Browsing by Author Whittle, Belinda
Showing results 1 to 20 of 31
A de novo Mutation in KMT2A (MLL) in monozygotic twins with Wiedemann-Steiner Syndrome
Author(s) | Dunkerton, Sophie; Field, Matthew; Cho, Eun, et al |
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Type | Journal article |
Date Published | 2015 |
Date Created | - |
A Missense Mutation in the Transcription Factor ETV5 Leads to Sterility, Increased Embryonic and Perinatal Death, Postnatal Growth Restriction, Renal Asymmetry and Polydactyly in the Mouse
Author(s) | Jamsai, Duangporn; Clark, Brett J.; Smith, Stephanie J., et al |
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Type | Journal article |
Date Published | 21-Oct-2013 |
Date Created | - |
A mutation in a chromosome condensin II subunit, kleisin, specifically disrupts T cell development
Author(s) | Gosling, Katharine; Makaroff, Lydia; Theodoratos, Angelo, et al |
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Type | Journal article |
Date Published | 2007 |
Date Created | - |
A recessive screen for genes regulating hematopoietic stem cells
Author(s) | Papathanasiou, Panagiotis; Tunningley, Robert; Pattabiraman, Diwakar, et al |
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Type | Journal article |
Date Published | 2010 |
Date Created | - |
A RING-type ubiquitin ligase family member required to repress follicular helper T cells and autoimmunity
Author(s) | Garcia De Vinuesa, Maria Carola; Cook, Matthew; Angelucci, C, et al |
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Type | Journal article |
Date Published | 2005 |
Date Created | - |
An essential role for Katanin p80 and microtubule severing in male gamete production
Author(s) | O'Donnell, Liza; Rhodes, Danielle; Smith, Stephanie J, et al |
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Type | Journal article |
Date Published | 24-May-2012 |
Date Created | - |
Arrested hematopoiesis and vascular relaxation defects in mice with a mutation in Dhfr
Author(s) | Thoms, Julie A. I.; Knezevic, Kathy; Liu, Jia Jenny, et al |
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Type | Journal article |
Date Published | 2016 |
Date Created | - |
ATP11C is critical for the internalization of phosphatidylserine and differentiation of B lymphocytes
Author(s) | Yabas, Mehmet; Teh, Charis; Frankenreiter, Sandra, et al |
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Type | Journal article |
Date Published | 2011 |
Date Created | - |
Autoimmunity in primary antibody deficiency is associated with protein tyrosine phosphatase nonreceptor type 22 (PTPN22)
Author(s) | Chew, Gary Y J; Sinha, Umang; Gatenby, Paul A, et al |
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Type | Journal article |
Date Published | Apr-2013 |
Date Created | - |
B cell survival, surface BCR and BAFFR expression, CD74 metabolism, and CD8-dendritic cells require the intramembrane endopeptidase SPPL2A
Author(s) | Bergmann, Hannes; Yabas, Mehmet; Short, Alanna, et al |
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Type | Journal article |
Date Published | 14-Jan-2013 |
Date Created | - |
Bulk Segregation Mapping of Mutations in Closely Related Strains of Mice
Author(s) | Xia, Yu; Won, Sungyong; Du, Xin, et al |
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Type | Journal article |
Date Published | 2010 |
Date Created | - |
Comparison of predicted and actual consequences of missense mutations
Author(s) | Miosge, Lisa; Field, Matthew; Sontani, Yovina, et al |
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Type | Journal article |
Date Published | 2015 |
Date Created | - |
Dock8 mutations cripple B cell immunological synapses, germinal centers and long-lived antibody production
Author(s) | Randall, Katrina; Lambe, Teresa; Johnson, Andy L, et al |
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Type | Journal article |
Date Published | 2009 |
Date Created | - |
ENU mutagenesis screen to establish motor phenotypes in wild-type mice and modifiers of a pre-existing motor phenotype in tau mutant mice
Author(s) | Liu, Xin; Dobbie, Michael S; Tunningley, Robert, et al |
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Type | Journal article |
Date Published | 2011 |
Date Created | - |
Genome-Wide ENU Mutagenesis in Combination with High Density SNP Analysis and Exome Sequencing Provides Rapid Identification of Novel Mouse Models of Developmental Disease
Author(s) | Caruana, Georgina; Farlie, Peter G; Hart, Adam H, et al |
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Type | Journal article |
Date Published | 1-Mar-2013 |
Date Created | - |
Identification of phenotypically and functionally heterogeneous mouse mucosal-associated invariant t cells using MR1 tetramers
Author(s) | Rahimpour, Azad; Koay, Hui Fern; Enders, Anselm, et al |
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Type | Journal article |
Date Published | 2015 |
Date Created | - |
LRGUK-1 is required for basal body and Manchette function during spermatogenesis and male fertility
Author(s) | Liu, Yan; DeBoer, Kathleen; de Kretser, David M., et al |
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Type | Journal article |
Date Published | 17-Mar-2015 |
Date Created | - |
Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models
Author(s) | Andrews, Thomas Daniel; Whittle, Belinda; Field, Matthew, et al |
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Type | Journal article |
Date Published | 2012 |
Date Created | - |
Memory T cell RNA rearrangement programmed by heterogeneous nuclear ribonucleoprotein hnRNPLL
Author(s) | Wu, Zuopeng; Jia, Xinying; de la Cruz, Laura, et al |
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Type | Journal article |
Date Published | 2008 |
Date Created | - |
Mitochondrial genome diversity among Papuan-speaking people of Papua New Guinea
Author(s) | Easteal, Simon; Whittle, Belinda; Mettenmeyer, Andrea, et al |
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Type | Book chapter |
Date Published | 2005 |
Date Created | - |
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