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🐬
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FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder.
Cecilia S. L. Lai,
D. Gerrelli,
A. Monaco,
S. Fisher,
A. Copp
|
8 |
2003 |
8
🐬
|
|
🐜
|
Convergent extension, planar-cell-polarity signalling and initiation of mouse neural tube closure
8 auth.
P. Ybot‐González,
D. Savery,
D. Gerrelli,
M. Signore,
Claire Mitchell,
Clare H. Faux,
...
N. Greene,
A. Copp
|
8 |
2007 |
8
🐜
|
|
🐜
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Heterozygous mutations of OTX2 cause severe ocular malformations.
24 auth.
Nicola K. Ragge,
Nicola K. Ragge,
Nicola K. Ragge,
Alison G. Brown,
C. Poloschek,
B. Lorenz,
R. Henderson,
Michael P. Clarke,
I. Russell-Eggitt,
A. Fielder,
...
D. Gerrelli,
J. Martínez-Barbera,
P. Ruddle,
J. Hurst,
J. Collin,
Alison Salt,
Alison Salt,
S. T. Cooper,
P. Thompson,
S. Sisodiya,
K. Williamson,
D. FitzPatrick,
V. Heyningen,
I. Hanson
|
8 |
2005 |
8
🐜
|
|
🐜
|
The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation.
15 auth.
H. Dawe,
U. Smith,
A. Cullinane,
D. Gerrelli,
P. Cox,
José L. Badano,
Sarah Blair-Reid,
N. Sriram,
N. Katsanis,
T. Attié-Bitach,
...
S. Afford,
A. Copp,
D. Kelly,
K. Gull,
Colin A. Johnson
|
8 |
2007 |
8
🐜
|
|
🐜
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Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways.
26 auth.
Preeti Bakrania,
M. Efthymiou,
J. Klein,
Alison Salt,
A. Salt,
D. Bunyan,
D. Bunyan,
A. Wyatt,
C. Ponting,
Angela M Martin,
Steven E Williams,
Victoria Lindley,
Joanne Gilmore,
M. Restori,
A. Robson,
...
M. Neveu,
G. Holder,
J. Collin,
D. Robinson,
D. Robinson,
P. Farndon,
H. Johansen-Berg,
D. Gerrelli,
N. Ragge,
N. Ragge,
N. Ragge
|
7 |
2008 |
7
🐜
|
|
🐜
|
SOX2 plays a critical role in the pituitary, forebrain, and eye during human embryonic development.
17 auth.
D. Kelberman,
Sandra C P De Castro,
Shuwen Huang,
J. Crolla,
R. Palmer,
J. Gregory,
David Taylor,
L. Cavallo,
M. Faienza,
R. Fischetto,
...
J. Achermann,
J. Martínez-Barbera,
K. Rizzoti,
R. Lovell-Badge,
I. Robinson,
D. Gerrelli,
M. Dattani
|
7 |
2008 |
7
🐜
|
|
🐬
|
Sonic hedgehog and the molecular regulation of mouse neural tube closure.
P. Ybot‐González,
P. Cogram,
D. Gerrelli,
A. Copp
|
7 |
2002 |
7
🐬
|
|
🐬
|
Abnormalities of floor plate, notochord and somite differentiation in the loop-tail (Lp) mouse: a model of severe neural tube defects
N. Greene,
D. Gerrelli,
H. V. Straaten,
A. Copp
|
7 |
1998 |
7
🐬
|
|
🐜
|
Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction.
16 auth.
M. McCabe,
C. Gaston-Massuet,
V. Tziaferi,
L. Gregory,
K. Alatzoglou,
M. Signore,
E. Puelles,
D. Gerrelli,
I. Farooqi,
J. Raza,
...
Joanna M. Walker,
Scott I. Kavanaugh,
P. Tsai,
N. Pitteloud,
J. Martínez-Barbera,
M. Dattani
|
6 |
2011 |
6
🐜
|
|
🐜
|
Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.
18 auth.
S. Twigg,
S. Versnel,
G. Nürnberg,
M. Lees,
M. Bhat,
P. Hammond,
R. Hennekam,
R. Hennekam,
R. Hennekam,
A. Hoogeboom,
...
J. Hurst,
David Johnson,
Alexis A. Robinson,
P. Scambler,
D. Gerrelli,
P. Nürnberg,
I. Mathijssen,
A. Wilkie
|
6 |
2009 |
6
🐜
|
|
🐜
|
Spatiotemporal expansion of primary progenitor zones in the developing human cerebellum
22 auth.
P. Haldipur,
K. Aldinger,
S. Bernardo,
Mei Deng,
A. Timms,
L. Overman,
Conrad Winter,
S. Lisgo,
F. Razavi,
E. Silvestri,
...
L. Manganaro,
H. Adle-Biasette,
Fabien Guilmiot,
Rosa Russo,
D. Kidron,
P. Hof,
D. Gerrelli,
S. Lindsay,
W. Dobyns,
I. Glass,
Paula Alexandre,
K. Millen
|
6 |
2019 |
6
🐜
|
