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Transcription factors in disease
scientific article published on June 1996
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
8791518
retrieved
26 September 2017
review article
1 reference
stated in
Europe PubMed Central
title
Transcription factors in disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
8791518
retrieved
26 September 2017
author
Veronica van Heyningen
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
8791518
retrieved
26 September 2017
author name string
D Engelkamp
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
8791518
retrieved
26 September 2017
publication date
1 June 1996
1 reference
stated in
Europe PubMed Central
PubMed ID
8791518
retrieved
26 September 2017
published in
Current Opinion in Genetics & Development
1 reference
stated in
Europe PubMed Central
PubMed ID
8791518
retrieved
26 September 2017
volume
6
1 reference
stated in
Europe PubMed Central
PubMed ID
8791518
retrieved
26 September 2017
page(s)
334-342
1 reference
stated in
Europe PubMed Central
PubMed ID
8791518
retrieved
26 September 2017
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
8791518
retrieved
26 September 2017
cites work
The role of activators in assembly of RNA polymerase II transcription complexes
1 reference
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Structure and function of DNA-binding proteins
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Structure and function of transcriptional activation domains
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Crossref
reference URL
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7 January 2021
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Transcriptional activation: a complex puzzle with few easy pieces
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Crossref
reference URL
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Knockouts. Targeting the mouse genome: a compendium of knockouts (Part I)
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reference URL
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Targeting the mouse genome: a compendium of knockouts (Part II)
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Crossref
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Targeting the mouse genome: a compendium of knockouts (Part III)
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Chromosomal translocations in human cancer.
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Pit-1 binding to specific DNA sites as a monomer or dimer determines gene-specific use of a tyrosine-dependent synergy domain
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The Ames dwarf gene is required for Pit-1 gene activation.
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Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4
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A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene.
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PAX genes: what's new in developmental biology and cancer?
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Crystal structure of a paired domain-DNA complex at 2.5 A resolution reveals structural basis for Pax developmental mutations
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High resolution crystal structure of a paired (Pax) class cooperative homeodomain dimer on DNA
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Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.
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Mutation of PAX2 in two siblings with renal-coloboma syndrome
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Patterning activities of vertebrate hedgehog proteins in the developing eye and brain.
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Pax6: more than meets the eye.
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Homology of the eyeless gene of Drosophila to the Small eye gene in mice and Aniridia in humans
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Patterning of the Caenorhabditis elegans head region by the Pax-6 family member vab-3.
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Specification of sense-organ identity by a Caenorhabditis elegans Pax-6 homologue.
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Induction of ectopic eyes by targeted expression of the eyeless gene in Drosophila
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Mutations in PAX3 that cause Waardenburg syndrome type I: ten new mutations and review of the literature
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Crossref
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A transgenic neuroanatomical marker identifies cranial neural crest deficiencies associated with the Pax3 mutant Splotch
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The mutational spectrum in Waardenburg syndrome.
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Insight into the microphthalmia gene
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The function and evolution of Msx genes: pointers and paradoxes
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A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
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Premature suture closure and ectopic cranial bone in mice expressing Msx2 transgenes in the developing skull
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Localization of craniosynostosis Adelaide type to 4p16.
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Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.
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Isolation and characterization of a cosmid contig for the GCPS gene region
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DNA binding capacity of the WT1 protein is abolished by Denys—Drash syndrome WT1 point mutations
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Subnuclear localization of WT1 in splicing or transcription factor domains is regulated by alternative splicing
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Resistance to thyroid hormone: an historical overview
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The androgen receptor gene mutations database.
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Evidence for a repressive function of the long polyglutamine tract in the human androgen receptor: possible pathogenetic relevance for the (CAG)n-expanded neuronopathies
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1 reference
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7 January 2021
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Syndromal mental retardation due to mutations in a regulator of gene expression
1 reference
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7 January 2021
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1 reference
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Crossref
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7 January 2021
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Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP
1 reference
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Crossref
reference URL
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7 January 2021
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1 reference
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reference URL
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7 January 2021
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1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
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1 reference
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Crossref
reference URL
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7 January 2021
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Dimerization and the control of transcription by Krüppel.
1 reference
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7 January 2021
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Synergy between transcription factors DBP and C/EBP compensates for a haemophilia B Leyden factor IX mutation
1 reference
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7 January 2021
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Increased gamma-globin expression in a nondeletion HPFH mediated by an erythroid-specific DNA-binding factor
1 reference
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Crossref
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7 January 2021
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Estrogen resistance caused by a mutation in the estrogen-receptor gene in a man
1 reference
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Crossref
reference URL
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7 January 2021
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inferred from DOI database lookup
p53 gene mutation: software and database.
1 reference
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Crossref
reference URL
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7 January 2021
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Germline p53 mutations and heritable cancer
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Influence of PAX6 gene dosage on development: overexpression causes severe eye abnormalities.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2980011-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
Deregulation of PAX-5 by translocation of the Emu enhancer of the IgH locus adjacent to two alternative PAX-5 promoters in a diffuse large-cell lymphoma
1 reference
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reference URL
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7 January 2021
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Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2980011-6
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7 January 2021
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Identifiers
DOI
10.1016/S0959-437X(96)80011-6
1 reference
stated in
Europe PubMed Central
PubMed ID
8791518
retrieved
26 September 2017
Fatcat ID
release_ysziko5nkrhx7aexllgur76s5y
1 reference
stated in
Fatcat
reference URL
https://api.fatcat.wiki/v0/release/ysziko5nkrhx7aexllgur76s5y
retrieved
24 November 2022
based on heuristic
mapped directly with Wikidata item
PubMed ID
8791518
1 reference
stated in
Europe PubMed Central
PubMed ID
8791518
retrieved
26 September 2017
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