Liu F - Search Results

1

Next generation sequencing as a rapid molecular diagnosis for Marfan syndrome in a Chinese family with mutations in the fibrillin-1 gene.

Xiao Y, Liu Y, Yang K, Yang Y, Zhou X, Lu C, Xiao J, Liu F, Zhang X. Xiao Y, et al. Among authors: liu y, liu f. Clin Chim Acta. 2015 Jan 15;439:58-60. doi: 10.1016/j.cca.2014.09.034. Epub 2014 Oct 7. Clin Chim Acta. 2015. PMID: 25304743 No abstract available.

2

Gross deletions in FBN1 results in variable phenotypes of Marfan syndrome.

Li J, Wu W, Lu C, Liu Y, Wang R, Si N, Liu F, Zhou J, Zhang S, Zhang X. Li J, et al. Among authors: liu y, liu f. Clin Chim Acta. 2017 Nov;474:54-59. doi: 10.1016/j.cca.2017.08.023. Epub 2017 Aug 24. Clin Chim Acta. 2017. PMID: 28842177

3

Novel missense mutations of ABCB6 in two chinese families with dyschromatosis universalis hereditaria.

Lu C, Liu J, Liu F, Liu Y, Ma D, Zhang X. Lu C, et al. Among authors: liu j, liu y, liu f. J Dermatol Sci. 2014 Dec;76(3):255-8. doi: 10.1016/j.jdermsci.2014.08.015. Epub 2014 Sep 11. J Dermatol Sci. 2014. PMID: 25288164 No abstract available.

4

Novel Phenotype-Genotype Correlations of Restrictive Cardiomyopathy With Myosin-Binding Protein C (MYBPC3) Gene Mutations Tested by Next-Generation Sequencing.

Wu W, Lu CX, Wang YN, Liu F, Chen W, Liu YT, Han YC, Cao J, Zhang SY, Zhang X. Wu W, et al. Among authors: liu yt, liu f. J Am Heart Assoc. 2015 Jul 10;4(7):e001879. doi: 10.1161/JAHA.115.001879. J Am Heart Assoc. 2015. PMID: 26163040 Free PMC article.

5

Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies.

Lu C, Wu W, Liu F, Yang K, Li J, Liu Y, Wang R, Si N, Gao P, Liu Y, Zhang S, Zhang X. Lu C, et al. Among authors: liu y, liu f. J Transl Med. 2018 Aug 30;16(1):241. doi: 10.1186/s12967-018-1605-5. J Transl Med. 2018. PMID: 30165862 Free PMC article.

6

CHCHD10 is not a frequent causative gene in Chinese ALS patients.

Li XL, Shu S, Li XG, Liu Q, Liu F, Cui B, Liu MS, Peng B, Cui LY, Zhang X. Li XL, et al. Among authors: liu ms, liu q, liu f. Amyotroph Lateral Scler Frontotemporal Degener. 2016 Jul-Aug;17(5-6):458-60. doi: 10.3109/21678421.2016.1170151. Epub 2016 Apr 14. Amyotroph Lateral Scler Frontotemporal Degener. 2016. PMID: 27077676

7

Mutation screening of NEK1 in Chinese ALS patients.

Shu S, Lei X, Liu F, Cui B, Liu Q, Ding Q, Liu MS, Li XG, Cui L, Zhang X. Shu S, et al. Among authors: liu ms, liu q, liu f. Neurobiol Aging. 2018 Nov;71:267.e1-267.e4. doi: 10.1016/j.neurobiolaging.2018.06.022. Epub 2018 Jun 28. Neurobiol Aging. 2018. PMID: 30093141

8

Screening of the TBK1 gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin.

Shu S, Li XL, Liu Q, Liu F, Cui B, Liu MS, Cui LY, Li XG, Zhang X. Shu S, et al. Among authors: liu ms, liu q, liu f. Amyotroph Lateral Scler Frontotemporal Degener. 2016 Oct-Nov;17(7-8):605-607. doi: 10.1080/21678421.2016.1183681. Epub 2016 Jun 3. Amyotroph Lateral Scler Frontotemporal Degener. 2016. PMID: 27260353

9

Mutation spectrum of Chinese patients with familial and sporadic amyotrophic lateral sclerosis.

Liu Q, Liu F, Cui B, Lu CX, Guo XN, Wang RR, Liu MS, Li XG, Cui LY, Zhang X. Liu Q, et al. Among authors: liu ms, liu f. J Neurol Neurosurg Psychiatry. 2016 Nov;87(11):1272-1274. doi: 10.1136/jnnp-2016-313337. Epub 2016 Jun 16. J Neurol Neurosurg Psychiatry. 2016. PMID: 27313233 No abstract available.

10

Identification of a novel loss-of-function C9orf72 splice site mutation in a patient with amyotrophic lateral sclerosis.

Liu F, Liu Q, Lu CX, Cui B, Guo XN, Wang RR, Liu MS, Li XG, Cui LY, Zhang X. Liu F, et al. Among authors: liu ms, liu q. Neurobiol Aging. 2016 Nov;47:219.e1-219.e5. doi: 10.1016/j.neurobiolaging.2016.07.027. Epub 2016 Aug 8. Neurobiol Aging. 2016. PMID: 27595458

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

36,274 results

Search Page

Filters