Ann-Marie Mallon
Ann-Marie Mallon
MRC Harwell
Email verificata su
Citata da
Citata da
High-throughput discovery of novel developmental phenotypes
ME Dickinson, AM Flenniken, X Ji, L Teboul, MD Wong, JK White, ...
Nature 537 (7621), 508-514, 2016
Promoting coherent minimum reporting guidelines for biological and biomedical investigations: the MIBBI project
CF Taylor, D Field, SA Sansone, J Aerts, R Apweiler, M Ashburner, ...
Nature biotechnology 26 (8), 889-896, 2008
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains
MM Simon, S Greenaway, JK White, H Fuchs, V Gailus-Durner, S Wells, ...
Genome biology 14, 1-22, 2013
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31
P Mburu, M Mustapha, A Varela, D Weil, A El-Amraoui, RH Holme, ...
Nature genetics 34 (4), 421-428, 2003
The International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping data
G Koscielny, G Yaikhom, V Iyer, TF Meehan, H Morgan, J Atienza-Herrero, ...
Nucleic acids research 42 (D1), D802-D809, 2014
Using ontologies to describe mouse phenotypes
GV Gkoutos, ECJ Green, AM Mallon, JM Hancock, D Davidson
Genome biology 6, 1-10, 2005
Prevalence of sexual dimorphism in mammalian phenotypic traits
NA Karp, J Mason, AL Beaudet, Y Benjamini, L Bower, RE Braun, ...
Nature communications 8 (1), 15475, 2017
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium
TF Meehan, N Conte, DB West, JO Jacobsen, J Mason, J Warren, ...
Nature genetics 49 (8), 1231-1238, 2017
The fantasy of authenticity: Touring with Lacan
DC Knudsen, JM Rickly, ES Vidon
Annals of Tourism Research 58, 33-45, 2016
The gene mutated in bare patches and striated mice encodes a novel 3β-hydroxysteroid dehydrogenase
XY Liu, AW Dangel, RI Kelley, W Zhao, P Denny, M Botcherby, ...
Nature genetics 22 (2), 182-187, 1999
Mouse large-scale phenotyping initiatives: Overview of the European mouse disease clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project
A Ayadi, MC Birling, J Bottomley, J Bussell, H Fuchs, M Fray, ...
Mammalian Genome 23, 600-610, 2012
The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease
T Groza, FL Gomez, HH Mashhadi, V Muoz-Fuentes, O Gunes, R Wilson, ...
Nucleic acids research 51 (D1), D1038-D1045, 2023
Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics
M Hrabě de Angelis, G Nicholson, M Selloum, JK White, H Morgan, ...
Nature genetics 47 (9), 969-978, 2015
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction
MR Bowl, MM Simon, NJ Ingham, S Greenaway, L Santos, H Cater, ...
Nature communications 8 (1), 886, 2017
Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair
J Miann, L Chessum, S Kumar, C Aguilar, G Codner, M Hutchison, ...
Genome medicine 8, 1-12, 2016
Accelerating the evolution of nonhuman primate neuroimaging
M Milham, CI Petkov, DS Margulies, CE Schroeder, MA Basso, P Belin, ...
Neuron 105 (4), 600-603, 2020
The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation
V Muoz-Fuentes, P Cacheiro, TF Meehan, JA Aguilar-Pimentel, ...
Conservation genetics 19, 995-1005, 2018
Novel gene function revealed by mouse mutagenesis screens for models of age-related disease
PK Potter, MR Bowl, P Jeyarajan, L Wisby, A Blease, ME Goldsworthy, ...
Nature communications 7 (1), 12444, 2016
Applying the ARRIVE guidelines to an in vivo database
NA Karp, TF Meehan, H Morgan, JC Mason, A Blake, N Kurbatova, ...
PLoS biology 13 (5), e1002151, 2015
The regulatory factor ZFHX3 modifies circadian function in SCN via an AT motif-driven axis
MJ Parsons, M Brancaccio, S Sethi, ES Maywood, R Satija, JK Edwards, ...
Cell 162 (3), 607-621, 2015
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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