A citation-based method for searching scientific literature

Shannon E Powers, Kenichiro Taniguchi, Weiwei Yen, Tiffany A Melhuish, Jun Shen, Christopher A Walsh, Ann E Sutherland, David Wotton. Development 2010
Times Cited: 49







List of co-cited articles
305 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
304
38

A Smad transcriptional corepressor.
D Wotton, R S Lo, S Lee, J Massagué. Cell 1999
453
36

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
61
34

Multiple modes of repression by the Smad transcriptional corepressor TGIF.
D Wotton, R S Lo, L A Swaby, J Massagué. J Biol Chem 1999
157
32


TGIF2 interacts with histone deacetylase 1 and represses transcription.
T A Melhuish, C M Gallo, D Wotton. J Biol Chem 2001
100
28

TGIF inhibits retinoid signaling.
Laurent Bartholin, Shannon E Powers, Tiffany A Melhuish, Samuel Lasse, Michael Weinstein, David Wotton. Mol Cell Biol 2006
91
28


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
39
33



The Smad transcriptional corepressor TGIF recruits mSin3.
D Wotton, P S Knoepfler, C D Laherty, R N Eisenman, J Massagué. Cell Growth Differ 2001
103
22

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
57
22

Expression and functional analysis of Tgif during mouse midline development.
Jiu-Zhen Jin, Shi Gu, Patrick McKinney, Jixiang Ding. Dev Dyn 2006
29
34

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
84
20

Smad transcription factors.
Joan Massagué, Joan Seoane, David Wotton. Genes Dev 2005
20

The novel E3 ubiquitin ligase Tiul1 associates with TGIF to target Smad2 for degradation.
Su Ryeon Seo, François Lallemand, Nathalie Ferrand, Marcia Pessah, Sébastien L'Hoste, Jacques Camonis, Azeddine Atfi. EMBO J 2004
125
20

The Tgif2 gene contains a retained intron within the coding sequence.
Tiffany A Melhuish, David Wotton. BMC Mol Biol 2006
26
34

The molecular genetics of holoprosencephaly.
Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
160
16

Drosophila TGIF proteins are transcriptional activators.
Cathy A Hyman, Laurent Bartholin, Stuart J Newfeld, David Wotton. Mol Cell Biol 2003
33
24

Tgif1 represses apolipoprotein gene expression in liver.
Tiffany A Melhuish, David D Chung, Glen A Bjerke, David Wotton. J Cell Biochem 2010
17
41



Nuclear retention of the tumor suppressor cPML by the homeodomain protein TGIF restricts TGF-beta signaling.
Su Ryeon Seo, Nathalie Ferrand, Nourdine Faresse, Céline Prunier, Lucile Abécassis, Marcia Pessah, Marie-Francoise Bourgeade, Azeddine Atfi. Mol Cell 2006
59
14

TGIF governs a feed-forward network that empowers Wnt signaling to drive mammary tumorigenesis.
Ming-Zhu Zhang, Olivier Ferrigno, Zhe Wang, Mutsuko Ohnishi, Céline Prunier, Laurence Levy, Mohammed Razzaque, Williams C Horne, Damian Romero, Guri Tzivion,[...]. Cancer Cell 2015
41
17

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
12

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
859
12

Smad transcriptional corepressors in TGF beta family signaling.
D Wotton, J Massagué. Curr Top Microbiol Immunol 2001
91
12

Preparation of PCR-quality mouse genomic DNA with hot sodium hydroxide and tris (HotSHOT).
G E Truett, P Heeger, R L Mynatt, A A Truett, J A Walker, M L Warman. Biotechniques 2000
836
12

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
34
17

Mouse Shh is required for prechordal plate maintenance during brain and craniofacial morphogenesis.
Kazushi Aoto, Yayoi Shikata, Hajime Imai, Daisuke Matsumaru, Tomoyuki Tokunaga, Seiji Shioda, Gen Yamada, Jun Motoyama. Dev Biol 2009
63
12



Premature senescence and increased TGFβ signaling in the absence of Tgif1.
Brad J Zerlanko, Laurent Bartholin, Tiffany A Melhuish, David Wotton. PLoS One 2012
21
28

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
68
12


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
70
10

Analysis of genotype-phenotype correlations in human holoprosencephaly.
Benjamin D Solomon, Sandra Mercier, Jorge I Vélez, Daniel E Pineda-Alvarez, Adrian Wyllie, Nan Zhou, Christèle Dubourg, Veronique David, Sylvie Odent, Erich Roessler,[...]. Am J Med Genet C Semin Med Genet 2010
108
10


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
267
10

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
265
10

Pathogenesis of holoprosencephaly.
Xin Geng, Guillermo Oliver. J Clin Invest 2009
61
10

Efficient gene modulation in mouse epiblast using a Sox2Cre transgenic mouse strain.
Shigemi Hayashi, Paula Lewis, Larysa Pevny, Andrew P McMahon. Mech Dev 2002
308
10

Genetics of ventral forebrain development and holoprosencephaly.
M Muenke, P A Beachy. Curr Opin Genet Dev 2000
203
10

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
104
10

TG-interacting factor 1 acts as a transcriptional repressor of sterol O-acyltransferase 2.
Camilla Pramfalk, Tiffany A Melhuish, David Wotton, Zhao-Yan Jiang, Mats Eriksson, Paolo Parini. J Lipid Res 2014
10
50

Tgif1 Counterbalances the Activity of Core Pluripotency Factors in Mouse Embryonic Stem Cells.
Bum-Kyu Lee, Wenwen Shen, Jiwoon Lee, Catherine Rhee, Haewon Chung, Kun-Yong Kim, In-Hyun Park, Jonghwan Kim. Cell Rep 2015
20
25

Tgif1 and Tgif2 Repress Expression of the RabGAP Evi5l.
Anoush E Anderson, Kenichiro Taniguchi, Yi Hao, Tiffany A Melhuish, Anant Shah, Stephen D Turner, Ann E Sutherland, David Wotton. Mol Cell Biol 2017
11
45

TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and Phenotype.
A A Keaton, B D Solomon, E F Kauvar, K B El-Jaick, A L Gropman, Y Zafer, J M Meck, S J Bale, D K Grange, B R Haddad,[...]. Mol Syndromol 2010
13
30



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.