Human DNA repair diseases: From genome instability to cancer
Autor(a) principal: | |
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Data de Publicação: | 1997 |
Outros Autores: | |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Journal of Genetics |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-84551997000400032 |
Resumo: | Several human genetic syndromes have long been recognized to be defective in DNA repair mechanisms. This was first discovered by Cleaver (1968), who showed that cells from patients with xeroderma pigmentosum (XP) were defective for the ability to remove ultraviolet (UV)-induced lesions from their genome. Since then, new discoveries have promoted DNA repair studies to one of the most exciting areas of molecular biology. The present work intends to give a brief summary of the main known human genetic diseases related to DNA repair and how they may be linked to acquired diseases such as cancer |
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oai:scielo:S0100-84551997000400032 |
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Brazilian Journal of Genetics |
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Human DNA repair diseases: From genome instability to cancerSeveral human genetic syndromes have long been recognized to be defective in DNA repair mechanisms. This was first discovered by Cleaver (1968), who showed that cells from patients with xeroderma pigmentosum (XP) were defective for the ability to remove ultraviolet (UV)-induced lesions from their genome. Since then, new discoveries have promoted DNA repair studies to one of the most exciting areas of molecular biology. The present work intends to give a brief summary of the main known human genetic diseases related to DNA repair and how they may be linked to acquired diseases such as cancerSociedade Brasileira de Genética1997-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-84551997000400032Brazilian Journal of Genetics v.20 n.4 1997reponame:Brazilian Journal of Geneticsinstname:Sociedade Brasileira de Genética (SBG)instacron:SBG10.1590/S0100-84551997000400032info:eu-repo/semantics/openAccessMachado,Carlos R.Menck,Carlos F.M.eng1998-10-06T00:00:00Zoai:scielo:S0100-84551997000400032Revistahttps://www.gmb.org.br/brazilian-journal-of-geneticsONGhttps://old.scielo.br/oai/scielo-oai.phpsede@sgb.org.br || sede@sgb.org.br0100-84550100-8455opendoar:1998-10-06T00:00Brazilian Journal of Genetics - Sociedade Brasileira de Genética (SBG)false |
dc.title.none.fl_str_mv |
Human DNA repair diseases: From genome instability to cancer |
title |
Human DNA repair diseases: From genome instability to cancer |
spellingShingle |
Human DNA repair diseases: From genome instability to cancer Machado,Carlos R. |
title_short |
Human DNA repair diseases: From genome instability to cancer |
title_full |
Human DNA repair diseases: From genome instability to cancer |
title_fullStr |
Human DNA repair diseases: From genome instability to cancer |
title_full_unstemmed |
Human DNA repair diseases: From genome instability to cancer |
title_sort |
Human DNA repair diseases: From genome instability to cancer |
author |
Machado,Carlos R. |
author_facet |
Machado,Carlos R. Menck,Carlos F.M. |
author_role |
author |
author2 |
Menck,Carlos F.M. |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Machado,Carlos R. Menck,Carlos F.M. |
description |
Several human genetic syndromes have long been recognized to be defective in DNA repair mechanisms. This was first discovered by Cleaver (1968), who showed that cells from patients with xeroderma pigmentosum (XP) were defective for the ability to remove ultraviolet (UV)-induced lesions from their genome. Since then, new discoveries have promoted DNA repair studies to one of the most exciting areas of molecular biology. The present work intends to give a brief summary of the main known human genetic diseases related to DNA repair and how they may be linked to acquired diseases such as cancer |
publishDate |
1997 |
dc.date.none.fl_str_mv |
1997-12-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-84551997000400032 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-84551997000400032 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0100-84551997000400032 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Genética |
publisher.none.fl_str_mv |
Sociedade Brasileira de Genética |
dc.source.none.fl_str_mv |
Brazilian Journal of Genetics v.20 n.4 1997 reponame:Brazilian Journal of Genetics instname:Sociedade Brasileira de Genética (SBG) instacron:SBG |
instname_str |
Sociedade Brasileira de Genética (SBG) |
instacron_str |
SBG |
institution |
SBG |
reponame_str |
Brazilian Journal of Genetics |
collection |
Brazilian Journal of Genetics |
repository.name.fl_str_mv |
Brazilian Journal of Genetics - Sociedade Brasileira de Genética (SBG) |
repository.mail.fl_str_mv |
sede@sgb.org.br || sede@sgb.org.br |
_version_ |
1754734879275220993 |