Các bài viết có thể truy cập công khai - Carol WiseTìm hiểu thêm
Không có ở bất kỳ nơi nào: 4
Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis
I Kou, Y Takahashi, TA Johnson, A Takahashi, L Guo, J Dai, X Qiu, ...
Nature genetics 45 (6), 676-679, 2013
Các cơ quan ủy nhiệm: US National Institutes of Health
A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups
D Londono, I Kou, TA Johnson, S Sharma, Y Ogura, T Tsunoda, ...
Journal of medical genetics 51 (6), 401-406, 2014
Các cơ quan ủy nhiệm: US National Institutes of Health, National Natural Science Foundation of China
Epistasis amongst PTPN2 and genes of the vitamin D pathway contributes to risk of juvenile idiopathic arthritis
JA Ellis, KJ Scurrah, YR Li, AL Ponsonby, RA Chavez, A Pezic, T Dwyer, ...
The Journal of Steroid Biochemistry and Molecular Biology 145, 113-120, 2015
Các cơ quan ủy nhiệm: US National Institutes of Health, Australian Research Council, National …
The association of PTPN22 rs2476601 with juvenile idiopathic arthritis is specific to females
RC Chiaroni-Clarke, YR Li, JE Munro, RA Chavez, KJ Scurrah, A Pezic, ...
Genes & Immunity 16 (7), 495-498, 2015
Các cơ quan ủy nhiệm: US National Institutes of Health, Australian Research Council, National …
Có tại một số nơi: 68
Genome-wide scan reveals association of psoriasis with IL-23 and NF-κB pathways
RP Nair, KC Duffin, C Helms, J Ding, PE Stuart, D Goldgar, ...
Nature genetics 41 (2), 199-204, 2009
Các cơ quan ủy nhiệm: US National Institutes of Health, Canadian Institutes of Health Research
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity
LC Tsoi, SL Spain, J Knight, E Ellinghaus, PE Stuart, F Capon, J Ding, ...
Nature genetics 44 (12), 1341-1348, 2012
Các cơ quan ủy nhiệm: US National Institutes of Health, Canadian Institutes of Health Research …
A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci
Y Liu, C Helms, W Liao, LC Zaba, S Duan, J Gardner, C Wise, A Miner, ...
PLoS genetics 4 (4), e1000041, 2008
Các cơ quan ủy nhiệm: US National Institutes of Health
Rare and common variants in CARD14, encoding an epidermal regulator of NF-kappaB, in psoriasis
CT Jordan, L Cao, EDO Roberson, S Duan, CA Helms, RP Nair, KC Duffin, ...
The American Journal of Human Genetics 90 (5), 796-808, 2012
Các cơ quan ủy nhiệm: US National Institutes of Health, Canadian Institutes of Health Research
The infevers autoinflammatory mutation online registry: update with new genes and functions
F Milhavet, L Cuisset, HM Hoffman, R Slim, H El‐Shanti, I Aksentijevich, ...
Human mutation 29 (6), 803-808, 2008
Các cơ quan ủy nhiệm: US National Institutes of Health
Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases
YR Li, J Li, SD Zhao, JP Bradfield, FD Mentch, SM Maggadottir, C Hou, ...
Nature medicine 21 (9), 1018-1027, 2015
Các cơ quan ủy nhiệm: US National Institutes of Health, Howard Hughes Medical Institute, UK …
Association of TALS developmental disorder with defect in minor splicing component U4atac snRNA
P Edery, C Marcaillou, M Sahbatou, A Labalme, J Chastang, R Touraine, ...
Science 332 (6026), 240-243, 2011
Các cơ quan ủy nhiệm: US National Institutes of Health, National Institute of Health and Medical …
Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes
S Sharma, X Gao, D Londono, SE Devroy, KN Mauldin, JT Frankel, ...
Human molecular genetics 20 (7), 1456-1466, 2011
Các cơ quan ủy nhiệm: US National Institutes of Health
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome
LS Bicknell, S Walker, A Klingseisen, T Stiff, A Leitch, C Kerzendorfer, ...
Nature genetics 43 (4), 350-355, 2011
Các cơ quan ủy nhiệm: Cancer Research UK
Asymmetric lower-limb malformations in individuals with homeobox PITX1 gene mutation
CA Gurnett, F Alaee, LM Kruse, DM Desruisseau, JT Hecht, CA Wise, ...
The American Journal of Human Genetics 83 (5), 616-622, 2008
Các cơ quan ủy nhiệm: US National Institutes of Health
ptk7 mutant zebrafish models of congenital and idiopathic scoliosis implicate dysregulated Wnt signalling in disease
M Hayes, X Gao, LX Yu, N Paria, RM Henkelman, CA Wise, B Ciruna
Nature communications 5 (1), 4777, 2014
Các cơ quan ủy nhiệm: US National Institutes of Health, Canadian Institutes of Health Research
The susceptibility loci juvenile idiopathic arthritis shares with other autoimmune diseases extend to PTPN2, COG6, and ANGPT1
SD Thompson, M Sudman, PS Ramos, MC Marion, M Ryan, M Tsoras, ...
Arthritis & Rheumatism 62 (11), 3265-3276, 2010
Các cơ quan ủy nhiệm: US National Institutes of Health
A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
S Sharma, D Londono, WL Eckalbar, X Gao, D Zhang, K Mauldin, I Kou, ...
Nature communications 6 (1), 6452, 2015
Các cơ quan ủy nhiệm: US National Institutes of Health
Regulatory polymorphisms modulate the expression of HLA class II molecules and promote autoimmunity
P Raj, E Rai, R Song, S Khan, BE Wakeland, K Viswanathan, C Arana, ...
elife 5, e12089, 2016
Các cơ quan ủy nhiệm: US National Institutes of Health
Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis
CA Martin, JE Murray, P Carroll, A Leitch, KJ Mackenzie, M Halachev, ...
Genes & development 30 (19), 2158-2172, 2016
Các cơ quan ủy nhiệm: UK Biotechnology and Biological Sciences Research Council, UK Medical …
Fine-mapping the MHC locus in juvenile idiopathic arthritis (JIA) reveals genetic heterogeneity corresponding to distinct adult inflammatory arthritic diseases
A Hinks, J Bowes, J Cobb, HC Ainsworth, MC Marion, ME Comeau, ...
Annals of the rheumatic diseases 76 (4), 765-772, 2017
Các cơ quan ủy nhiệm: US National Institutes of Health, Canadian Institutes of Health Research …
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