Spontaneous mutation in Mitf gene causes osteopetrosis in silver homozygote quail

Developmental Dynamics

Volumn 220, Issue 2, 2001, Pages 133-140

  Kawaguchi, Nanako ^a   Ono, Tamao ^b   Mochii, Makoto ^c   Noda, Masaki ^a  

^a TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

^b SHINSHU UNIVERSITY   (Japan)

^c Himeji Technological University   (Japan)

Author keywords

BHLH; Mi; Microphthalmia; Mitf; Osteoclast; Osteoclastogene sis; Osteopetrosis; Quail; Silver; Transcription factor

Indexed keywords

GENE PRODUCT;

ALBERS SCHOENBERG DISEASE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BONE DEFECT; BONE RADIOGRAPHY; CONTROLLED STUDY; GENE EXPRESSION; GENE MUTATION; GENETIC TRANSFECTION; HOMOZYGOSITY; MELANOGENESIS; NONHUMAN; OSTEOCLAST; OSTEOLYSIS; PIGMENT DISORDER; PIGMENTATION; PRIORITY JOURNAL; QUAIL; TIBIA; TRABECULAR BONE;

AGING; ANIMALS; BIRD DISEASES; COTURNIX; DNA-BINDING PROTEINS; HOMOZYGOTE; MICROPHTHALMIA-ASSOCIATED TRANSCRIPTION FACTOR; MUTATION; OSTEOCLASTS; OSTEOPETROSIS; TIBIA; TOMOGRAPHY, X-RAY COMPUTED; TRANSCRIPTION FACTORS;

GALLUS GALLUS; PHASIANIDAE;

EID: 0035142015     PISSN: 10588388     EISSN: None     Source Type: Journal    
DOI: 10.1002/1097-0177(2000)9999:9999<::AID-DVDY1095>3.0.CO;2-7     Document Type: Article

References (32)

1. Neonatal reductions in osteoclast number and function account for the transient nature of osteopetrosis in the rat mutation microphthalmia blanc(mib)
2. Bone metabolism in the osteopetrotic rat mutation microphthalmia blanc
3. c-Fos: A key regulator osteoclast-macrophage lineage determination and bone remodeling
4. Microphthalmia, a critical factor in melanocyte development, defines a discrete transcription factor family
5. Mutation at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein
6. Coturnix in biological research
7. A helixloop-helix transcription factor-like gene is located at the mi locus
8. Adaptor plasmids simplify the insertion of foreign DNA into helper-independent vectors
9. Osteoblastic cells regulate mi gene expression in cultured bone marrow cells
10. Mitf is expressed in osteoclast progenitors in vitro
11. wh allele on phenotype of murine mast cells
12. The hematogenous origin of osteoclasts: Experimental evidence from osteopetrotic (microphthalmic) mice treated with spleen cells from beige mouse donors
13. Spontaneous transdifferentiation of quail pigmented epithelial cell is accompanied by a mutation in the Mitf gene
14. Role of Mitf in differentiation and transdifferentiation of chicken pigmented epithelial cell
15. Insight into the microphthalmia gene
16. Mild osteopetrosis in the microphthalmia-oak ridge mouse. A model for intermediate autosomal recessive osteopetrosis in humans
17. TEEC is a macrophage-restricted member of the microphthalmia-TFE subfamily of basic helix-loop-helix leucine zipper transcription factors
18. Microphthalmia-associated transcription factor interacts with PU.1 and c-Fos: Determination of their subcellular localization
19. The coat colors of mice
20. Effect of the mi allele on mast cells, basophils, natural killer cells, and osteoclasts in C57Bl/6J mice
21. Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotype consequences
22. Mutation of osteoclast mutation
23. Osteoblastic cells are involved in osteoclast formation
24. Osteoclast-like cell formation and its regulation by osteotropic hormones in mouse bone marrow cultures
25. The recessive phenotype displayed by a dominant negative microphthalmia-associated transcription factor mutant is a result of impaired nuclear localization potential
26. Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene
27. Fusion disability of embryonic osteoclast precursor cells and macrophages in the microphthalmic osteopetrotic mice
28. Osteopetrosis in mice lacking haematopoietic transcription factor-PU.1
29. Age-resolving osteopetrosis: A rat model implicating microphthalmia and the related transcription factor TFE3
30. High-resolution micro CT (micro-computed tomography) analysis of the abnormal trabecular bone structures in klotho gene mutant mice
31. Functional analysis of microphthalmia-associated transcription factor in pigment cell-specific transcription of the human tyrosinase family genes