A R Lehmann|S Kirk-Bell - JoVE Visualize

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Mutation Research|February 1, 1995

G2 phase repair of X-ray-induced chromosomal DNA damage in trichothiodystrophy cellsK K Sanford, R Parshad, F M Price, et al.

Journal of Medical Genetics|August 1, 1993

Cockayne's syndrome: correlation of clinical features with cellular sensitivity of RNA synthesis to UV irradiationA R Lehmann, A F Thompson, S A Harcourt, et al.

Mutation Research|January 1, 1980

The induction and characterization of mouse lymphoma L5178Y cell lines resistant to 1-beta-d-arabinofuranosylcytosineA M Rogers, R Hill, A R Lehmann, et al.

Mutation Research|March 1, 1989

Mutagenic treatments result in inactivation of expression of a transfected bacterial gene integrated into a human cell lineA R Lehmann, C F Arlett, S A Harcourt, et al.

American Journal of Human Genetics|October 3, 1998

Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy: site of mutation correlates with repair deficiency, but gene dosage appears to determine clinical severityE Botta, T Nardo, B C Broughton, et al.

Experimental Cell Research|August 1, 1989

Instability of extrachromosomal cosmid DNA in SV40-transformed human (ataxia-telangiectasia) cellsS W Dean, L Kincla, H R Sykes, et al.

The EMBO Journal|December 1, 1995

Fission yeast rad17: a homologue of budding yeast RAD24 that shares regions of sequence similarity with DNA polymerase accessory proteinsD J Griffiths, N C Barbet, S McCready, et al.

Mutation Research|December 1, 1975

A comparison of the 8-azaguanine and ouabain-resistance systems for the selection of induced mutant Chinese hamster cellsC F Arlett, D Turnbull, S A Harcourt, et al.

Human Mutation|January 1, 1997

Confirmation of homozygosity for a single nucleotide substitution mutation in a Cockayne syndrome patient using monoallelic mutation analysis in somatic cell hybridsL D McDaniel, R Legerski, A R Lehmann, et al.

Lancet (London, England)|June 20, 1992

Growth retardation and immunodeficiency in a patient with mutations in the DNA ligase I geneA D Webster, D E Barnes, C F Arlett, et al.

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Showing results (51-60 of 126) with videos related to

Sort By:

Pageof 13

Mutation Research|February 1, 1995

G2 phase repair of X-ray-induced chromosomal DNA damage in trichothiodystrophy cellsK K Sanford, R Parshad, F M Price, et al.

Journal of Medical Genetics|August 1, 1993

Cockayne's syndrome: correlation of clinical features with cellular sensitivity of RNA synthesis to UV irradiationA R Lehmann, A F Thompson, S A Harcourt, et al.

Mutation Research|January 1, 1980

The induction and characterization of mouse lymphoma L5178Y cell lines resistant to 1-beta-d-arabinofuranosylcytosineA M Rogers, R Hill, A R Lehmann, et al.

Mutation Research|March 1, 1989

Mutagenic treatments result in inactivation of expression of a transfected bacterial gene integrated into a human cell lineA R Lehmann, C F Arlett, S A Harcourt, et al.

American Journal of Human Genetics|October 3, 1998

Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy: site of mutation correlates with repair deficiency, but gene dosage appears to determine clinical severityE Botta, T Nardo, B C Broughton, et al.

Experimental Cell Research|August 1, 1989

Instability of extrachromosomal cosmid DNA in SV40-transformed human (ataxia-telangiectasia) cellsS W Dean, L Kincla, H R Sykes, et al.

The EMBO Journal|December 1, 1995

Fission yeast rad17: a homologue of budding yeast RAD24 that shares regions of sequence similarity with DNA polymerase accessory proteinsD J Griffiths, N C Barbet, S McCready, et al.

Mutation Research|December 1, 1975

A comparison of the 8-azaguanine and ouabain-resistance systems for the selection of induced mutant Chinese hamster cellsC F Arlett, D Turnbull, S A Harcourt, et al.

Human Mutation|January 1, 1997

Confirmation of homozygosity for a single nucleotide substitution mutation in a Cockayne syndrome patient using monoallelic mutation analysis in somatic cell hybridsL D McDaniel, R Legerski, A R Lehmann, et al.

Lancet (London, England)|June 20, 1992

Growth retardation and immunodeficiency in a patient with mutations in the DNA ligase I geneA D Webster, D E Barnes, C F Arlett, et al.

Pageof 13