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kaiyong liang
(4 results)?
GPR37 expression as a prognostic marker in gliomas: a bioinformatics-based analysis.
Aging (Albany NY). 2023 Oct 13;15(19):10146-10167. doi: 10.18632/aging.205063. Epub 2023 Oct 13.
Aging (Albany NY). 2023.
PMID: 37837549
Free PMC article.
Mendelian Randomization Analyses Accounting for Causal Effect of COVID-19 on Brain Imaging-Derived Phenotypes.
Lu J, Huang R, Peng Y, Zhang J, Liang K, Wang Y, Feng Y, Wang Z.
Lu J, et al. Among authors: liang k.
J Alzheimers Dis. 2023;96(3):1059-1070. doi: 10.3233/JAD-230626.
J Alzheimers Dis. 2023.
PMID: 37955088
Item in Clipboard
Comprehensive analysis of the prognostic and immunological signature of eight Tripartitemotif (TRIM) family molecules in human gliomas.
Lu J, Liang K, Zou R, Peng Y, Wang H, Huang R, Zeng Z, Feng Z, Fan Y, Zhang S, Ji Y, Pang X, Wang Y, Zhang H, Wang Z.
Lu J, et al. Among authors: liang k.
Aging (Albany NY). 2023 Jun 24;15(12):5798-5825. doi: 10.18632/aging.204841. Epub 2023 Jun 24.
Aging (Albany NY). 2023.
PMID: 37367937
Free PMC article.
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Elevated LILRB1 expression predicts poor prognosis and is associated with tumor immune infiltration in patients with glioma.
Zou R, Zhong X, Liang K, Zhi C, Chen D, Xu Z, Zhang J, Liao D, Lai M, Weng Y, Peng H, Pang X, Ji Y, Ke Y, Zhang H, Wang Z, Wang Y.
Zou R, et al. Among authors: liang k.
BMC Cancer. 2023 May 4;23(1):403. doi: 10.1186/s12885-023-10906-2.
BMC Cancer. 2023.
PMID: 37142967
Free PMC article.
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Identification of one novel pathogenic ITGB3 mutation and two known mutations in two Chinese pedigrees with hereditary Glanzmann thrombasthenia.
Lu Z, Nikuze L, Zhong Z, Li F, Zhang F, Liang K, Wei M, Wei H.
Lu Z, et al. Among authors: liang k.
Platelets. 2020;31(3):355-359. doi: 10.1080/09537104.2019.1615614. Epub 2019 May 14.
Platelets. 2020.
PMID: 31088191
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Identification of two novel mutations in three children with congenital factor VII deficiency.
Liang K, Nikuze L, Zhang F, Lu Z, Wei M, Wei H.
Liang K, et al.
Blood Coagul Fibrinolysis. 2021 Jul 1;32(5):340-343. doi: 10.1097/MBC.0000000000001022.
Blood Coagul Fibrinolysis. 2021.
PMID: 33587484
Free PMC article.
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Identification of novel pathogenic F13A1 mutation and novel NBEAL2 gene missense mutation in a pedigree with hereditary congenital factor XIII deficiency.
Jia S, He Y, Lu M, Liao N, Lei Y, Lauriane N, Liang K, Wei H.
Jia S, et al. Among authors: liang k.
Gene. 2019 Jun 20;702:143-147. doi: 10.1016/j.gene.2019.03.067. Epub 2019 Mar 29.
Gene. 2019.
PMID: 30935919
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