Zfp521 promotes B-cell viability and cyclin D1 gene expression in a B cell culture system

Por Al Dallal, Salma, Wolton, Kathryn, Hentges, Kathryn E.
Publicado no Leuk Res (2016)

Locus heterogeneity disease genes encode proteins with high interconnectivity in the human protein interaction network

Por Keith, Benjamin P., Robertson, David L., Hentges, Kathryn E.
Publicado no Front Genet (2014)

The Use of Scenario-Based-Learning Interactive Software to Create Custom Virtual Laboratory Scenarios for Teaching Genetics

Por Breakey, Kate M., Levin, Daniel, Miller, Ian, Hentges, Kathryn E.
Publicado em 2008

The Essentiality Status of Mouse Duplicate Gene Pairs Correlates with Developmental Co-Expression Patterns

Por Kabir, Mitra, Wenlock, Stephanie, Doig, Andrew J., Hentges, Kathryn E.
Publicado no Sci Rep (2019)

Regional Variation in the Density of Essential Genes in Mice

Por Hentges, Kathryn E, Pollock, David D, Liu, Bin, Justice, Monica J
Publicado em 2007

Correlation of microsynteny conservation and disease gene distribution in mammalian genomes

Por Lovell, Simon C, Li, Xiting, Weerasinghe, Nimmi R, Hentges, Kathryn E
Publicado em 2009

Defining the Role of Essential Genes in Human Disease

Por Dickerson, Jonathan E., Zhu, Ana, Robertson, David L., Hentges, Kathryn E.
Publicado em 2011

Enforced Expression of Hoxa3 Inhibits Classical and Promotes Alternative Activation of Macrophages In Vitro and In Vivo

Por Al Sadoun, Hadeel, Burgess, Matthew, Hentges, Kathryn E., Mace, Kimberly A.
Publicado no J Immunol (2016)

Properties of genes essential for mouse development

Por Kabir, Mitra, Barradas, Ana, Tzotzos, George T., Hentges, Kathryn E., Doig, Andrew J.
Publicado no PLoS One (2017)

Identifying mouse developmental essential genes using machine learning

Por Tian, David, Wenlock, Stephanie, Kabir, Mitra, Tzotzos, George, Doig, Andrew J., Hentges, Kathryn E.
Publicado no Dis Model Mech (2018)

FRAP/mTOR is required for proliferation and patterning during embryonic development in the mouse

Por Hentges, Kathryn E., Sirry, Baheya, Gingeras, Anne-Claude, Sarbassov, Dos, Sonenberg, Nahum, Sabatini, David, Peterson, Andrew S.
Publicado em 2001

The functional diversity of essential genes required for mammalian cardiac development

Por Clowes, Christopher, Boylan, Michael GS, Ridge, Liam A, Barnes, Emma, Wright, Jayne A, Hentges, Kathryn E
Publicado em 2014

Gene Duplication and Environmental Adaptation within Yeast Populations

Por Ames, Ryan M., Rash, Bharat M., Hentges, Kathryn E., Robertson, David L., Delneri, Daniela, Lovell, Simon C.
Publicado em 2010

Integration of Large-Scale Genomic Data Sources With Evolutionary History Reveals Novel Genetic Loci for Congenital Heart Disease

Por Fotiou, Elisavet, Williams, Simon, Martin-Geary, Alexandra, Robertson, David L., Tenin, Gennadiy, Hentges, Kathryn E., Keavney, Bernard
Publicado no Circ Genom Precis Med (2019)

Erbb2 Is Required for Cardiac Atrial Electrical Activity during Development

Por Tenin, Gennadiy, Clowes, Christopher, Wolton, Kathryn, Krejci, Eliska, Wright, Jayne A., Lovell, Simon C., Sedmera, David, Hentges, Kathryn E.
Publicado em 2014

Retroviral insertions in the VISION database identify molecular pathways in mouse lymphoid leukemia and lymphoma

Por Weiser, Keith C., Liu, Bin, Hansen, Gwenn M., Skapura, Darlene, Hentges, Kathryn E., Yarlagadda, Sujatha, Morse III, Herbert C., Justice, Monica J.
Publicado em 2007

Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1–BP2) deletion in the UK Biobank

Por Williams, Simon G., Nakev, Apostol, Guo, Hui, Frain, Simon, Tenin, Gennadiy, Liakhovitskaia, Anna, Saha, Priyanka, Priest, James R., Hentges, Kathryn E., Keavney, Bernard D.
Publicado no Eur J Hum Genet (2020)

Transcriptional regulation of the proto‐oncogene Zfp521 by SPI1 (PU.1) and HOXC13

Por Yu, Ming, Al‐Dallal, Salma, Al‐Haj, Latifa, Panjwani, Shiraj, McCartney, Akina S., Edwards, Sarah M., Manjunath, Pooja, Walker, Catherine, Awgulewitsch, Alexander, Hentges, Kathryn E.
Publicado no Genesis (2016)

A missense mutation of ErbB2 produces a novel mouse model of stillbirth associated with a cardiac abnormality but lacking abnormalities of placental structure

Por Shawer, Heba, Aiyelaagbe, Esther, Clowes, Christopher, Lean, Samantha C., Lu, Yinhui, Kadler, Karl E., Kerby, Alan, Dilworth, Mark R., Hentges, Kathryn E., Heazell, Alexander E. P.
Publicado no PLoS One (2020)

Disease modeling of core pre-mRNA splicing factor haploinsufficiency

Por Wood, Katherine A, Rowlands, Charlie F, Qureshi, Wasay Mohiuddin Shaikh, Thomas, Huw B, Buczek, Weronika A, Briggs, Tracy A, Hubbard, Simon J, Hentges, Kathryn E, Newman, William G, O’Keefe, Raymond T
Publicado no Hum Mol Genet (2019)