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62.
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Transcript Analysis Reveals a Hypoxic Inflammatory Environment in Human Chronic Otitis Media With Effusion. [electronic resource] by
- Bhutta, Mahmood F
- Lambie, Jane
- Hobson, Lindsey
- Williams, Debbie
- Tyrer, Hayley E
- Nicholson, George
- Brown, Steve D M
- Brown, Helen
- Piccinelli, Chiara
- Devailly, Guillaume
- Ramsden, James
- Cheeseman, Michael T
Publication details: Frontiers in genetics 2019
In:
Frontiers in genetics vol. 10
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63.
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An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda. [electronic resource] by
- Barbaric, Ivana
- Perry, Mark J
- Dear, T Neil
- Rodrigues Da Costa, Alexandra
- Salopek, Daniela
- Marusic, Ana
- Hough, Tertius
- Wells, Sara
- Hunter, A Jackie
- Cheeseman, Michael
- Brown, Steve D M
Producer: 20080428
In:
Physiological genomics vol. 32
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64.
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Genetic analysis of the mouse brain proteome. [electronic resource] by
- Klose, Joachim
- Nock, Christina
- Herrmann, Marion
- Stühler, Kai
- Marcus, Katrin
- Blüggel, Martin
- Krause, Eberhard
- Schalkwyk, Leonard C
- Rastan, Sohaila
- Brown, Steve D M
- Büssow, Konrad
- Himmelbauer, Heinz
- Lehrach, Hans
Producer: 20020502
In:
Nature genetics vol. 30
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65.
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Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Signaling Pathway. [electronic resource] by
- Esapa, Christopher T
- Piret, Sian E
- Nesbit, M Andrew
- Loh, Nellie Y
- Thomas, Gethin
- Croucher, Peter I
- Brown, Matthew A
- Brown, Steve D M
- Cox, Roger D
- Thakker, Rajesh V
Producer: 20170629
In:
PloS one vol. 11
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66.
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N-ethyl-N-Nitrosourea (ENU) induced mutations within the klotho gene lead to ectopic calcification and reduced lifespan in mouse models. [electronic resource] by
- Esapa, Christopher T
- Hannan, Fadil M
- Babinsky, Valerie N
- Potter, Paul
- Thomas, Gethin P
- Croucher, Peter I
- Brown, Matthew A
- Brown, Steve D M
- Cox, Roger D
- Thakker, Rajesh V
Producer: 20160331
In:
PloS one vol. 10
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67.
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Establishing normal plasma and 24-hour urinary biochemistry ranges in C3H, BALB/c and C57BL/6J mice following acclimatization in metabolic cages. [electronic resource] by
- Stechman, Michael J
- Ahmad, Bushra N
- Loh, Nellie Y
- Reed, Anita A C
- Stewart, Michelle
- Wells, Sara
- Hough, Tertius
- Bentley, Liz
- Cox, Roger D
- Brown, Steve D M
- Thakker, Rajesh V
Producer: 20100928
In:
Laboratory animals vol. 44
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68.
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Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair. [electronic resource] by
- Mianné, Joffrey
- Chessum, Lauren
- Kumar, Saumya
- Aguilar, Carlos
- Codner, Gemma
- Hutchison, Marie
- Parker, Andrew
- Mallon, Ann-Marie
- Wells, Sara
- Simon, Michelle M
- Teboul, Lydia
- Brown, Steve D M
- Bowl, Michael R
Producer: 20161012
In:
Genome medicine vol. 8
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69.
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Modification of an aggressive model of Alport Syndrome reveals early differences in disease pathogenesis due to genetic background. [electronic resource] by
- Falcone, Sara
- Wisby, Laura
- Nicol, Thomas
- Blease, Andrew
- Starbuck, Becky
- Parker, Andrew
- Sanderson, Jeremy
- Brown, Steve D M
- Scudamore, Cheryl L
- Pusey, Charles D
- Tam, Frederick W K
- Potter, Paul K
Producer: 20201110
In:
Scientific reports vol. 9
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70.
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A mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutation. [electronic resource] by
- Piret, Sian E
- Esapa, Christopher T
- Gorvin, Caroline M
- Head, Rosie
- Loh, Nellie Y
- Devuyst, Olivier
- Thomas, Gethin
- Brown, Steve D M
- Brown, Matthew
- Croucher, Peter
- Cox, Roger
- Thakker, Rajesh V
Producer: 20130215
In:
PloS one vol. 7
Availability: No items available.
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71.
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Novel ENU-induced eye mutations in the mouse: models for human eye disease. [electronic resource] by
- Thaung, Caroline
- West, Katrine
- Clark, Brian J
- McKie, Lisa
- Morgan, Joanne E
- Arnold, Karen
- Nolan, Patrick M
- Peters, Jo
- Hunter, A Jackie
- Brown, Steve D M
- Jackson, Ian J
- Cross, Sally H
Producer: 20020911
In:
Human molecular genetics vol. 11
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72.
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Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2. [electronic resource] by
- Hough, Tertius A
- Polewski, Monika
- Johnson, Kristen
- Cheeseman, Michael
- Nolan, Patrick M
- Vizor, Lucie
- Rastan, Sohaila
- Boyde, Alan
- Pritzker, Kenneth
- Hunter, A Jackie
- Fisher, Elizabeth M C
- Terkeltaub, Robert
- Brown, Steve D M
Producer: 20071113
In:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 22
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73.
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Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population. [electronic resource] by
- Ouyang, Xiao Mei
- Yan, Denise
- Du, Li Lin
- Hejtmancik, J Fielding
- Jacobson, Samuel G
- Nance, Walter E
- Li, An Ren
- Angeli, Simon
- Kaiser, Muriel
- Newton, Valerie
- Brown, Steve D M
- Balkany, Thomas
- Liu, Xue Zhong
Producer: 20050418
In:
Human genetics vol. 116
Availability: No items available.
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74.
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Comparative visualization of genotype-phenotype relationships. [electronic resource] by
- Yaikhom, Gagarine
- Morgan, Hugh
- Sneddon, Duncan
- Retha, Ahmad
- Atienza-Herrero, Julian
- Blake, Andrew
- Brown, James
- Di Fenza, Armida
- Fiegel, Tanja
- Horner, Neil
- Ring, Natalie
- Santos, Luis
- Westerberg, Henrik
- Brown, Steve D M
- Mallon, Ann-Marie
Producer: 20151022
In:
Nature methods vol. 12
Availability: No items available.
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75.
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MouseBook: an integrated portal of mouse resources. [electronic resource] by
- Blake, Andrew
- Pickford, Karen
- Greenaway, Simon
- Thomas, Steve
- Pickard, Amanda
- Williamson, Christine M
- Adams, Niels C
- Walling, Alison
- Beck, Tim
- Fray, Martin
- Peters, Jo
- Weaver, Tom
- Brown, Steve D M
- Hancock, John M
- Mallon, Ann-Marie
Producer: 20100201
In:
Nucleic acids research vol. 38
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76.
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IGF-1 receptor antagonism inhibits autophagy. [electronic resource] by
- Renna, Maurizio
- Bento, Carla F
- Fleming, Angeleen
- Menzies, Fiona M
- Siddiqi, Farah H
- Ravikumar, Brinda
- Puri, Claudia
- Garcia-Arencibia, Moises
- Sadiq, Oana
- Corrochano, Silvia
- Carter, Sarah
- Brown, Steve D M
- Acevedo-Arozena, Abraham
- Rubinsztein, David C
Producer: 20140603
In:
Human molecular genetics vol. 22
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77.
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PRIME importance of pathology expertise. [electronic resource] by
- Schofield, Paul N
- Brown, Steve D M
- Sundberg, John P
- Arends, Mark
- Warren, Madhuri V
- Dubus, Pierre
- Ellender, Michele
- Fiette, Laurence
- Rozell, Bjorn
- Quintanilla-Martinez, Leticia
- Raspa, Marcello
- Song, Ji-Ying
- van der Valk, Martin
- McKerlie, Colin
Producer: 20090427
In:
Nature biotechnology vol. 27
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78.
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Mouse Models of NMNAT1-Leber Congenital Amaurosis (LCA9) Recapitulate Key Features of the Human Disease. [electronic resource] by
- Greenwald, Scott H
- Charette, Jeremy R
- Staniszewska, Magdalena
- Shi, Lan Ying
- Brown, Steve D M
- Stone, Lisa
- Liu, Qin
- Hicks, Wanda L
- Collin, Gayle B
- Bowl, Michael R
- Krebs, Mark P
- Nishina, Patsy M
- Pierce, Eric A
Producer: 20170512
In:
The American journal of pathology vol. 186
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79.
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CIB2 interacts with TMC1 and TMC2 and is essential for mechanotransduction in auditory hair cells. [electronic resource] by
- Giese, Arnaud P J
- Tang, Yi-Quan
- Sinha, Ghanshyam P
- Bowl, Michael R
- Goldring, Adam C
- Parker, Andrew
- Freeman, Mary J
- Brown, Steve D M
- Riazuddin, Saima
- Fettiplace, Robert
- Schafer, William R
- Frolenkov, Gregory I
- Ahmed, Zubair M
Producer: 20171116
In:
Nature communications vol. 8
Availability: No items available.
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80.
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A genetic modifier suggests that endurance exercise exacerbates Huntington's disease. [electronic resource] by
- Corrochano, Silvia
- Blanco, Gonzalo
- Williams, Debbie
- Wettstein, Jessica
- Simon, Michelle
- Kumar, Saumya
- Moir, Lee
- Agnew, Thomas
- Stewart, Michelle
- Landman, Allison
- Kotiadis, Vassilios N
- Duchen, Michael R
- Wackerhage, Henning
- Rubinsztein, David C
- Brown, Steve D M
- Acevedo-Arozena, Abraham
Producer: 20190214
In:
Human molecular genetics vol. 27
Availability: No items available.
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