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Akira Ishiguro et al.
SCIENTIFIC REPORTS (2018)
Genetic and Molecular Analyses indicate independent effects of TGIFs on Nodal and Gli3 in neural tube patterning
Kenichiro Taniguchi et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2017)
Tgif1 and Tgif2 Repress Expression of the RabGAP Evi5l
Anoush E. Anderson et al.
MOLECULAR AND CELLULAR BIOLOGY (2017)
Homeodomain proteins: an update
Thomas R. Buerglin et al.
CHROMOSOMA (2016)
Zic2 mutation causes holoprosencephaly via disruption of NODAL signalling
Rob Houtmeyers et al.
HUMAN MOLECULAR GENETICS (2016)
Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway
Christele Dubourg et al.
HUMAN MUTATION (2016)
Analysis of protein-coding genetic variation in 60,706 humans
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Tgif1 and Tgif2 Regulate Axial Patterning in Mouse
Tiffany A. Melhuish et al.
PLOS ONE (2016)
Transcriptional Control by the SMADs
Caroline S. Hill
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2016)
TGIF Governs a Feed-Forward Network that Empowers Wnt Signaling to Drive Mammary Tumorigenesis
Ming-Zhu Zhang et al.
CANCER CELL (2015)
Tgif1 Counterbalances the Activity of Core Pluripotency Factors in Mouse Embryonic Stem Cells
Bum-Kyu Lee et al.
CELL REPORTS (2015)
TGIF1 is a negative regulator of MLL-rearranged acute myeloid leukemia
A. Willer et al.
LEUKEMIA (2015)
Nuclear Receptors, RXR, and the Big Bang
Ronald M. Evans et al.
CELL (2014)
被撤回的出版物: miR-34a blocks osteoporosis and bone metastasis by inhibiting osteoclastogenesis and Tgif2 (Retracted article. See vol. 582, pg. 134, 2020)
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NATURE (2014)
Otitis media in the Tgif knockout mouse implicates TGF signalling in chronic middle ear inflammatory disease
Hilda Tateossian et al.
HUMAN MOLECULAR GENETICS (2013)
Utilizing prospective sequence analysis of SHH, ZIC2, SIX3 and TGIF in holoprosencephaly probands to describe the parameters limiting the observed frequency of mutant gene x gene interactions
Erich Roessler et al.
MOLECULAR GENETICS AND METABOLISM (2012)
Premature Senescence and Increased TGFβ Signaling in the Absence of Tgif1
Brad J. Zerlanko et al.
PLOS ONE (2012)
Loss of Tgif Function Causes Holoprosencephaly by Disrupting the Shh Signaling Pathway
Kenichiro Taniguchi et al.
PLOS GENETICS (2012)
New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases
Sandra Mercier et al.
JOURNAL OF MEDICAL GENETICS (2011)
The Molecular Genetics of Holoprosencephaly
Erich Roessler et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2010)
Tgif1 and Tgif2 regulate Nodal signaling and are required for gastrulation
Shannon E. Powers et al.
DEVELOPMENT (2010)
Tgif1 Represses Apolipoprotein Gene Expression in Liver
Tiffany A. Melhuish et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2010)
The primary cilium: a signalling centre during vertebrate development
Sarah C. Goetz et al.
NATURE REVIEWS GENETICS (2010)
TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and Phenotype
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MOLECULAR SYNDROMOLOGY (2010)
Mouse Shh is required for prechordal plate maintenance during brain and craniofacial morphogenesis
Kazushi Aoto et al.
DEVELOPMENTAL BIOLOGY (2009)
Pathogenesis of holoprosencephaly
Xin Geng et al.
JOURNAL OF CLINICAL INVESTIGATION (2009)
Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly
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AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Genomic structure, alternative splicing and expression of TG-interacting factor, in human myeloid leukemia blasts and cell lines
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BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS (2008)
Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance systems:: Searching for population variations
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BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2008)
The Gata5 target, TGIF2, defines the pancreatic region by modulating BMP signals within the endoderm
Francesca M. Spagnoli et al.
DEVELOPMENT (2008)
Maternal Tgif is required for vascularization of the embryonic placenta
Laurent Bartholin et al.
DEVELOPMENTAL BIOLOGY (2008)
Haploinsufficiency of Six3 fails to activate sonic hedgehog expression in the ventral forebrain and causes holoprosencephaly
Xin Geng et al.
DEVELOPMENTAL CELL (2008)
Genome-wide identification of Smad/Foxh1 targets reveals a role for Foxh1 in retinoic acid regulation and forebrain development
Cristoforo Silvestri et al.
DEVELOPMENTAL CELL (2008)
Maternal Tgif1 Regulates nodal Gene Expression in Xenopus
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DEVELOPMENTAL DYNAMICS (2008)
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NATURE GENETICS (2008)
Zebrafish model of holoprosencephaly demonstrates a key role for TGIF in regulating retinoic acid metabolism
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HUMAN MOLECULAR GENETICS (2008)
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JOURNAL OF MOLECULAR EVOLUTION (2007)
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FASEB JOURNAL (2007)
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MOLECULAR GENETICS AND METABOLISM (2007)
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INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2007)
Intragenic deletion of Tgif causes defects in brain development
Chenzhong Kuang et al.
HUMAN MOLECULAR GENETICS (2006)
Morphogen to mitogen: the multiple roles of hedgehog signalling in vertebrate neural development
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NATURE REVIEWS NEUROSCIENCE (2006)
Nuclear retention of the tumor suppressor cPML by the homeodomain protein TGIF restricts TGF-β signaling
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MOLECULAR CELL (2006)
FGF signalling generates ventral telencephalic cells independently of SHH
Grigoriy Gutin et al.
DEVELOPMENT (2006)
Embryonic fibroblasts from mice lacking Tgif were defective in cell cycling
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MOLECULAR AND CELLULAR BIOLOGY (2006)
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DEVELOPMENT (2006)
TGIF inhibits retinoid signaling
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MOLECULAR AND CELLULAR BIOLOGY (2006)
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DEVELOPMENTAL DYNAMICS (2006)
The Tgif2 gene contains a retained intron within the coding sequence
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BMC MOLECULAR BIOLOGY (2006)
Targeted disruption of Tgif, the mouse ortholog of a human holoprosencephaly gene, does not result in holoprosencephaly in mice
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MOLECULAR AND CELLULAR BIOLOGY (2005)
The novel E3 ubiquitin ligase Tiul1 associates with TGIF to target Smad2 for degradation
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EMBO JOURNAL (2004)
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MOLECULAR AND CELLULAR BIOLOGY (2003)
Efficient gene modulation in mouse epiblast using a Sox2Cre transgenic mouse strain
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Mouse GLI3 regulates Fgf8 expression and apoptosis in the developing neural tube, face, and limb bud
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A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects
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HUMAN GENETICS (2002)
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MOLECULAR CELL (2002)
Dickkopf1 is required for embryonic head induction and limb morphogenesis in the mouse
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DEVELOPMENTAL CELL (2001)
TGIF2 interacts with histone deacetylase I and represses transcription
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JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Physical and functional interactions between Zic and Gli proteins
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JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
The interaction of the carboxyl terminus-binding protein with the Smad corepressor TGIF is disrupted by a holoprosencephaly mutation in TGIF
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JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Amplification and overexpression of TGIF2, a novel homeobox gene of the TALE superclass, in ovarian cancer cell lines
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BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2000)
Three-amino acid extension loop homeodomain proteins Meis2 and TGIF differentially regulate transcription
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JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination
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NATURE GENETICS (2000)
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DEVELOPMENTAL BIOLOGY (2000)
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