Items where Subject is "Molecular Medicine Unit"
- UCL Eprints (16692)
- UCL Departments and Research Centres (8563)
- UCL Biomedical Sciences (1510)
- Institute of Child Health (252)
- Genes, Development and Disease (33)
- Molecular Medicine Unit (10)
- Genes, Development and Disease (33)
- Institute of Child Health (252)
- UCL Biomedical Sciences (1510)
- UCL Departments and Research Centres (8563)
Number of items at this level: 10.
2010
Robinson, R.A.;
(2010)
Genetic analysis of human absence epilepsy.
Doctoral thesis , UCL (University College London).
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2009
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Schwarz, Q;
Maden, CH;
Vieira, JM;
Ruhrberg, C;
(2009)
Neuropilin 1 signaling guides neural crest cells to coordinate pathway choice with cell specification.
P NATL ACAD SCI USA
, 106
(15)
6164 - 6169.
10.1073/pnas.0811521106.
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Tobin, J.;
(2009)
A functional and therapeutic investigation of ciliopathy proteins and ciliopathies.
Doctoral thesis , UCL (University College London).
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2008
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Schwarz, Q;
Vieira, JM;
Howard, B;
Eickholt, BJ;
Ruhrberg, C;
(2008)
Neuropilin 1 and 2 control cranial gangliogenesis and axon guidance through neural crest cells.
DEVELOPMENT
, 135
(9)
1605 - 1613.
10.1242/dev.015412.
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2007
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Everett, K;
Chioza, B;
Aicardi, J;
Aschauer, H;
Brouwer, O;
Callenbach, P;
Covanis, A;
... Gardiner, M; + view all
(2007)
Linkage and mutational analysis of CLCN2 in childhood absence epilepsy.
EPILEPSY RESEARCH
, 75
(2-3)
pp. 145-153.
10.1016/j.eplepsyres.2007.05.004.
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Everett, KV;
Chioza, B;
Aicardi, J;
Aschauer, H;
Brouwer, O;
Callenbach, P;
Covanis, A;
... Gardiner, M; + view all
(2007)
Linkage and association analysis of CACNG3 in childhood absence epilepsy.
EUR J HUM GENET
, 15
(4)
463 - 472.
10.1038/sj.ejhg.5201783.
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2006
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Chioza, B;
Everett, K;
Aschauer, H;
Brouwer, O;
Callenbach, P;
Covanis, A;
Dulac, O;
... Gardiner, RM; + view all
(2006)
Evaluation of CACNA1H in European patients with childhood absence epilepsy.
Epilepsy Research
, 69
(2)
pp. 177-181.
10.1016/j.eplepsyres.2006.01.009.
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2005
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Spencer, H;
Rampling, D;
Aurora, P;
Bonnet, D;
Hart, SL;
Jaffe, A;
(2005)
Transbronchial biopsies provide longitudinal evidence for epithelial chimerism in children following sex mismatched lung transplantation.
THORAX
, 60
(1)
60 - 62.
10.1136/thx.2004.029678.
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2003
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Lemonde, HA;
Custard, EJ;
Bouquet, J;
Duran, M;
Overmars, H;
Scambler, PJ;
Clayton, PT;
(2003)
Mutations in SRD5B1 (AKR1D1), the gene encoding Delta(4)-3-oxosteroid 5 beta-reductase, in hepatitis and liver failure in infancy.
GUT
, 52
(10)
1494 - 1499.
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2001
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Hammond, P;
Hutton, TJ;
Nelson-Moon, ZL;
Hunt, NP;
Madgwick, AJA;
(2001)
Classifying vertical facial deformity using supervised and unsupervised learning.
Methods of Information in Medicine
, 40
(5)
pp. 365-372.
10.1055/s-0038-1634194.
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