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Ruijuan Hao

Researcher at Guangdong Ocean University

Publications -  28
Citations -  575

Ruijuan Hao is an academic researcher from Guangdong Ocean University. The author has contributed to research in topics: Transplantation & Environmental pollution. The author has an hindex of 11, co-authored 28 publications receiving 369 citations.

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The pearl oyster Pinctada fucata martensii genome and multi-omic analyses provide insights into biomineralization.

TL;DR: The highly polymorphic genome of the pearl oyster is sequenced and a large set of novel proteins participating in matrix-framework formation are identified, including components similar to that found in vertebrate bones such as collagen-related VWA-containing proteins, chondroitin sulfotransferases, and regulatory elements.
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Integrated application of transcriptomics and metabolomics provides insights into unsynchronized growth in pearl oyster Pinctada fucata martensii.

TL;DR: Integrated transcriptome and metabolome analyses showed that fast-growing individuals exhibited higher biomineralization activity than the slow-growing group, which consumed more energy than the fast- growing group in response to environmental stress.
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Effect of vitamin D3 on immunity and antioxidant capacity of pearl oyster Pinctada fucata martensii after transplantation: Insights from LC-MS-based metabolomics analysis.

TL;DR: Investigation of the effect of dietary vitamin D3 levels on immunity and antioxidant capacity of pearl oyster Pinctada fucata martensii during postoperative care suggested that pearl oysters in EG5 regulated the pentose phosphate pathway, glutathione metabolism, sphingolipid metabolism, and arachidonic acid metabolism in response to stress generated from excessive VD3.
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Response to different dietary carbohydrate and protein levels of pearl oysters (Pinctada fucata martensii) as revealed by GC-TOF/MS-based metabolomics.

TL;DR: Integrated key metabolic pathway analysis showed that C45P25 regulated starch and sucrose metabolism, alanine, aspartate and glutamate metabolism and glycine, serine and threonine metabolism to meet the energy demand and increase the glucogenic amino acid, thereby promoting protein synthesis and reducing fatty acid β-oxidation in comparison with C30P40.