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🐜
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Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein
25 auth.
L. McGregor,
V. Makela,
S. Darling,
S. Vrontou,
G. Chalepakis,
C. Roberts,
N. Smart,
P. Rutland,
N. Prescott,
J. Hopkins,
E. Bentley,
A. Shaw,
E. Roberts,
R. Mueller,
S. Jadeja,
...
N. Philip,
J. Nelson,
C. Francannet,
A. Pérez-Aytés,
A. Mégarbané,
B. Kerr,
B. Wainwright,
A. Woolf,
R. Winter,
P. Scambler
|
7 |
2003 |
7
🐜
|
|
🐬
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HIRA, a mammalian homologue of Saccharomyces cerevisiae transcriptional co-repressors, interacts with Pax3
P. Magnaghi,
C. Roberts,
S. Lorain,
M. Lipinski,
P. Scambler
|
7 |
1998 |
7
🐬
|
|
🦁
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Targeted Mutagenesis of the Hira Gene Results in Gastrulation Defects and Patterning Abnormalities of Mesoendodermal Derivatives Prior to Early Embryonic Lethality
9 auth.
C. Roberts,
H. Sutherland,
H. Farmer,
W. Kimber,
S. Halford,
A. Carey,
...
J. Brickman,
A. Wynshaw-Boris,
P. Scambler
|
7 |
2002 |
7
🦁
|
|
🐜
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Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice.
17 auth.
Victoria Randall,
K. McCue,
C. Roberts,
V. Kyriakopoulou,
S. Beddow,
A. Barrett,
F. Vitelli,
K. Prescott,
C. Shaw-Smith,
K. Devriendt,
...
Erika A. Bosman,
Georg Steffes,
K. Steel,
S. Simrick,
M. A. Basson,
E. Illingworth,
P. Scambler
|
7 |
2009 |
7
🐜
|
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🐜
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Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease.
18 auth.
Stephanle Halford,
R. Wadey,
C. Roberts,
S. Daw,
Jennifer A. Whiting,
Hllary O'Donnell,
Ian Dunham,
David Bentley,
Elizabeth A. Lindsay,
Antonio Baldini,
...
Fiona Francis,
Hans Lehrach,
Robert Williamson,
D. Wilson,
J. Goodship,
I. Cross,
J. Burn,
Peter J. Scambler
|
7 |
1993 |
7
🐜
|
|
🦁
|
Retinoic acid down‐regulates Tbx1 expression in vivo and in vitro
C. Roberts,
S. Ivins,
C. James,
P. Scambler
|
6 |
2005 |
6
🦁
|
|
🦁
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Cyp26 genes a1, b1 and c1 are down-regulated in Tbx1 null mice and inhibition of Cyp26 enzyme function produces a phenocopy of DiGeorge Syndrome in the chick.
C. Roberts,
S. Ivins,
Andrew C. Cook,
A. Baldini,
P. Scambler
|
6 |
2006 |
6
🦁
|
|
🐜
|
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1.
8 auth.
S. Ivins,
Kelly Lammerts van Beuren,
C. Roberts,
C. James,
E. Lindsay,
A. Baldini,
...
P. Ataliotis,
P. Scambler
|
6 |
2005 |
6
🐜
|
|
🦁
|
Cloning and developmental expression analysis of chick Hira (Chira), a candidate gene for DiGeorge syndrome.
C. Roberts,
S. Daw,
Stephanie Halford,
P. J. Scambler
|
6 |
1997 |
6
🦁
|
|
🐜
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Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome
10 auth.
Kelly Lammerts van Bueren,
I. Papangeli,
F. Rochais,
K. Pearce,
C. Roberts,
A. Calmont,
...
D. Szumska,
R. Kelly,
S. Bhattacharya,
P. Scambler
|
6 |
2010 |
6
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|
