AbstractThe gene mutated in Nijmegen breakage syndrome, a chromosome instability disorder, has been identified and sequenced. The protein product of this gene forms a complex with hMre11 and hRad50 – proteins that are involved in repairing double-strand breaks in DNA
Alterations of the NBS1 gene are responsible for Nijmegen breakage syndrome (NBS), which is characte...
We have previously shown that mutations in the genes encoding DNA Ligase IV (LIGIV) and RAD50, invol...
We have previously shown that mutations in the genes encoding DNA Ligase IV (LIGIV) and RAD50, invol...
AbstractThe gene mutated in Nijmegen breakage syndrome, a chromosome instability disorder, has been ...
AbstractNijmegen breakage syndrome (NBS) is an autosomal recessive disorder characterized by increas...
The present report deals with the functional relationships among protein complexes which, when mutat...
Nijmegen breakage syndrome (NBS) is an autosomal recessive chromosomal instability syndrome characte...
The DNA-double strand break (DSB) repair has an essential importance for the genomic integrity maint...
AbstractNijmegen breakage syndrome (NBS) is an autosomal recessive chromosomal instability syndrome ...
Review on Nijmegen breakage syndrome, with data on clinics, and the genes involved
The human genetic disorder, Nijmegen breakage syn-drome (NBS), is characterized by radiosensitivity,...
Genomic instability in ataxia telangiectasia-like disorder and Nijmegen breakage syndrome is due to ...
Review on NBS1 (Nijmegen breakage syndrome 1), with data on DNA, on the protein encoded, and where t...
Nijmegen breakage syndrome (NBS) with NBS1 germ-line mutation is a human autosomal recessive disease...
In this work we have studied cells derived from five Italian patients characterised by growth delay,...
Alterations of the NBS1 gene are responsible for Nijmegen breakage syndrome (NBS), which is characte...
We have previously shown that mutations in the genes encoding DNA Ligase IV (LIGIV) and RAD50, invol...
We have previously shown that mutations in the genes encoding DNA Ligase IV (LIGIV) and RAD50, invol...
AbstractThe gene mutated in Nijmegen breakage syndrome, a chromosome instability disorder, has been ...
AbstractNijmegen breakage syndrome (NBS) is an autosomal recessive disorder characterized by increas...
The present report deals with the functional relationships among protein complexes which, when mutat...
Nijmegen breakage syndrome (NBS) is an autosomal recessive chromosomal instability syndrome characte...
The DNA-double strand break (DSB) repair has an essential importance for the genomic integrity maint...
AbstractNijmegen breakage syndrome (NBS) is an autosomal recessive chromosomal instability syndrome ...
Review on Nijmegen breakage syndrome, with data on clinics, and the genes involved
The human genetic disorder, Nijmegen breakage syn-drome (NBS), is characterized by radiosensitivity,...
Genomic instability in ataxia telangiectasia-like disorder and Nijmegen breakage syndrome is due to ...
Review on NBS1 (Nijmegen breakage syndrome 1), with data on DNA, on the protein encoded, and where t...
Nijmegen breakage syndrome (NBS) with NBS1 germ-line mutation is a human autosomal recessive disease...
In this work we have studied cells derived from five Italian patients characterised by growth delay,...
Alterations of the NBS1 gene are responsible for Nijmegen breakage syndrome (NBS), which is characte...
We have previously shown that mutations in the genes encoding DNA Ligase IV (LIGIV) and RAD50, invol...
We have previously shown that mutations in the genes encoding DNA Ligase IV (LIGIV) and RAD50, invol...
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