(Q54307155)

27 May 2018

title

Use of inverse PCR to amplify and sequence breakpoints of HPRT deletion and translocation mutations. (English)

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27 May 2018

author name string

Williams M

series ordinal

1

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27 May 2018

Rainville IR

series ordinal

2

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27 May 2018

Nicklas JA

series ordinal

3

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27 May 2018

publication date

1 January 2002

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27 May 2018

Environmental and Molecular Mutagenesis

published in

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27 May 2018

volume

39

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27 May 2018

issue

1

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27 May 2018

page(s)

22-32

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27 May 2018

In vivo somatic mutations in humans: measurement and analysis

cites work

1 reference

Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints

21 January 2018

1 reference

The chronic myelogenous leukemia-specific P210 protein is the product of the bcr/abl hybrid gene

21 January 2018

1 reference

Molecular analysis of a t(11;22) translocation junction in a case of Ewing's sarcoma

21 January 2018

1 reference

Molecular mechanisms for CMT1A duplication and HNPP deletion

21 January 2018

1 reference

Site-specific deletions involving the tal-1 and sil genes are restricted to cells of the T cell receptor alpha/beta lineage: T cell receptor delta gene deletion mechanism affects multiple genes.

21 January 2018

1 reference

Molecular description of three macro-deletions and an Alu-Alu recombination-mediated duplication in the HPRT gene in four patients with Lesch-Nyhan disease.

21 January 2018

1 reference

Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome

21 January 2018

1 reference

Inverse PCR amplification of rare T cell receptor delta messages from mucosal biopsy specimens

21 January 2018

1 reference

High-frequency deletion event at aprt locus of CHO cells: detection and characterization of endpoints.

21 January 2018

1 reference

Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.

21 January 2018

1 reference

AT-rich palindromes mediate the constitutional t(11;22) translocation.

21 January 2018

1 reference

Selection and sequencing of interchromosomal rearrangements from gamma-irradiated normal human fibroblasts

21 January 2018

1 reference

A novel PCR method for amplifying exons (or genes) over intragenic (or intergenic) regions in the genome

21 January 2018

1 reference

V(D)J recombinase-mediated deletion of the hprt gene in T-lymphocytes from adult humans

21 January 2018

1 reference

Multiplex DNA deletion detection and exon sequencing of the hypoxanthine phosphoribosyltransferase gene in Lesch-Nyhan families

21 January 2018

1 reference

Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation

21 January 2018

1 reference

The involvement of Alu repeats in recombination events at the alpha-globin gene cluster: characterization of two alphazero-thalassaemia deletion breakpoints.

21 January 2018

1 reference

Identification of a novel 4.6-kb genomic deletion in presenilin-1 gene which results in exclusion of exon 9 in a Finnish early onset Alzheimer's disease family: an Alu core sequence-stimulated recombination?

21 January 2018

1 reference

The genomic breakpoint and chimeric transcripts in the EWSR1-ETV4/E1AF gene fusion in Ewing sarcoma

21 January 2018

1 reference

The BCR gene recombines preferentially with Alu elements in complex BCR-ABL translocations of chronic myeloid leukaemia.

21 January 2018

1 reference

The second case of a t(17;22) in a family with neurofibromatosis type 1: sequence analysis of the breakpoint regions

21 January 2018

1 reference

An Alu-mediated large deletion of the FUT2 gene in individuals with the ABO-Bombay phenotype.

21 January 2018

1 reference

Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment

21 January 2018

1 reference

Duplication of seven exons in LDL receptor gene caused by Alu-Alu recombination in a subject with familial hypercholesterolemia

21 January 2018

1 reference

Large deletions partially external to the human hprt gene result in chimeric transcripts.

21 January 2018

1 reference

LINE-I element insertion at the t(11;22) translocation breakpoint of a desmoplastic small round cell tumor.

21 January 2018

1 reference

Duplication in the hypoxanthine phosphoribosyl-transferase gene caused by Alu-Alu recombination in a patient with Lesch Nyhan syndrome.

21 January 2018

1 reference

Inactivation of the cholinesterase gene by Alu insertion: possible mechanism for human gene transposition

21 January 2018

1 reference

Study of human foamy virus proviral integration in chronically infected murine cells

21 January 2018

1 reference

Molecular analysis of in vivo hprt mutations in human T lymphocytes. V. Effects of total body irradiation secondary to radioimmunoglobulin therapy (RIT)

21 January 2018

1 reference

Clonal integration and expression of human T-cell lymphotropic virus type I in carriers detected by polymerase chain reaction and inverse PCR.

21 January 2018

1 reference

Refinement of a T-lymphocyte cloning assay to quantify the in vivo thioguanine-resistant mutant frequency in humans.

21 January 2018

1 reference

Southern-blot analyses of human T-lymphocyte mutants induced in vitro by gamma-irradiation.

21 January 2018

1 reference

In vitro induction, expression and selection of thioguanine-resistant mutants with human T-lymphocytes.

21 January 2018

1 reference

Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletion

21 January 2018

1 reference

Breakpoints and junctional regions of intragenic deletions in the HPRT gene in human T-Cells

21 January 2018

1 reference

Mosaicism of a microdeletion of 486 bp involving the CGG repeat of the FMR1 gene due to misalignment of GTT tandem repeats at chi-like elements flanking both breakpoints and a full mutation.

21 January 2018

1 reference

Frameshift mutations and the genetic code. This paper is dedicated to Professor Theodosius Dobzhansky on the occasion of his 66th birthday

21 January 2018

1 reference

A procedure for in vitro amplification of DNA segments that lie outside the boundaries of known sequences

21 January 2018

1 reference

The t(14;18) chromosome translocations involved in B-cell neoplasms result from mistakes in VDJ joining.

21 January 2018

1 reference

Topoisomerase I and II consensus sequences in a 17-kb deletion junction of the COL4A5 and COL4A6 genes and immunohistochemical analysis of esophageal leiomyomatosis associated with Alport syndrome

21 January 2018

1 reference

Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).

21 January 2018

1 reference

A revised sequence of the human beta7 integrin gene (ITGB7) promoter region obtained by inverse PCR.

21 January 2018

1 reference

TAL2, a helix-loop-helix gene activated by the (7;9)(q34;q32) translocation in human T-cell leukemia

21 January 2018

1 reference

Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements

21 January 2018

1 reference

Novel chimaeric protein expressed in Philadelphia positive acute lymphoblastic leukaemia

21 January 2018

1 reference

Structural analysis of PAX3 genomic rearrangements in alveolar rhabdomyosarcoma

21 January 2018

1 reference

Deletion analysis of the simple tandem repeat loci physically linked to the spinal muscular atrophy locus

21 January 2018

2 references

21 January 2018

inferred from DOI database lookup

7 January 2021

based on heuristic

The molecular basis of leukemia

1 reference

Determination of the breakpoint of the common alpha-thalassaemia deletion in Filipinos in Hawaii

21 January 2018

1 reference

Two long homologous retroviral sequence blocks in proximal Yq11 cause AZFa microdeletions as a result of intrachromosomal recombination events

21 January 2018

1 reference

Molecular characterization and PCR diagnosis of Thailand deletion of alpha-globin gene cluster

21 January 2018

1 reference

Alu-mediated PCR artifacts and the constitutional t(11;22) breakpoint

21 January 2018

1 reference

Physical mapping of the human hprt chromosomal region (Xq26)

21 January 2018

1 reference

Pulsed field analysis of hprt T-cell large deletions: telomeric region breakpoint spectrum

21 January 2018

1 reference

Molecular analyses of in vivo hprt mutations in human T-lymphocytes. III. Longitudinal study of hprt gene structural alterations and T-cell clonal origins

21 January 2018

1 reference

Sequence analysis of deletion mutations at the HPRT locus of human T-lymphocytes: association of a palindromic structure with a breakpoint cluster in exon 2

21 January 2018

1 reference

DNA sequence analysis of in vivo hprt mutation in human T lymphocytes

21 January 2018

1 reference

Molecular characterization of the genomic breakpoint junction in the t(11;18) (q21;q21) translocation of a gastric MALT lymphoma

21 January 2018

1 reference

Development of long PCR techniques to analyze deletion mutations of the human hprt gene

21 January 2018

1 reference

Novel bcl-2 breakpoints in patients with follicular lymphoma

21 January 2018

1 reference

Microclustering of TEL-AML1 translocation breakpoints in childhood acute lymphoblastic leukemia

21 January 2018

1 reference

Modified inverse PCR method for cloning the flanking sequences from human cell pools

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/EM.10040

1 reference

27 May 2018

PubMed ID

11813293

1 reference

27 May 2018