Výsledky vyhledávání - "Katrina M, Wood"

Calcium oxalate crystal deposition in the kidney: identification, causes and consequences

Autor: John A. Sayer, R Geraghty, Katrina M Wood

Publikováno v: Urolithiasis

Calcium oxalate (CaOx) crystal deposition within the tubules is often a perplexing finding on renal biopsy of both native and transplanted kidneys. Understanding the underlying causes may help diagnosis and future management. The most frequent cause

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b6d7b12ee522120b010665ac082fb38
https://doi.org/10.1007/s00240-020-01202-w

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Genomic abnormalities of TP53 define distinct risk groups of paediatric B-cell non-Hodgkin lymphoma

Publikováno v: Leukemia. 36(3)

Children with B-cell non-Hodgkin lymphoma (B-NHL) have an excellent chance of survival, however, current clinical risk stratification places as many as half of patients in a high-risk group receiving very intensive chemo-immunotherapy. TP53 alteratio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d0fc5580417cb3f92949ca35052e769
https://pubmed.ncbi.nlm.nih.gov/34675373

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Transplantation for congenital heart disease is associated with an increased risk of Epstein-Barr virus-related post-transplant lymphoproliferative disorder in children

Autor: Kevin Windebank, Chris M. Bacon, Malcolm Brodlie, Julie Flett, Asif Hasan, Jason Powell, Andrew R. Gennery, Jessica Roberts, Vikki Rand, Gareth Parry, Katrina M Wood, Ugonna T. Offor, Terry Hewitt, Simon Bomken, Zdenka Reinhardt

Publikováno v: The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation. 40(1)

Children undergoing heart transplant are at higher risk of developing post-transplant lymphoproliferative disorder (PTLD) than other solid organ recipients. The factors driving that risk are unclear. This study investigated risk factors for PTLD in c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2a1dac1f614e32e5031e49299f7f323
https://pubmed.ncbi.nlm.nih.gov/33339556

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High-dose chemotherapy and autologous stem cell transplantation in enteropathy-associated and other aggressive T-cell lymphomas: a UK NCRI/Cancer Research UK Phase II Study

Autor: Gail Jones, Elizabeth H Phillips, Katrina M Wood, Paul Smith, Andre Lopes, Humra Chadwick, Nick Chadwick, Michal Sieniawski, Laura Clifton-Hadley, Anthony Lawrie, Michelle Lannon, Anne Lennard, Andrew Davies

Publikováno v: Bone Marrow Transplantation. 54:465-468

In the original version of this article, the mention of ‘ifosfamide 1500 mg/m2 days 1–3’ should, in fact, read ‘ifosfamide 1500 mg/m2 bd days 1–3’. This has now been updated in the original version of the article.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e5d95ca91c07b8eed021b4967f0831be
https://doi.org/10.1038/s41409-018-0294-2

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Human urine-derived renal epithelial cells provide insights into kidney-specific alternate splicing variants

Autor: Shreya Raman, Eva Decker, Simon A. Ramsbottom, John A. Sayer, Sumaya Alkanderi, Colin G. Miles, Shalabh Srivastava, Holly Mabillard, Colin A. Johnson, James Tellez, Elisa Molinari, Katrina M Wood, Caroline Kempf, Friedhelm Hildebrandt, Carsten Bergmann

Publikováno v: European Journal of Human Genetics

The majority of multi-exon genes undergo alternative splicing to produce different mRNA transcripts and this may occur in a tissue-specific manner. Assessment of mRNA transcripts isolated from blood samples may sometimes be unhelpful in determining t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dee9ba4165cd1db1282cc6e27a3f4705
https://doi.org/10.1038/s41431-018-0212-5

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Akademický článek

Atypical haemolytic uraemic syndrome associated with a hybrid complement gene.

Autor: Julian P Venables, Lisa Strain, Danny Routledge, David Bourn, Helen M Powell, Paul Warwicker, Martha L Diaz-Torres, Anne Sampson, Paul Mead, Michelle Webb, Yves Pirson, Michael S Jackson, Anne Hughes, Katrina M Wood, Judith A Goodship, Timothy H J Goodship

Publikováno v: PLoS Medicine, Vol 3, Iss 10, p e431 (2006)

BACKGROUND: Sequence analysis of the regulators of complement activation (RCA) cluster of genes at chromosome position 1q32 shows evidence of several large genomic duplications. These duplications have resulted in a high degree of sequence identity b

Externí odkaz: https://doaj.org/article/209c2f92f798427db3774ee714ab993d

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Rare genetic variants in Shiga toxin-associated haemolytic uraemic syndrome: genetic analysis prior to transplantation is essential

Autor: Vicky Brocklebank, Katrina M Wood, David J. Kavanagh, Frances Dowen, Alison L. Brown, Jennifer Palfrey

Publikováno v: Clinical Kidney Journal

We present a case of haemolytic uraemic syndrome (HUS) in a 16-year-old female with serological evidence of acute Escherichia coli O157:H7 infection. She progressed to established renal failure and received a deceased donor kidney transplant. Shiga t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b81dfbf88e2d08151663ddb9fc0efa49
https://doi.org/10.1093/ckj/sfx030

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