Zobrazeno 1 - 10
of 54
pro vyhledávání: '"George Rebello"'
Autor:
Safiye Yildiz, Takudzwa N. Musarurwa, Ursula Algar, Ramadhani Chambuso, George Rebello, Paul A. Goldberg, Raj Ramesar
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
IntroductionThe increase in incidence of colorectal cancer in young patients of African ancestry coupled with increased aggressiveness has warranted investigation of the heritable nature of these cancers. Only a limited number of published reports of
Externí odkaz:
https://doaj.org/article/bb66de43fbfb493f8fc1bc8f1b6c00d2
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
The development of cervical cancer has been shown to involve both viral and host factors. The host factors are those that determine the specific response to human papillomavirus (HPV) infection by the patient's immune system. The immune responses to
Externí odkaz:
https://doaj.org/article/da6afbabd55046b9ac82973330a69d6c
Autor:
Ramadhani Chambuso, Evelyn Kaambo, Lynette Denny, Clive M. Gray, Anna-Lise Williamson, Monika Migdalska-Sęk, Gloudi Agenbag, George Rebello, Raj Ramesar
Publikováno v:
Frontiers in Oncology, Vol 9 (2019)
Background: A subgroup of women who are co-infected with human immunodeficiency virus type 1 (HIV-1) and human papillomavirus (HPV) progress rapidly to cervical disease regardless of high CD4 counts. Chromosomal loss of heterozygosity (LOH) and micro
Externí odkaz:
https://doaj.org/article/5f7b67f048284ff0946314dd5de55805
Publikováno v:
Genetics in Medicine. 24:1148-1150
Autor:
Kebashni Thandrayen, Alvera Vorster, Gameda Benefeld, Safiye Yildiz, Raj Ramesar, Jorge da Rocha, George Rebello, Alina I. Esterhuizen, Stephanie Julius, Peter Beighton, Lisa Roberts, John M. Pettifor, S. L. Sellars, Shrinav Dawlat, Komala Pillay, Surita Meldau
Publikováno v:
Human Mutation. 41:1871-1876
More than two decades ago, a recessive syndromic phenotype affecting kidneys, eyes, and ears, was first described in the endogamous Afrikaner population of South Africa. Using whole-exome sequencing of DNA from two affected siblings (and their carrie
Autor:
Michel Michaelides, Michael E. Cheetham, Marco Aben, Alison J. Hardcastle, Hannie Kremer, Daniele Ottaviani, Stefan Mundlos, Graeme C.M. Black, Susan M Downes, Robert K. Koenekoop, Julio C. Corral-Serrano, Jordi Corominas, Gavin Arno, Andrew R. Webster, Claire E. L. Smith, Uirá Souto Melo, Carlo Rivolta, Suzanne E. de Bruijn, Chris F. Inglehearn, Raj Ramesar, L. Ingeborgh van den Born, Susanne Roosing, Christian Gilissen, Nikolas Pontikos, Musa M. Mhlanga, Jacquie Greenberg, F. Lucy Raymond, Frans P.M. Cremers, Alessia Fiorentino, Timo W. F. Mulders, Stephanie Fanucchi, Silvia Albert, Simon Mead, Lisa Roberts, Michalis Georgiou, George Rebello, Carel B. Hoyng
Publikováno v:
American Journal of Human Genetics, 107, 5, pp. 802-814
American Journal of Human Genetics, 107, 802-814
American Journal of Human Genetics
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
American Journal of Human Genetics, 107, 802-814
American Journal of Human Genetics
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
© 2020 The Authors. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)
The cause of autosomal-dominant retinitis pigmentosa (adRP), which leads to loss of vision and blindness, was investigated
The cause of autosomal-dominant retinitis pigmentosa (adRP), which leads to loss of vision and blindness, was investigated
Autor:
Jordi, Maggi, Lisa, Roberts, Samuel, Koller, George, Rebello, Wolfgang, Berger, Rajkumar, Ramesar
Publikováno v:
Genes
RPGR exon ORF15 variants are one of the most frequent causes for inherited retinal disorders (IRDs), in particular retinitis pigmentosa. The low sequence complexity of this mutation hotspot makes it prone to indels and challenging for sequence data a
Publikováno v:
Advances in experimental medicine and biology. 1185
There is a glaring disparity in the populations included in genetic research; the majority of work involves European-derived cohorts, while other global populations - including Africans - are underrepresented. This is also true for the study of inher
Publikováno v:
Frontiers in Oncology
Frontiers in Oncology, Vol 10 (2020)
Frontiers in Oncology, Vol 10 (2020)
The development of cervical cancer has been shown to involve both viral and host factors. The host factors are those that determine the specific response to human papillomavirus (HPV) infection by the patient's immune system. The immune responses to
Publikováno v:
Oncomedicine. 3:82-93