A citation-based method for searching scientific literature

Lynn Mar, Pamela A Hoodless. Mol Cell Biol 2006
Times Cited: 35







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



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
91
77

A Smad transcriptional corepressor.
D Wotton, R S Lo, S Lee, J Massagué. Cell 1999
453
71


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
60


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
54

Expression and functional analysis of Tgif during mouse midline development.
Jiu-Zhen Jin, Shi Gu, Patrick McKinney, Jixiang Ding. Dev Dyn 2006
29
58

TGIF2 interacts with histone deacetylase 1 and represses transcription.
T A Melhuish, C M Gallo, D Wotton. J Biol Chem 2001
100
45

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
42


Smad transcription factors.
Joan Massagué, Joan Seoane, David Wotton. Genes Dev 2005
37

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
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
49
34

The Tgif2 gene contains a retained intron within the coding sequence.
Tiffany A Melhuish, David Wotton. BMC Mol Biol 2006
26
42


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
31

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
28

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
26

Drosophila TGIF proteins are transcriptional activators.
Cathy A Hyman, Laurent Bartholin, Stuart J Newfeld, David Wotton. Mol Cell Biol 2003
33
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
61
25

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
81
22

Genetics of ventral forebrain development and holoprosencephaly.
M Muenke, P A Beachy. Curr Opin Genet Dev 2000
203
22

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
22

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
22

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
370
20

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
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
68
20

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
161
17

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
39
17

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
17

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
17


Mutations in holoprosencephaly.
D Wallis, M Muenke. Hum Mutat 2000
138
17



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
17

Tgif1 represses apolipoprotein gene expression in liver.
Tiffany A Melhuish, David D Chung, Glen A Bjerke, David Wotton. J Cell Biochem 2010
17
35

Expression pattern of TG-interacting factor 2 during mouse development.
Lei Jin, Yunhua Zhou, Chenzhong Kuang, Lin Lin, Yan Chen. Gene Expr Patterns 2005
14
35

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
238
14

c-Jun interacts with the corepressor TG-interacting factor (TGIF) to suppress Smad2 transcriptional activity.
M Pessah, C Prunier, J Marais, N Ferrand, A Mazars, F Lallemand, J M Gauthier, A Atfi. Proc Natl Acad Sci U S A 2001
73
14


Mouse GLI3 regulates Fgf8 expression and apoptosis in the developing neural tube, face, and limb bud.
Kazushi Aoto, Tamiko Nishimura, Kazuhiro Eto, Jun Motoyama. Dev Biol 2002
160
14

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
110
14

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
14

Negative regulation of TGF-beta receptor/Smad signal transduction.
Susumu Itoh, Peter ten Dijke. Curr Opin Cell Biol 2007
302
14


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
14




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.