Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Soruba Sivamoorthy"'
Autor:
Catherine S. Choong, John Beilby, Joan Uzaraga, Karen J. Woodward, Vicki Chabros, Fabiana Ramos Vasques Walters, Dimitar N. Azmanov, Sarah L. Nickerson, Dagmara A. Kennedy, Tanya Grumball, Joanne Peverall, Gillian M. Arscott, Tracey Edwards, Rebecca E. Brereton, Vanessa Marchin, Soruba Sivamoorthy, Sharron Townshend
Publikováno v:
American Journal of Medical Genetics Part A. 185:3136-3145
Silver-Russell syndrome (SRS) is a rare genetic condition primarily characterized by growth restriction and facial dysmorphisms. While hypomethylation of H19/IGF2:IG-DMR (imprinting control region 1 [IC1]) located at 11p15.5 and maternal uniparental
Autor:
Hashika Rijhumal, Nathan T. Harvey, Joanne Peverall, Alyssa Fruvall, Benjamin A. Wood, Tamazin Leecy, Joan Uzaraga, Dagmara Kennedy, Shalinder Singh, Soruba Sivamoorthy, Peter I A McQuillan, Nima Mesbah Ardakani, Chris van Vliet
Publikováno v:
Pathology. 52:431-438
A group of melanomas characterised by predominant growth as large nests within the epidermis has been described. These cases present a diagnostic challenge, as many traditional architectural criteria for the recognition of melanoma are absent. We rep
Autor:
Simon Williams, Clarissa Yates, Helen Wright, Joanne Peverall, Peter Shipman, David Ravine, John Beilby, Hamid Alinejad-Rokny, Gareth Baynam, Soruba Sivamoorthy, Julian Ik-Tsen Heng, Karen J. Woodward, Cathryn Poulton
Publikováno v:
Molecular Genetics & Genomic Medicine
Background Pallister-Killian syndrome (PKS) is a rare multisystem developmental syndrome usually caused by mosaic tetrasomy of chromosome 12p that is known to be associated with neurological defects. Methods We describe two patients with PKS, one of
Autor:
Soruba Sivamoorthy, Lakshmi Nagarajan, Tanya Grumball, Julian Ik-Tsen Heng, Ashleigh Murch, Joanne Peverall, Sabine Afchani, John Wray, Matthew S. Edwards, Julie Stampalia, Hamid Alinejad-Rokny, Cathy Kiraly-Borri, Jacqueline Scurlock, Hashika Rijhumal, Fiona Haslam McKenzie, Gareth Baynam, John Beilby, Kim Potts, Hannah Vanyai, Andrew J. O. Whitehouse, Fiona Taylor, Karen J. Woodward
Publikováno v:
Molecular Genetics & Genomic Medicine
Background Chromosome 22q11.2 is susceptible to genomic rearrangements and the most frequently reported involve deletions and duplications between low copy repeats LCR22A to LCR22D. Atypical nested deletions and duplications are rarer and can provide
Autor:
Josephine P. Mansfield, Cassandra M. James, Jason C Lenzo, Vanessa S. Cull, Soruba Sivamoorthy, Emmalene J. Bartlett
Publikováno v:
Immunology and cell biology. 82(2)
Gene therapy using DNA encoding type I IFN subtypes IFNA6, IFNA9 and IFNB suppresses murine cytomegalovirus (MCMV)-myocarditis, a predominantly cell-mediated disease in BALB/c mice. CD8(+) T cells are the principal cell type within the inflamed myoca
Autor:
Josephine P. Mansfield, Soruba Sivamoorthy, Cassandra M. James, Jason C Lenzo, Vanessa S. Cull
Publikováno v:
Cellular immunology. 223(1)
Cytomegalovirus-induced myocarditis is largely immune-mediated. BALB/c mice produced higher levels of IL-4 in the heart indicative of a Th2-like response. Although IL-6, IL-10, IL-18, and TNF-alpha were produced in the heart during acute infection, B