Search results - ORA - Oxford University Research Archive

1 - 7 of 7

1

Journal article

SEDLIN forms homodimers: characterisation of SEDLIN mutations and their interactions with transcription factors MBP1, PITX1 and SF1.

Jeyabalan, J, Nesbit, M, Galvanovskis, J, et al.
2010-01-01

2

Journal article

Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome.

Zahirieh, A, Nesbit, M, Ali, A, et al.
2005-04-01

3

Journal article

CLC-5 and KIF3B interact to facilitate CLC-5 plasma membrane expression, endocytosis, and microtubular transport: relevance to pathophysiology of Dent's disease.

Reed, A, Loh, N, Terryn, S, et al.
2010-02-01

4

Journal article

Structure of the leukemia oncogene LMO2: implications for the assembly of a hematopoietic transcription factor complex.

El Omari, K, Hoosdally, S, Tuladhar, K, et al.
2011-02-01

5

Journal article

Menin interacts directly with the homeobox-containing protein Pem.

Lemmens, I, Forsberg, L, Pannett, A, et al.
2001-08-01

6

Journal article

Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome.

Nesbit, M, Bowl, MR, Harding, B, et al.
2004-05-01

7

Conference item

AMP-activated protein kinase phosphorylates cardiac troponin I and alters contractility of murine ventricular myocytes.

Oliveira, S, Zhang, Y, Solis, R, et al.
2012-04-01

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