skip to main content
Show Results with:

Results 1 - 10 of 33  for Explore Further

results 1 2 3 4 next page
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Material Type:
Article
Add to My workspace

Differences in UGT1A1 , UGT1A7 , and UGT1A9 Polymorphisms between Uzbek and Japanese Populations

Molecular Diagnosis & Therapy, 2014, Vol.18(3), pp.333-342 [Peer Reviewed Journal]

Full text available

View all versions
2
Material Type:
Article
Add to My workspace

A Meta-Analysis of PTGS1 and PTGS2 Polymorphisms and NSAID Intake on the Risk of Developing Cancer

PLoS One, Aug 2013, p.e71126 [Peer Reviewed Journal]

Full text available

View all versions
3
Material Type:
Article
Add to My workspace

Genetic variants at 1q32.1, 10q11.2 and 19q13.41 are associated with prostate-specific antigen for prostate cancer screening in two Korean population-based cohort studies

Gene, 10 February 2015, Vol.556(2), pp.199-205 [Peer Reviewed Journal]

No full-text

View all versions
4
Material Type:
Article
Add to My workspace

Clinical characteristics and genetic analysis of childhood acute lymphoblastic leukemia with hemophagocytic lymphohistiocytosis: a Japanese retrospective study by the Kyushu–Yamaguchi Children’s Cancer Study Group

International Journal of Hematology, 2014, Vol.100(1), pp.70-78 [Peer Reviewed Journal]

No full-text

View all versions
5
Material Type:
Article
Add to My workspace

The course of gastric cancer following surgery is associated with genetic variations of the interleukin-1 receptor antagonist and interleukin-1[beta]

Gastric Cancer, Jan 2015, pp.77-83 [Peer Reviewed Journal]

No full-text

View all versions
6
Material Type:
Article
Add to My workspace

Nonparametric estimation of LOH using Affymetrix SNP genotyping arrays for unpaired samples

Journal of Human Genetics, 2008, Vol.53(11), pp.983-990 [Peer Reviewed Journal]

No full-text

View all versions
7
Material Type:
Article
Add to My workspace

Association study of the C3 gene with adult and childhood asthma

Journal of Human Genetics, 2008, Vol.53(8), pp.728-738 [Peer Reviewed Journal]

No full-text

View all versions
8
Material Type:
Article
Add to My workspace

G6PD deficiency assessment in Freetown, Sierra Leone, reveals further insight into the molecular heterogeneity of G6PD A-.

Journal of human genetics, 2008, Vol.53(7), pp.675-679 [Peer Reviewed Journal]

No full-text

View all versions
9
Material Type:
Article
Add to My workspace

Association study to evaluate the serotonin transporter and apolipoprotein E genes in frontotemporal lobar degeneration in Italy.

Journal of human genetics, 2008, Vol.53(11-12), pp.1029-1033 [Peer Reviewed Journal]

No full-text

View all versions
10
Material Type:
Article
Add to My workspace

Molecular basis of complement factor I (CFI) polymorphism: one of two polymorphic suballeles responsible for CFI A is Japanese-specific.

Journal of human genetics, 2008, Vol.53(11-12), pp.1016-1021 [Peer Reviewed Journal]

No full-text

View all versions

Results 1 - 10 of 33  for Explore Further

results 1 2 3 4 next page

Refine Search Results

Creation date 

From To

Try a new search

Ignore my search and look for everything

by this Author/Contributor:

  1. Ohashi, Jun
  2. Tokunaga, Katsushi
  3. Nishida, Nao
  4. Inada, Hiroko
  5. Okamura, Jun

Searching Remote Databases, Please Wait