Characterization of mouse Frizzled-3 expression in hair follicle development and identification of the human homolog in keratinocytes

Journal of Investigative Dermatology

Volumn 116, Issue 6, 2001, Pages 940-946

  Hung, Betsy S ^a   Wang, Xue Qing ^a   Cam, Graham R ^a   Rothnagel, Joseph A ^b  

^a UNIVERSITY OF QUEENSLAND   (Australia)

^b CSIRO   (Australia)

Author keywords

Chromosome mapping; Gene expression; Wnt signaling

Indexed keywords

GENE PRODUCT; MEMBRANE PROTEIN; MESSENGER RNA; PROTEIN FRIZZLED 3; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; CELL LINE; CHROMOSOME 8; CHROMOSOME ARM; CHROMOSOME MAP; EMBRYO; EPIDERMIS; GENE EXPRESSION; GENE LOCATION; GENE LOCUS; HAIR FOLLICLE; HAIR GROWTH; HUMAN; HUMAN CELL; HYPOTRICHOSIS; IN SITU HYBRIDIZATION; KERATINOCYTE; MOUSE; NEWBORN; NONHUMAN; NORTHERN BLOTTING; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN EXPRESSION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY;

EID: 0034990096     PISSN: 0022202X     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1523-1747.2001.01336.x     Document Type: Article

References (37)

1. Alopecia universalis associated with a mutation in the human hairless gene
2. Frizzled proteins constitute a novel family of G protein-coupled receptors, most closely related to the secretin family
3. Normal keratinization in a spontaneously immortalized aneuploid human keratinocyte cell line
4. A common human skin tumour is caused by activating mutations in beta-catenin
5. Two homologs of the Drosophila polarity gene frizzled (fz) are widely expressed in mammalian tissues
6. Rapid production of full-length cDNAs from rare transcripts: Amplification using a single gene-specific oligonucleotide primer
7. De Novo hair follicle morphogenesis and hair tumors in mice expressing a truncated beta-catenin in skin
8. Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in LEF-1-deficient mice
9. Identification and characterization of the familial adenomatous polyposis coli gene
10. A radiation hybrid map of the human genome
11. The development of mouse hair in vitro with some observations on pigmentation
12. Molecular cloning and genomic structure of human frizzled- 3 at chromosome 8p21
13. Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis
14. WNT signaling in the control of hair growth and structure
15. Activation of beta-catenin-Tcf signaling in colon cancer by mutations in beta-catenin or APC
16. Keratin gene expression in mouse epidermis and cultured epidermal cells
17. Stabilization of beta-catenin by genetic defects in melanoma cell lines
18. Molecular cloning, differential expression, and chromosomal localization of human frizzled-1, frizzled-2, and frizzled-7
19. Identification, gene structure, and expression of human frizzled-3 (FZD3)
20. AXIN1 mutations in hepatocellular carcinomas, and growth suppression in cancer cells by virus-mediated transfer of AXIN 1
21. Biochemical interactions in the wnt pathway
22. Atrichia with papular lesions resulting from a nonsense mutation within the human hairless gene
23. Marie Unna hereditary hypotrichosis gene maps to human chromosome 8p21 near hairless
24. The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: Exclusion of the hr gene by cDNA and genomic sequencing
25. A novel frizzled gene identified in human esophageal carcinoma mediates APC/beta-catenin signals
26. Metallothionein mRNA in the testis and prostate of the rat detected by digoxigenin-labeled riboprobe
27. Ueber Hypotrichosis congenita hereditaria
28. Molecular genetic studies of Wn: Signaling in the mouse
29. A large family of putative transmembrane receptors homologous to the product of the Drosophila tissue polarity gene frizzled
30. A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23
31. Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome
32. Early events in skin appendage formation: Induction of epithelial placodes and condensation of dermal mesenchyme
33. Mechanisms of Wnt signaling in development
34. Lymphoid enhancer factor 1 directs hair follicle patterning and epithelial cell fate
35. Congenital atrichia in five Arab Palestinian families resulting from a deletion mutation in the human hairless gene