Generation of sequence-tagged sites from Xp22.3 by isolating common Alu-PCR products of radiation hybrids retaining overlapping human X chromosome fragments

scientific article published in May 1996

Generation of sequence-tagged sites from Xp22.3 by isolating common Alu-PCR products of radiation hybrids retaining overlapping human X chromosome fragments is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1007/S004390050102
P698PubMed publication ID8655139

P2093author name stringI A Glass
P H Yen
L J Shapiro
E C Salido
T Mohandas
M Passage
L Bernatowicz
P2860cites workSegregation of the Huntington disease region of human chromosome 4 in a somatic cell hybridQ45295513
The distribution of interspersed repetitive DNA sequences in the human genomeQ46186808
A common language for physical mapping of the human genomeQ46940837
Sixty-five radiation hybrids for the short arm of human chromosome 6: Their value as a mapping panel and as a source for rapid isolation of new probes using repeat element-mediated PCRQ56909393
Rapid isolation of human chromosome-specific DNA probes from a somatic cell hybridQ57337249
High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)Q57339579
New method for mapping genes in human chromosomesQ59082669
Hypervariable telomeric sequences from the human sex chromosomes are pseudoautosomalQ59085522
A method for generating hybrids containing nonselected fragments of human chromosomesQ69651224
A pseudoautosomal gene in manQ69889517
Human DNA polymerase alpha gene expression is cell proliferation dependent and its primary structure is similar to both prokaryotic and eukaryotic replicative DNA polymerasesQ24298233
Structure of the human phosphoglycerate kinase gene and the intron-mediated evolution and dispersal of the nucleotide-binding domainQ24609342
Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplificationQ24633695
Sequencing of the variant thyroxine-binding globulin (TBG)-Quebec reveals two nucleotide substitutionsQ24679512
Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemiaQ27861076
Human and mouse amelogenin gene loci are on the sex chromosomesQ28276905
The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: evidence for an inversion of the Y chromosome during primate evolutionQ28292894
Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridizationQ29616823
Ligation-independent cloning of PCR products (LIC-PCR)Q29618962
Directed isolation of human genes that escape X inactivationQ31047770
An optimized Alu-PCR primer pair for human-specific amplification of YACs and somatic cell hybridsQ31157633
Isolation of human transcribed sequences from human-rodent somatic cell hybridsQ31160101
Coincidence cloning of Alu PCR productsQ33351174
X/Y translocations resulting from recombination between homologous sequences on Xp and Yq.Q33412558
Long-range restriction map of the terminal part of the short arm of the human X chromosomeQ33579172
Fluorescence in situ hybridization with Alu and L1 polymerase chain reaction probes for rapid characterization of human chromosomes in hybrid cell linesQ33763867
Exchange of terminal portions of X- and Y-chromosomal short arms in human XY femalesQ33847127
Automated DNA sequencing of the human HPRT locusQ34035590
Isolation of a new gene from the distal short arm of the human X chromosome that escapes X-inactivationQ34211839
Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sourcesQ34301388
Rapid cloning and characterization of new chromosome 10 DNA markers by Alu element-mediated PCR.Q34856475
Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reactionQ34993293
A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm.Q35280432
Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletionQ37541303
The mammalian pseudoautosomal regionQ38768001
Dinucleotide repeat polymorphisms at the DXS453, DXS454 and DXS458 lociQ40518362
Characterization and expression of a murine gene homologous to human EPA/TIMP: a virus-induced gene in the mouseQ41335462
Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elementsQ41733959
Isolation and characterization of cell hybrids containing human Xp-chromosome fragmentsQ41751527
Use of Alu-PCR to characterize hybrids containing multiple fragments and to generate new Xp21.3–p22.2 markersQ42618174
Generation of novel sequence tagged sites (STSs) from discrete chromosomal regions using Alu-PCR.Q44385949
Chromosome mapping and expression of a putative testis-determining gene in mouseQ45243633
P433issue5
P304page(s)604-610
P577publication date1996-05-01
P1433published inHuman GeneticsQ5937167
P1476titleGeneration of sequence-tagged sites from Xp22.3 by isolating common Alu-PCR products of radiation hybrids retaining overlapping human X chromosome fragments
P478volume97

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