A mouse with an ENU-induced mutation (Tyr209Asn) in the natriuretic peptide receptor 3 (Npr3) develops autosomal recessive kyphosis

Christopher Esapa; Rosie Head; Gethin Thomas; Matthew Brown; Peter Croucher; Roger Cox; Steve Brown; Rajesh Thakker

A mouse with an ENU-induced mutation (Tyr209Asn) in the natriuretic peptide receptor 3 (Npr3) develops autosomal recessive kyphosis

Christopher Esapa, Rosie Head, Gethin Thomas, Matthew Brown, Peter Croucher, Roger Cox, Steve Brown, Rajesh Thakker

Research output: Other contribution to conference › Abstract › peer-review

Abstract

Kyphosis is a common spinal disorder affecting up to 8.3% of the population, and associated with significant morbidity. Familial and twin studies have implicated a genetic involvement. However, the causative genes have not been identified.

Original language	English
Pages	25
Number of pages	1
Publication status	Published - 2011
Event	Society for Endocrinology BES 2010 - Manchester, United Kingdom Duration: 14 Mar 2010 → 17 Mar 2010 https://web.archive.org/web/20100403001113/http://www.endocrinology.org:80/meetings/2010/SFEBES2010/

Conference

Conference	Society for Endocrinology BES 2010
Country	United Kingdom
City	Manchester
Period	14/03/10 → 17/03/10
Internet address	https://web.archive.org/web/20100403001113/http://www.endocrinology.org:80/meetings/2010/SFEBES2010/

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http://www.endocrine-abstracts.org/ea/0025/ea0025OC4.1.htm

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Esapa, C., Head, R., Thomas, G., Brown, M., Croucher, P., Cox, R., Brown, S., & Thakker, R. (2011). A mouse with an ENU-induced mutation (Tyr209Asn) in the natriuretic peptide receptor 3 (Npr3) develops autosomal recessive kyphosis. 25. Abstract from Society for Endocrinology BES 2010, Manchester, United Kingdom. http://www.endocrine-abstracts.org/ea/0025/ea0025OC4.1.htm

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title = "A mouse with an ENU-induced mutation (Tyr209Asn) in the natriuretic peptide receptor 3 (Npr3) develops autosomal recessive kyphosis",

abstract = "Kyphosis is a common spinal disorder affecting up to 8.3% of the population, and associated with significant morbidity. Familial and twin studies have implicated a genetic involvement. However, the causative genes have not been identified. ",

author = "Christopher Esapa and Rosie Head and Gethin Thomas and Matthew Brown and Peter Croucher and Roger Cox and Steve Brown and Rajesh Thakker",

year = "2011",

language = "English",

pages = "25",

note = "Society for Endocrinology BES 2010 ; Conference date: 14-03-2010 Through 17-03-2010",

url = "https://web.archive.org/web/20100403001113/http://www.endocrinology.org:80/meetings/2010/SFEBES2010/",

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Esapa, C, Head, R, Thomas, G, Brown, M, Croucher, P, Cox, R, Brown, S & Thakker, R 2011, 'A mouse with an ENU-induced mutation (Tyr209Asn) in the natriuretic peptide receptor 3 (Npr3) develops autosomal recessive kyphosis', Society for Endocrinology BES 2010, Manchester, United Kingdom, 14/03/10 - 17/03/10 pp. 25. <http://www.endocrine-abstracts.org/ea/0025/ea0025OC4.1.htm>

A mouse with an ENU-induced mutation (Tyr209Asn) in the natriuretic peptide receptor 3 (Npr3) develops autosomal recessive kyphosis. / Esapa, Christopher; Head, Rosie; Thomas, Gethin; Brown, Matthew; Croucher, Peter; Cox, Roger; Brown, Steve; Thakker, Rajesh.

2011. 25 Abstract from Society for Endocrinology BES 2010, Manchester, United Kingdom.

Research output: Other contribution to conference › Abstract › peer-review

TY - CONF

T1 - A mouse with an ENU-induced mutation (Tyr209Asn) in the natriuretic peptide receptor 3 (Npr3) develops autosomal recessive kyphosis

AU - Esapa, Christopher

AU - Head, Rosie

AU - Thomas, Gethin

AU - Brown, Matthew

AU - Croucher, Peter

AU - Cox, Roger

AU - Brown, Steve

AU - Thakker, Rajesh

PY - 2011

Y1 - 2011

N2 - Kyphosis is a common spinal disorder affecting up to 8.3% of the population, and associated with significant morbidity. Familial and twin studies have implicated a genetic involvement. However, the causative genes have not been identified.

AB - Kyphosis is a common spinal disorder affecting up to 8.3% of the population, and associated with significant morbidity. Familial and twin studies have implicated a genetic involvement. However, the causative genes have not been identified.

M3 - Abstract

SP - 25

T2 - Society for Endocrinology BES 2010

Y2 - 14 March 2010 through 17 March 2010

ER -