Hao XD - Search Results

1

Large-scale mtDNA screening reveals a surprising matrilineal complexity in east Asia and its implications to the peopling of the region.

Kong QP, Sun C, Wang HW, Zhao M, Wang WZ, Zhong L, Hao XD, Pan H, Wang SY, Cheng YT, Zhu CL, Wu SF, Liu LN, Jin JQ, Yao YG, Zhang YP. Kong QP, et al. Among authors: hao xd. Mol Biol Evol. 2011 Jan;28(1):513-22. doi: 10.1093/molbev/msq219. Epub 2010 Aug 16. Mol Biol Evol. 2011. PMID: 20713468

2

Uncovering the profile of somatic mtDNA mutations in Chinese colorectal cancer patients.

Wang CY, Li H, Hao XD, Liu J, Wang JX, Wang WZ, Kong QP, Zhang YP. Wang CY, et al. Among authors: hao xd. PLoS One. 2011;6(6):e21613. doi: 10.1371/journal.pone.0021613. Epub 2011 Jun 28. PLoS One. 2011. PMID: 21738732 Free PMC article.

3

Mitochondrial DNA haplogroup Y is associated to Leigh syndrome in Chinese population.

Hao XD, Yang YL, Tang NL, Kong QP, Wu SF, Zhang YP. Hao XD, et al. Gene. 2013 Jan 10;512(2):460-3. doi: 10.1016/j.gene.2012.10.054. Epub 2012 Oct 27. Gene. 2013. PMID: 23111160 Clinical Trial.

4

Evidence for positive selection on the Osteogenin (BMP3) gene in human populations.

Wu DD, Jin W, Hao XD, Tang NL, Zhang YP. Wu DD, et al. Among authors: hao xd. PLoS One. 2010 Jun 4;5(6):e10959. doi: 10.1371/journal.pone.0010959. PLoS One. 2010. PMID: 20532035 Free PMC article.

5

Correlation of telomere length shortening with TP53 somatic mutations, polymorphisms and allelic loss in breast tumors and esophageal cancer.

Hao XD, Yang Y, Song X, Zhao XK, Wang LD, He JD, Kong QP, Tang NL, Zhang YP. Hao XD, et al. Oncol Rep. 2013 Jan;29(1):226-36. doi: 10.3892/or.2012.2098. Epub 2012 Oct 22. Oncol Rep. 2013. PMID: 23124483

6

Mitochondrial DNA copy number, but not haplogroup is associated with keratoconus in Han Chinese population.

Hao XD, Chen P, Wang Y, Li SX, Xie LX. Hao XD, et al. Exp Eye Res. 2015 Mar;132:59-63. doi: 10.1016/j.exer.2015.01.016. Epub 2015 Jan 19. Exp Eye Res. 2015. PMID: 25613073

7

Evaluating the Association between Keratoconus and Reported Genetic Loci in a Han Chinese Population.

Hao XD, Chen P, Chen ZL, Li SX, Wang Y. Hao XD, et al. Ophthalmic Genet. 2015 Jun;36(2):132-6. doi: 10.3109/13816810.2015.1005317. Epub 2015 Feb 12. Ophthalmic Genet. 2015. PMID: 25675348

8

Mutations in the ABCA3 gene are associated with cataract-microcornea syndrome.

Chen P, Dai Y, Wu X, Wang Y, Sun S, Xiao J, Zhang Q, Guan L, Zhao X, Hao X, Wu R, Xie L. Chen P, et al. Invest Ophthalmol Vis Sci. 2014 Nov 18;55(12):8031-43. doi: 10.1167/iovs.14-14098. Invest Ophthalmol Vis Sci. 2014. PMID: 25406294

9

Decreased Integrity, Content, and Increased Transcript Level of Mitochondrial DNA Are Associated with Keratoconus.

Hao XD, Chen ZL, Qu ML, Zhao XW, Li SX, Chen P. Hao XD, et al. PLoS One. 2016 Oct 26;11(10):e0165580. doi: 10.1371/journal.pone.0165580. eCollection 2016. PLoS One. 2016. PMID: 27783701 Free PMC article.

10

Uncovering the profile of mutations of transforming growth factor beta-induced gene in Chinese corneal dystrophy patients.

Hao XD, Zhang YY, Chen P, Li SX, Wang Y. Hao XD, et al. Int J Ophthalmol. 2016 Feb 18;9(2):198-203. doi: 10.18240/ijo.2016.02.03. eCollection 2016. Int J Ophthalmol. 2016. PMID: 26949635 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

68 results

Search Page

Filters