A long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes.

No abstract is available for this paper.

• Publication year

  1990

• Venue

  American Journal of Human Genetics

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  PMID 2309701PMCID PMC1683630
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  1990cited by this paper
• Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q.

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• A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19.

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• Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19.

  1989cited by this paper
• Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM)

  1989cited by this paper
• Refined mapping of the three DNA repair genes, ERCC1, ERCC2, and XRCC1, on human chromosome 19.

  1989cited by this paper
• Definition of subchromosomal intervals around the myotonic dystrophy locus at 19q.

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• Sensitive, high-resolution chromatin and chromosome mapping in situ: presence and orientation of two closely integrated copies of EBV in a lymphoma line.

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• A primary map of ten DNA markers and two serological markers for human chromosome 19.

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• Isolation and characterization of alphoid DNA sequences specific for the pericentric regions of chromosomes 4, 5, 9, and 19.

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• Genetic and physical demarcation of the locus for dystrophia myotonica.

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• NcoI RFLP at the creatine kinase-muscle type gene locus (CKMM, chromosome 19).

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• Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase.

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• Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

  1988cited by this paper
• Molecular cloning and biological characterization of a human gene, ERCC2, that corrects the nucleotide excision repair defect in CHO UV5 cells

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• Toward early diagnosis of myotonic dystrophy: construction and characterization of a somatic cell hybrid with a single human der(19) chromosome.

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• Partial reactivation of a human inactive X chromosome in human-mouse somatic cell hybrids.

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  2005cites this paper
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  2001cites this paper
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  2001cites this paper
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• Genotype-phenotype correlation in myotonic dystrophy.

  1998cites this paper
• Disruption of the mouse xeroderma pigmentosum group D DNA repair/basal transcription gene results in preimplantation lethality.

  1998cites this paper
• Myotonic dystrophy: molecular genetics and diagnosis.

  1998cites this paper
• Genotype ‐phenotype correlation in myotonic dystrophy

  1998cites this paper
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  1997cites this paper
• Sequence analysis of the ERCC2 gene regions in human, mouse, and hamster reveals three linked genes.

  1996cites this paper
• Gene for progressive familial heart block type I maps to chromosome 19q13.

  1995cites this paper
• Repair of oxidative damage to DNA: enzymology and biology.

  1994cites this paper
• The 1.5-Mb region spanning the myotonic dystrophy locus shows uniform recombination frequency.

  1994cites this paper
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  1994cites this paper
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  1994cites this paper
• Molecular and Cell Biology of Muscular Dystrophy

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• [Direct genotypic analysis of myotonic dystrophy: detection of an unstable DNA fragment in carriers].

  1993cites this paper
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• Molecular genetic aspects of cardiomyopathy.

  1993cites this paper
• Genetic analysis of nucleotide excision repair in mammalian cells.

  1993cites this paper
• Inheritance and pathogenicity of myotonic dystrophy.

  1993cites this paper
• An informative panel of somatic cell hybrids for physical mapping on human chromosome 19q.

  1993cites this paper
• Genes controlling nucleotide excision repair in eukaryotic cells

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• Expression of excision repair genes in non-malignant bone marrow from cancer patients.

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• Regional localization of the selenocysteine tRNA gene (TRSP) on human chromosome 19.

  1992cites this paper
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  1992cites this paper
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  1991cites this paper
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  1991cites this paper
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  1991cites this paper
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  1991cites this paper
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  1991cites this paper
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  1991cites this paper
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  1990cites this paper
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  1990cites this paper
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  1990cites this paper
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  1990cites this paper