Search results - ORA - Oxford University Research Archive

1 - 8 of 8

1

Journal article

A gating mutation at the internal mouth of the Kir6.2 pore is associated with DEND syndrome.

Proks, P, Girard, C, Haider, S, et al.
2005-05-01

2

Journal article

SLC2A9 is a high-capacity urate transporter in humans.

Caulfield, M, Munroe, P, O'Neill, D, et al.
2008-10-01

3

Journal article

Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent'sJapan disease.

Igarashi, T, Günther, W, Sekine, T, et al.
1998-12-01

4

Journal article

Alpha7-acetylcholine receptor antibodies in two patients with Rasmussen encephalitis.

Watson, R, Jepson, J, Bermudez, I, et al.
2005-12-01

5

Journal article

Characterization of renal chloride channel (CLCN5) mutations in Dent's disease.

Yamamoto, K, Cox, J, Friedrich, T, et al.
2000-08-01

6

Journal article

Expression of K channels in Xenopus laevis oocytes injected with poly(A+) mRNA from the insulin-secreting beta-cell line, HIT T15.

Ashcroft, F, Ashcroft, S, Berggren, P, et al.
1988-11-01

7

Journal article

Relapsing diabetes can result from moderately activating mutations in KCNJ11.

Gloyn, A, Reimann, F, Girard, C, et al.
2005-04-01

8

Journal article

Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features.

Proks, P, Antcliff, J, Lippiat, J, et al.
2004-12-01

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