Yan AZ - Search Results

1

Further identification of a 140bp sequence from amid intron 9 of human FMR1 gene as a new exon.

Yang WJ, Yan AZ, Xu YJ, Guo XY, Fu XG, Li D, Liao J, Zhang D, Lan FH. Yang WJ, et al. Among authors: yan az. BMC Genet. 2020 Jun 18;21(1):63. doi: 10.1186/s12863-020-00870-2. BMC Genet. 2020. PMID: 32552710 Free PMC article.

2

Splicing of exon 9a in FMR1 transcripts results in a truncated FMRP with altered subcellular distribution.

Fu XG, Yan AZ, Xu YJ, Liao J, Guo XY, Zhang D, Yang WJ, Zheng DZ, Lan FH. Fu XG, et al. Among authors: yan az. Gene. 2020 Mar 20;731:144359. doi: 10.1016/j.gene.2020.144359. Epub 2020 Jan 11. Gene. 2020. PMID: 31935509

3

Alternatively spliced products lacking exon 12 dominate the expression of fragile X mental retardation 1 gene in human tissues.

Fu X, Zheng D, Liao J, Li Q, Lin Y, Zhang D, Yan A, Lan F. Fu X, et al. Mol Med Rep. 2015 Aug;12(2):1957-62. doi: 10.3892/mmr.2015.3574. Epub 2015 Mar 31. Mol Med Rep. 2015. PMID: 25847585

4

[Mutation analysis of SMN gene in a patient and his family with spinal muscular atrophy].

Zeng J, Lin YH, Yan AZ, Cai MY, Ke LF, Lan FH. Zeng J, et al. Among authors: yan az. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Apr;26(2):139-43. doi: 10.3760/cma.j.issn.1003-9406.2009.02.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19350502 Chinese.

5

[Analysis of APC gene mutation in a familial adenomatous polyposis pedigree].

Zhang M, Wang Z, Lin Y, Lin Y, Li X, Yan A, Fu X, Zhong F, Lan F. Zhang M, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Dec;31(6):757-60. doi: 10.3760/cma.j.issn.1003-9406.2014.06.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25449083 Chinese.

6

[Phenotypic and genetic analysis of an inv dup(15) case with a BP3:BP3 rearrangement].

Zhong F, Lan F, Zhang X, Lin Y, Lin Y, Yan A, Tu X. Zhong F, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Jun 10;34(3):402-405. doi: 10.3760/cma.j.issn.1003-9406.2017.03.020. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28604965 Chinese.

7

[Molecular diagnosis of a Chinese pedigree with osteogenesis imperfecta type I].

Ke LF, Zheng LW, Xie HH, Yan AZ, Zhu ZY, Lan FH. Ke LF, et al. Among authors: yan az. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Feb;26(1):50-3. doi: 10.3760/cma.j.issn.1003-9406.2009.01.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19199251 Chinese.

8

Establishment of a molecular diagnostic system for spinal muscular atrophy experience from a clinical laboratory in china.

Zeng J, Lin Y, Yan A, Ke L, Zhu Z, Lan F. Zeng J, et al. J Mol Diagn. 2011 Jan;13(1):41-7. doi: 10.1016/j.jmoldx.2010.11.009. Epub 2010 Dec 23. J Mol Diagn. 2011. PMID: 21227393 Free PMC article.

9

Whole-exome sequencing identifies compound heterozygous mutations in ARSA of two siblings presented with atypical onset of metachromatic leukodystrophy from a Chinese pedigree.

Wang Z, Lin Y, Zheng D, Yan A, Tu X, Lin J, Lan F. Wang Z, et al. Clin Chim Acta. 2016 Sep 1;460:135-7. doi: 10.1016/j.cca.2016.06.038. Epub 2016 Jun 30. Clin Chim Acta. 2016. PMID: 27374302

10

Pre-symptomatic molecular diagnosis of X-linked adrenoleukodystrophy in Chinese families.

Wang Z, Ke L, Xie H, Yan A, Huang L, Lan F. Wang Z, et al. Neurol Res. 2010 Sep;32(7):695-9. doi: 10.1179/016164109X12445616596364. Epub 2009 Aug 5. Neurol Res. 2010. PMID: 19660195

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