Ding'an Zhou

5PUBLICATIONS
1CO-AUTHORS
Medical molecular engineering of nucleic acids and proteinsPhotochemistryEpigenetics (incl. genome methylation and epigenomics)Gene and molecular therapy
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Publications (5)

|May 21, 2025
The p.W651fsX666 mutation on COL10A1 results in impaired trimerization of normal collagen X to induce Schmid type Metaphyseal chondrodysplasia.

Jingye Yang, Jing Zhang, Qingxiang Lu

|Feb 27, 2024
A novel genomic rearrangement on chr19q13.42 leads to PRPF31-associated retinitis pigmentosa.

Qingxiang Lu, Jingye Yang, Yu Xiong

|Jun 24, 2023
Retyping and molecular pathology diagnosis of dyschromatosis universalis hereditaria.

Ding'an Zhou, Pingping Yang, Hongyu Chen

|Feb 15, 2023
The PER3rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria.

Hongyu Chen, Pingping Yang, Dan Yang

|Apr 07, 2017
p53 regulates ERK1/2/CREB cascade via a novel SASH1/MAP2K2 crosstalk to induce hyperpigmentation.

Ding'an Zhou, Zhongshu Kuang, Xing Zeng

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Frequent Collaborators

1 joint publications

Jingye Yang