Characterization of molecular defects in xeroderma pigmentosum group C (Q28259157)

xeroderma pigmentosum group C

inferred from title

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L Li

1

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E S Bales

series ordinal

2

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C A Peterson

series ordinal

3

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R J Legerski

series ordinal

4

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language of work or name

English

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publication date

December 1993

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published in

Nature Genetics

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volume

5

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issue

4

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page(s)

413-7

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exact match

https://scigraph.springernature.com/pub.10.1038/ng1293-413

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cites work

Xeroderma pigmentosum. An inherited diseases with sun sensitivity, multiple cutaneous neoplasms, and abnormal DNA repair

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

21 January 2018

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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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Xeroderma pigmentosum neurological abnormalities correlate with colony-forming ability after ultraviolet radiation

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Defective Repair Replication of DNA in Xeroderma Pigmentosum

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Molecular cloning of a mouse DNA repair gene that complements the defect of group-A xeroderma pigmentosum

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Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C

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Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

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Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

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Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

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Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

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Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

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A de novo Alu insertion results in neurofibromatosis type 1

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Isolation of an active human transposable element

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High-frequency transformation of human repair-deficient cell lines by an Epstein-Barr virus-based cDNA expression vector

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