Ma D - Search Results

1

A novel loss-of-function heterozygous BRCA2 c.8946_8947delAG mutation found in a Chinese woman with family history of breast cancer.

Ma J, Yang J, Jian W, Wang X, Xiao D, Xia W, Xiong L, Ma D. Ma J, et al. Among authors: ma d. J Cancer Res Clin Oncol. 2017 Apr;143(4):631-637. doi: 10.1007/s00432-016-2327-9. Epub 2017 Jan 5. J Cancer Res Clin Oncol. 2017. PMID: 28058502

2

Grhl1 deficiency affects inner ear development in zebrafish.

Liu F, Yang F, Wen D, Xia W, Hao L, Hu J, Zong J, Shen X, Ma J, Jiang N, Sun S, Zhang J, Wang H, Wang X, Ma Z, Ma D. Liu F, et al. Among authors: ma d, ma j, ma z. Int J Dev Biol. 2015;59(10-12):417-23. doi: 10.1387/ijdb.140230FL. Int J Dev Biol. 2015. PMID: 25896282 Free article.

3

Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss.

Liu F, Hu J, Xia W, Hao L, Ma J, Ma D, Ma Z. Liu F, et al. Among authors: ma d, ma j, ma z. PLoS One. 2015 May 11;10(5):e0126602. doi: 10.1371/journal.pone.0126602. eCollection 2015. PLoS One. 2015. PMID: 25961296 Free PMC article.

4

Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in Zebrafish.

Liu F, Xia W, Hu J, Wang Y, Yang F, Sun S, Zhang J, Jiang N, Wang H, Tian W, Wang X, Ma D. Liu F, et al. Among authors: ma d. PLoS One. 2015 Sep 16;10(9):e0136832. doi: 10.1371/journal.pone.0136832. eCollection 2015. PLoS One. 2015. PMID: 26375458 Free PMC article.

5

Down-regulation of msrb3 and destruction of normal auditory system development through hair cell apoptosis in zebrafish.

Shen X, Liu F, Wang Y, Wang H, Ma J, Xia W, Zhang J, Jiang N, Sun S, Wang X, Ma D. Shen X, et al. Among authors: ma d, ma j. Int J Dev Biol. 2015;59(4-6):195-203. doi: 10.1387/ijdb.140200md. Int J Dev Biol. 2015. PMID: 26505252 Free article.

6

Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss.

Hu J, Liu F, Xia W, Hao L, Lan J, Zhu Z, Ye J, Ma D, Ma Z. Hu J, et al. Among authors: ma d, ma z. J Transl Med. 2016 Jan 28;14:29. doi: 10.1186/s12967-016-0780-5. J Transl Med. 2016. PMID: 26822030 Free PMC article.

7

Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness.

Xia W, Liu F, Ma D. Xia W, et al. Among authors: ma d. Front Med. 2016 Jun;10(2):137-42. doi: 10.1007/s11684-016-0449-8. Epub 2016 May 3. Front Med. 2016. PMID: 27142990 Review.

8

Conditional knockout of TFPI-1 in VSMCs of mice accelerates atherosclerosis by enhancing AMOT/YAP pathway.

Xiao J, Jin K, Wang J, Ma J, Zhang J, Jiang N, Wang H, Luo X, Fei J, Wang Z, Yang X, Ma D. Xiao J, et al. Among authors: ma d, ma j. Int J Cardiol. 2017 Feb 1;228:605-614. doi: 10.1016/j.ijcard.2016.11.195. Epub 2016 Nov 12. Int J Cardiol. 2017. PMID: 27875740

9

SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss.

Ma Z, Xia W, Liu F, Ma J, Sun S, Zhang J, Jiang N, Wang X, Hu J, Ma D. Ma Z, et al. Among authors: ma d, ma j. Hum Mol Genet. 2017 Jan 15;26(2):383-394. doi: 10.1093/hmg/ddw394. Hum Mol Genet. 2017. PMID: 28013291

10

Changes in lncRNAs and related genes in β-thalassemia minor and β-thalassemia major.

Ma J, Liu F, Du X, Ma D, Xiong L. Ma J, et al. Among authors: ma d. Front Med. 2017 Mar;11(1):74-86. doi: 10.1007/s11684-017-0503-1. Epub 2017 Mar 2. Front Med. 2017. PMID: 28251479

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