Impact of LIMK1, MMP2 and TNF-α variations for intracranial aneurysm in Japanese population.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 211, doi. 10.1038/jhg.2010.169
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- Publication type:
- Article
Works matching IS 14345161 AND DT 2011 AND VI 56 AND IP 3
Results: 16
1
2
Knowledge gaining by human genetic studies on tuberculosis susceptibility.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 177, doi. 10.1038/jhg.2010.164
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- Publication type:
- Article
3
A common variant in the CDKN2B gene on chromosome 9p21 protects against coronary artery disease in Americans of African ancestry.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 224, doi. 10.1038/jhg.2010.171
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- Publication type:
- Article
4
A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 250, doi. 10.1038/jhg.2010.163
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- Publication type:
- Article
5
Association of HLA-A<sup>*</sup>02:06 and HLA-DRB1<sup>*</sup>04:05 with clinical subtypes of juvenile idiopathic arthritis.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 196, doi. 10.1038/jhg.2010.159
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- Publication type:
- Article
6
KEAP1 gene mutations and NRF2 activation are common in pulmonary papillary adenocarcinoma.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 230, doi. 10.1038/jhg.2010.172
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- Publication type:
- Article
7
Association of CARD8 with inflammatory bowel disease in Koreans.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 217, doi. 10.1038/jhg.2010.170
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- Publication type:
- Article
8
Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 247, doi. 10.1038/jhg.2010.162
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- Publication type:
- Article
9
Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 183, doi. 10.1038/jhg.2010.156
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- Publication type:
- Article
10
Positive selection on mitochondrial M7 lineages among the Gelong people in Hainan.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 253, doi. 10.1038/jhg.2010.165
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- Publication type:
- Article
11
Association of ADAM33 gene polymorphisms with asthma in Indian children.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 188, doi. 10.1038/jhg.2010.157
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- Publication type:
- Article
12
A regulatory SNP in AKAP13 is associated with blood pressure in Koreans.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 205, doi. 10.1038/jhg.2010.167
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- Publication type:
- Article
13
Mitochondrial DNA and Y-chromosomal stratification in Iran: relationship between Iran and the Arabian Peninsula.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 235, doi. 10.1038/jhg.2010.174
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- Publication type:
- Article
14
Hypophosphatasia now draws more attention of both clinicians and researchers: A Commentary on prevelance of c. 1559delT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasias in Japanese and effects of the mutation on heterozygous carriers
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 174, doi. 10.1038/jhg.2011.6
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- Publication type:
- Article
15
A Commentary on Identification of novel MLC1 mutations in Chinese patients with megalencephalic leukoencephalopathy with subcortical cysts (MLC).
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 173, doi. 10.1038/jhg.2011.5
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- Publication type:
- Article
16
No association between TNFSF15 and IL23R with ulcerative colitis in Koreans.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 200, doi. 10.1038/jhg.2010.166
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- Publication type:
- Article