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For: Aldaz CM, Hussain T. WWOX Loss of Function in Neurodevelopmental and Neurodegenerative Disorders. Int J Mol Sci 2020;21:E8922. [PMID: 33255508 DOI: 10.3390/ijms21238922] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 6.0] [Reference Citation Analysis]
Number Citing Articles
1 Lin Y, Shih Y, Yap YV, Chen Y, Kuo H, Liu T, Hsu L, Kuo Y, Chang N. Zfra Inhibits the TRAPPC6AΔ-Initiated Pathway of Neurodegeneration. IJMS 2022;23:14510. [DOI: 10.3390/ijms232314510] [Reference Citation Analysis]
2 Zhao C, Jia X, Wang Y, Luo Z, Fan J, Shi X, Yang Y. Overlapping genetic susceptibility of seven autoimmune diseases:SPU tests based on genome-wide association summary statistics. Gene 2022. [DOI: 10.1016/j.gene.2022.147036] [Reference Citation Analysis]
3 Baryła I, Kośla K, Bednarek AK. WWOX and metabolic regulation in normal and pathological conditions. J Mol Med (Berl) 2022. [PMID: 36271927 DOI: 10.1007/s00109-022-02265-5] [Reference Citation Analysis]
4 Chaudhary S, Chaudhary S, Rawat S, Kulkarni A, Bilgrami AL, Perveen A, Alghamdi BS, Zughaibi TA, Ashraf GM, Alam MZ, Hussain T. Galectins—Potential Therapeutic Targets for Neurodegenerative Disorders. IJMS 2022;23:11012. [DOI: 10.3390/ijms231911012] [Reference Citation Analysis]
5 Liu T, Nagarajan G, Chiang M, Huang S, Lin T, Chen Y, Sze C, Chang N. WWOX Controls Cell Survival, Immune Response and Disease Progression by pY33 to pS14 Transition to Alternate Signaling Partners. Cells 2022;11:2137. [DOI: 10.3390/cells11142137] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Goodspeed K, Bailey RM, Prasad S, Sadhu C, Cardenas JA, Holmay M, Bilder DA, Minassian BA. Gene Therapy: Novel Approaches to Targeting Monogenic Epilepsies. Front Neurol 2022;13:805007. [DOI: 10.3389/fneur.2022.805007] [Reference Citation Analysis]
7 Sukkar G, Alzahrani RM, Altirkistani BA, Al lohaibi RS. Novel Mutation With Literature Review WW Domain-Containing Oxidoreductase (WWOX) Gene. Cureus 2022. [DOI: 10.7759/cureus.25003] [Reference Citation Analysis]
8 Dong W, Wong KH, Liu Y, Levy-Sakin M, Hung WC, Li M, Li B, Jin SC, Choi J, Lopez-Giraldez F, Vaka D, Poon A, Chu C, Lao R, Balamir M, Movsesyan I, Malloy MJ, Zhao H, Kwok PY, Kane JP, Lifton RP, Pullinger CR. Whole Exome Sequencing Reveals Damaging Gene Variants Associated with Hypoalphalipoproteinemia. J Lipid Res 2022;:100209. [PMID: 35460704 DOI: 10.1016/j.jlr.2022.100209] [Reference Citation Analysis]
9 Li JP, Chang JT, Ju PC, Hsieh MH, Chao YH, Tsao TC, Hsieh MJ, Yang SF. Effect of WW Domain-Containing Oxidoreductase Gene Polymorphism on Clinicopathological Characteristics of Patients with EGFR Mutant Lung Adenocarcinoma in Taiwan. Int J Environ Res Public Health 2021;18:13136. [PMID: 34948746 DOI: 10.3390/ijerph182413136] [Reference Citation Analysis]
10 Repudi S, Kustanovich I, Abu-Swai S, Stern S, Aqeilan RI. Neonatal neuronal WWOX gene therapy rescues Wwox null phenotypes. EMBO Mol Med 2021;13:e14599. [PMID: 34747138 DOI: 10.15252/emmm.202114599] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Steinberg DJ, Aqeilan RI. WWOX-Related Neurodevelopmental Disorders: Models and Future Perspectives. Cells 2021;10:3082. [PMID: 34831305 DOI: 10.3390/cells10113082] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
12 Hsu CY, Lee KT, Sun TY, Sze CI, Huang SS, Hsu LJ, Chang NS. WWOX and Its Binding Proteins in Neurodegeneration. Cells 2021;10:1781. [PMID: 34359949 DOI: 10.3390/cells10071781] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
13 Taouis K, Driouch K, Lidereau R, Lallemand F. Molecular Functions of WWOX Potentially Involved in Cancer Development. Cells 2021;10:1051. [PMID: 33946771 DOI: 10.3390/cells10051051] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
14 Banne E, Abudiab B, Abu-Swai S, Repudi SR, Steinberg DJ, Shatleh D, Alshammery S, Lisowski L, Gold W, Carlen PL, Aqeilan RI. Neurological Disorders Associated with WWOX Germline Mutations-A Comprehensive Overview. Cells 2021;10:824. [PMID: 33916893 DOI: 10.3390/cells10040824] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 7.0] [Reference Citation Analysis]