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From mouse to man: generating megabase chromosome rearrangements
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
11377795
retrieved
1 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
From mouse to man: generating megabase chromosome rearrangements
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
11377795
retrieved
1 August 2017
author name string
Mills AA
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
11377795
retrieved
1 August 2017
Bradley A
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
11377795
retrieved
1 August 2017
publication date
1 June 2001
1 reference
stated in
Europe PubMed Central
PubMed ID
11377795
retrieved
1 August 2017
published in
Trends in Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
11377795
retrieved
1 August 2017
volume
17
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stated in
Europe PubMed Central
PubMed ID
11377795
retrieved
1 August 2017
page(s)
331-339
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stated in
Europe PubMed Central
PubMed ID
11377795
retrieved
1 August 2017
issue
6
1 reference
stated in
Europe PubMed Central
PubMed ID
11377795
retrieved
1 August 2017
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A chromosome 14 inversion in a T-cell lymphoma is caused by site-specific recombination between immunoglobulin and T-cell receptor loci
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Frequency and nature of specific-locus mutations induced in female mice by radiations and chemicals: a review
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Mouse albino-deletions: from genetics to genes in development
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Genetic and molecular analysis of chlorambucil-induced germ-line mutations in the mouse
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Chromosomal deletion complexes in mice by radiation of embryonic stem cells
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Genotype-based screen for ENU-induced mutations in mouse embryonic stem cells
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Chromosome engineering in mice
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A site-directed chromosomal translocation induced in embryonic stem cells by Cre-loxP recombination.
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Site-specific DNA recombination in mammalian cells by the Cre recombinase of bacteriophage P1
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Cre-mediated chromosome loss in mice
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Congenital heart disease in mice deficient for the DiGeorge syndrome region
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Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice
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Engineering mouse chromosomes with Cre-loxP: range, efficiency, and somatic applications
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Introducing defined chromosomal rearrangements into the mouse genome
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Engineering a mouse balancer chromosome
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A comprehensive genetic map of the mouse genome.
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A system for rapid generation of coat color-tagged knockouts and defined chromosomal rearrangements in mice
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Target frequency and integration pattern for insertion and replacement vectors in embryonic stem cells
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Using targeted large deletions and high-efficiency N-ethyl-N-nitrosourea mutagenesis for functional analyses of the mammalian genome
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1 reference
stated in
Crossref
reference URL
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Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation.
1 reference
stated in
Crossref
reference URL
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retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0168-9525(01)02321-6
1 reference
stated in
Europe PubMed Central
PubMed ID
11377795
retrieved
1 August 2017
PubMed ID
11377795
1 reference
stated in
Europe PubMed Central
PubMed ID
11377795
retrieved
1 August 2017
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