growth factor-induced differentiation of PC12 cells by preventing the induction of some but not all late-response genes |
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