Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Katrina Soderquest"'
Autor:
Katrina Soderquest, Arnulf Hertweck, Claudia Giambartolomei, Stephen Henderson, Rami Mohamed, Rimma Goldberg, Esperanza Perucha, Lude Franke, Javier Herrero, Vincent Plagnol, Richard G Jenner, Graham M Lord
Publikováno v:
PLoS Genetics, Vol 13, Iss 2, p e1006587 (2017)
The polarization of CD4+ T cells into distinct T helper cell lineages is essential for protective immunity against infection, but aberrant T cell polarization can cause autoimmunity. The transcription factor T-bet (TBX21) specifies the Th1 lineage an
Externí odkaz:
https://doaj.org/article/1b047c1f9aaf46738e2b7b4684f706e9
Autor:
P. Dean, Graham M. Lord, Caroline Jones, Carol Inward, Gavin I. Welsh, Ania Koziell, Moin A. Saleem, Maggie Williams, Hugh J. McCarthy, Ruth Rollason, Katrina Soderquest, Michael A. Simpson, Elizabeth Colby, Agnieszka Bierzynska
Publikováno v:
Bierzynska, A, Soderquest, K, Dean, P, Colby, E, Rollason, R, Jones, C, Inward, C, McCarthy, H, Simpson, M A, Lord, G M, Williams, M, Welsh, G, Koziell, A & Saleem, M 2017, ' MAGI2 Mutations Cause Congenital Nephrotic Syndrome ', Journal of the American Society of Nephrology, vol. 28, no. 5, pp. 1614-1621 . https://doi.org/10.1681/ASN.2016040387
Bierzynska, A, Soderquest, K, Dean, P, Colby, E, Rollason, R, Jones, C, Inward, C D, McCarthy, H J, Simpson, M A, Lord, G M, Williams, M, Welsh, G I, Koziell, A B & Saleem, M A 2017, ' MAGI2 mutations cause congenital nephrotic syndrome ', Journal of the American Society of Nephrology, vol. 28, no. 5, pp. 1614-1621 . https://doi.org/10.1681/ASN.2016040387
Bierzynska, A, Soderquest, K, Dean, P, Colby, E, Rollason, R, Jones, C, Inward, C D, McCarthy, H J, Simpson, M A, Lord, G M, Williams, M, Welsh, G I, Koziell, A B & Saleem, M A 2017, ' MAGI2 mutations cause congenital nephrotic syndrome ', Journal of the American Society of Nephrology, vol. 28, no. 5, pp. 1614-1621 . https://doi.org/10.1681/ASN.2016040387
Steroid-resistant nephrotic syndrome (SRNS), a heterogeneous disorder of the renal glomerular filtration barrier, results in impairment of glomerular permselectivity. Inheritance of genetic SRNS may be autosomal dominant or recessive, with a subset o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5969c0133dfd87bda0271297773ebc45
https://hdl.handle.net/1983/7cef385e-33c4-4af0-aa5f-8112ecc1fe55
https://hdl.handle.net/1983/7cef385e-33c4-4af0-aa5f-8112ecc1fe55
Autor:
Katrina Soderquest, Ethan S Sen, Stephen D. Marks, Michael A. Simpson, Milos Ognjanovic, Caroline Jones, Rodney D. Gilbert, David Hughes, Gavin I. Welsh, Larissa Kerecuk, Hugh J. McCarthy, Manish D. Sinha, Agnieszka Bierzynska, Elizabeth Colby, Shivram Hegde, Moin A. Saleem, Nicholas J. A. Webb, Graham M. Lord, Wen Y. Ding, Sally Feather, Martin Christian, Ania Koziell, Marwa M. Nabhan
Publikováno v:
Bierzynska, A, McCarthy, H, Soderquest, K, Sen, E, Colby, E, Ding, W, Nabhan, M, Kerecuk, L, Welsh, G, Saleem, M, Hedge, S, Hughes, D, Marks, S, Feather, S, Jones, C, Webb, N J A, Ognjanovic, M, Christian, M, Gilbert, R D, Sinha, M, Lord, G M, Simpson, M A & Koziell, A 2017, ' Genomic and clinical profiling of a national Nephrotic Syndrome cohort advocates a precision medicine approach to disease management ', Kidney International, vol. 91, no. 4, pp. 937–947 . https://doi.org/10.1016/j.kint.2016.10.013
Steroid Resistant Nephrotic Syndrome (SRNS) in children and young adults has differing etiologies with monogenic disease accounting for 2.9–30% in selected series. Using whole exome sequencing we sought to stratify a national population of children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c233c30b48723bfe6a5827875b2d2e9
https://research-information.bris.ac.uk/en/publications/c730c0d6-5527-435a-8c27-a99fd990a0e8
https://research-information.bris.ac.uk/en/publications/c730c0d6-5527-435a-8c27-a99fd990a0e8
Autor:
Thierry Walzer, Nico van Rooijen, Frederic Geissmann, Nick Powell, Carmelo Luci, Andrés Hidalgo, Graham M. Lord, Katrina Soderquest, Alfonso Martín-Fontecha
Publikováno v:
Blood, 117(17), 4511-4518. American Society of Hematology
Europe PubMed Central
Soderquest, K, Powell, N, Luci, C, van Rooijen, N, Hidalgo, A, Geissmann, F, Walzer, T, Lord, G M & Martin-Fontecha, A 2011, ' Monocytes control natural killer cell differentiation to effector phenotypes ', Blood, vol. 117, no. 17, pp. 4511-4518 . https://doi.org/10.1182/blood-2010-10-312264
Europe PubMed Central
Soderquest, K, Powell, N, Luci, C, van Rooijen, N, Hidalgo, A, Geissmann, F, Walzer, T, Lord, G M & Martin-Fontecha, A 2011, ' Monocytes control natural killer cell differentiation to effector phenotypes ', Blood, vol. 117, no. 17, pp. 4511-4518 . https://doi.org/10.1182/blood-2010-10-312264
Natural killer (NK) cells play a major role in immunologic surveillance of cancer. Whether NK-cell subsets have specific roles during antitumor responses and what the signals are that drive their terminal maturation remain unclear. Using an in vivo m
Publikováno v:
Frontiers in Endocrinology
After decades of primarily morphological study, positional cloning of the NPHS1 gene was the landmark event that established aberrant podocyte genetics as a pivotal cause of malfunction of the glomerular filter. This ended any uncertainty whether gen
Autor:
Bojan Polić, Thierry Walzer, Biljana Zafirova, Eric Vivier, Alfonso Martín-Fontecha, Linda S. Klavinskis, Katrina Soderquest, Graham M. Lord
Publikováno v:
Journal of Immunology
Journal of Immunology, 2011, 186 (6), pp.3304-8. ⟨10.4049/jimmunol.1004122⟩
Journal of Immunology, Publisher : Baltimore : Williams & Wilkins, c1950-. Latest Publisher : Bethesda, MD : American Association of Immunologists, 2011, 186 (6), pp.3304-8. ⟨10.4049/jimmunol.1004122⟩
Journal of Immunology, 2011, 186 (6), pp.3304-8. ⟨10.4049/jimmunol.1004122⟩
Journal of Immunology, Publisher : Baltimore : Williams & Wilkins, c1950-. Latest Publisher : Bethesda, MD : American Association of Immunologists, 2011, 186 (6), pp.3304-8. ⟨10.4049/jimmunol.1004122⟩
It is uncertain whether NK cells modulate T cell memory differentiation. By using a genetic model that allows the selective depletion of NK cells, we show in this study that NK cells shape CD8+ T cell fate by killing recently activated CD8+ T cells i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b635309d5cca4e09d2f9e71c00235643
https://hal.science/hal-00608178
https://hal.science/hal-00608178
Autor:
Graham M. Lord, Katrina Soderquest
Publikováno v:
Science Translational Medicine. 2
In the United Kingdom, many foundations and institutions and the government have made substantial investments in translational research. We examine the structures that surround this support and consider some of the results of this prodigious push tow
Autor:
Gavin I. Welsh, Agnieszka Bierzynska, Moin A. Saleem, Michael A. Simpson, Elizabeth Colby, Ania Koziell, Katrina Soderquest, Hugh J. McCarthy, Ethan S Sen
Publikováno v:
Nephrology Dialysis Transplantation. 30:iii382-iii382
Publikováno v:
The Journal of Immunology. 186:6071-6072
In our recent publication in The Journal of Immunology , we proposed that NK cells shape CD8+ T cell responses by migrating to s.c. lymph nodes and by killing Ag-primed CD8+ T cells. We are happy to reply to the questions raised by Dr. Manjili and Dr