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A Quantitative Trait Locus in Major Histocompatibility Complex Determining Latent Period of Mouse Lymphomas
The effects of two host genes on retro virus‐induced murine lymphoma were evaluated by studying 114 F2 intercross mice between SL/Kh and AKR/Ms mice. Out of 47 T‐lymphoma‐bearing F2 mice, 45 had the AKR‐derived dominant allele at Tlsm‐1. The length of the lymphoma latent period was not related to ty...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1996
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921108/ https://www.ncbi.nlm.nih.gov/pubmed/8641972 http://dx.doi.org/10.1111/j.1349-7006.1996.tb00236.x |
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author | Kamoto, Toshiyuki Shisa, Hayase Pataer, Abujiang Lu, Ling‐min Yoshida, Osamu Yamada, Yoshihiro Hiai, Hiroshi |
author_facet | Kamoto, Toshiyuki Shisa, Hayase Pataer, Abujiang Lu, Ling‐min Yoshida, Osamu Yamada, Yoshihiro Hiai, Hiroshi |
author_sort | Kamoto, Toshiyuki |
collection | PubMed |
description | The effects of two host genes on retro virus‐induced murine lymphoma were evaluated by studying 114 F2 intercross mice between SL/Kh and AKR/Ms mice. Out of 47 T‐lymphoma‐bearing F2 mice, 45 had the AKR‐derived dominant allele at Tlsm‐1. The length of the lymphoma latent period was not related to type of tumor. Instead, it was significantly shortened by a recessive SL/Kh‐derived allele at a major histocompatibility complex (MHC)‐linked locus on Chr. 17. A quantitative trait analysis of the latent period yielded a maximal logarithm of likelihood ratio for linkage (LOD) score of 7.06 at a class II gene within MHC. The SL/Kh‐derived recessive gene was named lla (lymphoma latency acceleration). |
format | Online Article Text |
id | pubmed-5921108 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1996 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59211082018-05-11 A Quantitative Trait Locus in Major Histocompatibility Complex Determining Latent Period of Mouse Lymphomas Kamoto, Toshiyuki Shisa, Hayase Pataer, Abujiang Lu, Ling‐min Yoshida, Osamu Yamada, Yoshihiro Hiai, Hiroshi Jpn J Cancer Res Article The effects of two host genes on retro virus‐induced murine lymphoma were evaluated by studying 114 F2 intercross mice between SL/Kh and AKR/Ms mice. Out of 47 T‐lymphoma‐bearing F2 mice, 45 had the AKR‐derived dominant allele at Tlsm‐1. The length of the lymphoma latent period was not related to type of tumor. Instead, it was significantly shortened by a recessive SL/Kh‐derived allele at a major histocompatibility complex (MHC)‐linked locus on Chr. 17. A quantitative trait analysis of the latent period yielded a maximal logarithm of likelihood ratio for linkage (LOD) score of 7.06 at a class II gene within MHC. The SL/Kh‐derived recessive gene was named lla (lymphoma latency acceleration). Blackwell Publishing Ltd 1996-04 /pmc/articles/PMC5921108/ /pubmed/8641972 http://dx.doi.org/10.1111/j.1349-7006.1996.tb00236.x Text en |
spellingShingle | Article Kamoto, Toshiyuki Shisa, Hayase Pataer, Abujiang Lu, Ling‐min Yoshida, Osamu Yamada, Yoshihiro Hiai, Hiroshi A Quantitative Trait Locus in Major Histocompatibility Complex Determining Latent Period of Mouse Lymphomas |
title | A Quantitative Trait Locus in Major Histocompatibility Complex Determining Latent Period of Mouse Lymphomas |
title_full | A Quantitative Trait Locus in Major Histocompatibility Complex Determining Latent Period of Mouse Lymphomas |
title_fullStr | A Quantitative Trait Locus in Major Histocompatibility Complex Determining Latent Period of Mouse Lymphomas |
title_full_unstemmed | A Quantitative Trait Locus in Major Histocompatibility Complex Determining Latent Period of Mouse Lymphomas |
title_short | A Quantitative Trait Locus in Major Histocompatibility Complex Determining Latent Period of Mouse Lymphomas |
title_sort | quantitative trait locus in major histocompatibility complex determining latent period of mouse lymphomas |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921108/ https://www.ncbi.nlm.nih.gov/pubmed/8641972 http://dx.doi.org/10.1111/j.1349-7006.1996.tb00236.x |
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