Zobrazeno 1 - 10
of 214
pro vyhledávání: '"McLean WHI"'
Autor:
McAleer, MA, Jakasa, I, Hurault, G, Sarvari, P, McLean, WHI, Tanaka, RJ, Kezic, S, Irvine, AD
Background Biomarkers of atopic dermatitis (AD) are largely lacking, especially in infant AD. Those that have been examined to date have focused mostly on serum cytokines, with few on noninvasive biomarkers in the skin. Objectives We aimed to explore
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::2bacd234f2496b35fd1132a8fbd0a986
https://www.bib.irb.hr/987685
https://www.bib.irb.hr/987685
Autor:
McAleer, MA, Jakasa, I, Hurault, G, Sarvari, P, McLean, WHI, Tanaka, RJ, Kezic, S, Irvine, AD
BACKGROUND: Biomarkers of atopic dermatitis (AD) are largely lacking, especially in infant AD. Those that have been examined to date have focused mostly on serum cytokines with few on non-invasive biomarkers in the skin. OBJECTIVES: We aimed to explo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1032::3ca47b0b4b2547819f4f325d41a70359
http://hdl.handle.net/10044/1/62001
http://hdl.handle.net/10044/1/62001
Autor:
Aleksandar Rajkovic, S. Christin-Maitre, Anu Bashamboo, Liliana Dain, Caroline Schluth-Bolard, McLean Whi, ossetti R, Caroline Eozenou, Svetlana A. Yatsenko, Inas Mazen, Etienne Patin, Selma F. Witchel, Ralf Jauch, Rajpert-De Meyts E, Joelle Bignon-Topalovic, Kristian Almstrup, Ken McElreavey, Marie-Charlotte Dumargne, Louis-Sylvestre C, Sandra Chantot-Bastaraud, de Malleray Pichard C, Jean-Pierre Siffroi, Célia Ravel, Violeta A. Chiauzzi, Capucine Hyon, John C. Achermann, Hassan Rouba, Stuart A. MacGowan, Reyes-ugica M, Andrew J. Duncan, Eduardo H. Charreau, Leila Fusee, Marie-France Portnoi, Sandra Rojo, Luca Persani, Raja Brauner, Validire P, Yogesh Srivastava
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Human Molecular Genetics
Human Molecular Genetics, 2018, 27 (7), pp.1228-1240. ⟨10.1093/hmg/ddy037⟩
Human molecular genetics, vol 27, iss 7
Human Molecular Genetics, Oxford University Press (OUP), 2018, 27 (7), pp.1228-1240. ⟨10.1093/hmg/ddy037⟩
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Human Molecular Genetics
Human Molecular Genetics, 2018, 27 (7), pp.1228-1240. ⟨10.1093/hmg/ddy037⟩
Human molecular genetics, vol 27, iss 7
Human Molecular Genetics, Oxford University Press (OUP), 2018, 27 (7), pp.1228-1240. ⟨10.1093/hmg/ddy037⟩
SOX8 is an HMG-box transcription factor closely related to SRY and SOX9. Deletion of the gene encoding Sox8 in mice causes reproductive dysfunction but the role of SOX8 in humans is unknown. Here, we show that SOX8 is expressed in the somatic cells o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c3735ed6276ab345f922c6d19eef946
https://academic.oup.com/hmg/article/27/7/1228/4823478
https://academic.oup.com/hmg/article/27/7/1228/4823478
Autor:
Deeny, HA, Murphy, AM, O'Rourke, D, Gallagher, S, Rea, G, Ware, JS, Lightman, EG, Walsh, R, John, S, Homfray, T, Till, J, Prasad, S, Buchan, R, Wilkinson, S, Barton, PJR, Cook, SA, McVeigh, TP, Cody, N, Meany, M, Carroll, C, O'Shea, R, Gallagher, DJ, Clabby, C, Green, AJ, Casey, J, Crushell, E, Hughes, J, Losty, E, Slattery, D, Green, A, Ennis, S, Lynch, SA, Kirk, CW, McKee, S, Project, DDD, Al Shehhi, M, Shen, S, Gallagher, L, Betts, DR, McArdle, L, Quinn, EM, Coleman, C, Molloy, B, Dominguez Castro, P, Trimble, V, Mahmud, N, McManus, R, Jung, S, Salzman, D, Kerin, MJ, Nallur, S, Dookwah, M, Nemec, AA, Sadofsky, J, Paranjape, T, Kelly, O, Chan, E., Miller, N, Sweeney, KJ, Zelterman, D, Sweasy, J, Pilarski, R, Telesca, D, Weidhaas, JB, Stapleton, CP, McCormack, M, Connaughton, D, Phelan, PJ, Cavalleri, GL, Conlon, PJ, Gilbert, E, O'Reilly, S, Merrigan, M, McGettigan, D, Cavalleri, G, Heavin, SB, Slattery, L, Walley, N, Avbersek, A, Novy, J, Sinha, S, Alarts, N, Legros, B, Radtke, R, Doherty, C, Depondt, C, Sisodiya, S, Goldstein, D, Delanty, N, Nesbit, MA, Courtney, DG, Allen, EHA, Atkinson, SD, Maurizi, E, Moore, JE, Pedrioli, DM Leslie, McLean, WHI, Moore, CBT, Petyrka, J, Vieira, M, Donnelly, DE, O'Neill, T, Hardy, R, Morrison, PJ, Hegarty, M, Irvine, M, Dabir, T, Zhang, X, Dineen, T, Flanagan, J, Kovacs, A, Mihart, R, O'Callaghan, J, Culligan, J, Daly, N, McAuliffe, D, Waterstone, J, Owens, P, Guerin, C, Quill, D, Bell, M, Lowery, AJ, Bradley, L, Barton, DE, Matthews, J, Turner, J, O'Byrne, JJ, Fitzsimons, PE, Unger, S, Croft, J, Mayne, PD, Moylette, E, McDonnell, C, Parker, VE, Al-Shehhi, M, Kelly, PM, Costigan, C, Hegarty, A, Knox, R, Byrne, S, Semple, LRK., Irvine, A, McDaid, J, Ryan, H, Dunne, A, Lambert, DM, Treacy, EP, Lynch, SM, McKenna, MM, Walsh, CP, McKenna, DJ, Whitton, L, Cosgrove, D, Clarkson, C, Gill, M, Corvin, A, Rea, S, Donohoe, G, Morris, D, Neville, J, Ryan, AM, Hand, CK, Ryan, E, Ryan, F, Barton, D, O'Dwyer, V, Neylan, D, Nesbitt, H, Byrne, NM, Worthington, J, Mc Keown, SR, Mc Kenna, DJ, Harold, D, Holland, J, Mothershill, O, Allen, EH, Leslie Pedrioli, DM, Courtney, D, Cole, A, Cox, S, Jeong, C, Droma, Y, Hanaoka, M, Ota, M, Gasparini, P, Montgomery, H, Di Rienzo, A, Robbins, P, L. Cavalleri, G, Heavin, S, Buckley, P, Irwin, RE, Thakur, A, O’ Neill, KM, Cummins, Paul, Mackin, SJ, O'Neill, K, Walsh, C, Schiroli, D, Mulligan, R, Sebag, F, Ozaki, M, Molloy, AM, Mills, JL, Fan, R, Wang, Y, Gibney, ER, Shane, B, Brody, LC, Parle-Mcdermott, A, O'Halloran, ET, Ebrahim, A, Meydan, C, Mason, C, Magalhães, TR
Publikováno v:
The Ulster Medical Journal
Aims The Irish DNA Atlas is a DNA collection being assembled with the aim of describing the fine-scale population structure in Ireland. Understanding such structure can inform on optimal design of clinical genetic studies as well as the history of th
Autor:
Lee, JYW, Hsu, C-K, Michael, M, Nanda, A, Liu, L, McMillan, Pourreyron, C, Takeichi, T, Tolar, J, Reid, E, Hayday, T, Blumen, SC, Abu-Mouch, S, Straussberg, R, Basel-Vanagaite, L, Barhum, Y, Zouabi, Y, Al-Ajmi, H, Huang, H-Y, Lin, T-C, Akiyama, M, Lee, JYY, McLean, WHI, Simpson, MA, Parsons, M, McGrath, JA
Publikováno v:
Lee, J Y W, Hsu, C K, Michael, M, Nanda, A, Liu, L, McMillan, J R, Pourreyron, C, Takeichi, T, Tolar, J, Reid, E, Hayday, T, Blumen, S C, Abu-Mouch, S, Straussberg, R, Basel-Vanagaite, L, Barhum, Y, Zouabi, Y, Al-Ajmi, H, Huang, H Y, Lin, T C, Akiyama, M, Lee, J Y Y, McLean, W H I, Simpson, M A, Parsons, M & McGrath, J A 2017, ' Large Intragenic Deletion in DSTYK Underlies Autosomal-Recessive Complicated Spastic Paraparesis, SPG23 ', American Journal of Human Genetics, vol. 100, no. 2, pp. 364-370 . https://doi.org/10.1016/j.ajhg.2017.01.014
SPG23 is an autosomal-recessive neurodegenerative subtype of lower limb spastic paraparesis with additional diffuse skin and hair dyspigmentation at birth followed by further patchy pigment loss during childhood. Previously, genome-wide linkage in an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49a4284259470725b7f5834809ad7a7d
https://www.repository.cam.ac.uk/handle/1810/263193
https://www.repository.cam.ac.uk/handle/1810/263193
Autor:
Casey, JP, Murphy, H, Ennis, S, Lynch, SA, Bradley, L, Mabrouk, R, Paterson, A, McAuley, D, Dabir, T, Dobson, MG, Darlow, JM, Darlay, R, Cordell, HJ, Green, AJ, Puri, P, Barton, DE, McCormack, M, Chaila, E, Shawan, A, Conroy, J, Heinzen, E, Goldstein, DB, Delanty, N, Caldecott, K, Cavalleri, GL, McConnell, VPM, Fitzpatrick, DJ, Shah, N, Ryan, CJ, Greene, D, Shields, DC, Courtney, DG, Atkinson, SD, Allen, EHA, Moore, JE, Maurizi, E, Pellegrini, G, Black, GC, Mason, FD, Yam, G, McLean, WHI, Moore, CBT, McKay, GJ, Kavanagh, DH, Maxwell, AP, O’Neill, KM, Walsh, CP, Anney, R, Ning, Z., O’Keeffe, G, Moore, T, Magee, AC, Stewart, FJ, Muir, A, McOsker, J, Jardine, T, Wilson, A, McKeown, P, McKay, L, Scala, S, Winship, I, Jeffers, L, Thornton, C, Morrison, PJ, Ward, A, Turner, J, Byrne, M, Casey, J, J Toner, G, Harrison, A, Pentieva, K, McNulty, H, Parle-McDermott, A, MacEwen, CJ, Ozaki, M., Parle-McDermott, A., Cattell, N, Duffy, S, McKnight, AJ, Heagerty, AHM, Leigh, IM, Pourreyron, C, Szeverenyi, I, Smith, FJ, Swan, EJ, Smyth, LJ, Kilner, J, Connolly, S, Heron, E, Fahey, C, Byrne, S, McLaughlin, R, Kenna, K, Bradley, D G, Gill, M, Hardiman, O, Corvin, AP, Morris, DW, Evenepoel, L
Publikováno v:
The Ulster Medical Journal
Autor:
Perkin, MR, Craven, J, Logan, K, Strachan, D, Marrs, T, Radulovic, S, Campbell, LE, MacCallum, SF, McLean, WHI, Lack, G, Flohr, C, Enquiring About Tolerance Study Team
BACKGROUND: Domestic water hardness and chlorine have been suggested as important risk factors for atopic dermatitis (AD). OBJECTIVE: We sought to examine the link between domestic water calcium carbonate (CaCO3) and chlorine concentrations, skin bar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::364a7b87584e88cb317d2cd1fe860b4e
Autor:
Paternoster, L, Standl, M, Waage, J, Baurecht, H, Hotze, M, Strachan, DP, Curtin, JA, Bonnelykke, K, Tian, C, Takahashi, A, Esparza-Gordillo, J, Alves, AC, Thyssen, JP, den Dekker, HT, Ferreira, MA, Altmaier, E, Sleiman, PMA, Xiao, FL, Gonzalez, JR, Marenholz, I, Kalb, B, Pino-Yanes, M, Xu, C-J, Carstensen, L, Groen-Blokhuis, MM, Venturini, C, Pennell, CE, Barton, SJ, Levin, AM, Curjuric, I, Bustamante, M, Kreiner-Moller, E, Lockett, GA, Bacelis, J, Bunyavanich, S, Myers, RA, Matanovic, A, Kumar, A, Tung, JY, Hirota, T, Kubo, M, McArdle, WL, Henderson, AJ, Kemp, JP, Zheng, J, Smith, GD, Rueschendorf, F, Bauerfeind, A, Lee-Kirsch, MA, Arnold, A, Homuth, G, Schmidt, CO, Mangold, E, Cichon, S, Keil, T, Rodriguez, E, Peters, A, Franke, A, Lieb, W, Novak, N, Foelster-Holst, R, Horikoshi, M, Pekkanen, J, Sebert, S, Husemoen, LL, Grarup, N, De Jongste, JC, Rivadeneira, F, Hofman, A, Jaddoe, VWV, Pasmans, SGMA, Elbert, NJ, Uitterlinden, AG, Marks, GB, Thompson, PJ, Matheson, MC, Robertson, CF, Ried, JS, Li, J, Zuo, XB, Zheng, XD, Yin, XY, Sun, LD, McAleer, MA, O'Regan, GM, Fahy, CMR, Campbell, LE, Macek, M, Kurek, M, Hu, D, Eng, C, Postma, DS, Feenstra, B, Geller, F, Hottenga, JJ, Middeldorp, CM, Hysi, P, Bataille, V, Spector, T, Tiesler, CMT, Thiering, E, Pahukasahasram, B, Yang, JJ, Imboden, M, Huntsman, S, Vilor-Tejedor, N, Relton, CL, Myhre, R, Nystad, W, Custovic, A, Weiss, ST, Meyers, DA, Soederhaell, C, Melen, E, Ober, C, Raby, BA, Simpson, A, Jacobsson, B, Holloway, JW, Bisgaard, H, Sunyer, J, Probst-Hensch, NM, Williams, LK, Godfrey, KM, Wang, CA, Boomsma, DI, Melbye, M, Koppelman, GH, Jarvis, D, McLean, WHI, Irvine, AD, Zhang, XJ, Hakonarson, H, Gieger-, C, Burchard, EG, Martin, NG, Duijts, L, Linneberg, A, Jarvelin, M-R, Noethen, MM, Lau, S, Huebner, N, Lee, Y-A, Tamari, M, Hinds, DA, Glass, D, Brown, SJ, Heinrich, J, Evans, DM, Weidinger, S, AAGC, AAGC, Epidemio, EGL
Publikováno v:
Nature Genetics
Genetic association studies have identified 21 loci associated with atopic dermatitis risk predominantly in populations of European ancestry. To identify further susceptibility loci for this common, complex skin disease, we performed a meta-analysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::fe015907bf2695c75e6d9e570aa8583c
https://openaccess.sgul.ac.uk/id/eprint/107705/7/NG-LE40675R1_Paternoster_200815_with_fig.pdf
https://openaccess.sgul.ac.uk/id/eprint/107705/7/NG-LE40675R1_Paternoster_200815_with_fig.pdf
Publikováno v:
The British Journal of Dermatology
Autor:
Baclig, Alvin, Schut, TCB, O'Regan, GM, Irvine, AD, McLean, WHI, Puppels, Gerwin, Caspers, Peter
Publikováno v:
Journal of Raman Spectroscopy, 44(3), 340-345. John Wiley & Sons Ltd.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::3e58f38dc3075aa2c703830bc96b334e
https://pure.eur.nl/en/publications/3c08c3c2-81f4-44a2-a19a-a0d66646b6f2
https://pure.eur.nl/en/publications/3c08c3c2-81f4-44a2-a19a-a0d66646b6f2