Role of DNA secondary structures in fragile site breakage along human chromosome 10 - Wikidata - awgldk - TriplyDB

Role of DNA secondary structures in fragile site breakage along human chromosome 10

Role of DNA secondary structures in fragile site breakage along human chromosome 10

http://www.wikidata.org/entity/Q36682494

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Replication stress in Mammalian cells and its consequences for mitosis Endogenous florendoviruses are major components of plant genomes and hallmarks of virus evolution Environmental and chemotherapeutic agents induce breakage at genes involved in leukemia-causing gene rearrangements in human hematopoietic stem/progenitor cells.DNA secondary structure at chromosomal fragile sites in human disease.Phenotypic diversity of breast cancer-related mutations in metalloproteinase-disintegrin ADAM12 A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder DNA topoisomerases participate in fragility of the oncogene RET.Translocation and deletion breakpoints in cancer genomes are associated with potential non-B DNA-forming sequences Replication initiation and genome instability: a crossroads for DNA and RNA synthesis.Updating the mechanisms of common fragile site instability: how to reconcile the different views?Evolution of the Genome 3D Organization: Comparison of Fused and Segregated Globin Gene Clusters.Alternative DNA secondary structure formation affects RNA polymerase II promoter-proximal pausing in human.

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Role of DNA secondary structures in fragile site breakage along human chromosome 10

http://www.wikidata.org/entity/Q36682494

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2013 nî lūn-bûn

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2013年の論文

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2013年論文

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Role of DNA secondary structures in fragile site breakage along human chromosome 10

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Role of DNA secondary structures in fragile site breakage along human chromosome 10

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Role of DNA secondary structures in fragile site breakage along human chromosome 10

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Role of DNA secondary structures in fragile site breakage along human chromosome 10

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Role of DNA secondary structures in fragile site breakage along human chromosome 10

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Role of DNA secondary structures in fragile site breakage along human chromosome 10

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Human Molecular Genetics

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Role of DNA secondary structures in fragile site breakage along human chromosome 10

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Laura W Dillon

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Levi C T Pierce

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Maggie C Y Ng

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Yuh-Hwa Wang

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Initial sequencing and analysis of the human genome

B cell lymphoma-associated chromosomal translocation involves candidate oncogene lyt-10, homologous to NF-kappa B p50

A comprehensive functional analysis of PTEN mutations: implications in tumor- and autism-related syndromes

Mfold web server for nucleic acid folding and hybridization prediction

Molecular basis for expression of common and rare fragile sites

Chromosome fragile sites

Human chromosome fragility

The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data

DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes

The molecular basis of common and rare fragile sites

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1443-1456

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scholarly article

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10.1093/HMG/DDS561

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7

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22

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234087129

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23297364

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3596854

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