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1

Journal article

Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing

Nicod, J, Davies, R, Cai, N, et al.
2016-07-01

2

Journal article

Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemia.

Harding, B, Lemos, M, Reed, A, et al.
2009-12-01

3

Conference item

A Mouse with a Ser1386Pro Mutation in the C-propeptide Domain of col2aI Provides a Model for Spondyloepiphyseal Dysplasia Congenita

Esapa, C, Hough, T, Testori, S, et al.
2008-09-01

4

Journal article

An N-ethyl-n-nitrosourea induced corticotropin-releasing hormone promoter mutation provides a mouse model for endogenous glucocorticoid excess

Bentley, L, Esapa, C, Nesbit, M, et al.
2014-03-01

5

Journal article

A mouse with an N-Ethyl-N-nitrosourea (ENU) Induced Trp589Arg Galnt3 mutation represents a model for hyperphosphataemic familial tumoural calcinosis

Esapa, C, Head, R, Jeyabalan, J, et al.
2012-08-13

6

Journal article

Next-generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson's syndrome.

Bull, K, Mason, T, Rimmer, A, et al.
2014-05-01

7

Journal article

Activating calcium-sensing receptor mutation in the mouse is associated with cataracts and ectopic calcification.

Hough, T, Bogani, D, Cheeseman, M, et al.
2004-09-01

8

Journal article

A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutation.

Esapa, C, Hough, T, Testori, S, et al.
2012-02-01

9

Journal article

A mutation in the mitochondrial fission gene Dnm1l leads to cardiomyopathy

Ashrafian, H, Docherty, L, Leo, V, et al.
2010-06-01

10

Journal article

HIF-VEGF pathways are critical for chronic otitis media in Junbo and Jeff mouse mutants.

Cheeseman, M, Tyrer, H, Williams, D, et al.
2011-10-01

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