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Literature DB >> 1483924

Precise localization of the excision repair gene, ERCC5, to human chromosome 13q32.3-q33.1 by direct R-banding fluorescence in situ hybridization.

Abstract

The genomic DNA fragment encoding the excision repair gene, ERCC5, was mapped by direct R-banding fluorescence in situ hybridization. The signals were localized to human chromosome 13q32.3-q33.1. This result was in agreement with previous reports, and the gene was assigned to a narrower region.

Entities: CellLine Disease Gene Species

Mesh：

Substances：
DNA Probes
DNA

Year: 1992 PMID： 1483924 PMCID： PMC5918714 DOI： 10.1111/j.1349-7006.1992.tb02731.x

Source DB: PubMed Journal: Jpn J Cancer Res ISSN： 0910-5050

17 in total

1. Molecular characterization of the human excision repair gene ERCC-1: cDNA cloning and amino acid homology with the yeast DNA repair gene RAD10.

Authors: M van Duin; J de Wit; H Odijk; A Westerveld; A Yasui; M H Koken; J H Hoeijmakers; D Bootsma
Journal: Cell Date: 1986-03-28 Impact factor: 41.582

2. Molecular cloning of the human DNA excision repair gene ERCC-6.

Authors: C Troelstra; H Odijk; J de Wit; A Westerveld; L H Thompson; D Bootsma; J H Hoeijmakers
Journal: Mol Cell Biol Date: 1990-11 Impact factor: 4.272

3. Molecular cloning and biological characterization of the human excision repair gene ERCC-3.

Authors: G Weeda; R C van Ham; R Masurel; A Westerveld; H Odijk; J de Wit; D Bootsma; A J van der Eb; J H Hoeijmakers
Journal: Mol Cell Biol Date: 1990-06 Impact factor: 4.272

4. Identification of nucleotide-excision-repair genes on human chromosomes 2 and 13 by functional complementation in hamster-human hybrids.

Authors: L H Thompson; A V Carrano; K Sato; E P Salazar; B F White; S A Stewart; J L Minkler; M J Siciliano
Journal: Somat Cell Mol Genet Date: 1987-09

5. An eighth complementation group of rodent cells hypersensitive to ultraviolet radiation.

Authors: L H Thompson; T Shiomi; E P Salazar; S A Stewart
Journal: Somat Cell Mol Genet Date: 1988-11

6. Regional assignment of the human thymidylate synthase (TS) gene to chromosome band 18p11.32 by nonisotopic in situ hybridization.

Authors: T Hori; E Takahashi; D Ayusawa; K Takeishi; S Kaneda; T Seno
Journal: Hum Genet Date: 1990-10 Impact factor: 4.132

Precise localization of the excision repair gene, ERCC5, to human chromosome 13q32.3-q33.1 by direct R-banding fluorescence in situ hybridization.

1. Molecular characterization of the human excision repair gene ERCC-1: cDNA cloning and amino acid homology with the yeast DNA repair gene RAD10.

2. Molecular cloning of the human DNA excision repair gene ERCC-6.

3. Molecular cloning and biological characterization of the human excision repair gene ERCC-3.

4. Identification of nucleotide-excision-repair genes on human chromosomes 2 and 13 by functional complementation in hamster-human hybrids.

5. An eighth complementation group of rodent cells hypersensitive to ultraviolet radiation.

6. Regional assignment of the human thymidylate synthase (TS) gene to chromosome band 18p11.32 by nonisotopic in situ hybridization.

7. Cell fusion-mediated improvement in transfection competence for repair-deficient mutant of mouse T cell line.

8. Replication timing of genes and middle repetitive sequences.

9. Human chromosome 13 compensates a DNA repair defect in UV-sensitive mouse cells by mouse--human cell hybridization.

10. Novel Chinese hamster ultraviolet-sensitive mutants for excision repair form complementation groups 9 and 10.

1. Mapping of a congenital microcoria locus to 13q31-q32.

2. Polymorphisms in the XPG gene and risk of gastric cancer in Chinese populations.

3. The human XPG gene: gene architecture, alternative splicing and single nucleotide polymorphisms.

Review 4. XPG: its products and biological roles.

5. The 13q- syndrome: the molecular definition of a critical deletion region in band 13q32.