Zobrazeno 1 - 10
of 17
pro vyhledávání: '"C. M. Coleman"'
Autor:
S. G. P. Funnell, W. E. Dowling, C. Muñoz-Fontela, P.-S. Gsell, D. E. Ingber, G. A. Hamilton, L. Delang, J. Rocha-Pereira, S. Kaptein, K. H. Dallmeier, J. Neyts, K. Rosenke, E. de Wit, H. Feldmann, P. Maisonnasse, R. Le Grand, M. B. Frieman, C. M. Coleman
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-4 (2020)
There is an urgent need for drugs, therapies and vaccines to be available to protect the human population against COVID-19. One of the first approaches taken in the COVID-19 global response was to consider repurposing licensed drugs. This commentary
Externí odkaz:
https://doaj.org/article/16f0fbaa1ef74b81ae8f7a0d0a46c7fa
Autor:
Donald E. Ingber, H. Feldmann, Kyle Rosenke, César Muñoz-Fontela, Joana Rocha-Pereira, Pierre Stéphane Gsell, Matthew B. Frieman, Simon G. P. Funnell, Kai Dallmeier, Suzanne J.F. Kaptein, E. de Wit, Johan Neyts, Leen Delang, R. Le Grand, Pauline Maisonnasse, W. E. Dowling, G. A. Hamilton, C. M. Coleman
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-4 (2020)
Nature Communications
Nature Communications, Nature Publishing Group, 2020, 11 (1), pp.4253. ⟨10.1038/s41467-020-17907-w⟩
Nature Communications, 2020, 11 (1), pp.4253. ⟨10.1038/s41467-020-17907-w⟩
Nature Communications
Nature Communications, Nature Publishing Group, 2020, 11 (1), pp.4253. ⟨10.1038/s41467-020-17907-w⟩
Nature Communications, 2020, 11 (1), pp.4253. ⟨10.1038/s41467-020-17907-w⟩
There is an urgent need for drugs, therapies and vaccines to be available to protect the human population against COVID-19. One of the first approaches taken in the COVID-19 global response was to consider repurposing licensed drugs. This commentary
Autor:
Susan A. Gerbi, Nanyan Lu, John M. Urban, Jacob E. Bliss, C. M. Coleman, Michael S. Foulk, Reza Mazloom, Susan J. Brown, Allan C. Spradling
The lower Dipteran fungus fly,Sciara coprophila, has many unique biological features. For example,Sciaraundergoes paternal chromosome elimination and maternal X chromosome nondisjunction during spermatogenesis, paternal X elimination during embryogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8c07ceb9cd753307997dd7b650019d4
https://doi.org/10.1101/2020.02.24.963009
https://doi.org/10.1101/2020.02.24.963009
Publikováno v:
Journal of Animal Science. 87:2653-2663
Three hundred forty-seven crossbred heifers (330 +/- 11 kg initial BW) were used in a randomized complete block study to identify the optimal level of dried corn distillers grains with solubles (DGS) in flaked corn finishing diets. Fifty-four pens we
Autor:
T. Gabrielle H. S. Ashton, John A. McGrath, C. M. Coleman, Neil V. Whittock, Robin A.J. Eady, K. M. Acland, Whi McLean
Publikováno v:
Journal of Investigative Dermatology. 115:694-698
Naegeli-Franceschetti-Jadassohn syndrome is a rare autosomal dominant form of ectodermal dysplasia affecting sweat glands, nails, teeth, and skin. We have studied a multigeneration family of Anglo-Saxon British descent using microsatellite markers to
Autor:
Jouni Uitto, Marcel F. Jonkman, H. Van Goor, C. M. Coleman, Whi McLean, S. P. Covello, Fjd Smith
Publikováno v:
Human Molecular Genetics, 7(7), 1143-1148. Oxford University Press
Type I and type II keratins form the heteropolymeric intermediate filament cytoskeleton, which is the main stress-bearing structure within epithelial cells. Pachyonychia congenita (PC) is a group of autosomal dominant disorders whose most prominent p
Publikováno v:
Journal of animal science. 87(8)
Three hundred forty-seven crossbred heifers (330 +/- 11 kg initial BW) were used in a randomized complete block study to identify the optimal level of dried corn distillers grains with solubles (DGS) in flaked corn finishing diets. Fifty-four pens we
Autor:
Fjd Smith, Graeme C.M. Black, Whi McLean, S J Morgan, Alan D. Irvine, J H McCarthy, Johnny Moore, C. M. Coleman, Ole Swensson
Publikováno v:
The British journal of ophthalmology. 86(7)
Background: The molecular basis of Meesmann9s epithelial corneal dystrophy (MECD) has recently been attributed to mutations in the cornea specific keratin genes KRT3 and KRT12. The mechanisms by which these mutations cause the Meesmann9s phenotype ar
Autor:
Sadeer B. Hannush, C. M. Coleman, Frances J.D. Smith, Seana P. Covello, W.H. Irwin McLean, Jouni Uitto
Publikováno v:
American journal of ophthalmology. 128(6)
PURPOSE: Meesmann corneal dystrophy is an autosomal dominant disorder characterized by fragility of the anterior corneal epithelium. We have previously demonstrated that this disease can be caused by mutations in the genes encoding keratins K3 or K12
Publikováno v:
The British journal of dermatology. 140(3)
Epidermolytic palmoplantar keratoderma (EPPK) is an autosomal dominant genodermatosis characterized by diffuse keratoderma, typically with an erythematous border. Histologically, palmoplantar epidermis shows suprabasal cytolysis and ultrastructurally