%0 Journal Article %1 Schwartz.1994 %A Schwartz, F. %A Neve, R. %A Eisenman, R. %A Gessler, M. %A Bruns, G. %D 1994 %J Hum Genet %K *Gene Blotting;Northern Brain/*embryology Chromosome Deletion Expression Gene Humans Mapping RNA/analysis Syndrome/*genetics Transcription;Genetic/*genetics WAGR %N 6 %P 658--664 %T A WAGR region gene between PAX-6 and FSHB expressed in fetal brain %V 94 %X Developmental delay or mental retardation is a frequent component of multi-system anomaly syndromes associated with chromosomal deletions. Isolation of genes involved in the mental dysfunction in these disorders should define loci important in brain formation or function. We have identified a highly conserved locus in the distal part of 11p13 that is prominently expressed in fetal brain. Minimal expression is observed in a number of other fetal tissues. The gene maps distal to PAX-6 but proximal to the loci for brain-derived neurotrophic factor (BDNF) and the beta subunit of follicle stimulating hormone (FSHB), within a region previously implicated in the mental retardation component of some WAGR syndrome patients. Within fetal brain, the corresponding transcript is prominent in frontal, motor and primary visual cortex as well as in the caudate-putamen. The characteristics of this gene, including the striking evolutionary conservation at the locus, suggest that the encoded protein may function in brain development.

@article{Schwartz.1994, abstract = {Developmental delay or mental retardation is a frequent component of multi-system anomaly syndromes associated with chromosomal deletions. Isolation of genes involved in the mental dysfunction in these disorders should define loci important in brain formation or function. We have identified a highly conserved locus in the distal part of 11p13 that is prominently expressed in fetal brain. Minimal expression is observed in a number of other fetal tissues. The gene maps distal to PAX-6 but proximal to the loci for brain-derived neurotrophic factor (BDNF) and the beta subunit of follicle stimulating hormone (FSHB), within a region previously implicated in the mental retardation component of some WAGR syndrome patients. Within fetal brain, the corresponding transcript is prominent in frontal, motor and primary visual cortex as well as in the caudate-putamen. The characteristics of this gene, including the striking evolutionary conservation at the locus, suggest that the encoded protein may function in brain development.}, added-at = {2013-01-29T13:47:26.000+0100}, author = {Schwartz, F. and Neve, R. and Eisenman, R. and Gessler, M. and Bruns, G.}, biburl = {https://www.bibsonomy.org/bibtex/223ef7543f9435b8ae5427d6c012622bc/ebch}, interhash = {35d6ba12b1eb3b614b37094bf696698a}, intrahash = {23ef7543f9435b8ae5427d6c012622bc}, journal = {Hum Genet}, keywords = {*Gene Blotting;Northern Brain/*embryology Chromosome Deletion Expression Gene Humans Mapping RNA/analysis Syndrome/*genetics Transcription;Genetic/*genetics WAGR}, number = 6, pages = {658--664}, timestamp = {2013-01-29T13:47:28.000+0100}, title = {A WAGR region gene between PAX-6 and FSHB expressed in fetal brain}, volume = 94, year = 1994 }