| P2093 | author name string | Christopher A Walsh | |
| | Jun Shen | |
| P2860 | cites work | TGF-beta signal transduction | Q22003891 |
| | Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired | Q22003954 |
| | Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly | Q22009990 |
| | Amplification and overexpression of TGIF2, a novel homeobox gene of the TALE superclass, in ovarian cancer cell lines | Q24290321 |
| | Drosophila TGIF is essential for developmentally regulated transcription in spermatogenesis. | Q47070669 |
| | Requirement for two nearly identical TGIF-related homeobox genes in Drosophila spermatogenesis | Q47072212 |
| | Epidemiology of holoprosencephaly and phenotypic characteristics of affected children: New York State, 1984-1989. | Q47636876 |
| | Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly | Q48058539 |
| | Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion | Q48197794 |
| | The human-specific Yp11.2/Xq21.3 homology block encodes a potentially functional testis-specific TGIF-like retroposon. | Q48283505 |
| | Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain. | Q48340477 |
| | Expression of a novel murine homeobox gene in the developing cerebellar external granular layer during its proliferation | Q49018217 |
| | Teratogenicity of low doses of all-trans retinoic acid in presomite mouse embryos. | Q52208261 |
| | Multiple modes of repression by the Smad transcriptional corepressor TGIF | Q73279910 |
| | Prenatal diagnosis of holoprosencephaly (HPE) in a fetus with a recombinant (18)dup(18q)inv(18)(p11.31q11.2)mat | Q73290757 |
| | Phenotypic and molecular variability of the holoprosencephalic spectrum | Q80364155 |
| | A novel homeobox protein which recognizes a TGT core and functionally interferes with a retinoid-responsive motif | Q24313957 |
| | Regulation of TG-interacting factor by transforming growth factor-beta | Q24529895 |
| | Epidermal growth factor signaling via Ras controls the Smad transcriptional co-repressor TGIF. | Q24540358 |
| | The novel E3 ubiquitin ligase Tiul1 associates with TGIF to target Smad2 for degradation | Q24563226 |
| | Physical mapping of the holoprosencephaly critical region in 18p11.3 | Q24671971 |
| | Six3 repression of Wnt signaling in the anterior neuroectoderm is essential for vertebrate forebrain development | Q24672772 |
| | Mechanisms of TGF-beta signaling from cell membrane to the nucleus | Q27860785 |
| | Primer3 on the WWW for general users and for biologist programmers | Q27861030 |
| | The interaction of the carboxyl terminus-binding protein with the Smad corepressor TGIF is disrupted by a holoprosencephaly mutation in TGIF | Q28139069 |
| | A Smad transcriptional corepressor | Q28141283 |
| | Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination | Q28145579 |
| | The Smad transcriptional corepressor TGIF recruits mSin3 | Q28188642 |
| | 5'TG3' interacting factor interacts with Sin3A and represses AR-mediated transcription | Q28202494 |
| | Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations | Q28202625 |
| | TGIF2 interacts with histone deacetylase 1 and represses transcription | Q28203909 |
| | Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly | Q28213823 |
| | Molecular diagnosis of a novel heterozygous 268C-->T (R90C) mutation in TGIF gene in a fetus with holoprosencephaly and premaxillary agenesis | Q28216639 |
| | Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function | Q28291924 |
| | Patterning of the dorsal telencephalon and cerebral cortex by a roof plate-Lhx2 pathway | Q28508424 |
| | Zic2 regulates the kinetics of neurulation | Q28509004 |
| | Meis homeoproteins directly regulate Pax6 during vertebrate lens morphogenesis | Q28589322 |
| | Sonic hedgehog, a member of a family of putative signaling molecules, is implicated in the regulation of CNS polarity | Q29616632 |
| | Transcriptional control by the TGF-beta/Smad signaling system | Q29618985 |
| | Drosophila TGIF proteins are transcriptional activators | Q30450957 |
| | Holoprosencephaly: birth data, benetic and demographic analyses of 30 families | Q30725458 |
| | Monosomy 18p and pure trisomy 18p in a family with translocation (7;18). | Q33670873 |
| | Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis | Q34255682 |
| | Homo- and heterodimers of the retinoid X receptor (RXR) activated transcription in yeast | Q34808006 |
| | Multiple hits during early embryonic development: digenic diseases and holoprosencephaly | Q34978312 |
| | Postgastrulation Smad2-deficient embryos show defects in embryo turning and anterior morphogenesis | Q36547210 |
| | Trisomy 18 and 18p- features in a case of isochromosome 18q [46,XY,i(18q)]: prenatal diagnosis and autopsy report. | Q37692731 |
| | Smad2 role in mesoderm formation, left-right patterning and craniofacial development | Q41027581 |
| | Regulation of retinoid signalling by receptor polarity and allosteric control of ligand binding | Q41436527 |
| | SMADs: mediators and regulators of TGF-beta signaling | Q41732765 |
| | Holoprosencephaly: the Maastricht experience | Q41923353 |
| | Holoprosencephaly in human embryos: Epidemiologic studies of 150 cases | Q45159232 |
| | Holoprosencephaly: epidemiologic and clinical characteristics of a California population | Q46047771 |
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | holoprosencephaly | Q1459821 |
| P304 | page(s) | 3639-3647 | |
| P577 | publication date | 2005-05-01 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | Targeted disruption of Tgif, the mouse ortholog of a human holoprosencephaly gene, does not result in holoprosencephaly in mice | |
| P478 | volume | 25 | |