Wu J - Search Results

1

Identification of Two Novel Variants of the DMD Gene in Chinese Families with Duchenne Muscular Dystrophy.

Wu J, Ren L, Huang X, Hu L, Zhang L, Xie D, Li Z, Han N, Huang S. Wu J, et al. Pharmgenomics Pers Med. 2023 Aug 17;16:759-766. doi: 10.2147/PGPM.S416294. eCollection 2023. Pharmgenomics Pers Med. 2023. PMID: 37609034 Free PMC article.

2

Whole-exome sequencing identified five novel de novo variants in patients with unexplained intellectual disability.

Zhang W, Hu L, Huang X, Xie D, Wu J, Fu X, Liang D, Huang S. Zhang W, et al. Among authors: wu j. J Clin Lab Anal. 2022 Sep;36(9):e24587. doi: 10.1002/jcla.24587. Epub 2022 Jul 15. J Clin Lab Anal. 2022. PMID: 35837997 Free PMC article.

3

Application of third-generation sequencing for genetic testing of thalassemia in Guizhou Province, Southwest China.

Wu J, Xie D, Wang L, Kuang Y, Luo S, Ren L, Li D, Mao A, Li J, Chen L, An B, Huang S. Wu J, et al. Hematology. 2022 Dec;27(1):1305-1311. doi: 10.1080/16078454.2022.2156720. Hematology. 2022. PMID: 36519257 Free article.

4

A novel heterozygous mutation of the NPHS1 gene in a Chinese child with congenital nephrotic syndrome: A case report.

Xie D, Wu J, Zhang W, Jin T, Wu P, An B, Huang S. Xie D, et al. Among authors: wu p, wu j. Medicine (Baltimore). 2023 Feb 17;102(7):e32970. doi: 10.1097/MD.0000000000032970. Medicine (Baltimore). 2023. PMID: 36800604 Free PMC article.

5

A Rare Case of Abnormal Hemoglobin Variant Hb Mizuho: [HBB: c.206T > C β 68(E12) Leu-Pro]: A First Report in the Chinese Population.

Chen YP, Wu P, Wang H, Wu JF, Xie D, Wang L, An B, Huang S. Chen YP, et al. Hemoglobin. 2023 May;47(3):130-134. doi: 10.1080/03630269.2023.2231851. Epub 2023 Jul 28. Hemoglobin. 2023. PMID: 37501630

6

Long Non-Coding RNA H19 Leads to Upregulation of γ-Globin Gene Expression during Erythroid Differentiation.

Xie D, Han Y, Zhang W, Wu J, An B, Huang S, Sun F. Xie D, et al. Among authors: wu j. Hemoglobin. 2024 Jan;48(1):4-14. doi: 10.1080/03630269.2023.2284950. Epub 2024 Feb 29. Hemoglobin. 2024. PMID: 38419555 Free article.

7

Identification of Novel Hb Guiyang [HBA2: c.151C > A α2 50 (CE8) His- Asn] and Phenotype- Genotype Correlation of Abnormal Hemoglobins in Guizhou, Southwest China.

Chen YP, Wang H, Wang L, Xie D, Guo M, Wu JF, An BQ, Huang SW. Chen YP, et al. J Blood Med. 2024 Jun 14;15:265-273. doi: 10.2147/JBM.S458057. eCollection 2024. J Blood Med. 2024. PMID: 38895162 Free PMC article.

8

A novel variant c.902C>A (p. A301D) in KCNQ4 associated with non-syndromic deafness 2A in a Chinese family.

Ren L, Wu J, Kuang Y, Chen K, Jiang M, Zhuo Z, Cao Z, Huang S. Ren L, et al. Among authors: wu j. Mol Genet Genomic Med. 2024 Jul;12(7):e2446. doi: 10.1002/mgg3.2446. Mol Genet Genomic Med. 2024. PMID: 38980994 Free PMC article.

9

Psychometric Testing of the Protocol for Responding to and Assessing Patient Assets, Risks, and Experiences (PRAPARE) in Patients With Heart Failure and Coronary Heart Disease.

Thapa A, Rayens MK, Chung ML, Biddle MJ, Wu JR, Lin CY, Kang J, Moser DK. Thapa A, et al. Among authors: wu jr. Res Nurs Health. 2025 Jan 7. doi: 10.1002/nur.22440. Online ahead of print. Res Nurs Health. 2025. PMID: 39764771

10

Spontaneous Catalytic Reaction of a Surfactant in the Interfacial Microenvironment of Colloidal Gold Nanoparticles.

Pan SQ, Luo P, Huang Q, Xue J, Tian XD, Xu B, Wu J, Chen J, Xie J, Yang N, Zhang XG, Tian ZQ, Liu GK. Pan SQ, et al. Among authors: wu j. J Am Chem Soc. 2025 Jan 7. doi: 10.1021/jacs.4c16796. Online ahead of print. J Am Chem Soc. 2025. PMID: 39764761

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