(Q41536261)

2 October 2017

1 reference

title

Homeobox genes and disease (English)

1 reference

2 October 2017

Boncinelli E

1

1 reference

2 October 2017

publication date

1 June 1997

1 reference

Current Opinion in Genetics & Development

2 October 2017

published in

1 reference

2 October 2017

volume

7

1 reference

2 October 2017

issue

3

1 reference

2 October 2017

page(s)

331-337

1 reference

Checklist: vertebrate homeobox genes

2 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

RNA recognition and translational regulation by a homeodomain protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

RNA binding and translational suppression by bicoid

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Transcription factor hoxa-5 is taken up by cells in culture and conveyed to their nuclei.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

EMX1 homeoprotein is expressed in cell nuclei of the developing cerebral cortex and in the axons of the olfactory sensory neurons

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Homeobox genes and axial patterning

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Patterning the vertebrate neuraxis

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Early mouse development: lessons from gene targeting

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Transcription factors in disease

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Hox genes in vertebrate development

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

HOX gene activation by retinoic acid

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated families

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Disruption of the Hoxd-13 gene induces localized heterochrony leading to mice with neotenic limbs

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Synpolydactyly in mice with a targeted deficiency in the HoxD complex

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Gene transpositions in the HoxD complex reveal a hierarchy of regulatory controls.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Altered segmental identity and abnormal migration of motor neurons in mice lacking Hoxb-1.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Reprogramming Hox expression in the vertebrate hindbrain: influence of paraxial mesoderm and rhombomere transposition.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Transcription factors and head formation in vertebrates

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Nested expression domains of four homeobox genes in developing rostral brain

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Homeobox genes in vertebrate gastrulation

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Mouse Otx2 functions in the formation and patterning of rostral head.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Requirement for Lim1 in head-organizer function

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Epilepsy and brain abnormalities in mice lacking the Otx1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Otx1 function overlaps with Otx2 in development of mouse forebrain and midbrain.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Targeting epilepsy genes

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Emx1 and Emx2 show different patterns of expression during proliferation and differentiation of the developing cerebral cortex in the mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Mutation of the Emx-1 homeobox gene disrupts the corpus callosum

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Familial schizencephaly associated with EMX2 mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Homeobox genes are expressed in the retina and brain of adult goldfish

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Developmental expression of a novel murine homeobox gene (Chx10): evidence for roles in determination of the neuroretina and inner nuclear layer

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

PAX genes in human developmental anomalies

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Pax proteins and eye development

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Pax6: more than meets the eye.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Influence of PAX6 gene dosage on development: overexpression causes severe eye abnormalities.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

The function and evolution of Msx genes: pointers and paradoxes

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Rostral optic tectum acquires caudal characteristics following ectopic engrailed expression

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Coordinate regulation of HOX genes in human hematopoietic cells

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

Inactivation of the zebrafish homologue of Chx10 by antisense oligonucleotides causes eye malformations similar to the ocular retardation phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980146-3

7 January 2021

10.1016/S0959-437X(97)80146-3

Identifiers

DOI

1 reference

2 October 2017

1 reference