Identifying genes within microdissected genomic DNA: Isolation of brain expressed genes from a translocation region associated with inherited mental illness

ISSN:
1432-1777
Source:
Springer Online Journal Archives 1860-2000
Topics:
Biology
Medicine
Notes:
Abstract An improved protocol has been developed for physical enrichment of cDNA sequences by hybridization to genomic DNA. When applied to microdissection recombinants derived from a translocation breakpoint region associated with inherited mental illness, a single cycle of the procedure permitted enriched cDNAs to be visualized directly by agarose gel electrophoresis. Hybridization screening of a library of clones derived from the enriched cDNAs, employing the genomic resource as a probe, led to the identification of six novel gene fragments. This general approach to the isolation of regionally encoded genes could be applied to any subchromosomal interval as a first step towards global transcription map construction.
Type of Medium:
Electronic Resource
URL:
_version_ 1798297661034463232
autor Brookes, A. J.
Slorach, E. M.
Evans, K. L.
Thomson, M. L.
Gosden, C. M.
Muir, W. J.
Porteous, D. J.
autorsonst Brookes, A. J.
Slorach, E. M.
Evans, K. L.
Thomson, M. L.
Gosden, C. M.
Muir, W. J.
Porteous, D. J.
book_url http://dx.doi.org/10.1007/BF00352412
datenlieferant nat_lic_papers
hauptsatz hsatz_simple
identnr NLM207330360
issn 1432-1777
journal_name Mammalian genome
materialart 1
notes Abstract An improved protocol has been developed for physical enrichment of cDNA sequences by hybridization to genomic DNA. When applied to microdissection recombinants derived from a translocation breakpoint region associated with inherited mental illness, a single cycle of the procedure permitted enriched cDNAs to be visualized directly by agarose gel electrophoresis. Hybridization screening of a library of clones derived from the enriched cDNAs, employing the genomic resource as a probe, led to the identification of six novel gene fragments. This general approach to the isolation of regionally encoded genes could be applied to any subchromosomal interval as a first step towards global transcription map construction.
package_name Springer
publikationsjahr_anzeige 1995
publikationsjahr_facette 1995
publikationsjahr_intervall 8004:1995-1999
publikationsjahr_sort 1995
publisher Springer
reference 6 (1995), S. 257-262
search_space articles
shingle_author_1 Brookes, A. J.
Slorach, E. M.
Evans, K. L.
Thomson, M. L.
Gosden, C. M.
Muir, W. J.
Porteous, D. J.
shingle_author_2 Brookes, A. J.
Slorach, E. M.
Evans, K. L.
Thomson, M. L.
Gosden, C. M.
Muir, W. J.
Porteous, D. J.
shingle_author_3 Brookes, A. J.
Slorach, E. M.
Evans, K. L.
Thomson, M. L.
Gosden, C. M.
Muir, W. J.
Porteous, D. J.
shingle_author_4 Brookes, A. J.
Slorach, E. M.
Evans, K. L.
Thomson, M. L.
Gosden, C. M.
Muir, W. J.
Porteous, D. J.
shingle_catch_all_1 Brookes, A. J.
Slorach, E. M.
Evans, K. L.
Thomson, M. L.
Gosden, C. M.
Muir, W. J.
Porteous, D. J.
Identifying genes within microdissected genomic DNA: Isolation of brain expressed genes from a translocation region associated with inherited mental illness
Abstract An improved protocol has been developed for physical enrichment of cDNA sequences by hybridization to genomic DNA. When applied to microdissection recombinants derived from a translocation breakpoint region associated with inherited mental illness, a single cycle of the procedure permitted enriched cDNAs to be visualized directly by agarose gel electrophoresis. Hybridization screening of a library of clones derived from the enriched cDNAs, employing the genomic resource as a probe, led to the identification of six novel gene fragments. This general approach to the isolation of regionally encoded genes could be applied to any subchromosomal interval as a first step towards global transcription map construction.
1432-1777
14321777
Springer
shingle_catch_all_2 Brookes, A. J.
Slorach, E. M.
Evans, K. L.
Thomson, M. L.
Gosden, C. M.
Muir, W. J.
Porteous, D. J.
Identifying genes within microdissected genomic DNA: Isolation of brain expressed genes from a translocation region associated with inherited mental illness
Abstract An improved protocol has been developed for physical enrichment of cDNA sequences by hybridization to genomic DNA. When applied to microdissection recombinants derived from a translocation breakpoint region associated with inherited mental illness, a single cycle of the procedure permitted enriched cDNAs to be visualized directly by agarose gel electrophoresis. Hybridization screening of a library of clones derived from the enriched cDNAs, employing the genomic resource as a probe, led to the identification of six novel gene fragments. This general approach to the isolation of regionally encoded genes could be applied to any subchromosomal interval as a first step towards global transcription map construction.
1432-1777
14321777
Springer
shingle_catch_all_3 Brookes, A. J.
Slorach, E. M.
Evans, K. L.
Thomson, M. L.
Gosden, C. M.
Muir, W. J.
Porteous, D. J.
Identifying genes within microdissected genomic DNA: Isolation of brain expressed genes from a translocation region associated with inherited mental illness
Abstract An improved protocol has been developed for physical enrichment of cDNA sequences by hybridization to genomic DNA. When applied to microdissection recombinants derived from a translocation breakpoint region associated with inherited mental illness, a single cycle of the procedure permitted enriched cDNAs to be visualized directly by agarose gel electrophoresis. Hybridization screening of a library of clones derived from the enriched cDNAs, employing the genomic resource as a probe, led to the identification of six novel gene fragments. This general approach to the isolation of regionally encoded genes could be applied to any subchromosomal interval as a first step towards global transcription map construction.
1432-1777
14321777
Springer
shingle_catch_all_4 Brookes, A. J.
Slorach, E. M.
Evans, K. L.
Thomson, M. L.
Gosden, C. M.
Muir, W. J.
Porteous, D. J.
Identifying genes within microdissected genomic DNA: Isolation of brain expressed genes from a translocation region associated with inherited mental illness
Abstract An improved protocol has been developed for physical enrichment of cDNA sequences by hybridization to genomic DNA. When applied to microdissection recombinants derived from a translocation breakpoint region associated with inherited mental illness, a single cycle of the procedure permitted enriched cDNAs to be visualized directly by agarose gel electrophoresis. Hybridization screening of a library of clones derived from the enriched cDNAs, employing the genomic resource as a probe, led to the identification of six novel gene fragments. This general approach to the isolation of regionally encoded genes could be applied to any subchromosomal interval as a first step towards global transcription map construction.
1432-1777
14321777
Springer
shingle_title_1 Identifying genes within microdissected genomic DNA: Isolation of brain expressed genes from a translocation region associated with inherited mental illness
shingle_title_2 Identifying genes within microdissected genomic DNA: Isolation of brain expressed genes from a translocation region associated with inherited mental illness
shingle_title_3 Identifying genes within microdissected genomic DNA: Isolation of brain expressed genes from a translocation region associated with inherited mental illness
shingle_title_4 Identifying genes within microdissected genomic DNA: Isolation of brain expressed genes from a translocation region associated with inherited mental illness
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source_archive Springer Online Journal Archives 1860-2000
timestamp 2024-05-06T10:11:32.252Z
titel Identifying genes within microdissected genomic DNA: Isolation of brain expressed genes from a translocation region associated with inherited mental illness
titel_suche Identifying genes within microdissected genomic DNA: Isolation of brain expressed genes from a translocation region associated with inherited mental illness
topic W
WW-YZ
uid nat_lic_papers_NLM207330360