Zobrazeno 1 - 10
of 86
pro vyhledávání: '"Josephine Peters"'
Autor:
Lee B Smith, Laura Milne, Nancy Nelson, Sharon Eddie, Pamela Brown, Nina Atanassova, Moira K O'Bryan, Liza O'Donnell, Danielle Rhodes, Sara Wells, Diane Napper, Patrick Nolan, Zuzanna Lalanne, Michael Cheeseman, Josephine Peters
Publikováno v:
PLoS Genetics, Vol 8, Iss 5, p e1002697 (2012)
Spermatogenesis is a complex process reliant upon interactions between germ cells (GC) and supporting somatic cells. Testicular Sertoli cells (SC) support GCs during maturation through physical attachment, the provision of nutrients, and protection f
Externí odkaz:
https://doaj.org/article/05d4d8773d914772b7862b40f7d997eb
Autor:
Leila Katirayi, Thulani Maphosa, Lloyd Chilikutali, Rachel K Chamanga, Josephine Petersson, Sarah Khatib, Boswell Munthali, Rose Nyirenda, Eddie Matiya, Laywell Nyirenda, Appolinaire Tiam, Lise Denoeud-Ndam
Publikováno v:
BMC Public Health, Vol 23, Iss 1, Pp 1-10 (2023)
Abstract Background Despite tremendous progress in improving antiretroviral therapy (ART) access, advanced HIV disease (AHD) still remains a challenge globally. Reasons for delayed presentation to care and ART adherence may be affected by gender. We
Externí odkaz:
https://doaj.org/article/86d44ac876fe47ae8ab275c974df2473
Autor:
Daniel Yominiya Peters, Wahab Stephens Adepoju, Olubunmi Josephine Peters, Jide Nosakare Ogunbo
Publikováno v:
SEG Technical Program Expanded Abstracts 2018.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::942423f09e8946c62552535e191efd62
https://doi.org/10.1190/segam2018-2959359.1
https://doi.org/10.1190/segam2018-2959359.1
Autor:
S. P. Parkinson, J. H. Edwards, T. P. Dalton, Mary F. Lyon, Edward P. Evans, Josephine Peters, A.G. Searle
Publikováno v:
Clinical Genetics. 20:407-415
Chromosome displays and listings are presented showing loci whose position is known in both man and mouse, in similar manner to our previous report (Dalton et al. 1981). There is now evidence for at least 27 conserved autosomal segments with two or m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b00b27634b4af19487c89d9df6764506
https://doi.org/10.1111/j.1399-0004.1981.tb01050.x
https://doi.org/10.1111/j.1399-0004.1981.tb01050.x
Autor:
Phimon Atsawasuwan, Simon Ball, Julieta Gentiletti, Josephine Peters, Mitsuo Yamauchi, Louis J. Soslowsky, Paul J. Christner, David E. Birk, David P. Beason
Publikováno v:
Journal of Investigative Dermatology. 126:595-602
The Sagg /+ mouse is an ethylnitrosourea-derived mutant with a dermal phenotype similar to some of the subtypes of Ehlers–Danlos syndrome (EDS) and cutis laxa. The dermis of the Sagg /+ mouse has less dense and more disorganized collagen fibers com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6289473cf71784027b0b348af893d19d
https://doi.org/10.1038/sj.jid.5700100
https://doi.org/10.1038/sj.jid.5700100
Autor:
Josephine Peters, Laura J. McCloskey, Carol M. Artlett, Paul J. Christner, Julieta Gentiletti, Sergio A. Jimenez
Publikováno v:
The Journal of Immunology. 175:2418-2426
The tight skin-2 (Tsk2/+) mouse has been proposed as an animal model of systemic sclerosis (SSc) because this animal exhibits increased collagen synthesis and accumulation in the dermis. The Tsk2/+ mouse also has been reported to have a mononuclear c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0846489e8d5f1c221ba13c6a8581febc
https://doi.org/10.4049/jimmunol.175.4.2418
https://doi.org/10.4049/jimmunol.175.4.2418
Autor:
Josephine Peters, Derek Thomson, Permphan Dharmasaroja, Catherine M. Abbott, Thomas H. Gillingwater, Stephen B. Wharton, Helen J Newbery, Richard R. Ribchester
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 64:295-303
Wasted (wst) is a spontaneous autosomal recessive mutation in which the gene encoding translation factor eEF1A2 is deleted. Homozygous mice show tremors and disturbances of gait shortly after weaning, followed by motor neuron degeneration, paralysis,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::712415aa0fe3844b105e21c610aaabe9
https://doi.org/10.1093/jnen/64.4.295
https://doi.org/10.1093/jnen/64.4.295
Publikováno v:
Mammalian Genome. 14:495-505
When paternally transmitted, two independent ENU-induced mutations showed reduced whole body wet weight soon after birth. The mutations were mapped to Chromosome 9 (Chr 9) between the markers D9Mit208 and D9Mit215. Their map position and imprinted st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fa87cb01446a9256114f96312fdaded
https://doi.org/10.1007/s00335-002-2258-4
https://doi.org/10.1007/s00335-002-2258-4
Autor:
Carolina Medina-Gomez, Karol Estrada, Marjoline Josephine Peters, Albert Hofman, Vincent W. V. Jaddoe, Fernando Rivadeneira, Cornelia M. van Duijn, Liesbeth Duijts, Claudia J. Kruithof, Janine F. Felix, Lizbeth Herrera, Andreas Gerardus Uitterlinden
Publikováno v:
European Journal of Epidemiology
European Journal of Epidemiology, 30(4), 317-330. Springer Netherlands
European Journal of Epidemiology, 30(4), 317-330. Springer Netherlands
Genome-wide association studies (GWAS) have been successful in identifying loci associated with a wide range of complex human traits and diseases. Up to now, the majority of GWAS have focused on European populations. However, the inclusion of other e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4d82c36827ff49e9effdb5fbbde1706
https://pubmed.ncbi.nlm.nih.gov/25762173
https://pubmed.ncbi.nlm.nih.gov/25762173
Autor:
Philomena Mburu, Joanne E. Martin, Simon Greenaway, Josephine Peters, Mark A. Strivens, Ian C. Gray, P. Roby, Jean-Louis Guénet, Patrick M. Nolan, Carole D. Nickols, Stéphanie Voegeling, Xue Zhong Liu, R Selley, Adrian M. Isaacs, Stefan L. McCormack, Elizabeth M. C. Fisher, C Thornton, M Browne, Alexandra Erven, Ruth M. Arkell, Tertius Hough, Zuzanna Tymowska-Lalanne, Jackie Hunter, Karen P. Steel, Peter H. Glenister, Kay E. Davies, Rachel E. Hardisty, D Brooker, R Sadri, Nigel K. Spurr, E Whitehill, Lucie Vizor, J A Stevenson, K Pickford, Christine A. Wells, Amy E. Kiernan, M Hewitt, Steve D.M. Brown, Sohaila Rastan, Derek C. Rogers, Caroline Thaung, Jim J. Hagan, R Washbourne, M Nasse
Publikováno v:
Nature Genetics. 25:440-443
As the human genome project approaches completion, the challenge for mammalian geneticists is to develop approaches for the systematic determination of mammalian gene function. Mouse mutagenesis will be a key element of studies of gene function. Phen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25d69b10742c4b2938bb2e4430adf5d1
https://doi.org/10.1038/78140
https://doi.org/10.1038/78140