Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Gurdeep Matharu Lall"'
Autor:
Emily C. Patterson, Gurdeep Matharu Lall, Rita Neumann, Barbara Ottolini, Chiara Batini, Federico Sacchini, Aiden P. Foster, Jon H. Wetton, Mark A. Jobling
Publikováno v:
BMC Genomics, Vol 24, Iss 1, Pp 1-12 (2023)
Abstract Background As a population genetic tool, mitochondrial DNA is commonly divided into the ~ 1-kb control region (CR), in which single nucleotide variant (SNV) diversity is relatively high, and the coding region, in which selective constraint i
Externí odkaz:
https://doaj.org/article/c7d3685ce1584fdf81c7529c7562562e
Autor:
Rebecca C Allsopp, Karen Page, Bana Ambasager, Marc K Wadsley, Emmanuel Acheampong, Tumisang P Ntereke, Qi Guo, Gurdeep Matharu Lall, Kelly L T Gleason, Evie Wren, Georgios Nteliopoulos, Amelia J Rushton, R Charles Coombes, Jacqueline A Shaw
Publikováno v:
Clinical Chemistry. 69:510-518
Background Somatic copy number alterations (sCNAs) acquired during the evolution of breast cancer provide valuable prognostic and therapeutic information. Here we present a workflow for screening sCNAs using picogram amounts of cell-free DNA (cfDNA)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e944b78ecb25a6e2ffa9168bd02f9cf
https://doi.org/10.1093/clinchem/hvac220
https://doi.org/10.1093/clinchem/hvac220
Autor:
Chiara Batini, Chris Tyler-Smith, Sigurd Aase, Hayley Dunn, Walter F. Bodmer, Horolma Pamjav, Maciej Tomaszewski, Marta Pereira Verdugo, Berit Myhre Dupuy, Joanna Story, Jon H. Wetton, Daniel Zadik, Patricia Balaresque, Andreas O. Tillmar, Turi E. King, Anders D. Børglum, Pille Hallast, Gurdeep Matharu Lall, Pragya Vohra, Harald Løvvik, Mark A. Jobling, Tina Baker, Stephen E. Harding, Bruce Winney, Peter de Knijff, Tunde I. Huszar, Maarten Larmuseau
Publikováno v:
European Journal of Human Genetics
European Journal of Human Genetics, Nature Publishing Group, 2020, ⟨10.1038/s41431-020-00747-z⟩
European Journal of Human Genetics, Nature Publishing Group, 2020, 29 (3), pp.512-523. ⟨10.1038/s41431-020-00747-z⟩
European Journal of Human Genetics, Nature Publishing Group, 2021, 29 (3), pp.512-523. ⟨10.1038/s41431-020-00747-z⟩
European Journal of Human Genetics, 29, 512-523. SPRINGERNATURE
Lall, G M, Larmuseau, M H D, Wetton, J H, Batini, C, Hallast, P, Huszar, T I, Zadik, D, Aase, S, Baker, T, Balaresque, P, Bodmer, W, Børglum, A D, de Knijff, P, Dunn, H, Harding, S E, Løvvik, H, Dupuy, B M, Pamjav, H, Tillmar, A O, Tomaszewski, M, Tyler-Smith, C, Verdugo, M P, Winney, B, Vohra, P, Story, J, King, T E & Jobling, M A 2021, ' Subdividing Y-chromosome haplogroup R1a1 reveals Norse Viking dispersal lineages in Britain ', European Journal of Human Genetics, vol. 29, no. 3, pp. 512-523 . https://doi.org/10.1038/s41431-020-00747-z
Lall, G M, Larmuseau, M H D, Wetton, J H, Batini, C, Hallast, P, Huszar, T I, Zadik, D, Aase, S, Baker, T, Balaresque, P, Bodmer, W, Børglum, A D, De Knijff, P, Dunn, H, Harding, S E, Løvvik, H, Dupuy, B M, Pamjav, H, Tillmar, A O, Tomaszewski, M, Tyler-smith, C, Verdugo, M P, Winney, B, Vohra, P, Story, J, King, T E & Jobling, M A 2020, ' Subdividing Y-chromosome haplogroup R1a1 reveals Norse Viking dispersal lineages in Britain ', European Journal of Human Genetics . https://doi.org/10.1038/s41431-020-00747-z
European Journal of Human Genetics, Nature Publishing Group, 2020, ⟨10.1038/s41431-020-00747-z⟩
European Journal of Human Genetics, Nature Publishing Group, 2020, 29 (3), pp.512-523. ⟨10.1038/s41431-020-00747-z⟩
European Journal of Human Genetics, Nature Publishing Group, 2021, 29 (3), pp.512-523. ⟨10.1038/s41431-020-00747-z⟩
European Journal of Human Genetics, 29, 512-523. SPRINGERNATURE
Lall, G M, Larmuseau, M H D, Wetton, J H, Batini, C, Hallast, P, Huszar, T I, Zadik, D, Aase, S, Baker, T, Balaresque, P, Bodmer, W, Børglum, A D, de Knijff, P, Dunn, H, Harding, S E, Løvvik, H, Dupuy, B M, Pamjav, H, Tillmar, A O, Tomaszewski, M, Tyler-Smith, C, Verdugo, M P, Winney, B, Vohra, P, Story, J, King, T E & Jobling, M A 2021, ' Subdividing Y-chromosome haplogroup R1a1 reveals Norse Viking dispersal lineages in Britain ', European Journal of Human Genetics, vol. 29, no. 3, pp. 512-523 . https://doi.org/10.1038/s41431-020-00747-z
Lall, G M, Larmuseau, M H D, Wetton, J H, Batini, C, Hallast, P, Huszar, T I, Zadik, D, Aase, S, Baker, T, Balaresque, P, Bodmer, W, Børglum, A D, De Knijff, P, Dunn, H, Harding, S E, Løvvik, H, Dupuy, B M, Pamjav, H, Tillmar, A O, Tomaszewski, M, Tyler-smith, C, Verdugo, M P, Winney, B, Vohra, P, Story, J, King, T E & Jobling, M A 2020, ' Subdividing Y-chromosome haplogroup R1a1 reveals Norse Viking dispersal lineages in Britain ', European Journal of Human Genetics . https://doi.org/10.1038/s41431-020-00747-z
The influence of Viking-Age migrants to the British Isles is obvious in archaeological and place-names evidence, but their demographic impact has been unclear. Autosomal genetic analyses support Norse Viking contributions to parts of Britain, but sho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8ab224737b2d25b065d7863bf3a5e44
https://hal.archives-ouvertes.fr/hal-03039180
https://hal.archives-ouvertes.fr/hal-03039180
Publikováno v:
Science & Justice. 57:331-335
In developed countries, DNA profiling routinely forms part of the forensic strategy in the investigation of sexual violence. Medical examinations provide opportunities for recovering DNA evidence from intimate swabs, which can be particularly probati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9cb9973ce7045d8f6b9767153ce28a2
https://doi.org/10.1016/j.scijus.2017.07.004
https://doi.org/10.1016/j.scijus.2017.07.004
Publikováno v:
Forensic Science International: Genetics. 27:149-155
DNA variation in 402 bp of the mitochondrial control region flanked by repeat sequences RS2 and RS3 was evaluated by Sanger sequencing in 152 English domestic cats, in order to determine the significance of matching DNA sequences between hairs found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bb33ad30f514760961bceadae66b198
https://doi.org/10.1016/j.fsigen.2016.12.008
https://doi.org/10.1016/j.fsigen.2016.12.008