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Jump to: B | F | G | K | L | S | T | Y
Number of items: 16.

B

Bibb, LC and Holt, JKL and Tarttelin, E and Lucas, R and Hodges, M and Gregory-Evans, K and Sowden, JC and Gregory-Evans, CY (2001) Expression of the CRX gene in Human Retina during early eye development. In: Genet Res Camb.

Bibb, LC and Holt, JKL and Tarttelin, EE and Hodges, MD and Gregory-Evans, K and Rutherford, A and Lucas, RJ and Sowden, JC and Gregory-Evans, CY (2001) Temporal and spatial expression patterns of the CRX transcription factor and its downstream targets. Critical differences during human and mouse eye development. HUM MOL GENET , 10 (15) 1571 - 1579.

F

Ferretti, P and Zhang, F and Santos-Ruiz, L and Clarke, JDW (2001) FGF signalling and blastema growth during amphibian tail regeneration. INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY , 45 S127 - S128.

G

Gouge, A and Holt, J and Hardy, AP and Sowden, JC and Smith, HK (2001) Foxn4 - a new member of the forkhead gene family is expressed in the retina. MECH DEVELOP , 107 (1-2) 203 - 206.

K

Kelberman, D and Tyson, J and Chandler, DC and McInerney, A and Slee, J and Calvert, M and Goldblatt, J and Haan, EA and Laing, NG and Malcolm, S and Singer, SL and Winter, RM and Bitner-Glindzicz, M (2001) Genetic heterogeneity in hemifacial microsomia: evidence for three loci at 14q32, 2q35 and 11q12-q13. In: AM J HUM GENET. (pp. 514 - 514). UNIV CHICAGO PRESS

Kelberman, D and Tyson, J and Chandler, DC and McInerney, AM and Slee, J and Albert, D and Aymat, A and Botma, M and Calvert, M and Goldblatt, J and Haan, EA and Laing, NG and Lim, J and Malcolm, S and Singer, SL and Winter, RM and Bitner-Glindzicz, M (2001) Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome. HUM GENET , 109 (6) 638 - 645.

L

Lehman, OJ and Jordan, TL and Ebenezer, N and Ocaka, L and Hitchings, RA and Khaw, PT and Sowden, JC and Povey, S and Walter, MA and Bhattacharya, SS (2001) Progress with FOXC1 gene dosage. In: Inves Ophthalomol Vis Sci. (pp. 2846 - ?).

Lehmann, OJ and Ebenezer, N and Jordan, TL and Ekong, R and Hitchings, RA and Khaw, PT and Sowden, J and Povey, S and Walter, MA and Bhattacharya, SS (2001) Paired interstitial duplications and deletions: a novel cause of ocular developmental abnormalities and glaucoma. In: American Journal of Human Genetics. (pp. 928 - ?).

S

Sarkar, S and Petiot, A and Copp, A and Ferretti, P and Thorogood, P (2001) FGF2 promotes skeletogenic differentiation of cranial neural crest cells. Development , 128 (11) 2143 - 2152.

Sarkar, S and Petiot, A and Copp, A and Ferretti, P and Thorogood, P (2001) FGF2 promotes skeletogenic differentiation of cranial neural crest cells. DEVELOPMENT , 128 (11) 2143 - 2152.

Sowden, JC and Holt, JKL and Meins, A and Smith, HK and Bhattacharya, SS (2001) Expression of Drosophila omb-related T-box genes in the developing human and mouse neural retina. INVEST OPHTH VIS SCI , 42 (13) 3095 - 3102.

T

Tarttelin, E and Gregory-Evans, K and Sowden, JC and Gregory-Evans, CY (2001) Investigation of the role of the EFEMP1 gene in the developing retina and retina disease. In: Genet Res Camb. (pp. 202 - ?).

Tyson, J and Kelberman, D and Brady, A and Garrett, C and Botma, M and Lim, J and Calvert, M and Gorlin, R and Malcolm, S and Winter, RM and Bitner-Glindzicz, M (2001) Hemifacial microsomia: Progress in understanding the genetic basis of a multifactorial condition. In: J MED GENET. (pp. S72 - S72). BRITISH MED JOURNAL PUBL GROUP

Y

Yip, GW and Ferretti, P and Copp, AJ (2001) Abnormal accumulation of chondroitin sulphate in the splotch (Sp(2H)) mouse mutant. In: GLYCOBIOLOGY. (pp. 881 - 882). OXFORD UNIV PRESS INC

Yip, GW and Ferretti, P and Copp, AJ (2001) Abnormal accumulation of chondroitin sulphate in the splotch (Sp(2H)) mouse mutant. In: (pp. 56 - ?).

This list was generated on Wed Jun 12 10:19:30 2013 BST.