Detalles de la búsqueda
1.
Smek1 deficiency exacerbates experimental autoimmune encephalomyelitis by activating proinflammatory microglia and suppressing the IDO1-AhR pathway.
J Neuroinflammation
; 18(1): 145, 2021 Jun 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-34183017
2.
Cervical Spinal Involvement in a Chinese Pedigree With Pontine Autosomal Dominant Microangiopathy and Leukoencephalopathy Caused by a 3' Untranslated Region Mutation of COL4A1 Gene.
Stroke
; 50(9): 2307-2313, 2019 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-31366314
3.
Correction: Smek1 deficiency exacerbates experimental autoimmune encephalomyelitis by activating proinflammatory microglia and suppressing the IDO1-AhR pathway.
J Neuroinflammation
; 20(1): 160, 2023 Jul 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-37407996
4.
Association of polymorphisms in SPARC and NLRP2 genes with rheumatoid arthritis in a Chinese Han population.
Mod Rheumatol
; 25(1): 67-71, 2015 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-24754275
5.
Diagnostic signatures and immune cell infiltration characteristics in anti-GABABR encephalitis.
J Neuroimmunol
; 388: 578296, 2024 03 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-38309225
6.
[Association of two SNPs in 3'UTR of ETS1 gene with systemic lupus erythematosus in a northern Chinese Han population].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 30(4): 477-80, 2013 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-23926020
7.
Two single nucleotide polymorphisms in TSLP gene are associated with asthma susceptibility in Chinese Han population.
Exp Lung Res
; 38(8): 375-82, 2012 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-22913730
8.
[Association study between TNFSF4 and coronary heart disease].
Yi Chuan
; 33(3): 239-45, 2011 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-21402531
9.
Two single nucleotide polymorphisms in ALOX15 are associated with risk of coronary artery disease in a Chinese Han population.
Heart Vessels
; 25(5): 368-73, 2010 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-20676957
10.
[Association of rs2298212 polymorphism in OX40 gene with coronary atherosclerotic disease in Chinese Han population].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 27(2): 171-5, 2010 Apr.
Artículo
en Zh
| MEDLINE | ID: mdl-20376799
11.
[Association of the ABCG1 gene polymorphism with the susceptibility and severity of coronary atherosclerotic disease].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 27(5): 506-11, 2010 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-20931526
12.
[Clinical investigation of a family with brachydactyly type A1 and the identification of the disease gene].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 26(3): 267-71, 2009 Jun.
Artículo
en Zh
| MEDLINE | ID: mdl-19504437
13.
The effect of ZnO nanoparticles on liver function in rats.
Int J Nanomedicine
; 11: 4275-85, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-27621621
14.
[Analysis on genetic polymorphism of 5 STR loci selected from X chromosome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 22(1): 54-7, 2005 Feb.
Artículo
en Zh
| MEDLINE | ID: mdl-15696480
15.
Lipoprotein lipase gene Hind III polymorphism was associated with hemorrhagic stroke.
Int J Clin Exp Med
; 8(6): 9575-9, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26309627
16.
[Characterization of genomic structure and mutation analysis of SMARCA1 gene in a Smith-Fineman-Myers syndrome family].
Yi Chuan Xue Bao
; 31(2): 114-8, 2004 Feb.
Artículo
en Zh
| MEDLINE | ID: mdl-15473299
17.
[Polymorphic loci and polymorphism analysis of short tandem repeats within XNP gene].
Yi Chuan Xue Bao
; 29(3): 201-5, 2002.
Artículo
en Zh
| MEDLINE | ID: mdl-12182071
18.
[Application of homozygosity mapping to the fine mapping of the osteoporosis-pseudoglioma syndrome locus].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 20(1): 53-5, 2003 Feb.
Artículo
en Zh
| MEDLINE | ID: mdl-12579502
19.
[Fine mapping of Smith-Fineman-Myers syndrome and exclusion of GPC3, GPCR2 MST4 and GLUD2 as candidate genes].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 21(3): 198-202, 2004 Jun.
Artículo
en Zh
| MEDLINE | ID: mdl-15192816
20.
Features of a Chinese family with cerebral cavernous malformation induced by a novel CCM1 gene mutation.
Chin Med J (Engl)
; 126(18): 3427-32, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-24034083