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Number of items: 32.
A
Adams, D;
Baldock, R;
Bhattacharya, S;
Copp, AJ;
Dickinson, M;
Greene, NDE;
Henkelman, M;
... West, D; + view all
(2013)
Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screening.
Disease Models and Mechanisms
, 6
(3)
pp. 571-579.
10.1242/dmm.011833.
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Alvarez-Gonzalez, C;
Duggleby, R;
Vagaska, B;
Querol, S;
Gomez, SG;
Ferretti, P;
Madrigal, A;
(2013)
Cord Blood Lin−CD45− Embryonic-Like Stem Cells Are a Heterogeneous Population That Lack Self-Renewal Capacity.
PLoS One
, 8
(6)
, Article e67968. 10.1371/journal.pone.0067968.
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C
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Carnaghan, H;
Roberts, T;
Savery, D;
Norris, FC;
McCann, CJ;
Copp, AJ;
Scambler, PJ;
... Eaton, S; + view all
(2013)
Novel exomphalos genetic mouse model: The importance of accurate phenotypic classification.
J Pediatr Surg
, 48
(10)
2036 - 2042.
10.1016/j.jpedsurg.2013.04.010.
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Copp, AJ;
Greene, NDE;
(2013)
Neural tube defects-disorders of neurulation and related embryonic processes.
Wiley Interdisciplinary Reviews: Developmental Biology
, 2
(2)
pp. 213-227.
10.1002/wdev.71.
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Copp, AJ;
Stanier, P;
Greene, NDE;
(2013)
Neural tube defects: recent advances, unsolved questions, and controversies.
The Lancet Neurology
, 12
(8)
pp. 799-810.
10.1016/S1474-4422(13)70110-8.
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D
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Danovi, D;
Folarin, A;
Gogolok, S;
Ender, C;
Elbatsh, AM;
Engström, PG;
Stricker, SH;
... Pollard, SM; + view all
(2013)
A High-Content Small Molecule Screen Identifies Sensitivity of Glioblastoma Stem Cells to Inhibition of Polo-Like Kinase 1.
PLoS One
, 8
(10)
, Article e77053. 10.1371/journal.pone.0077053.
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E
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Escobedo, N;
Contreras, O;
Muñoz, R;
Farías, M;
Carrasco, H;
Hill, C;
Tran, U;
... Larraín, J; + view all
(2013)
Syndecan 4 interacts genetically with Vangl2 to regulate neural tube closure and planar cell polarity.
Development
, 140
(14)
3008 - 3017.
10.1242/dev.091173.
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F
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Fishman, JM;
(2013)
Characterisation and immunomodulatory effect of a decellularised skeletal muscle scaffold for tissue engineering.
Doctoral thesis , UCL (University College London).
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G
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Ghazi-Noori, S;
(2013)
Generating and Characterising Knockout and Transgenic Mouse Models of Frontotemporal Dementia Caused by CHMP2B Mutation.
Doctoral thesis (PhD), UCL (University College London).
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H
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Halbritter, J;
Bizet, AA;
Schmidts, M;
Porath, JD;
Braun, DA;
Gee, HY;
McInerney-Leo, AM;
... Hildebrandt, F; + view all
(2013)
Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans.
Am J Hum Genet
, 93
(5)
pp. 915-925.
10.1016/j.ajhg.2013.09.012.
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Hallal, PC;
Reichert, FF;
Clark, VL;
Cordeira, KL;
Menezes, AM;
Eaton, S;
Ekelund, U;
(2013)
Energy expenditure compared to physical activity measured by accelerometry and self-report in adolescents: a validation study.
PLoS One
, 8
(11)
, Article e77036. 10.1371/journal.pone.0077036.
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Huang, JL;
(2013)
Polycystic kidney disease and the renal circulation.
Doctoral thesis , UCL (University College London).
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K
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Kinsler, VA;
Thomas, AC;
Ishida, M;
Bulstrode, NW;
Loughlin, S;
Hing, S;
Chalker, J;
... Moore, GE; + view all
(2013)
Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRAS.
Journal of Investigative Dermatology
, 133
(9)
pp. 2229-2236.
10.1038/jid.2013.70.
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L
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Lashkari, HP;
Nash, R;
Albanese, A;
Okoye, B;
Millar, R;
Pritchard-Jones, K;
(2013)
Treatment of high risk Sertoli-Leydig cell tumors of the ovary using a gonadotropin releasing hormone (GnRH) analog.
Pediatric Blood & Cancer
, 60
(6)
E16 - E18.
10.1002/pbc.24382.
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Leung, KY;
De Castro, SC;
Savery, D;
Copp, AJ;
Greene, ND;
(2013)
Nucleotide precursors prevent folic acid-resistant neural tube defects in the mouse.
Brain: A Journal of Neurology
, 136
(9)
pp. 2836-2841.
10.1093/brain/awt209.
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Long, DA;
Kolatsi-Joannou, M;
Price, KL;
Dessapt-Baradez, C;
Huang, JL;
Papakrivopoulou, E;
Hubank, M;
... Woolf, AS; + view all
(2013)
Albuminuria is associated with too few glomeruli and too much testosterone.
Kidney International
, 83
(6)
1118 -1129.
10.1038/ki.2013.45.
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M
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Maghsoudlou, P;
Georgiades, F;
Tyraskis, A;
Totonelli, G;
Loukogeorgakis, SP;
Orlando, G;
Shangaris, P;
... Coppi, PD; + view all
(2013)
Preservation of micro-architecture and angiogenic potential in a pulmonary acellular matrix obtained using intermittent intra-tracheal flow of detergent enzymatic treatment.
Biomaterials
, 34
(28)
6638- 6648.
10.1016/j.biomaterials.2013.05.015.
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Mansour, MR;
(2013)
Role of the Notch signalling pathway in acute leukaemia.
Doctoral thesis , UCL (University College London).
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McInerney-Leo, AM;
Schmidts, M;
Cortés, CR;
Leo, PJ;
Gener, B;
Courtney, AD;
Gardiner, B;
... Wicking, C; + view all
(2013)
Short-Rib Polydactyly and Jeune Syndromes Are Caused by Mutations in WDR60.
Am J Hum Genet
, 93
(3)
pp. 515-523.
10.1016/j.ajhg.2013.06.022.
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Mohun, T;
Adams, DJ;
Baldock, R;
Bhattacharya, S;
Copp, AJ;
Hemberger, M;
Houart, C;
... Weninger, W; + view all
(2013)
Deciphering the Mechanisms of Developmental Disorders (DMDD): a new programme for phenotyping embryonic lethal mice.
Disease Models & Mechanisms
, 6
(3)
562 -566.
10.1242/dmm.011957.
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Moulding, DA;
Record, J;
Malinova, D;
Thrasher, AJ;
(2013)
Actin cytoskeletal defects in immunodeficiency.
Immunological Reviews
, 256
(1)
282 - 299.
10.1111/imr.12114.
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O
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Onoufriadis, A;
Shoemark, A;
Munye, MM;
James, CT;
Schmidts, M;
Patel, M;
Rosser, EM;
... Mitchison, HM; + view all
(2013)
Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm.
Journal of Medical Genetics
10.1136/jmedgenet-2013-101938.
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P
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Peake, JN;
Copp, AJ;
Shawe, J;
(2013)
Knowledge and periconceptional use of folic acid for the prevention of neural tube defects in ethnic communities in the United Kingdom: Systematic review and meta-analysis.
Birth Defects Research
, 97
(7)
444 - 451.
10.1002/bdra.23154.
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Pulido, R;
Stoker, AW;
Hendriks, WJ;
(2013)
PTPs emerge as PIPs: protein tyrosine phosphatases with lipid-phosphatase activities in human disease.
Human Molecular Genetics
, 22
(R1)
R66 - R76.
10.1093/hmg/ddt347.
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R
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Roberts, C;
(2013)
The role of putative Tbx1 traget genes in the pathogenesis of the 22q11 Deletion Syndrome phenotype.
Doctoral thesis , UCL (University College London).
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Robinson, A;
Partridge, D;
Malhas, A;
De Castro, SC;
Gustavsson, P;
Thompson, DN;
Vaux, DJ;
... Greene, ND; + view all
(2013)
Is LMNB1 a susceptibility gene for neural tube defects in humans?
Birth Defects Research Part A: Clinical and Molecular Teratology
, 97
(6)
pp. 398-402.
10.1002/bdra.23141.
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S
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Schmidts, M;
Vodopiutz, J;
Christou-Savina, S;
Cortés, CR;
McInerney-Leo, AM;
Emes, RD;
Arts, HH;
... Mitchison, HM; + view all
(2013)
Mutations in the Gene Encoding IFT Dynein Complex Component WDR34 Cause Jeune Asphyxiating Thoracic Dystrophy.
The American Journal of Human Genetics
, 93
(5)
932 - 944.
10.1016/j.ajhg.2013.10.003.
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Shepherd, C;
Liu, J;
Goc, J;
Martinian, L;
Jacques, TS;
Sisodiya, SM;
Thom, M;
(2013)
A quantitative study of white matter hypomyelination and oligodendroglial maturation in focal cortical dysplasia type II.
Epilepsia
, 54
(5)
898 - 908.
10.1111/epi.12143.
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Shroff, RC;
Price, KL;
Kolatsi-Joannou, M;
Todd, AF;
Wells, D;
Deanfield, J;
Johnson, RJ;
... Long, DA; + view all
(2013)
Circulating angiopoietin-2 is a marker for early cardiovascular disease in children on chronic dialysis.
PLoS One
, 8
(2)
, Article e56273. 10.1371/journal.pone.0056273.
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Sugiyama, T;
Meakin, LB;
Galea, GL;
Lanyon, LE;
Price, JS;
(2013)
The cyclooxygenase-2 selective inhibitor NS-398 does not influence trabecular or cortical bone gain resulting from repeated mechanical loading in female mice.
Osteoporosis International
, 24
(1)
pp. 383-388.
10.1007/s00198-012-1922-0.
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W
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Waters, AM;
(2013)
Genetic and functional dissection of ciliary genes.
Doctoral thesis , UCL (University College London).
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Watson, JA;
Bryan, K;
Williams, R;
Popov, S;
Vujanic, G;
Coulomb, A;
Boccon-Gibod, L;
... O'Sullivan, M; + view all
(2013)
miRNA profiles as a predictor of chemoresponsiveness in Wilms' tumor blastema.
PLoS One
, 8
(1)
, Article e53417. 10.1371/journal.pone.0053417.
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