Five distinct novel transcripts (RES4-22,-23,-24,-25 and-26) that mapped to the 1-Mb interval between D4S180 and D4S183 on human chromosome 4pl6.3 close to the Huntington's disease (HD) gene were isolated, and the structure and exon/intron organization of each gene were thoroughly analyzed. The transcripts of the RES4-22,-23 and-24 genes each have several isoforms by alternative splicing and these have also been defined. Two transcripts, RES4-24 and RES4-25, reside in the same genomic region with opposite polarities and they also clearly overlap. Among these transcripts, RES4-26 was found to encode a novel zinc finger protein. The transcript map based upon our current level of analysis combined with data from previous studies reveals t...
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disease affecting approximatel...
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disease affecting approximatel...
Analysis of many families with linked DNA markers has provided support for the Huntington's disease ...
Huntington's disease (HD) is an inherited progressive neurodegenerative disorder caused by a patholo...
SUMMARY The recent discovery that the gene causing Huntington's disease (HD) resides on chromos...
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder caused by a CAG expans...
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have ...
The gene for Huntington disease, a neurodegenerative disorder with autosomal dominant inheritance, h...
The gene for Huntington disease, a neurodegenerative disorder with autosomal dominant inheritance, h...
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have ...
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have ...
With the completion of the sequencing of the human genome near, the next phase will be to identify a...
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have ...
The sequences of three cosmids (90 kilobases) from the Huntington's disease region in chromosome 4p1...
The Huntington’s disease (HD) gene has been mapped in 4~16.3 but has eluded identification. We have ...
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disease affecting approximatel...
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disease affecting approximatel...
Analysis of many families with linked DNA markers has provided support for the Huntington's disease ...
Huntington's disease (HD) is an inherited progressive neurodegenerative disorder caused by a patholo...
SUMMARY The recent discovery that the gene causing Huntington's disease (HD) resides on chromos...
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder caused by a CAG expans...
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have ...
The gene for Huntington disease, a neurodegenerative disorder with autosomal dominant inheritance, h...
The gene for Huntington disease, a neurodegenerative disorder with autosomal dominant inheritance, h...
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have ...
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have ...
With the completion of the sequencing of the human genome near, the next phase will be to identify a...
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have ...
The sequences of three cosmids (90 kilobases) from the Huntington's disease region in chromosome 4p1...
The Huntington’s disease (HD) gene has been mapped in 4~16.3 but has eluded identification. We have ...
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disease affecting approximatel...
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disease affecting approximatel...
Analysis of many families with linked DNA markers has provided support for the Huntington's disease ...