Detalhe da pesquisa
1.
Sex-specific analysis in Behçet's disease reveals higher genetic risk in male patients.
J Autoimmun
; 132: 102882, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35987173
2.
Polymorphism of the apolipoprotein B gene and association with plasma lipid and lipoprotein levels in the Mongolian Buryat.
Biochem Genet
; 50(3-4): 249-68, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21952877
3.
Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet's Disease.
Arthritis Rheumatol
; 73(7): 1244-1252, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33393726
4.
Genetic association of HLA-A*2601 with ocular Behçet's disease in Japanese patients.
Clin Exp Rheumatol
; 28(4 Suppl 60): S39-44, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20868569
5.
HERC1 polymorphisms: population-specific variations in haplotype composition.
Cell Biochem Funct
; 27(6): 402-5, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19618402
6.
Markedly different clinical features in 2 diabetes mellitus patients with extremely high tissue levels of the mitochondrial DNA A3243G mutation.
Gerontology
; 54(3): 168-72, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18417955
7.
Investigation of Japanese-specific alleles: most are of Jomon lineage.
Leg Med (Tokyo)
; 17(1): 52-5, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25239165
8.
Comparison of the level of mitochondrial DNA A3243G mutation in esophageal epithelium and myocardium from individuals of very advanced age.
Exp Gerontol
; 37(7): 917-23, 2002 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-12086700
9.
The mitochondrial DNA A3243G mutation in Werner's syndrome.
Exp Gerontol
; 38(3): 339-42, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12581800
10.
Single nucleotide polymorphisms in the human complement C6 and C7 genes.
Leg Med (Tokyo)
; 5 Suppl 1: S198-200, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12935588
11.
Spontaneous event of mitochondrial DNA mutation, A3243G, found in a family of identical twins.
Mitochondrial DNA
; 24(2): 158-62, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23072508
12.
A hypervariable STR polymorphism in the CFI gene: southern origin of East Asian-specific group H alleles.
Leg Med (Tokyo)
; 15(5): 239-43, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23688582
13.
Distribution of OCA2∗481Thr and OCA2∗615Arg, associated with hypopigmentation, in several additional populations.
Leg Med (Tokyo)
; 13(4): 215-7, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21565543
14.
A Japanese-specific allele in the GALNT11 gene.
Leg Med (Tokyo)
; 12(4): 208-11, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20547088
15.
Sequence analysis for HV I region of mitochondrial DNA using WGA (Whole Genome Amplification) method.
Leg Med (Tokyo)
; 11 Suppl 1: S115-8, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19278888
16.
Characteristics of the beta-globin gene cluster haplotypes of three Han Chinese populations at Beijing, Xi'an, and Kunming as compared with those of other Asian populations.
Biochem Genet
; 46(9-10): 566-82, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18553219
17.
Molecular basis of complement factor I (CFI) polymorphism: one of two polymorphic suballeles responsible for CFI A is Japanese-specific.
J Hum Genet
; 53(11-12): 1016-1021, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18825487
18.
OCA2 481Thr, a hypofunctional allele in pigmentation, is characteristic of northeastern Asian populations.
J Hum Genet
; 52(8): 690-693, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17568986
19.
Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes.
J Hum Genet
; 51(1): 47-58, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16328082
20.
Beta-globin gene cluster haplotype frequencies in Khalkhs and Buryats of Mongolia.
Hum Biol
; 78(6): 749-56, 2006 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17564253