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Browsing by Author Whittle, Belinda

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Showing results 1 to 20 of 32

A de novo Mutation in KMT2A (MLL) in monozygotic twins with Wiedemann-Steiner Syndrome

Author(s)Dunkerton, Sophie; Field, Matthew; Cho, Eun, et al
TypeJournal article
Date Published2015
Date Created-
01_Jamsai_A_Missense_Mutation_in_the_2013.pdf.jpg

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
TypeJournal article
Date Published21-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
TypeJournal article
Date Published2007
Date Created-

A recessive screen for genes regulating hematopoietic stem cells

Author(s)Papathanasiou, Panagiotis; Tunningley, Robert; Pattabiraman, Diwakar, et al
TypeJournal article
Date Published2010
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
TypeJournal article
Date Published2005
Date Created-
01_O'Donnell_An_essential_role_for_Katanin_2012.pdf.jpg

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
TypeJournal article
Date Published24-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
TypeJournal article
Date Published2016
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
TypeJournal article
Date Published2011
Date Created-
Journal of Allergy and Clinical Immunology.pdf.jpg

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
TypeJournal article
Date PublishedApr-2013
Date Created-

Autosomal-dominant B-cell deficiency with alopecia due to a mutation in NFKB2 that results in nonprocessable p100

Author(s)Lee, Cindy; Fulcher, David; Whittle, Belinda, et al
TypeJournal article
Date Published2014
Date Created-
BergmannetalBcellsurvival,surfaceBCR2013.pdf.jpg

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
TypeJournal article
Date Published14-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
TypeJournal article
Date Published2010
Date Created-

Comparison of predicted and actual consequences of missense mutations

Author(s)Miosge, Lisa; Field, Matthew; Sontani, Yovina, et al
TypeJournal article
Date Published2015
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
TypeJournal article
Date Published2009
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
TypeJournal article
Date Published2011
Date Created-
01_Caruana_Genome-Wide_ENU_Mutagenesis_in_2013.pdf.jpg

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
TypeJournal article
Date Published1-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
TypeJournal article
Date Published2015
Date Created-
Liu et al LRGUK-1 is Required 2015.pdf.jpg

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
TypeJournal article
Date Published17-Mar-2015
Date Created-
01_Andrews_Massively_parallel_sequencing_2012.pdf.jpg

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
TypeJournal article
Date Published2012
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
TypeJournal article
Date Published2008
Date Created-

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