(Q46989159)

27 December 2017

title

TGIF, a gene associated with human brain defects, regulates neuronal development (English)

1 reference

27 December 2017

author name string

Jessica L Knepper

series ordinal

1

1 reference

27 December 2017

Alison C James

series ordinal

2

1 reference

27 December 2017

Jeffrey E Ming

series ordinal

3

1 reference

27 December 2017

publication date

1 June 2006

1 reference

27 December 2017

published in

Developmental Dynamics

1 reference

27 December 2017

volume

235

1 reference

27 December 2017

issue

6

1 reference

27 December 2017

page(s)

1482-1490

1 reference

27 December 2017

Type I bone morphogenetic protein receptors are expressed on cerebellar granular neurons and a constitutively active form of the type IA receptor induces cerebellar abnormalities.

cites work

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Drosophila TGIF is essential for developmentally regulated transcription in spermatogenesis.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Msx1 is required for dorsal diencephalon patterning

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

A novel homeobox protein which recognizes a TGT core and functionally interferes with a retinoid-responsive motif

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Analysis of TALE superclass homeobox genes (MEIS, PBC, KNOX, Iroquois, TGIF) reveals a novel domain conserved between plants and animals

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Specification of neuronal fates in the ventral neural tube

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Patterning cell types in the dorsal spinal cord: what the mouse mutants say.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Molecular diagnosis of a novel heterozygous 268C-->T (R90C) mutation in TGIF gene in a fetus with holoprosencephaly and premaxillary agenesis

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Teratogenesis of holoprosencephaly

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Holoprosencephaly: epidemiologic and clinical characteristics of a California population

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Pax6 controls progenitor cell identity and neuronal fate in response to graded Shh signaling

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Ectopic bone morphogenetic proteins 5 and 4 in the chicken forebrain lead to cyclopia and holoprosencephaly

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Overexpression of ptc1 inhibits induction of Shh target genes and prevents normal patterning in the neural tube

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Crossinhibitory activities of Ngn1 and Math1 allow specification of distinct dorsal interneurons

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Vax1, a novel homeobox-containing gene, directs development of the basal forebrain and visual system

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

A series of normal stages in the development of the chick embryo

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Amplification and overexpression of TGIF2, a novel homeobox gene of the TALE superclass, in ovarian cancer cell lines

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Neuronal specification in the spinal cord: inductive signals and transcriptional codes

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genes

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

The T/ebp null mouse: thyroid-specific enhancer-binding protein is essential for the organogenesis of the thyroid, lung, ventral forebrain, and pituitary

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Retinoic acid embryopathy

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Distinct activities of Msx1 and Msx3 in dorsal neural tube development.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

TGFbeta signaling in growth control, cancer, and heritable disorders

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Holoprosencephaly in human embryos: Epidemiologic studies of 150 cases

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

The interaction of the carboxyl terminus-binding protein with the Smad corepressor TGIF is disrupted by a holoprosencephaly mutation in TGIF

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

TGIF2 interacts with histone deacetylase 1 and represses transcription

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Multiple hits during early embryonic development: digenic diseases and holoprosencephaly

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Genetics of ventral forebrain development and holoprosencephaly

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

A Requirement for Retinoic Acid-Mediated Transcriptional Activation in Ventral Neural Patterning and Motor Neuron Specification

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Sequential actions of BMP receptors control neural precursor cell production and fate

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

The generation and diversification of spinal motor neurons: signals and responses

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephaly

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Isolation and characterization of the chicken homeodomain protein AKR.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Targeted disruption of Tgif, the mouse ortholog of a human holoprosencephaly gene, does not result in holoprosencephaly in mice

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Teratogenicity of low doses of all-trans retinoic acid in presomite mouse embryos.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Regulation of cell proliferation by Smad proteins

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Requirement for two nearly identical TGIF-related homeobox genes in Drosophila spermatogenesis

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

A Smad transcriptional corepressor

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Multiple modes of repression by the Smad transcriptional corepressor TGIF

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

https://api.crossref.org/works/10.1002%2FDVDY.20725

1 reference

7 January 2021

Smoothened mutants reveal redundant roles for Shh and Ihh signaling including regulation of L/R symmetry by the mouse node

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20725

7 January 2021

Identifiers

DOI

10.1002/DVDY.20725

1 reference

27 December 2017

PubMed ID

16534781

1 reference

27 December 2017