受强制性开放获取政策约束的文章 - Zsolt Urban了解详情
无法在其他位置公开访问的文章：2 篇
Cutis laxa: a review
DR Berk, DD Bentley, SJ Bayliss, A Lind, Z Urban
Journal of the American Academy of Dermatology 66 (5), 842. e1-842. e17, 2012
强制性开放获取政策： US National Institutes of Health
DANCE/fibulin-5 promotes elastic fiber formation in a tropoelastin isoform-dependent manner
R Nonaka, S Onoue, H Wachi, F Sato, Z Urban, BC Starcher, Y Seyama
Clinical biochemistry 42 (7-8), 713-721, 2009
强制性开放获取政策： US National Institutes of Health
可在其他位置公开访问的文章：32 篇
Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2
U Kornak, E Reynders, A Dimopoulou, J Van Reeuwijk, B Fischer, ...
Nature genetics 40 (1), 32-34, 2008
强制性开放获取政策： Research Foundation (Flanders), German Research Foundation
A thrifty variant in CREBRF strongly influences body mass index in Samoans
RL Minster, NL Hawley, CT Su, G Sun, EE Kershaw, H Cheng, OD Buhule, ...
Nature genetics 48 (9), 1049-1054, 2016
强制性开放获取政策： US National Institutes of Health
Mechanisms and treatment of cardiovascular disease in Williams-Beuren syndrome
BR Pober, M Johnson, Z Urban
The Journal of clinical investigation 118 (5), 1606-1615, 2008
强制性开放获取政策： US National Institutes of Health
Mutations in LTBP4 cause a syndrome of impaired pulmonary, gastrointestinal, genitourinary, musculoskeletal, and dermal development
Z Urban, V Hucthagowder, N Schürmann, V Todorovic, L Zilberberg, ...
The American Journal of Human Genetics 85 (5), 593-605, 2009
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research
Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival
V Hucthagowder, E Morava, U Kornak, DJ Lefeber, B Fischer, ...
Human molecular genetics 18 (12), 2149-2165, 2009
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research
New insights into the pathogenesis of autosomal‐dominant cutis laxa with report of five ELN mutations
B Callewaert, M Renard, V Hucthagowder, B Albrecht, I Hausser, E Blair, ...
Human mutation 32 (4), 445-455, 2011
强制性开放获取政策： US National Institutes of Health, Research Foundation (Flanders)
Jagged1 (JAG1) mutations in patients with tetralogy of fallot or pulmonic stenosis
RC Bauer, AO Laney, R Smith, J Gerfen, JJD Morrissette, ...
Human mutation 31 (5), 594-601, 2010
强制性开放获取政策： US National Institutes of Health
Comprehensive clinical and molecular analysis of 12 families with type 1 recessive cutis laxa
B Callewaert, CT Su, T Van Damme, P Vlummens, F Malfait, O Vanakker, ...
Human mutation 34 (1), 111-121, 2013
强制性开放获取政策： US National Institutes of Health, Research Foundation (Flanders)
Bi-allelic mutations in the mitochondrial ribosomal protein MRPS2 cause sensorineural hearing loss, hypoglycemia, and multiple OXPHOS complex deficiencies
T Gardeitchik, M Mohamed, B Ruzzenente, D Karall, S Guerrero-Castillo, ...
The American Journal of Human Genetics 102 (4), 685-695, 2018
强制性开放获取政策： US National Institutes of Health, Netherlands Organisation for Scientific …
The complexity of elastic fibre biogenesis in the skin–a perspective to the clinical heterogeneity of cutis laxa
J Uitto, Q Li, Z Urban
Experimental dermatology 22 (2), 88-92, 2013
强制性开放获取政策： US National Institutes of Health
GLUT10 is required for the development of the cardiovascular system and the notochord and connects mitochondrial function to TGFβ signaling
A Willaert, S Khatri, BL Callewaert, PJ Coucke, SD Crosby, JGH Lee, ...
Human molecular genetics 21 (6), 1248-1259, 2012
强制性开放获取政策： US National Institutes of Health, Research Foundation (Flanders)
Integrin β3 inhibition is a therapeutic strategy for supravalvular aortic stenosis
A Misra, AQ Sheikh, A Kumar, J Luo, J Zhang, RB Hinton, L Smoot, ...
Journal of Experimental Medicine 213 (3), 451-463, 2016
强制性开放获取政策： US National Institutes of Health, American Heart Association
Cutis laxa: intersection of elastic fiber biogenesis, TGFβ signaling, the secretory pathway and metabolism
Z Urban, EC Davis
Matrix Biology 33, 16-22, 2014
强制性开放获取政策： US National Institutes of Health
Latent transforming growth factor binding protein 4 regulates transforming growth factor beta receptor stability
CT Su, JW Huang, CK Chiang, EC Lawrence, KL Levine, B Dabovic, ...
Human Molecular Genetics 24 (14), 4024-4036, 2015
强制性开放获取政策： US National Institutes of Health
Alternative splicing and tissue-specific elastin misassembly act as biological modifiers of human elastin gene frameshift mutations associated with dominant cutis laxa
H Sugitani, E Hirano, RH Knutsen, A Shifren, JE Wagenseil, C Ciliberto, ...
Journal of Biological Chemistry 287 (26), 22055-22067, 2012
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research
Mechanisms of emphysema in autosomal dominant cutis laxa
Q Hu, A Shifren, C Sens, J Choi, Z Szabo, BC Starcher, RH Knutsen, ...
Matrix Biology 29 (7), 621-628, 2010
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research
LTBP4 in Health and Disease
CT Su, Z Urban
Genes 12 (6), 795, 2021
强制性开放获取政策： US National Institutes of Health
EFEMP2-related cutis laxa
B Loeys, A De Paepe, Z Urban
强制性开放获取政策： Research Foundation (Flanders), European Commission, Dutch Heart Foundation
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