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Book Chapter: Chromosome-engineered mouse models

TitleChromosome-engineered mouse models
Authors
Issue Date2006
Citation
Genomic Disorders: The Genomic Basis of Disease, 2006, p. 373-387 How to Cite?
AbstractChromosome rearrangements cause genomic disorders and cancer in human. Region-specific low-copy repeats (LCRs) can mediate nonallelic homologous recombination (NAHR) that results in chromosome rearrangements. Using the Cre-loxP site-specific recombination system, chromosome rearrangements that cause genomic disorders and cancer can be recapitulated in the mouse. Technology advancements in mouse genetics, such as recombineering, will undoubtedly facilitate modeling genetic changes associated with genomic disorders in the mouse. © 2006 Humana Press Inc.
Persistent Identifierhttp://hdl.handle.net/10722/249092

 

DC FieldValueLanguage
dc.contributor.authorLiu, Pentao-
dc.date.accessioned2017-10-27T05:59:05Z-
dc.date.available2017-10-27T05:59:05Z-
dc.date.issued2006-
dc.identifier.citationGenomic Disorders: The Genomic Basis of Disease, 2006, p. 373-387-
dc.identifier.urihttp://hdl.handle.net/10722/249092-
dc.description.abstractChromosome rearrangements cause genomic disorders and cancer in human. Region-specific low-copy repeats (LCRs) can mediate nonallelic homologous recombination (NAHR) that results in chromosome rearrangements. Using the Cre-loxP site-specific recombination system, chromosome rearrangements that cause genomic disorders and cancer can be recapitulated in the mouse. Technology advancements in mouse genetics, such as recombineering, will undoubtedly facilitate modeling genetic changes associated with genomic disorders in the mouse. © 2006 Humana Press Inc.-
dc.languageeng-
dc.relation.ispartofGenomic Disorders: The Genomic Basis of Disease-
dc.titleChromosome-engineered mouse models-
dc.typeBook_Chapter-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1007/978-1-59745-039-3_26-
dc.identifier.scopuseid_2-s2.0-84891444139-
dc.identifier.spage373-
dc.identifier.epage387-

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