AbstractThe Bloom's syndrome (BS) gene, BLM, plays an important role in the maintenance of genomic stability in somatic cells. A candidate for BLM was identified by direct selection of a cDNA derived from a 250 kb segment of the genome to which BLM had been assigned by somatic crossover point mapping. In this novel mapping method, cells were used from persons with BS that had undergone intragenic recombination within BLM. cDNA analysis of the candidate gene identified a 4437 by cDNA that encodes a 1417 amino acid peptide with homology to the RecQ helicases, a sub-family of DExH box-containing DNA and RNA helicases. The presence of chain-terminating mutations in the candidate gene in persons with BS proved that it was BLM
BACKGROUND: Bloom syndrome is an autosomal recessive disorder characterized by extraordinary cancer ...
Bloom's syndrome (BS) is an autosomal recessive disorder associated with dwarfism, immunodeficiency,...
Defects in the human BLM gene cause Bloom syndrome, notable for early development of tumors in a bro...
Bloom syndrome (BS) is a rare autosomal recessive disorder characterized by growth deficiency, immun...
Bloom syndrome is a cancer predisposition disorder caused by mutations in the BLM helicase gene. Cel...
Bloom's syndrome (BS) is an autosomal recessive disorder associated with dwarfism, immunodeficiency,...
AbstractThe recent cloning of the gene defective in individuals with Bloom's syndrome has revealed a...
Bloom's syndrome is a rare autosomal recessive disorder characterised by an early onset of cancer of...
Genomic instability is a hallmark of disorders in which DNA replication and repair genes are dysfunc...
The RecQ family of DNA helicases has members in all organisms analysed. In humans, defects in three ...
Genomic instability driven by non-allelic homologous recombination (NAHR) provides a realistic mecha...
The RecQ family of DNA helicases is highly conserved in evolution from bacteria to humans. Of the fi...
SummaryThe gene BLM, mutated in Bloom syndrome (BS), encodes the nuclear protein BLM, which when abs...
Review on BLM (Bloom), with data on DNA, on the protein encoded, and where the gene is implicated
Bloom's syndrome (BS) is a recessive human genetic disorder characterized by short stature, immunode...
BACKGROUND: Bloom syndrome is an autosomal recessive disorder characterized by extraordinary cancer ...
Bloom's syndrome (BS) is an autosomal recessive disorder associated with dwarfism, immunodeficiency,...
Defects in the human BLM gene cause Bloom syndrome, notable for early development of tumors in a bro...
Bloom syndrome (BS) is a rare autosomal recessive disorder characterized by growth deficiency, immun...
Bloom syndrome is a cancer predisposition disorder caused by mutations in the BLM helicase gene. Cel...
Bloom's syndrome (BS) is an autosomal recessive disorder associated with dwarfism, immunodeficiency,...
AbstractThe recent cloning of the gene defective in individuals with Bloom's syndrome has revealed a...
Bloom's syndrome is a rare autosomal recessive disorder characterised by an early onset of cancer of...
Genomic instability is a hallmark of disorders in which DNA replication and repair genes are dysfunc...
The RecQ family of DNA helicases has members in all organisms analysed. In humans, defects in three ...
Genomic instability driven by non-allelic homologous recombination (NAHR) provides a realistic mecha...
The RecQ family of DNA helicases is highly conserved in evolution from bacteria to humans. Of the fi...
SummaryThe gene BLM, mutated in Bloom syndrome (BS), encodes the nuclear protein BLM, which when abs...
Review on BLM (Bloom), with data on DNA, on the protein encoded, and where the gene is implicated
Bloom's syndrome (BS) is a recessive human genetic disorder characterized by short stature, immunode...
BACKGROUND: Bloom syndrome is an autosomal recessive disorder characterized by extraordinary cancer ...
Bloom's syndrome (BS) is an autosomal recessive disorder associated with dwarfism, immunodeficiency,...
Defects in the human BLM gene cause Bloom syndrome, notable for early development of tumors in a bro...