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Author/Creator Hough, Tertius A

1. An N‐Ethyl‐N‐Nitrosourea (ENU)‐Induced Tyr265Stop Mutation of the DNA Polymerase Accessory Subunit Gamma 2 (Polg2) Is Associated With Renal Calcification in Mice. (14th December 2018)

Authors:
Gorvin, Caroline M; Ahmad, Bushra N; Stechman, Michael J; Loh, Nellie Y; Hough, Tertius A; Leo, Paul; Marshall, Mhairi; Sethi, Siddharth; Bentley, Liz; Piret, Sian E; Reed, Anita; Jeyabalan, Jeshmi; Christie, Paul T; Wells, Sara; Simon, Michelle M; Mallon, Ann‐Marie; Schulz, Herbert; Huebner, Nor...
Journal:
Journal of bone and mineral research
Issue:
Volume 34:Number 3(2019)
Page Start:
497
Record Type:
Journal Article
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2. Chronically elevated branched chain amino acid levels are pro-arrhythmic. Issue 7 (17th June 2021)

Authors:
Portero, Vincent; Nicol, Thomas; Podliesna, Svitlana; Marchal, Gerard A; Baartscheer, Antonius; Casini, Simona; Tadros, Rafik; Treur, Jorien L; Tanck, Michael W T; Cox, I Jane; Probert, Fay; Hough, Tertius A; Falcone, Sara; Beekman, Leander; Müller-Nurasyid, Martina; Kastenmüller, Gabi; Gieger, C...
Journal:
Cardiovascular research
Issue:
Volume 118:Issue 7(2022)
Page Start:
1742
Record Type:
Journal Article
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3. Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis. (4th March 2019)

Authors:
Gorvin, Caroline M; Loh, Nellie Y; Stechman, Michael J; Falcone, Sara; Hannan, Fadil M; Ahmad, Bushra N; Piret, Sian E; Reed, Anita AC; Jeyabalan, Jeshmi; Leo, Paul; Marshall, Mhairi; Sethi, Siddharth; Bass, Paul; Roberts, Ian; Sanderson, Jeremy; Wells, Sara; Hough, Tertius A; Bentley, Liz; Chris...
Journal:
Journal of bone and mineral research
Issue:
Volume 34:Number 7(2019)
Page Start:
1324
Record Type:
Journal Article
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4. Next‐generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson's syndrome. Issue 1 (6th February 2014)

Authors:
Bull, Katherine R; Mason, Thomas; Rimmer, Andrew J; Crockford, Tanya L; Silver, Karlee L; Bouriez‐Jones, Tiphaine; Hough, Tertius A; Chaudhry, Shirine; Roberts, Ian SD; Goodnow, Christopher C; Cornall, Richard J
Journal:
Journal of pathology
Issue:
Volume 233:Issue 1(2014)
Page Start:
18
Record Type:
Journal Article
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5. Next‐generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson's syndrome. Issue 1 (6th February 2014)

Authors:
Bull, Katherine R; Mason, Thomas; Rimmer, Andrew J; Crockford, Tanya L; Silver, Karlee L; Bouriez‐Jones, Tiphaine; Hough, Tertius A; Chaudhry, Shirine; Roberts, Ian SD; Goodnow, Christopher C; Cornall, Richard J
Journal:
Journal of pathology
Issue:
Volume 233:Issue 1(2014)
Page Start:
18
Record Type:
Journal Article
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6. N‐ethyl‐N‐nitrosourea–Induced Adaptor Protein 2 Sigma Subunit 1 (Ap2s1) Mutations Establish Ap2s1 Loss‐of‐Function Mice. (2nd May 2017)

Authors:
Gorvin, Caroline M; Rogers, Angela; Stewart, Michelle; Paudyal, Anju; Hough, Tertius A; Teboul, Lydia; Wells, Sara; Brown, Steve DM; Cox, Roger D; Thakker, Rajesh V
Journal:
JBMR plus
Issue:
Volume 1:Number 1(2017)
Page Start:
3
Record Type:
Journal Article
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