Literature DB >> 8764824

Novel transcribed sequences represented in the complex genomic region 5q13.

K E Morrison1, S J Qureshi, S Anderson, J P Borrett, A Theodosiou, N Rodrigues, D Blake, A Nesbit, K E Davies, D J Porteous, A J Brookes.   

Abstract

YACs from the complex repetitive human genomic region 5q13, spanning the spinal muscular atrophy (SMA) locus, have been searched for transcribed sequences using the method of End Ligation Coincident Sequence Cloning. Six transcripts (PT1-6) have been identified, three of which (PT4, PT5 and PT6) are novel. Five of these elements hybridise to multiple loci in 5q13, but PT5 is single copy and maps very close to markers that show linkage disequilibrium with SMA.

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Year:  1996        PMID: 8764824     DOI: 10.1016/0167-4781(96)00097-8

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  3 in total

Review 1.  Coincidence cloning. Taking the coincidences out of genome analysis.

Authors:  R S Devon; A J Brookes
Journal:  Mol Biotechnol       Date:  1996-06       Impact factor: 2.695

2.  The spinal muscular atrophy gene region at 5q13.1 has a paralogous chromosomal region at 6p21.3.

Authors:  J L Banyer; S Goldwurm; L Cullen; B van der Griend; A Zournazi; D J Smit; L W Powell; E C Jazwinska
Journal:  Mamm Genome       Date:  1998-03       Impact factor: 2.957

3.  Molecular diagnosis of spinal muscular atrophy.

Authors:  H Stewart; A Wallace; J McGaughran; R Mountford; H Kingston
Journal:  Arch Dis Child       Date:  1998-06       Impact factor: 3.791

  3 in total

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