Zobrazeno 1 - 10
of 285
pro vyhledávání: '"C. A. Poole"'
Autor:
C. Stayner, C. A. Poole, S. R. McGlashan, M. Pilanthananond, R. Brauning, D. Markie, B. Lett, L. Slobbe, A. Chae, A. C. Johnstone, C. G. Jensen, J. C. McEwan, K. Dittmer, K. Parker, A. Wiles, W. Blackburne, A. Leichter, M. Leask, A. Pinnapureddy, M. Jennings, J. A. Horsfield, R. J. Walker, M. R. Eccles
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-15 (2017)
Abstract Meckel syndrome (MKS) is an inherited autosomal recessive hepatorenal fibrocystic syndrome, caused by mutations in TMEM67, characterized by occipital encephalocoele, renal cysts, hepatic fibrosis, and polydactyly. Here we describe an ovine m
Externí odkaz:
https://doaj.org/article/edcafb5f13094ac2bfab71d2db069f8d
Publikováno v:
Journal of Micropalaeontology, Vol 42, Pp 57-81 (2023)
We describe Globigerinoides rublobatus n. sp., a new morphospecies of fossil planktonic foraminifera, from the Pleistocene sediments (∼810 ka) of the Indian Ocean and Pacific Ocean. We use image analysis and morphometry of 860 specimens from Intern
Externí odkaz:
https://doaj.org/article/375e06dd62a241d99f5599c3a48127e4
Autor:
Joy Garrett, Erin Metzger, Mark W. Dewhirst, Karen E. Pollok, John J. Turchi, Isabelle C. Le Poole, Kira Couch, Logan Lew, Anthony Sinn, Jeffrey M. Zaleski, Joseph R. Dynlacht
Publikováno v:
International Journal of Hyperthermia. 39:405-413
Publikováno v:
Journal of Investigative Dermatology. 141:S95
Autor:
Emilia R. Dellacecca, Rohan Shivde, I. C. Le Poole, Roopal V. Kundu, Stephanie M. Rangel, Cormac Cosgrove, Julia M. Mhlaba
Publikováno v:
Journal of Investigative Dermatology. 141:S41
Autor:
Julian Halcox, Ami Banerjee, M W Marcus, R Ghouse, N Rotheram, Jesse Dawson, P Dequen-O'byrne, David Keeling, S Webster, Neil Hawkins, Raza Alikhan, Rod S Taylor, David Scott, C D Poole, F D R Hobbs
Publikováno v:
European Heart Journal. 39
Publikováno v:
Clinical and Experimental Dermatology. 41:26-33
INTRODUCTION Pachyonychia congenita (PC) is a rare skin disorder caused by an autosomal dominant mutation in one of five genes encoding keratin (K6a, K6b, K6c, K16 or K17; each defining one PC subtype). Pain is a prominent symptom, but its severity a
Autor:
Anna Wiles, C. Anthony Poole, Anna Varone, Habiba Yasmin, Clare L. Thompson, Martin M. Knight
Publikováno v:
Journal of Orthopaedic Research. 33:1552-1559
Osteoarthritis is a chronic degenerative disease that affects the articular cartilage. Recent studies have demonstrated that lithium chloride exhibits significant efficacy as a chondroprotective agent, blocking cartilage degradation in response to in