Browse by UCL Departments and Centres
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Group by: Author | Type
Number of items: 19.
B
| Bockenhauer, D and Goldstein, SAN (2000) hTPKC1: A potassium channel with a masterswitch. PEDIATR RES , 47 (4) 444A - 444A. |
| Bockenhauer, D and Goldstein, SEN and Pausch, MH (2000) Improving the pore of a human 2 P domain potassium channel (hTPKC1) by random mutagenesis and selective pressure in S-cerevisiae. BIOPHYS J , 78 (1) 206A - 206A. |
| Bockenhauer, D and Nimmakayalu, MA and Ward, DC and Goldstein, SAN and Gallagher, PG (2000) Genomic organization and chromosomal localization of the murine 2 P domain potassium channel gene Kcnk8: conservation of gene structure in 2 P domain potassium channels. GENE , 261 (2) 365 - 372. |
| Borley, NC and Kimber, C and Ransley, PG (2000) An unusual cause of testicular ischaemia. BJU International , 85 (7) 971 - 971. |
C
| Cale, CM and Klein, NJ and Winyard, PJD and Woolf, AS (2000) Inflammatory mediators in human renal dysplasia. NEPHROL DIAL TRANSPL , 15 (2) 173 - 183. |
D
| Dana, A and Skarli, M and Papakrivopoulou, J and Yellon, DM (2000) Adenosine A(1) receptor induced delayed preconditioning in rabbits - Induction of p38 mitogen-activated protein kinase activation and Hsp27 phosphorylation via a tyrosine kinase- and protein kinase C-dependent mechanism. CIRC RES , 86 (9) 989 - 997. |
K
| Kari, JA and Gonzalez, C and Ledermann, SE and Shaw, V and Rees, L (2000) Outcome and growth of infants with severe chronic renal failure. KIDNEY INTERNATIONAL , 57 (4) 1681 - 1687. 10.1046/j.1523-1755.2000.00013.x. |
| Koziell, A and Charmandari, E and Hindmarsh, PC and Rees, L and Scambler, P and Brook, CGD (2000) Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy? CLIN ENDOCRINOL , 52 (4) 519 - 524. |
M
| Marks, SD and Rees, L (2000) Spontaneous clinical improvement in dense deposit disease. PEDIATRIC NEPHROLOGY , 14 (4) 322 - 324. |
| Maxwell, H and Amlot, P and Rees, L (2000) Growth hormone and markers of immune function in children with renal transplants. PEDIATRIC NEPHROLOGY , 14 (6) 473 - 475. |
N
| Nishizawa, S and Peters, J and Cuckow, PM and Winyard, PJD (2000) Congenital kidney and bladder malformations in the T(2;11)30H mouse. In: American Society of Nephrology. |
| Nishizawa, S and Peters, J and Cuckow, PM and Winyard, PJD (2000) Congenital kidney and bladder malformations in the T(2;11)30H mouse. UK Renal Association, London, April 2000 |
R
| Rees, L and Ward, G and Rigden, SPA (2000) Growth over 10 years following a 1-year trial of growth hormone therapy. PEDIATRIC NEPHROLOGY , 14 (4) 309 - 314. |
S
| Saleem, MA and Ramanan, AV and Rees, L (2000) Recurrent focal segmental glomerulosclerosis in grafts treated with plasma exchange and increased immunosuppression. PEDIATRIC NEPHROLOGY , 14 (5) 361 - 364. |
W
| Wilcon, DT and Ransley, PG (2000) Medicolegal aspects of hypospadias. BJU International , 86 (3) 327 - 331. |
| Winyard, PJD and Sidwell, R (2000) Renal. In: Sidwell, R and Thompson, M, (eds.) Concise Paediatrics. (211 - 246). Greenwich Medical Media |
| Woolf, AS and Winyard, PJD (2000) Gene expression and cell turnover in human renal dysplasia. HISTOL HISTOPATHOL , 15 (1) 159 - 166. |
Y
| Yang, SP and Woolf, AS and Yuan, HT and Scott, RJ and Risdon, RA and O'Hare, MJ and Winyard, PJD (2000) Biological role of transforming growth factor 1 in human congenital kidney malformations. In: Renal Association. |
| Yang, SP and Woolf, AS and Yuan, HT and Scott, RJ and Risdon, RA and O'Hare, MJ and Winyard, PJD (2000) Potential biological role of transforming growth factor-beta 1 in human congenital kidney malformations. AM J PATHOL , 157 (5) 1633 - 1647. |


