Jiu-Zhen Jin, Shi Gu, Patrick McKinney, Jixiang Ding. Dev Dyn 2006
Times Cited: 29
Times Cited: 29
Times Cited
Times Co-cited
Similarity
TGIF inhibits retinoid signaling.
Laurent Bartholin, Shannon E Powers, Tiffany A Melhuish, Samuel Lasse, Michael Weinstein, David Wotton. Mol Cell Biol 2006
Laurent Bartholin, Shannon E Powers, Tiffany A Melhuish, Samuel Lasse, Michael Weinstein, David Wotton. Mol Cell Biol 2006
82
Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination.
K W Gripp, D Wotton, M C Edwards, E Roessler, L Ades, P Meinecke, A Richieri-Costa, E H Zackai, J Massagué, M Muenke,[...]. Nat Genet 2000
K W Gripp, D Wotton, M C Edwards, E Roessler, L Ades, P Meinecke, A Richieri-Costa, E H Zackai, J Massagué, M Muenke,[...]. Nat Genet 2000
79
Targeted disruption of Tgif, the mouse ortholog of a human holoprosencephaly gene, does not result in holoprosencephaly in mice.
Jun Shen, Christopher A Walsh. Mol Cell Biol 2005
Jun Shen, Christopher A Walsh. Mol Cell Biol 2005
75
A novel homeobox protein which recognizes a TGT core and functionally interferes with a retinoid-responsive motif.
E Bertolino, B Reimund, D Wildt-Perinic, R G Clerc. J Biol Chem 1995
E Bertolino, B Reimund, D Wildt-Perinic, R G Clerc. J Biol Chem 1995
72
Embryonic fibroblasts from mice lacking Tgif were defective in cell cycling.
Lynn Mar, Pamela A Hoodless. Mol Cell Biol 2006
Lynn Mar, Pamela A Hoodless. Mol Cell Biol 2006
58
Functional analysis of mutations in TGIF associated with holoprosencephaly.
Kenia B El-Jaick, Shannon E Powers, Laurent Bartholin, Kenneth R Myers, Jin Hahn, Ieda M Orioli, Maia Ouspenskaia, Felicitas Lacbawan, Erich Roessler, David Wotton,[...]. Mol Genet Metab 2007
Kenia B El-Jaick, Shannon E Powers, Laurent Bartholin, Kenneth R Myers, Jin Hahn, Ieda M Orioli, Maia Ouspenskaia, Felicitas Lacbawan, Erich Roessler, David Wotton,[...]. Mol Genet Metab 2007
55
Multiple modes of repression by the Smad transcriptional corepressor TGIF.
D Wotton, R S Lo, L A Swaby, J Massagué. J Biol Chem 1999
D Wotton, R S Lo, L A Swaby, J Massagué. J Biol Chem 1999
51
TGIF2 interacts with histone deacetylase 1 and represses transcription.
T A Melhuish, C M Gallo, D Wotton. J Biol Chem 2001
T A Melhuish, C M Gallo, D Wotton. J Biol Chem 2001
48
The interaction of the carboxyl terminus-binding protein with the Smad corepressor TGIF is disrupted by a holoprosencephaly mutation in TGIF.
T A Melhuish, D Wotton. J Biol Chem 2000
T A Melhuish, D Wotton. J Biol Chem 2000
44
Intragenic deletion of Tgif causes defectsin brain development.
Chenzhong Kuang, Yan Xiao, Ling Yang, Qian Chen, Zhenzhen Wang, Simon J Conway, Yan Chen. Hum Mol Genet 2006
Chenzhong Kuang, Yan Xiao, Ling Yang, Qian Chen, Zhenzhen Wang, Simon J Conway, Yan Chen. Hum Mol Genet 2006
44
The Smad transcriptional corepressor TGIF recruits mSin3.
D Wotton, P S Knoepfler, C D Laherty, R N Eisenman, J Massagué. Cell Growth Differ 2001
D Wotton, P S Knoepfler, C D Laherty, R N Eisenman, J Massagué. Cell Growth Differ 2001
37
The Tgif2 gene contains a retained intron within the coding sequence.
Tiffany A Melhuish, David Wotton. BMC Mol Biol 2006
Tiffany A Melhuish, David Wotton. BMC Mol Biol 2006
42
Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function.
C Chiang, Y Litingtung, E Lee, K E Young, J L Corden, H Westphal, P A Beachy. Nature 1996
C Chiang, Y Litingtung, E Lee, K E Young, J L Corden, H Westphal, P A Beachy. Nature 1996
34
Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, S W Scherer, L C Tsui, M Muenke. Nat Genet 1996
E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, S W Scherer, L C Tsui, M Muenke. Nat Genet 1996
34
Drosophila TGIF proteins are transcriptional activators.
Cathy A Hyman, Laurent Bartholin, Stuart J Newfeld, David Wotton. Mol Cell Biol 2003
Cathy A Hyman, Laurent Bartholin, Stuart J Newfeld, David Wotton. Mol Cell Biol 2003
34
Tgif1 and Tgif2 regulate Nodal signaling and are required for gastrulation.
Shannon E Powers, Kenichiro Taniguchi, Weiwei Yen, Tiffany A Melhuish, Jun Shen, Christopher A Walsh, Ann E Sutherland, David Wotton. Development 2010
Shannon E Powers, Kenichiro Taniguchi, Weiwei Yen, Tiffany A Melhuish, Jun Shen, Christopher A Walsh, Ann E Sutherland, David Wotton. Development 2010
34
Genetics of ventral forebrain development and holoprosencephaly.
M Muenke, P A Beachy. Curr Opin Genet Dev 2000
M Muenke, P A Beachy. Curr Opin Genet Dev 2000
31
Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations.
Céline Aguilella, Christèle Dubourg, Jocelyne Attia-Sobol, Jacqueline Vigneron, Martine Blayau, Laurent Pasquier, Leila Lazaro, Sylvie Odent, Véronique David. Hum Genet 2003
Céline Aguilella, Christèle Dubourg, Jocelyne Attia-Sobol, Jacqueline Vigneron, Martine Blayau, Laurent Pasquier, Leila Lazaro, Sylvie Odent, Véronique David. Hum Genet 2003
27
The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
L Nanni, J E Ming, M Bocian, K Steinhaus, D W Bianchi, C Die-Smulders, A Giannotti, K Imaizumi, K L Jones, M D Campo,[...]. Hum Mol Genet 1999
L Nanni, J E Ming, M Bocian, K Steinhaus, D W Bianchi, C Die-Smulders, A Giannotti, K Imaizumi, K L Jones, M D Campo,[...]. Hum Mol Genet 1999
27
Multiple hits during early embryonic development: digenic diseases and holoprosencephaly.
Jeffrey E Ming, Maximilian Muenke. Am J Hum Genet 2002
Jeffrey E Ming, Maximilian Muenke. Am J Hum Genet 2002
27
Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired.
S A Brown, D Warburton, L Y Brown, C Y Yu, E R Roeder, S Stengel-Rutkowski, R C Hennekam, M Muenke. Nat Genet 1998
S A Brown, D Warburton, L Y Brown, C Y Yu, E R Roeder, S Stengel-Rutkowski, R C Hennekam, M Muenke. Nat Genet 1998
27
Amplification and overexpression of TGIF2, a novel homeobox gene of the TALE superclass, in ovarian cancer cell lines.
I Imoto, A Pimkhaokham, T Watanabe, F Saito-Ohara, E Soeda, J Inazawa. Biochem Biophys Res Commun 2000
I Imoto, A Pimkhaokham, T Watanabe, F Saito-Ohara, E Soeda, J Inazawa. Biochem Biophys Res Commun 2000
27
Loss of Tgif function causes holoprosencephaly by disrupting the SHH signaling pathway.
Kenichiro Taniguchi, Anoush E Anderson, Ann E Sutherland, David Wotton. PLoS Genet 2012
Kenichiro Taniguchi, Anoush E Anderson, Ann E Sutherland, David Wotton. PLoS Genet 2012
27
Coordinate regulation and synergistic actions of BMP4, SHH and FGF8 in the rostral prosencephalon regulate morphogenesis of the telencephalic and optic vesicles.
Y Ohkubo, C Chiang, J L R Rubenstein. Neuroscience 2002
Y Ohkubo, C Chiang, J L R Rubenstein. Neuroscience 2002
24
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
D E Wallis, E Roessler, U Hehr, L Nanni, T Wiltshire, A Richieri-Costa, G Gillessen-Kaesbach, E H Zackai, J Rommens, M Muenke. Nat Genet 1999
D E Wallis, E Roessler, U Hehr, L Nanni, T Wiltshire, A Richieri-Costa, G Gillessen-Kaesbach, E H Zackai, J Rommens, M Muenke. Nat Genet 1999
24
Physical mapping of the holoprosencephaly critical region in 18p11.3.
J Overhauser, H F Mitchell, E H Zackai, D B Tick, K Rojas, M Muenke. Am J Hum Genet 1995
J Overhauser, H F Mitchell, E H Zackai, D B Tick, K Rojas, M Muenke. Am J Hum Genet 1995
24
Smad2 role in mesoderm formation, left-right patterning and craniofacial development.
M Nomura, E Li. Nature 1998
M Nomura, E Li. Nature 1998
24
A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects.
June M de la Cruz, Richard N Bamford, Rebecca D Burdine, Erich Roessler, A James Barkovich, Dian Donnai, Alexander F Schier, Maximilian Muenke. Hum Genet 2002
June M de la Cruz, Richard N Bamford, Rebecca D Burdine, Erich Roessler, A James Barkovich, Dian Donnai, Alexander F Schier, Maximilian Muenke. Hum Genet 2002
24
Teratogenicity of low doses of all-trans retinoic acid in presomite mouse embryos.
K K Sulik, D B Dehart, J M Rogers, N Chernoff. Teratology 1995
K K Sulik, D B Dehart, J M Rogers, N Chernoff. Teratology 1995
24
Zebrafish model of holoprosencephaly demonstrates a key role for TGIF in regulating retinoic acid metabolism.
Patricia A Gongal, Andrew J Waskiewicz. Hum Mol Genet 2008
Patricia A Gongal, Andrew J Waskiewicz. Hum Mol Genet 2008
24
Maternal Tgif is required for vascularization of the embryonic placenta.
Laurent Bartholin, Tiffany A Melhuish, Shannon E Powers, Sophie Goddard-Léon, Isabelle Treilleux, Ann E Sutherland, David Wotton. Dev Biol 2008
Laurent Bartholin, Tiffany A Melhuish, Shannon E Powers, Sophie Goddard-Léon, Isabelle Treilleux, Ann E Sutherland, David Wotton. Dev Biol 2008
24
Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotype.
C Bendavid, B R Haddad, A Griffin, M Huizing, C Dubourg, I Gicquel, L R Cavalli, L Pasquier, A L Shanske, R Long,[...]. J Med Genet 2006
C Bendavid, B R Haddad, A Griffin, M Huizing, C Dubourg, I Gicquel, L R Cavalli, L Pasquier, A L Shanske, R Long,[...]. J Med Genet 2006
20
Three-amino acid extension loop homeodomain proteins Meis2 and TGIF differentially regulate transcription.
Y Yang, C K Hwang, U M D'Souza, S H Lee, E Junn, M M Mouradian. J Biol Chem 2000
Y Yang, C K Hwang, U M D'Souza, S H Lee, E Junn, M M Mouradian. J Biol Chem 2000
20
Molecular diagnosis of a novel heterozygous 268C-->T (R90C) mutation in TGIF gene in a fetus with holoprosencephaly and premaxillary agenesis.
Chih-Ping Chen, Schu-Rern Chern, Shin-Hua Du, Wayseen Wang. Prenat Diagn 2002
Chih-Ping Chen, Schu-Rern Chern, Shin-Hua Du, Wayseen Wang. Prenat Diagn 2002
21
Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly.
Jeffrey E Ming, Michelle E Kaupas, Erich Roessler, Han G Brunner, Mahin Golabi, Mustafa Tekin, Robert F Stratton, Eva Sujansky, Sherri J Bale, Maximilian Muenke. Hum Genet 2002
Jeffrey E Ming, Michelle E Kaupas, Erich Roessler, Han G Brunner, Mahin Golabi, Mustafa Tekin, Robert F Stratton, Eva Sujansky, Sherri J Bale, Maximilian Muenke. Hum Genet 2002
20
Molecular evaluation of foetuses with holoprosencephaly shows high incidence of microdeletions in the HPE genes.
Claude Bendavid, Christèle Dubourg, Isabelle Gicquel, Laurent Pasquier, Pascale Saugier-Veber, Marie-Renée Durou, Sylvie Jaillard, Thierry Frébourg, Bassem R Haddad, Catherine Henry,[...]. Hum Genet 2006
Claude Bendavid, Christèle Dubourg, Isabelle Gicquel, Laurent Pasquier, Pascale Saugier-Veber, Marie-Renée Durou, Sylvie Jaillard, Thierry Frébourg, Bassem R Haddad, Catherine Henry,[...]. Hum Genet 2006
20
Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.
Erich Roessler, Yang-Zhu Du, Jose L Mullor, Esther Casas, William P Allen, Gabriele Gillessen-Kaesbach, Elizabeth R Roeder, Jeffrey E Ming, Ariel Ruiz i Altaba, Maximilian Muenke. Proc Natl Acad Sci U S A 2003
Erich Roessler, Yang-Zhu Du, Jose L Mullor, Esther Casas, William P Allen, Gabriele Gillessen-Kaesbach, Elizabeth R Roeder, Jeffrey E Ming, Ariel Ruiz i Altaba, Maximilian Muenke. Proc Natl Acad Sci U S A 2003
20
Analysis of TALE superclass homeobox genes (MEIS, PBC, KNOX, Iroquois, TGIF) reveals a novel domain conserved between plants and animals.
T R Bürglin. Nucleic Acids Res 1997
T R Bürglin. Nucleic Acids Res 1997
20
20
Dorsoventral patterning of the telencephalon is disrupted in the mouse mutant extra-toes(J).
S Tole, C W Ragsdale, E A Grove. Dev Biol 2000
S Tole, C W Ragsdale, E A Grove. Dev Biol 2000
20
Dose-dependent functions of Fgf8 in regulating telencephalic patterning centers.
Elaine E Storm, Sonia Garel, Ugo Borello, Jean M Hebert, Salvador Martinez, Susan K McConnell, Gail R Martin, John L R Rubenstein. Development 2006
Elaine E Storm, Sonia Garel, Ugo Borello, Jean M Hebert, Salvador Martinez, Susan K McConnell, Gail R Martin, John L R Rubenstein. Development 2006
20
Haploinsufficiency of Six3 fails to activate Sonic hedgehog expression in the ventral forebrain and causes holoprosencephaly.
Xin Geng, Christina Speirs, Oleg Lagutin, Adi Inbal, Wei Liu, Lilianna Solnica-Krezel, Yongsu Jeong, Douglas J Epstein, Guillermo Oliver. Dev Cell 2008
Xin Geng, Christina Speirs, Oleg Lagutin, Adi Inbal, Wei Liu, Lilianna Solnica-Krezel, Yongsu Jeong, Douglas J Epstein, Guillermo Oliver. Dev Cell 2008
20
Zic2-associated holoprosencephaly is caused by a transient defect in the organizer region during gastrulation.
Nicholas Warr, Nicola Powles-Glover, Anna Chappell, Joan Robson, Dominic Norris, Ruth M Arkell. Hum Mol Genet 2008
Nicholas Warr, Nicola Powles-Glover, Anna Chappell, Joan Robson, Dominic Norris, Ruth M Arkell. Hum Mol Genet 2008
20
Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly.
Erich Roessler, Maia V Ouspenskaia, Jayaprakash D Karkera, Jorge I Vélez, Amy Kantipong, Felicitas Lacbawan, Peter Bowers, John W Belmont, Jeffrey A Towbin, Elizabeth Goldmuntz,[...]. Am J Hum Genet 2008
Erich Roessler, Maia V Ouspenskaia, Jayaprakash D Karkera, Jorge I Vélez, Amy Kantipong, Felicitas Lacbawan, Peter Bowers, John W Belmont, Jeffrey A Towbin, Elizabeth Goldmuntz,[...]. Am J Hum Genet 2008
20
Tgif1 represses apolipoprotein gene expression in liver.
Tiffany A Melhuish, David D Chung, Glen A Bjerke, David Wotton. J Cell Biochem 2010
Tiffany A Melhuish, David D Chung, Glen A Bjerke, David Wotton. J Cell Biochem 2010
35
Expression of a novel murine homeobox gene in the developing cerebellar external granular layer during its proliferation.
E Bertolino, S Wildt, G Richards, R G Clerc. Dev Dyn 1996
E Bertolino, S Wildt, G Richards, R G Clerc. Dev Dyn 1996
17
Epidermal growth factor signaling via Ras controls the Smad transcriptional co-repressor TGIF.
R S Lo, D Wotton, J Massagué. EMBO J 2001
R S Lo, D Wotton, J Massagué. EMBO J 2001
17
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.