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Allele diversity of the H-ras-1 variable number of tandem repeats in Norwegian lung cancer patients.
We have examined restriction fragment length polymorphisms of the H-ras-1 gene in germ-line DNA from 214 lung cancer patients and 309 unaffected controls. When DNA samples were digested with MspI/HpaII, Southern blot analysis revealed at least 22 different alleles, grouped according to their frequen...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
1992
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1519637/ https://www.ncbi.nlm.nih.gov/pubmed/1362538 |
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author | Ryberg, D Tefre, T Skaug, V Stangeland, L Ovrebø, S Naalsund, A Børresen, A L Haugen, A |
author_facet | Ryberg, D Tefre, T Skaug, V Stangeland, L Ovrebø, S Naalsund, A Børresen, A L Haugen, A |
author_sort | Ryberg, D |
collection | PubMed |
description | We have examined restriction fragment length polymorphisms of the H-ras-1 gene in germ-line DNA from 214 lung cancer patients and 309 unaffected controls. When DNA samples were digested with MspI/HpaII, Southern blot analysis revealed at least 22 different alleles, grouped according to their frequencies as common, intermediate, and rare. The frequency of rare alleles in lung cancer patients (16/428) is significantly different (p = 0.002) from that in the control group (5/618). Individuals with rare alleles were found to be at 4.7-fold greater risk of lung cancer than those with no rare alleles. |
format | Text |
id | pubmed-1519637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1992 |
record_format | MEDLINE/PubMed |
spelling | pubmed-15196372006-07-26 Allele diversity of the H-ras-1 variable number of tandem repeats in Norwegian lung cancer patients. Ryberg, D Tefre, T Skaug, V Stangeland, L Ovrebø, S Naalsund, A Børresen, A L Haugen, A Environ Health Perspect Research Article We have examined restriction fragment length polymorphisms of the H-ras-1 gene in germ-line DNA from 214 lung cancer patients and 309 unaffected controls. When DNA samples were digested with MspI/HpaII, Southern blot analysis revealed at least 22 different alleles, grouped according to their frequencies as common, intermediate, and rare. The frequency of rare alleles in lung cancer patients (16/428) is significantly different (p = 0.002) from that in the control group (5/618). Individuals with rare alleles were found to be at 4.7-fold greater risk of lung cancer than those with no rare alleles. 1992-11 /pmc/articles/PMC1519637/ /pubmed/1362538 Text en |
spellingShingle | Research Article Ryberg, D Tefre, T Skaug, V Stangeland, L Ovrebø, S Naalsund, A Børresen, A L Haugen, A Allele diversity of the H-ras-1 variable number of tandem repeats in Norwegian lung cancer patients. |
title | Allele diversity of the H-ras-1 variable number of tandem repeats in Norwegian lung cancer patients. |
title_full | Allele diversity of the H-ras-1 variable number of tandem repeats in Norwegian lung cancer patients. |
title_fullStr | Allele diversity of the H-ras-1 variable number of tandem repeats in Norwegian lung cancer patients. |
title_full_unstemmed | Allele diversity of the H-ras-1 variable number of tandem repeats in Norwegian lung cancer patients. |
title_short | Allele diversity of the H-ras-1 variable number of tandem repeats in Norwegian lung cancer patients. |
title_sort | allele diversity of the h-ras-1 variable number of tandem repeats in norwegian lung cancer patients. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1519637/ https://www.ncbi.nlm.nih.gov/pubmed/1362538 |
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