Congenital abnormalities of body patterning: embryology revisited (Q35207874)

7 August 2017

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title

Congenital abnormalities of body patterning: embryology revisited (English)

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7 August 2017

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Frances R Goodman

1

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PubMed ID

12944067

7 August 2017

language of work or name

English

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publication date

1 August 2003

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7 August 2017

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7 August 2017

362

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7 August 2017

9384

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7 August 2017

651-662

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Homeobox genes and axial patterning

7 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Developmental patterning genes and their conserved functions: from model organisms to humans

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Limb malformations and the human HOX genes

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Heart development in Drosophila and vertebrates: conservation of molecular mechanisms.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Cell biology of cardiac development

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Pax6: more than meets the eye.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Vertebrate eye development as modeled in Drosophila

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

A new concept of the cellular basis of immunity

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

The 22q11 deletion syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

1 reference

7 January 2021

Developing models of DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Closing time for CATCH22

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

A common molecular basis for rearrangement disorders on chromosome 22q11

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Chromosomal microdeletions: dissecting del22q11 syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Congenital heart disease in mice deficient for the DiGeorge syndrome region

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

T-box genes: what they do and how they do it.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Tbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch development

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/del22q11 syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Mutation analysis of TBX1 in non-deleted patients with features of DGS/VCFS or isolated cardiovascular defects

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Holoprosencephaly: from Homer to Hedgehog.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Induction of the zebrafish ventral brain and floorplate requires cyclops/nodal signalling.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

The EGF-CFC protein one-eyed pinhead is essential for nodal signaling

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Functional interactions of genes mediating convergent extension, knypek and trilobite, during the partitioning of the eye primordium in zebrafish.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Transducing Hedgehog: the story so far

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Sonic hedgehog in CNS development: one signal, multiple outputs

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Inhibition of sonic hedgehog signaling in vivo results in craniofacial neural crest cell death

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Teratogen-mediated inhibition of target tissue response to Shh signaling.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Hedgehog signaling and human disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Sonic hedgehog in the nervous system: functions, modifications and mechanisms

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Effects of oncogenic mutations in Smoothened and Patched can be reversed by cyclopamine

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Zic2 regulates the kinetics of neurulation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

TGFbeta signaling in growth control, cancer, and heritable disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Smad2 role in mesoderm formation, left-right patterning and craniofacial development

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Mutations in holoprosencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

The Hedgehog and Wnt signalling pathways in cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Gli and hedgehog in cancer: tumours, embryos and stem cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Human homolog of patched, a candidate gene for the basal cell nevus syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Activating Smoothened mutations in sporadic basal-cell carcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Basal cell carcinoma possibly originates from the outer root sheath and/or the bulge region of the vellus hair follicle

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Sonic hedgehog signaling is essential for hair development

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Induction of the hair growth phase in postnatal mice by localized transient expression of Sonic hedgehog

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Basal cell carcinomas in mice overexpressing sonic hedgehog

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Mutations in SUFU predispose to medulloblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Control of neuronal precursor proliferation in the cerebellum by Sonic Hedgehog

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Medulloblastoma growth inhibition by hedgehog pathway blockade

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Hox genes in vertebrate development

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Exploring the homeobox

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Homeobox genes in embryogenesis and pathogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Developmental functions of mammalian Hox genes

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Human HOX gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Of fingers, toes and penises.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree data

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype?

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

The molecular basis of hypodactyly (Hd): a deletion in Hoxa 13 leads to arrest of digital arch formation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Mutation of HOXA13 in hand-foot-genital syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Genetic interactions of Hox genes in limb development: learning from compound mutants.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Molecular models for vertebrate limb development

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Priming the search for HOX mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Amegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Haploinsufficiency of the HOXA gene cluster, in a patient with hand-foot-genital syndrome, velopharyngeal insufficiency, and persistent patent Ductus botalli

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

HoxB4 confers definitive lymphoid-myeloid engraftment potential on embryonic stem cell and yolk sac hematopoietic progenitors.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

HOX and non-HOX homeobox genes in leukemic hematopoiesis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Cooperative activation of Hoxa and Pbx1-related genes in murine myeloid leukaemias

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Hoxa9 transforms primary bone marrow cells through specific collaboration with Meis1a but not Pbx1b

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Overexpression of HOXA10 in murine hematopoietic cells perturbs both myeloid and lymphoid differentiation and leads to acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Overexpression of HOXB3 in hematopoietic cells causes defective lymphoid development and progressive myeloproliferation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Conditional immortalization of mouse myelomonocytic, megakaryocytic and mast cell progenitors by the Hox-2.4 homeobox gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Fusion of the NUP98 gene and the homeobox gene HOXC13 in acute myeloid leukemia with t(11;12)(p15;q13).

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

CREB binding protein interacts with nucleoporin-specific FG repeats that activate transcription and mediate NUP98-HOXA9 oncogenicity

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Molecular classification of cancer: class discovery and class prediction by gene expression monitoring

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

The oncoprotein E2A-Pbx1a collaborates with Hoxa9 to acutely transform primary bone marrow cells

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Upregulation of Meis1 and HoxA9 in acute lymphocytic leukemias with the t(4 : 11) abnormality

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Frequent co-expression of HoxA9 and Meis1 genes in infant acute lymphoblastic leukaemia with MLL rearrangement

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Homeobox genes in normal and malignant cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

HOXB7 constitutively activates basic fibroblast growth factor in melanomas

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

A serologically identified tumor antigen encoded by a homeobox gene promotes growth of ovarian epithelial cells

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Altered HOX and WNT7A expression in human lung cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Deregulated expression of homeobox-containing genes, HOXB6, B8, C8, C9, and Cdx-1, in human colon cancer cell lines

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Deregulated homeobox gene expression in cancer: cause or consequence?

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Compromised HOXA5 function can limit p53 expression in human breast tumours

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

Basal cell carcinomas in mice overexpressing Gli2 in skin

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914187-6

7 January 2021

10.1016/S0140-6736(03)14187-6

Identifiers

DOI

1 reference

7 August 2017

1 reference

PubMed ID

12944067