Literature DB >> 1639400

YAC mapping by FISH using Alu-PCR-generated probes.

M Breen1, B Arveiler, I Murray, J R Gosden, D J Porteous.   

Abstract

Human genomic mapping has been greatly advanced by the independent development of three new methods: large DNA fragment cloning in yeast artificial chromosomes, amplification from complex DNAs of human specific segments by Alu-PCR, and high-resolution localization of complex DNA probes by fluorescent in situ hybridization. We describe here the combination of these three analytical tools for efficient and accurate localization of randomly screened or especially selected human YAC recombinants to chromosome 11. We map a YAC clone encompassing the pepsinogen A (PGA) locus to 11q13.1-11q13.3.

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Year:  1992        PMID： 1639400     DOI： 10.1016/0888-7543(92)90148-l

Source DB:  PubMed          Journal:  Genomics        ISSN： 0888-7543            Impact factor:   5.736


  11 in total

1.  Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions.

Authors:  Marco Venturin; Cristina Gervasini; Francesca Orzan; Angela Bentivegna; Lucia Corrado; Patrizia Colapietro; Alessandra Friso; Romano Tenconi; Meena Upadhyaya; Lidia Larizza; Paola Riva
Journal:  Hum Genet       Date:  2004-04-21       Impact factor: 4.132

2.  Distribution of Alu and L1 repeats in human YAC recombinants.

Authors:  B Arveiler; D J Porteous
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

3.  Characterization and application of soybean YACs to molecular cytogenetics.

Authors:  T Zhu; I Shi; R P Funke; P M Gresshoff; P Keim
Journal:  Mol Gen Genet       Date:  1996-09-25

4.  Genome mapping by arbitrary amplification of yeast artificial chromosomes.

Authors:  A Di Rienzo; A Peterson; S Das; N B Freimer
Journal:  Mamm Genome       Date:  1993       Impact factor: 2.957

5.  Genetical and physical assignments of equine microsatellites--first integration of anchored markers in horse genome mapping.

Authors:  M Breen; G Lindgren; M M Binns; J Norman; Z Irvin; K Bell; K Sandberg; H Ellegren
Journal:  Mamm Genome       Date:  1997-04       Impact factor: 2.957

6.  Schizophrenia-associated chromosome 11q21 translocation: identification of flanking markers and development of chromosome 11q fragment hybrids as cloning and mapping resources.

Authors:  J M Fletcher; K Evans; D Baillie; P Byrd; D Hanratty; S Leach; C Julier; J R Gosden; W Muir; D J Porteous
Journal:  Am J Hum Genet       Date:  1993-03       Impact factor: 11.025

7.  Condensation behaviour of the human X chromosome in male germ cells and Sertoli cells examined by fluorescence in situ hybridization.

Authors:  S Kofman-Alfaro; R M Speed; S Boyle; A C Chandley
Journal:  Chromosome Res       Date:  1994-11       Impact factor: 5.239

8.  Mapping chromosome rearrangement breakpoints to the physical map of Caenorhabditis elegans by fluorescent in situ hybridization.

Authors:  D G Albertson
Journal:  Genetics       Date:  1993-05       Impact factor: 4.562

9.  NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes.

Authors:  P Riva; L Corrado; F Natacci; P Castorina; B L Wu; G H Schneider; M Clementi; R Tenconi; B R Korf; L Larizza
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

10.  FISH with locus-specific probes on stretched chromosomes: a useful tool for genome organization studies.

Authors:  A Bentivegna; M Venturin; C Gervasini; L Corrado; L Larizza; P Riva
Journal:  Chromosome Res       Date:  2001       Impact factor: 5.239
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