W A Paznekas, N Zhang, T Gridley, E W Jabs. Biochem Biophys Res Commun 1997
Times Cited: 11
Times Cited: 11
Times Cited
Times Co-cited
Similarity
Sequence analysis, identification of evolutionary conserved motifs and expression analysis of murine tcof1 provide further evidence for a potential function for the gene and its human homologue, TCOF1.
J Dixon, K Hovanes, R Shiang, M J Dixon. Hum Mol Genet 1997
J Dixon, K Hovanes, R Shiang, M J Dixon. Hum Mol Genet 1997
90
TCOF1 gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region.
C A Wise, L C Chiang, W A Paznekas, M Sharma, M M Musy, J A Ashley, M Lovett, E W Jabs. Proc Natl Acad Sci U S A 1997
C A Wise, L C Chiang, W A Paznekas, M Sharma, M M Musy, J A Ashley, M Lovett, E W Jabs. Proc Natl Acad Sci U S A 1997
81
The Treacher Collins syndrome (TCOF1) gene product, treacle, is targeted to the nucleolus by signals in its C-terminus.
S T Winokur, R Shiang. Hum Mol Genet 1998
S T Winokur, R Shiang. Hum Mol Genet 1998
72
Identification of the complete coding sequence and genomic organization of the Treacher Collins syndrome gene.
J Dixon, S J Edwards, I Anderson, A Brass, P J Scambler, M J Dixon. Genome Res 1997
J Dixon, S J Edwards, I Anderson, A Brass, P J Scambler, M J Dixon. Genome Res 1997
63
The mutational spectrum in Treacher Collins syndrome reveals a predominance of mutations that create a premature-termination codon.
S J Edwards, A J Gladwin, M J Dixon. Am J Hum Genet 1997
S J Edwards, A J Gladwin, M J Dixon. Am J Hum Genet 1997
63
Increased levels of apoptosis in the prefusion neural folds underlie the craniofacial disorder, Treacher Collins syndrome.
J Dixon, C Brakebusch, R Fässler, M J Dixon. Hum Mol Genet 2000
J Dixon, C Brakebusch, R Fässler, M J Dixon. Hum Mol Genet 2000
63
Mutations in the Treacher Collins syndrome gene lead to mislocalization of the nucleolar protein treacle.
K L Marsh, J Dixon, M J Dixon. Hum Mol Genet 1998
K L Marsh, J Dixon, M J Dixon. Hum Mol Genet 1998
54
Treacher Collins syndrome may result from insertions, deletions or splicing mutations, which introduce a termination codon into the gene.
A J Gladwin, J Dixon, S K Loftus, S Edwards, J J Wasmuth, R C Hennekam, M J Dixon. Hum Mol Genet 1996
A J Gladwin, J Dixon, S K Loftus, S Edwards, J J Wasmuth, R C Hennekam, M J Dixon. Hum Mol Genet 1996
45
Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome. The Treacher Collins Syndrome Collaborative Group.
. Nat Genet 1996
. Nat Genet 1996
45
High mutation detection rate in TCOF1 among Treacher Collins syndrome patients reveals clustering of mutations and 16 novel pathogenic changes.
A Splendore, E O Silva, L G Alonso, A Richieri-Costa, N Alonso, A Rosa, G Carakushanky, D P Cavalcanti, D Brunoni, M R Passos-Bueno. Hum Mutat 2000
A Splendore, E O Silva, L G Alonso, A Richieri-Costa, N Alonso, A Rosa, G Carakushanky, D P Cavalcanti, D Brunoni, M R Passos-Bueno. Hum Mutat 2000
45
Detection of an appropriate kinase activity in branchial arches I and II that coincides with peak expression of the Treacher Collins syndrome gene product, treacle.
N C Jones, P G Farlie, J Minichiello, D F Newgreen. Hum Mol Genet 1999
N C Jones, P G Farlie, J Minichiello, D F Newgreen. Hum Mol Genet 1999
36
Characterization of the nucleolar gene product, treacle, in Treacher Collins syndrome.
C Isaac, K L Marsh, W A Paznekas, J Dixon, M J Dixon, E W Jabs, U T Meier. Mol Biol Cell 2000
C Isaac, K L Marsh, W A Paznekas, J Dixon, M J Dixon, E W Jabs, U T Meier. Mol Biol Cell 2000
36
Canine TCOF1; cloning, chromosome assignment and genetic analysis in dogs with different head types.
K E Haworth, I Islam, M Breen, W Putt, E Makrinou, M Binns, D Hopkinson, Y Edwards. Mamm Genome 2001
K E Haworth, I Islam, M Breen, W Putt, E Makrinou, M Binns, D Hopkinson, Y Edwards. Mamm Genome 2001
36
Genetic background has a major effect on the penetrance and severity of craniofacial defects in mice heterozygous for the gene encoding the nucleolar protein Treacle.
Jill Dixon, Michael James Dixon. Dev Dyn 2004
Jill Dixon, Michael James Dixon. Dev Dyn 2004
36
Another face of the Treacher Collins syndrome (TCOF1) gene: identification of additional exons.
Rolando B So, Bianca Gonzales, Dale Henning, Jill Dixon, Michael J Dixon, Benigno C Valdez. Gene 2004
Rolando B So, Bianca Gonzales, Dale Henning, Jill Dixon, Michael J Dixon, Benigno C Valdez. Gene 2004
36
The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor.
Benigno C Valdez, Dale Henning, Rolando B So, Jill Dixon, Michael J Dixon. Proc Natl Acad Sci U S A 2004
Benigno C Valdez, Dale Henning, Rolando B So, Jill Dixon, Michael J Dixon. Proc Natl Acad Sci U S A 2004
36
Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches.
M Qiu, A Bulfone, I Ghattas, J J Meneses, L Christensen, P T Sharpe, R Presley, R A Pedersen, J L Rubenstein. Dev Biol 1997
M Qiu, A Bulfone, I Ghattas, J J Meneses, L Christensen, P T Sharpe, R Presley, R A Pedersen, J L Rubenstein. Dev Biol 1997
27
Null mutation of Dlx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain.
M Qiu, A Bulfone, S Martinez, J J Meneses, K Shimamura, R A Pedersen, J L Rubenstein. Genes Dev 1995
M Qiu, A Bulfone, S Martinez, J J Meneses, K Shimamura, R A Pedersen, J L Rubenstein. Genes Dev 1995
27
Proteomic analysis of human Nop56p-associated pre-ribosomal ribonucleoprotein complexes. Possible link between Nop56p and the nucleolar protein treacle responsible for Treacher Collins syndrome.
Toshiya Hayano, Mitsuaki Yanagida, Yoshio Yamauchi, Takashi Shinkawa, Toshiaki Isobe, Nobuhiro Takahashi. J Biol Chem 2003
Toshiya Hayano, Mitsuaki Yanagida, Yoshio Yamauchi, Takashi Shinkawa, Toshiaki Isobe, Nobuhiro Takahashi. J Biol Chem 2003
27
Clinical features, treatment and genetic background of Treacher Collins syndrome.
Bozena Marszałek, Piotr Wójcicki, Kazimierz Kobus, Wiesław H Trzeciak. J Appl Genet 2002
Bozena Marszałek, Piotr Wójcicki, Kazimierz Kobus, Wiesław H Trzeciak. J Appl Genet 2002
27
Craniofacial, vestibular and bone defects in mice lacking the Distal-less-related gene Dlx5.
D Acampora, G R Merlo, L Paleari, B Zerega, M P Postiglione, S Mantero, E Bober, O Barbieri, A Simeone, G Levi. Development 1999
D Acampora, G R Merlo, L Paleari, B Zerega, M P Postiglione, S Mantero, E Bober, O Barbieri, A Simeone, G Levi. Development 1999
18
Cranial paraxial mesoderm and neural crest cells of the mouse embryo: co-distribution in the craniofacial mesenchyme but distinct segregation in branchial arches.
P A Trainor, P P Tam. Development 1995
P A Trainor, P P Tam. Development 1995
18
Dlx5 regulates regional development of the branchial arches and sensory capsules.
M J Depew, J K Liu, J E Long, R Presley, J J Meneses, R A Pedersen, J L Rubenstein. Development 1999
M J Depew, J K Liu, J E Long, R Presley, J J Meneses, R A Pedersen, J L Rubenstein. Development 1999
18
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
18
Mandibulofacial dysostosis (Treacher Collins syndrome): a new proposal for its pathogenesis.
K K Sulik, M C Johnston, S J Smiley, H S Speight, B E Jarvis. Am J Med Genet 1987
K K Sulik, M C Johnston, S J Smiley, H S Speight, B E Jarvis. Am J Med Genet 1987
18
MANDIBULOFACIAL DYSOSTOSIS, A FAMILIAL STUDY OF FIVE GENERATIONS.
S ROVIN, S F DACHI, D B BORENSTEIN, W B COTTER. J Pediatr 1964
S ROVIN, S F DACHI, D B BORENSTEIN, W B COTTER. J Pediatr 1964
18
An early phase of embryonic Dlx5 expression defines the rostral boundary of the neural plate.
L Yang, H Zhang, G Hu, H Wang, C Abate-Shen, M M Shen. J Neurosci 1998
L Yang, H Zhang, G Hu, H Wang, C Abate-Shen, M M Shen. J Neurosci 1998
18
Effects of retinoic acid on the development of the facial skeleton in hamsters: early changes involving cranial neural crest cells.
M J Wiley, P Cauwenbergs, I M Taylor. Acta Anat (Basel) 1983
M J Wiley, P Cauwenbergs, I M Taylor. Acta Anat (Basel) 1983
18
The pathogenesis of the Treacher Collins syndrome (mandibulofacial dysostosis).
D Poswillo. Br J Oral Surg 1975
D Poswillo. Br J Oral Surg 1975
18
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
18
Comparison of the rat nucleolar protein nopp140 with its yeast homolog SRP40. Differential phosphorylation in vertebrates and yeast.
U T Meier. J Biol Chem 1996
U T Meier. J Biol Chem 1996
18
Older paternal age and fresh gene mutation: data on additional disorders.
K L Jones, D W Smith, M A Harvey, B D Hall, L Quan. J Pediatr 1975
K L Jones, D W Smith, M A Harvey, B D Hall, L Quan. J Pediatr 1975
18
18
Human Nopp140, which interacts with RNA polymerase I: implications for rRNA gene transcription and nucleolar structural organization.
H K Chen, C Y Pai, J Y Huang, N H Yeh. Mol Cell Biol 1999
H K Chen, C Y Pai, J Y Huang, N H Yeh. Mol Cell Biol 1999
18
Conserved composition of mammalian box H/ACA and box C/D small nucleolar ribonucleoprotein particles and their interaction with the common factor Nopp140.
Y Yang, C Isaac, C Wang, F Dragon, V Pogacic, U T Meier. Mol Biol Cell 2000
Y Yang, C Isaac, C Wang, F Dragon, V Pogacic, U T Meier. Mol Biol Cell 2000
18
Transformation of tooth type induced by inhibition of BMP signaling.
A S Tucker, K L Matthews, P T Sharpe. Science 1998
A S Tucker, K L Matthews, P T Sharpe. Science 1998
18
Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1.
Y Kurihara, H Kurihara, H Suzuki, T Kodama, K Maemura, R Nagai, H Oda, T Kuwaki, W H Cao, N Kamada. Nature 1994
Y Kurihara, H Kurihara, H Suzuki, T Kodama, K Maemura, R Nagai, H Oda, T Kuwaki, W H Cao, N Kamada. Nature 1994
18
The role of the neural crest in patterning of avian cranial skeletal, connective, and muscle tissues.
D M Noden. Dev Biol 1983
D M Noden. Dev Biol 1983
18
Early embryonic lethality in Bmp5;Bmp7 double mutant mice suggests functional redundancy within the 60A subgroup.
M J Solloway, E J Robertson. Development 1999
M J Solloway, E J Robertson. Development 1999
18
Expression of the mouse goosecoid gene during mid-embryogenesis may mark mesenchymal cell lineages in the developing head, limbs and body wall.
S J Gaunt, M Blum, E M De Robertis. Development 1993
S J Gaunt, M Blum, E M De Robertis. Development 1993
18
Barx1, a new mouse homeodomain transcription factor expressed in cranio-facial ectomesenchyme and the stomach.
J P Tissier-Seta, M L Mucchielli, M Mark, M G Mattei, C Goridis, J F Brunet. Mech Dev 1995
J P Tissier-Seta, M L Mucchielli, M Mark, M G Mattei, C Goridis, J F Brunet. Mech Dev 1995
18
Signaling pathways crucial for craniofacial development revealed by endothelin-A receptor-deficient mice.
D E Clouthier, S C Williams, H Yanagisawa, M Wieduwilt, J A Richardson, M Yanagisawa. Dev Biol 2000
D E Clouthier, S C Williams, H Yanagisawa, M Wieduwilt, J A Richardson, M Yanagisawa. Dev Biol 2000
18
The triple origin of skull in higher vertebrates: a study in quail-chick chimeras.
G F Couly, P M Coltey, N M Le Douarin. Development 1993
G F Couly, P M Coltey, N M Le Douarin. Development 1993
18
Segmental origin and migration of neural crest cells in the hindbrain region of the chick embryo.
A Lumsden, N Sprawson, A Graham. Development 1991
A Lumsden, N Sprawson, A Graham. Development 1991
18
Fgf-8 determines rostral-caudal polarity in the first branchial arch.
A S Tucker, G Yamada, M Grigoriou, V Pachnis, P T Sharpe. Development 1999
A S Tucker, G Yamada, M Grigoriou, V Pachnis, P T Sharpe. Development 1999
18
Dual genetic pathways of endothelin-mediated intercellular signaling revealed by targeted disruption of endothelin converting enzyme-1 gene.
H Yanagisawa, M Yanagisawa, R P Kapur, J A Richardson, S C Williams, D E Clouthier, D de Wit, N Emoto, R E Hammer. Development 1998
H Yanagisawa, M Yanagisawa, R P Kapur, J A Richardson, S C Williams, D E Clouthier, D de Wit, N Emoto, R E Hammer. Development 1998
18
Cranial and cardiac neural crest defects in endothelin-A receptor-deficient mice.
D E Clouthier, K Hosoda, J A Richardson, S C Williams, H Yanagisawa, T Kuwaki, M Kumada, R E Hammer, M Yanagisawa. Development 1998
D E Clouthier, K Hosoda, J A Richardson, S C Williams, H Yanagisawa, T Kuwaki, M Kumada, R E Hammer, M Yanagisawa. Development 1998
18
Cre-mediated gene inactivation demonstrates that FGF8 is required for cell survival and patterning of the first branchial arch.
A Trumpp, M J Depew, J L Rubenstein, J M Bishop, G R Martin. Genes Dev 1999
A Trumpp, M J Depew, J L Rubenstein, J M Bishop, G R Martin. Genes Dev 1999
18
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.