Search results - ORA - Oxford University Research Archive

1

Journal article

Studies of mice deleted for Sox3 and uc482: Relevance to X-linked hypoparathyroidism

Gaynor, KU, Grigorieva, IV, Mirczuk, SM, et al.
2020-02-01

2

Journal article

Cinacalcet corrects hypercalcemia in mice with an inactivating Gα11 mutation

Howles, S, Hannan, F, Gorvin, C, et al.
2017-10-19

3

Journal article

Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.

Potter, PK, Bowl, MR, Jeyarajan, P, et al.
2016-08-18

4

Journal article

A mouse model for inherited renal fibrosis associated with endoplasmic reticulum stress.

Piret, S, Olinger, E, Reed, A, et al.
2017-03-01

5

Journal article

N-ethyl-N-nitrosourea-induced adaptor protein 2 sigma subunit 1 ( Ap2s1 ) mutations establish Ap2s1 loss-of-function mice

Gorvin, C, Rogers, A, Stewart, M, et al.
2017-03-09

6

Journal article

Mutant mice with calcium-sensing receptor (CaSR) activation have hyperglycemia, that is rectified by calcilytic therapy

Babinsky, V, Hannan, F, Ramracheya, R, et al.
2017-06-02

7

Journal article

Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy

Gorvin, C, Hannan, F, Howles, S, et al.
2017-02-09

8

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

9

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

10

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

11

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

12

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

13

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

14

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

15

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

16

Journal article

A mutation in the mitochondrial fission gene Dnm1l leads to cardiomyopathy

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

17

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

18

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

19

Journal article

Gata3-deficient mice develop parathyroid abnormalities due to dysregulation of the parathyroid-specific transcription factor Gcm2.

Grigorieva, I, Mirczuk, S, Gaynor, K, et al.
2010-06-01

20

Journal article

A mutation in the mitochondrial fission gene Dnm1l leads to cardiomyopathy.

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

21

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

22

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.
2012-01-01

23

Journal article

A protocol for high-throughput phenotyping, suitable for quantitative trait analysis in mice.

Solberg, L, Valdar, W, Gauguier, D, et al.
2006-02-01

24

Conference item

Genetic models of bone disease using ENU mutagenesis

Brown, S, Esapa, C, Barbaric, I, et al.
2009-05-01

25

Journal article

Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5.

Loh, N, Bentley, L, Dimke, H, et al.
2013-01-01

26

Journal article

Establishing normal plasma and 24-hour urinary biochemistry ranges in C3H, BALB/c and C57BL/6J mice following acclimatization in metabolic cages.

Stechman, M, Ahmad, B, Loh, N, et al.
2010-07-01

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