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Congenital abnormalities of body patterning: embryology revisited
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12944067
retrieved
7 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Congenital abnormalities of body patterning: embryology revisited
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12944067
retrieved
7 August 2017
main subject
congenital disorder
0 references
author name string
Frances R Goodman
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12944067
retrieved
7 August 2017
language of work or name
English
0 references
publication date
1 August 2003
1 reference
stated in
Europe PubMed Central
PubMed ID
12944067
retrieved
7 August 2017
published in
The Lancet
1 reference
stated in
Europe PubMed Central
PubMed ID
12944067
retrieved
7 August 2017
volume
362
1 reference
stated in
Europe PubMed Central
PubMed ID
12944067
retrieved
7 August 2017
issue
9384
1 reference
stated in
Europe PubMed Central
PubMed ID
12944067
retrieved
7 August 2017
page(s)
651-662
1 reference
stated in
Europe PubMed Central
PubMed ID
12944067
retrieved
7 August 2017
cites work
Homeobox genes and axial patterning
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Developmental patterning genes and their conserved functions: from model organisms to humans
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
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7 January 2021
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Limb malformations and the human HOX genes
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
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Heart development in Drosophila and vertebrates: conservation of molecular mechanisms.
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
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7 January 2021
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Cell biology of cardiac development
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
Pax6: more than meets the eye.
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
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7 January 2021
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Vertebrate eye development as modeled in Drosophila
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reference URL
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7 January 2021
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A new concept of the cellular basis of immunity
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
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Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study
1 reference
stated in
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
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The 22q11 deletion syndromes
1 reference
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https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
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7 January 2021
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DiGeorge syndrome(s)
1 reference
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https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
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7 January 2021
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Developing models of DiGeorge syndrome
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
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7 January 2021
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Closing time for CATCH22
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stated in
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
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Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients
1 reference
stated in
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
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A common molecular basis for rearrangement disorders on chromosome 22q11
1 reference
stated in
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
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Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis
1 reference
stated in
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosomal microdeletions: dissecting del22q11 syndrome
1 reference
stated in
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital heart disease in mice deficient for the DiGeorge syndrome region
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
T-box genes: what they do and how they do it.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
Tbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/del22q11 syndromes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation analysis of TBX1 in non-deleted patients with features of DGS/VCFS or isolated cardiovascular defects
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Holoprosencephaly: from Homer to Hedgehog.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
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Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
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7 January 2021
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inferred from DOI database lookup
Induction of the zebrafish ventral brain and floorplate requires cyclops/nodal signalling.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
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7 January 2021
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The EGF-CFC protein one-eyed pinhead is essential for nodal signaling
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
Functional interactions of genes mediating convergent extension, knypek and trilobite, during the partitioning of the eye primordium in zebrafish.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the human Sonic Hedgehog gene cause holoprosencephaly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
Transducing Hedgehog: the story so far
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
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inferred from DOI database lookup
Sonic hedgehog in CNS development: one signal, multiple outputs
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inhibition of sonic hedgehog signaling in vivo results in craniofacial neural crest cell death
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Teratogen-mediated inhibition of target tissue response to Shh signaling.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hedgehog signaling and human disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sonic hedgehog in the nervous system: functions, modifications and mechanisms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effects of oncogenic mutations in Smoothened and Patched can be reversed by cyclopamine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Zic2 regulates the kinetics of neurulation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
TGFbeta signaling in growth control, cancer, and heritable disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Smad2 role in mesoderm formation, left-right patterning and craniofacial development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in holoprosencephaly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Hedgehog and Wnt signalling pathways in cancer
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gli and hedgehog in cancer: tumours, embryos and stem cells.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human homolog of patched, a candidate gene for the basal cell nevus syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Activating Smoothened mutations in sporadic basal-cell carcinoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Basal cell carcinoma possibly originates from the outer root sheath and/or the bulge region of the vellus hair follicle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sonic hedgehog signaling is essential for hair development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Induction of the hair growth phase in postnatal mice by localized transient expression of Sonic hedgehog
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Basal cell carcinomas in mice overexpressing sonic hedgehog
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in SUFU predispose to medulloblastoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Control of neuronal precursor proliferation in the cerebellum by Sonic Hedgehog
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Medulloblastoma growth inhibition by hedgehog pathway blockade
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hox genes in vertebrate development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exploring the homeobox
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homeobox genes in embryogenesis and pathogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Developmental functions of mammalian Hox genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hoxb-4 (Hox-2.6) mutant mice show homeotic transformation of a cervical vertebra and defects in the closure of the sternal rudiments
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human HOX gene mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Of fingers, toes and penises.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree data
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The molecular basis of hypodactyly (Hd): a deletion in Hoxa 13 leads to arrest of digital arch formation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation of HOXA13 in hand-foot-genital syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic interactions of Hox genes in limb development: learning from compound mutants.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular models for vertebrate limb development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mouse Hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Priming the search for HOX mutations
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Amegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Haploinsufficiency of the HOXA gene cluster, in a patient with hand-foot-genital syndrome, velopharyngeal insufficiency, and persistent patent Ductus botalli
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
HoxB4 confers definitive lymphoid-myeloid engraftment potential on embryonic stem cell and yolk sac hematopoietic progenitors.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
HOX and non-HOX homeobox genes in leukemic hematopoiesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cooperative activation of Hoxa and Pbx1-related genes in murine myeloid leukaemias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hoxa9 transforms primary bone marrow cells through specific collaboration with Meis1a but not Pbx1b
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Overexpression of HOXA10 in murine hematopoietic cells perturbs both myeloid and lymphoid differentiation and leads to acute myeloid leukemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Overexpression of HOXB3 in hematopoietic cells causes defective lymphoid development and progressive myeloproliferation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Conditional immortalization of mouse myelomonocytic, megakaryocytic and mast cell progenitors by the Hox-2.4 homeobox gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Single-translocation and double-chimeric transcripts: detection of NUP98-HOXA9 in myeloid leukemias with HOXA11 or HOXA13 breaks of the chromosomal translocation t(7;11)(p15;p15)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fusion of the NUP98 gene and the homeobox gene HOXC13 in acute myeloid leukemia with t(11;12)(p15;q13).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CREB binding protein interacts with nucleoporin-specific FG repeats that activate transcription and mediate NUP98-HOXA9 oncogenicity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular classification of cancer: class discovery and class prediction by gene expression monitoring
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The oncoprotein E2A-Pbx1a collaborates with Hoxa9 to acutely transform primary bone marrow cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Upregulation of Meis1 and HoxA9 in acute lymphocytic leukemias with the t(4 : 11) abnormality
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frequent co-expression of HoxA9 and Meis1 genes in infant acute lymphoblastic leukaemia with MLL rearrangement
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homeobox genes in normal and malignant cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
HOXB7 constitutively activates basic fibroblast growth factor in melanomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A serologically identified tumor antigen encoded by a homeobox gene promotes growth of ovarian epithelial cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Aberrant expression of homeobox gene HOXA7 is associated with müllerian-like differentiation of epithelial ovarian tumors and the generation of a specific autologous antibody response
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Altered HOX and WNT7A expression in human lung cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deregulated expression of homeobox-containing genes, HOXB6, B8, C8, C9, and Cdx-1, in human colon cancer cell lines
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deregulated homeobox gene expression in cancer: cause or consequence?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Compromised HOXA5 function can limit p53 expression in human breast tumours
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Basal cell carcinomas in mice overexpressing Gli2 in skin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(03)14187-6
1 reference
stated in
Europe PubMed Central
PubMed ID
12944067
retrieved
7 August 2017
PubMed ID
12944067
1 reference
stated in
Europe PubMed Central
PubMed ID
12944067
retrieved
7 August 2017
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