Liu D - Search Results

1

Perrault syndrome: Clinical report and retrospective analysis.

Pan Z, Xu H, Tian Y, Liu D, Liu H, Li R, Dou Q, Zuo B, Zhai R, Tang W, Lu W. Pan Z, et al. Among authors: liu h, liu d. Mol Genet Genomic Med. 2020 Oct;8(10):e1445. doi: 10.1002/mgg3.1445. Epub 2020 Aug 7. Mol Genet Genomic Med. 2020. PMID: 32767731 Free PMC article.

2

Early truncation of the N-terminal variable region of EYA4 gene causes dominant hearing loss without cardiac phenotype.

Mi Y, Liu D, Zeng B, Tian Y, Zhang H, Chen B, Zhang J, Xue H, Tang W, Zhao Y, Xu H. Mi Y, et al. Among authors: liu d. Mol Genet Genomic Med. 2021 Jan;9(1):e1569. doi: 10.1002/mgg3.1569. Epub 2020 Dec 10. Mol Genet Genomic Med. 2021. PMID: 33301229 Free PMC article.

3

Treacher Collins syndrome: Clinical report and retrospective analysis of Chinese patients.

Pan Z, Xu H, Chen B, Tian Y, Zhang L, Zhang S, Liu D, Liu H, Li R, Hu X, Guan J, Tang W, Lu W. Pan Z, et al. Among authors: liu h, liu d. Mol Genet Genomic Med. 2021 Feb;9(2):e1573. doi: 10.1002/mgg3.1573. Epub 2020 Dec 17. Mol Genet Genomic Med. 2021. PMID: 33332773 Free PMC article.

4

Auditory Neuropathy Spectrum Disorder (ANSD)-Clinical Characteristics and Pathogenic Variant Analysis of Three Nonsyndromic Deafness Families.

Zhai R, Feng H, Li Q, Lu W, Liu D, Tian Y, Liu H, Li R, Zuo B, Tang W, Xu H, Chen B. Zhai R, et al. Among authors: liu h, liu d. Biomed Res Int. 2020 Dec 21;2020:8843539. doi: 10.1155/2020/8843539. eCollection 2020. Biomed Res Int. 2020. PMID: 33426078 Free PMC article.

5

Dynamics of binding ability prediction between spike protein and human ACE2 reveals the adaptive strategy of SARS-CoV-2 in humans.

Xue X, Shi J, Xu H, Qin Y, Yang Z, Feng S, Liu D, Jian L, Hua L, Wang Y, Zhang Q, Huang X, Zhang X, Li X, Chen C, Guo J, Tang W, Liu J. Xue X, et al. Among authors: liu j, liu d. Sci Rep. 2021 Feb 4;11(1):3187. doi: 10.1038/s41598-021-82938-2. Sci Rep. 2021. PMID: 33542420 Free PMC article.

6

High Genetic Heterogeneity in Chinese Patients With Waardenburg Syndrome Revealed by Next-Generation Sequencing.

Zhang S, Xu H, Tian Y, Liu D, Hou X, Zeng B, Chen B, Liu H, Li R, Li X, Zuo B, Tang R, Tang W. Zhang S, et al. Among authors: liu h, liu d. Front Genet. 2021 Jun 4;12:643546. doi: 10.3389/fgene.2021.643546. eCollection 2021. Front Genet. 2021. PMID: 34149797 Free PMC article.

7

Increased diagnosis of enlarged vestibular aqueduct by multiplex PCR enrichment and next-generation sequencing of the SLC26A4 gene.

Tian Y, Xu H, Liu D, Zhang J, Yang Z, Zhang S, Liu H, Li R, Tian Y, Zeng B, Li T, Lin Q, Wang H, Li X, Lu W, Shi Y, Zhang Y, Zhang H, Jiang C, Xu Y, Chen B, Liu J, Tang W. Tian Y, et al. Among authors: liu j, liu h, liu d. Mol Genet Genomic Med. 2021 Aug;9(8):e1734. doi: 10.1002/mgg3.1734. Epub 2021 Jun 25. Mol Genet Genomic Med. 2021. PMID: 34170635 Free PMC article.

8

An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease.

Wang Z, Xu H, Xiang T, Liu D, Xu F, Zhao L, Feng Y, Xu L, Liu J, Fang Y, Liu H, Li R, Hu X, Guan J, Liu L, Feng G, Shen Q, Xu H, Frishman D, Tang W, Guo J, Rao J, Shang W. Wang Z, et al. Among authors: liu j, liu h, liu l, liu d. NPJ Genom Med. 2021 Jul 2;6(1):57. doi: 10.1038/s41525-021-00219-3. NPJ Genom Med. 2021. PMID: 34215756 Free PMC article.

9

Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype.

Li J, Xu H, Sun J, Tian Y, Liu D, Qin Y, Liu H, Li R, Neng L, Deng X, Xue B, Yu C, Tang W. Li J, et al. Among authors: liu h, liu d. Biomed Res Int. 2021 Mar 4;2021:6624744. doi: 10.1155/2021/6624744. eCollection 2021. Biomed Res Int. 2021. PMID: 34258273 Free PMC article.

10

Donor BMSC-derived small extracellular vesicles relieve acute rejection post-renal allograft through transmitting Loc108349490 to dendritic cells.

Wang ZG, Xu HE, Cheng FM, Zhang J, Feng YH, Liu DH, Shang WJ, Feng GW. Wang ZG, et al. Aging Cell. 2021 Oct;20(10):e13461. doi: 10.1111/acel.13461. Epub 2021 Sep 9. Aging Cell. 2021. PMID: 34499402 Free PMC article.

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