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Characterization of genomic structures and expression profiles of three tandem repeats of a mouse double homeobox gene: Duxbl
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
20063414
retrieved
24 January 2017
title
Characterization of genomic structures and expression profiles of three tandem repeats of a mouse double homeobox gene: Duxbl
(English)
1 reference
stated in
PubMed
PubMed ID
20063414
retrieved
24 January 2017
main subject
tandem repeat
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inferred from title
author name string
Shey-Lin Wu
series ordinal
1
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PubMed
PubMed ID
20063414
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24 January 2017
Ming-Shiun Tsai
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2
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PubMed
PubMed ID
20063414
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24 January 2017
Swee-Hee Wong
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3
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PubMed
PubMed ID
20063414
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24 January 2017
Hsiu-Mei Hsieh-Li
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4
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PubMed
PubMed ID
20063414
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24 January 2017
Tz-Shiu Tsai
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5
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PubMed
PubMed ID
20063414
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24 January 2017
Wei-Tang Chang
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PubMed
PubMed ID
20063414
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24 January 2017
Shin-Ling Huang
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7
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PubMed
PubMed ID
20063414
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24 January 2017
Chun-Ching Chiu
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8
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PubMed
PubMed ID
20063414
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24 January 2017
Sue-Hong Wang
series ordinal
9
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PubMed
PubMed ID
20063414
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24 January 2017
language of work or name
English
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publication date
1 March 2010
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PubMed
PubMed ID
20063414
retrieved
24 January 2017
published in
Developmental Dynamics
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PubMed
PubMed ID
20063414
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24 January 2017
volume
239
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PubMed
PubMed ID
20063414
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24 January 2017
issue
3
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PubMed
PubMed ID
20063414
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24 January 2017
page(s)
927–940
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PubMed
PubMed ID
20063414
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24 January 2017
cites work
Expression profiling of immature thymocytes revealed a novel homeobox gene that regulates double-negative thymocyte development
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Identification of differentially expressed genes in mouse spermatogenesis
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Active genes in junk DNA? Characterization of DUX genes embedded within 3.3 kb repeated elements
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7 January 2021
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Homeobox genes and disease
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Annotation, nomenclature and evolution of four novel homeobox genes expressed in the human germ line.
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Conservation of a large protein domain in the segmentation gene paired and in functionally related genes of Drosophila.
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7 January 2021
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An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
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Biphasic myopathic phenotype of mouse DUX, an ORF within conserved FSHD-related repeats.
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The role of Pax genes in the development of tissues and organs: Pax3 and Pax7 regulate muscle progenitor cell functions
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Homeobox genes in normal and malignant cells.
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Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy
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Whole-mount in situ hybridization to mouse embryos.
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MyoD, myogenin independent differentiation of primordial myoblasts in mouse somites
1 reference
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https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
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Characterization of a double homeodomain protein (DUX1) encoded by a cDNA homologous to 3.3 kb dispersed repeated elements
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
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DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1
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Crossref
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Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element
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Plac8 and Plac9, novel placental-enriched genes identified through microarray analysis
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Evolution of homeobox genes: Q50 Paired-like genes founded the Paired class
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Homeodomain-DNA recognition
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
based on heuristic
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Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy.
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
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The evolution of homeobox genes: Implications for the study of brain development
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Classification and nomenclature of all human homeobox genes.
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The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
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Interpreting cDNA sequences: some insights from studies on translation
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Pax genes in eye development and evolution
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Crossref
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7 January 2021
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A novel maternally transcribed homeobox gene, Eso-1, is preferentially expressed in oocytes and regulated by cytoplasmic polyadenylation
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
The Rx homeobox gene is essential for vertebrate eye development
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
based on heuristic
inferred from DOI database lookup
Homeobox genes and axial patterning
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
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inferred from DOI database lookup
Expression of a novel aristaless related homeobox gene 'Arx' in the vertebrate telencephalon, diencephalon and floor plate.
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation and characterization of Vsx1, a novel mouse CVC paired-like homeobox gene expressed during embryogenesis and in the retina
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
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Intracellular trafficking and dynamics of double homeodomain proteins.
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
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Identification, characterization and metagenome analysis of oocyte-specific genes organized in clusters in the mouse genome
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
based on heuristic
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Paired-type homeodomain transcription factors are imported into the nucleus by karyopherin 13
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
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inferred from DOI database lookup
A high-copy T7 Escherichia coli expression vector for the production of recombinant proteins with a minimal N-terminal His-tagged fusion peptide.
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
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Expression of two myogenic regulatory factors myogenin and MyoDl during mouse embryogenesis
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
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The birth of muscle progenitor cells in the mouse: spatiotemporal considerations
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of facioscapulohumeral muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
based on heuristic
inferred from DOI database lookup
FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22210
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel NK-type homeobox gene, ENK (early embryo specific NK), preferentially expressed in embryonic stem cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22210
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7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22210
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22210
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1002/DVDY.22210
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PubMed ID
20063414
1 reference
stated in
PubMed
PubMed ID
20063414
retrieved
24 January 2017
ResearchGate publication ID
40901080
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