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Showing 25 to 36 of 820 entries
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Identification of PSMD7 as a prognostic factor correlated with immune infiltration in head and neck squamous cell carcinoma.

Bioscience reports

Zhang S, Yu S, Wang J, Cheng Z.
PMID: 33687056
Biosci Rep. 2021 Mar 26;41(3). doi: 10.1042/BSR20203829.

BACKGROUND: Recurrent locally advanced or metastatic head and neck squamous cell carcinoma (HNSCC) is associated with dismal prognosis because of its highly invasive behavior and resistance to conventional intensive chemotherapy. The identification of effective markers for early diagnosis and...

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Zhang S, Yu S, Wang J, et al. Identification of PSMD7 as a prognostic factor correlated with immune infiltration in head and neck squamous cell carcinoma. Biosci Rep. 2021;41(3)doi: 10.1042/BSR20203829.
Zhang, S., Yu, S., Wang, J., & Cheng, Z. (2021). Identification of PSMD7 as a prognostic factor correlated with immune infiltration in head and neck squamous cell carcinoma. Bioscience reports, 41(3), . https://doi.org/10.1042/BSR20203829
Zhang, Si, et al. "Identification of PSMD7 as a prognostic factor correlated with immune infiltration in head and neck squamous cell carcinoma." Bioscience reports vol. 41,3 (2021). doi: https://doi.org/10.1042/BSR20203829
Zhang S, Yu S, Wang J, Cheng Z. Identification of PSMD7 as a prognostic factor correlated with immune infiltration in head and neck squamous cell carcinoma. Biosci Rep. 2021 Mar 26;41(3). doi: 10.1042/BSR20203829. PMID: 33687056; PMCID: PMC7990087.
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High glucose represses the proliferation of tendon fibroblasts by inhibiting autophagy activation in tendon injury.

Bioscience reports

Song FC, Yuan JQ, Zhu MD, Li Q, Liu SH, Zhang L, Zhao C.
PMID: 34398191
Biosci Rep. 2021 Aug 16; doi: 10.1042/BSR20210640. Epub 2021 Aug 16.

Diabetic foot ulcer (DFU) is a kind of common and disabling complications of Diabetes Mellitus (DM). Emerging studies have demonstrated that tendon fibroblasts play a crucial role in remodeling phase of wound healing. However, little is known about the...

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Song FC, Yuan JQ, Zhu MD, et al. High glucose represses the proliferation of tendon fibroblasts by inhibiting autophagy activation in tendon injury. Biosci Rep. 2021;doi: 10.1042/BSR20210640.
Song, F. C., Yuan, J. Q., Zhu, M. D., Li, Q., Liu, S. H., Zhang, L., & Zhao, C. (2021). High glucose represses the proliferation of tendon fibroblasts by inhibiting autophagy activation in tendon injury. Bioscience reports, . https://doi.org/10.1042/BSR20210640
Song, Fu-Chen, et al. "High glucose represses the proliferation of tendon fibroblasts by inhibiting autophagy activation in tendon injury." Bioscience reports vol. (2021). doi: https://doi.org/10.1042/BSR20210640
Song FC, Yuan JQ, Zhu MD, Li Q, Liu SH, Zhang L, Zhao C. High glucose represses the proliferation of tendon fibroblasts by inhibiting autophagy activation in tendon injury. Biosci Rep. 2021 Aug 16; doi: 10.1042/BSR20210640. Epub 2021 Aug 16. PMID: 34398191.
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Retraction: MicroRNA-506 inhibits rheumatoid arthritis fibroblast-like synoviocytes proliferation and induces apoptosis by targeting TLR4.

Bioscience reports

[No authors listed]
PMID: 34319391
Biosci Rep. 2021 Jul 30;41(7). doi: 10.1042/BSR-2018-2500_RET.

No abstract available.

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Retraction: MicroRNA-506 inhibits rheumatoid arthritis fibroblast-like synoviocytes proliferation and induces apoptosis by targeting TLR4. Biosci Rep. 2021;41(7)doi: 10.1042/BSR-2018-2500_RET.
(2021). Retraction: MicroRNA-506 inhibits rheumatoid arthritis fibroblast-like synoviocytes proliferation and induces apoptosis by targeting TLR4. Bioscience reports, 41(7), . https://doi.org/10.1042/BSR-2018-2500_RET
"Retraction: MicroRNA-506 inhibits rheumatoid arthritis fibroblast-like synoviocytes proliferation and induces apoptosis by targeting TLR4." Bioscience reports vol. 41,7 (2021). doi: https://doi.org/10.1042/BSR-2018-2500_RET
Retraction: MicroRNA-506 inhibits rheumatoid arthritis fibroblast-like synoviocytes proliferation and induces apoptosis by targeting TLR4. Biosci Rep. 2021 Jul 30;41(7). doi: 10.1042/BSR-2018-2500_RET. PMID: 34319391.
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KMT2D deficiency disturbs the proliferation and cell cycle activity of dental epithelial cell line (LS8) partially via Wnt signaling.

Bioscience reports

Pang L, Tian H, Gao X, Wang W, Wang X, Zhang Z.
PMID: 34724040
Biosci Rep. 2021 Nov 26;41(11). doi: 10.1042/BSR20211148.

Lysine methyltransferase 2D (KMT2D), as one of the key histone methyltransferases responsible for histone 3 lysine 4 methylation (H3K4me), has been proved to be the main pathogenic gene of Kabuki syndrome disease. Kabuki patients with KMT2D mutation frequently present...

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Pang L, Tian H, Gao X, et al. KMT2D deficiency disturbs the proliferation and cell cycle activity of dental epithelial cell line (LS8) partially via Wnt signaling. Biosci Rep. 2021;41(11)doi: 10.1042/BSR20211148.
Pang, L., Tian, H., Gao, X., Wang, W., Wang, X., & Zhang, Z. (2021). KMT2D deficiency disturbs the proliferation and cell cycle activity of dental epithelial cell line (LS8) partially via Wnt signaling. Bioscience reports, 41(11), . https://doi.org/10.1042/BSR20211148
Pang, Liping, et al. "KMT2D deficiency disturbs the proliferation and cell cycle activity of dental epithelial cell line (LS8) partially via Wnt signaling." Bioscience reports vol. 41,11 (2021). doi: https://doi.org/10.1042/BSR20211148
Pang L, Tian H, Gao X, Wang W, Wang X, Zhang Z. KMT2D deficiency disturbs the proliferation and cell cycle activity of dental epithelial cell line (LS8) partially via Wnt signaling. Biosci Rep. 2021 Nov 26;41(11). doi: 10.1042/BSR20211148. PMID: 34724040; PMCID: PMC8607332.
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Integrated bioinformatics analysis revealed the regulation of angiogenesis by tumor cells in hepatocellular carcinoma.

Bioscience reports

Huo M, Yu K, Zheng Y, Liu L, Zhao H, Li X, Huang C, Zhang J.
PMID: 34151937
Biosci Rep. 2021 Jul 30;41(7). doi: 10.1042/BSR20210126.

Hepatocellular carcinoma (HCC) is one of the leading causes of cancer mortality, metastasis accounts for most of the cases. Angiogenesis plays an important role in cancer metastasis, but how tumor cells affect the function of endothelial cells by dictating...

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Huo M, Yu K, Zheng Y, et al. Integrated bioinformatics analysis revealed the regulation of angiogenesis by tumor cells in hepatocellular carcinoma. Biosci Rep. 2021;41(7)doi: 10.1042/BSR20210126.
Huo, M., Yu, K., Zheng, Y., Liu, L., Zhao, H., Li, X., Huang, C., & Zhang, J. (2021). Integrated bioinformatics analysis revealed the regulation of angiogenesis by tumor cells in hepatocellular carcinoma. Bioscience reports, 41(7), . https://doi.org/10.1042/BSR20210126
Huo, Meisi, et al. "Integrated bioinformatics analysis revealed the regulation of angiogenesis by tumor cells in hepatocellular carcinoma." Bioscience reports vol. 41,7 (2021). doi: https://doi.org/10.1042/BSR20210126
Huo M, Yu K, Zheng Y, Liu L, Zhao H, Li X, Huang C, Zhang J. Integrated bioinformatics analysis revealed the regulation of angiogenesis by tumor cells in hepatocellular carcinoma. Biosci Rep. 2021 Jul 30;41(7). doi: 10.1042/BSR20210126. PMID: 34151937; PMCID: PMC8252189.
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Retraction: Long noncoding RNA TUG1 promotes proliferation and inhibits apoptosis in multiple myeloma by inhibiting miR-29b-3p.

Bioscience reports

[No authors listed]
PMID: 34151939
Biosci Rep. 2021 Jun 25;41(6). doi: 10.1042/BSR-2018-2489_RET.

No abstract available.

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Retraction: Long noncoding RNA TUG1 promotes proliferation and inhibits apoptosis in multiple myeloma by inhibiting miR-29b-3p. Biosci Rep. 2021;41(6)doi: 10.1042/BSR-2018-2489_RET.
(2021). Retraction: Long noncoding RNA TUG1 promotes proliferation and inhibits apoptosis in multiple myeloma by inhibiting miR-29b-3p. Bioscience reports, 41(6), . https://doi.org/10.1042/BSR-2018-2489_RET
"Retraction: Long noncoding RNA TUG1 promotes proliferation and inhibits apoptosis in multiple myeloma by inhibiting miR-29b-3p." Bioscience reports vol. 41,6 (2021). doi: https://doi.org/10.1042/BSR-2018-2489_RET
Retraction: Long noncoding RNA TUG1 promotes proliferation and inhibits apoptosis in multiple myeloma by inhibiting miR-29b-3p. Biosci Rep. 2021 Jun 25;41(6). doi: 10.1042/BSR-2018-2489_RET. PMID: 34151939.
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Serum HBV pregenomic RNA exhibited opposite associations with NKdim and NKbright cell immunity in treatment-naïve chronic hepatitis B patients.

Bioscience reports

Gu Y, Huang Z, Li X, Chen Y, Liao C, Bi Y, Huang Y.
PMID: 34151357
Biosci Rep. 2021 Jul 30;41(7). doi: 10.1042/BSR20210600.

Hepatitis B virus (HBV) pregenomic RNA (pgRNA) is a new biomarker that reflects HBV replication, but its relationship with natural killer (NK) cell immunity in chronic hepatitis B (CHB) is unknown. We assessed serum HBV pgRNA levels in 323...

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Gu Y, Huang Z, Li X, et al. Serum HBV pregenomic RNA exhibited opposite associations with NKdim and NKbright cell immunity in treatment-naïve chronic hepatitis B patients. Biosci Rep. 2021;41(7)doi: 10.1042/BSR20210600.
Gu, Y., Huang, Z., Li, X., Chen, Y., Liao, C., Bi, Y., & Huang, Y. (2021). Serum HBV pregenomic RNA exhibited opposite associations with NKdim and NKbright cell immunity in treatment-naïve chronic hepatitis B patients. Bioscience reports, 41(7), . https://doi.org/10.1042/BSR20210600
Gu, Yurong, et al. "Serum HBV pregenomic RNA exhibited opposite associations with NKdim and NKbright cell immunity in treatment-naïve chronic hepatitis B patients." Bioscience reports vol. 41,7 (2021). doi: https://doi.org/10.1042/BSR20210600
Gu Y, Huang Z, Li X, Chen Y, Liao C, Bi Y, Huang Y. Serum HBV pregenomic RNA exhibited opposite associations with NKdim and NKbright cell immunity in treatment-naïve chronic hepatitis B patients. Biosci Rep. 2021 Jul 30;41(7). doi: 10.1042/BSR20210600. PMID: 34151357; PMCID: PMC8255538.
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Evaluation of anticancer effects of Juniperus communis extract on hepatocellular carcinoma cells in vitro and in vivo.

Bioscience reports

Huang NC, Huang RL, Huang XF, Chang KF, Lee CJ, Hsiao CY, Lee SC, Tsai NM.
PMID: 34151367
Biosci Rep. 2021 Jul 30;41(7). doi: 10.1042/BSR20211143.

Hepatocellular carcinoma (HCC) is the most common type of primary liver cancer and accounts for the fourth leading cause of all cancer deaths. Scientific evidence has found that plant extracts seem to be a reliable choice due to their...

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Huang NC, Huang RL, Huang XF, et al. Evaluation of anticancer effects of Juniperus communis extract on hepatocellular carcinoma cells in vitro and in vivo. Biosci Rep. 2021;41(7)doi: 10.1042/BSR20211143.
Huang, N. C., Huang, R. L., Huang, X. F., Chang, K. F., Lee, C. J., Hsiao, C. Y., Lee, S. C., & Tsai, N. M. (2021). Evaluation of anticancer effects of Juniperus communis extract on hepatocellular carcinoma cells in vitro and in vivo. Bioscience reports, 41(7), . https://doi.org/10.1042/BSR20211143
Huang, Nan-Chieh, et al. "Evaluation of anticancer effects of Juniperus communis extract on hepatocellular carcinoma cells in vitro and in vivo." Bioscience reports vol. 41,7 (2021). doi: https://doi.org/10.1042/BSR20211143
Huang NC, Huang RL, Huang XF, Chang KF, Lee CJ, Hsiao CY, Lee SC, Tsai NM. Evaluation of anticancer effects of Juniperus communis extract on hepatocellular carcinoma cells in vitro and in vivo. Biosci Rep. 2021 Jul 30;41(7). doi: 10.1042/BSR20211143. PMID: 34151367; PMCID: PMC8276093.
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Construction of a five-gene prognostic model based on immune-related genes for the prediction of survival in pancreatic cancer.

Bioscience reports

Liu B, Fu T, He P, Du C, Xu K.
PMID: 34143198
Biosci Rep. 2021 Jul 30;41(7). doi: 10.1042/BSR20204301.

PURPOSE: To identify differentially expressed immune-related genes (DEIRGs) and construct a model with survival-related DEIRGs for evaluating the prognosis of patients with pancreatic cancer (PC).METHODS: Six microarray gene expression datasets of PC from the Gene Expression Omnibus (GEO) and...

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Liu B, Fu T, He P, et al. Construction of a five-gene prognostic model based on immune-related genes for the prediction of survival in pancreatic cancer. Biosci Rep. 2021;41(7)doi: 10.1042/BSR20204301.
Liu, B., Fu, T., He, P., Du, C., & Xu, K. (2021). Construction of a five-gene prognostic model based on immune-related genes for the prediction of survival in pancreatic cancer. Bioscience reports, 41(7), . https://doi.org/10.1042/BSR20204301
Liu, Bo, et al. "Construction of a five-gene prognostic model based on immune-related genes for the prediction of survival in pancreatic cancer." Bioscience reports vol. 41,7 (2021). doi: https://doi.org/10.1042/BSR20204301
Liu B, Fu T, He P, Du C, Xu K. Construction of a five-gene prognostic model based on immune-related genes for the prediction of survival in pancreatic cancer. Biosci Rep. 2021 Jul 30;41(7). doi: 10.1042/BSR20204301. PMID: 34143198; PMCID: PMC8252190.
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Conditioned medium of IGF1-induced synovial membrane mesenchymal stem cells increases chondrogenic and chondroprotective markers in chondrocyte inflammation.

Bioscience reports

Marlina M, Rahmadian R, Armenia A, Aviani JK, Sholihah IA, Kusuma HSW, Azizah AM, Elida N, Widowati W.
PMID: 34143208
Biosci Rep. 2021 Jul 30;41(7). doi: 10.1042/BSR20202038.

Recently, mesenchymal stem cells (MSCs) have been the most explored cells for cell therapy for osteoarthritis (OA) that can be obtained from various sources. Synovial membrane MSCs (SMMSCs) provide best potential for OA therapy, however they are not widely...

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Marlina M, Rahmadian R, Armenia A, et al. Conditioned medium of IGF1-induced synovial membrane mesenchymal stem cells increases chondrogenic and chondroprotective markers in chondrocyte inflammation. Biosci Rep. 2021;41(7)doi: 10.1042/BSR20202038.
Marlina, M., Rahmadian, R., Armenia, A., Aviani, J. K., Sholihah, I. A., Kusuma, H. S. W., Azizah, A. M., Elida, N., & Widowati, W. (2021). Conditioned medium of IGF1-induced synovial membrane mesenchymal stem cells increases chondrogenic and chondroprotective markers in chondrocyte inflammation. Bioscience reports, 41(7), . https://doi.org/10.1042/BSR20202038
Marlina, Marlina, et al. "Conditioned medium of IGF1-induced synovial membrane mesenchymal stem cells increases chondrogenic and chondroprotective markers in chondrocyte inflammation." Bioscience reports vol. 41,7 (2021). doi: https://doi.org/10.1042/BSR20202038
Marlina M, Rahmadian R, Armenia A, Aviani JK, Sholihah IA, Kusuma HSW, Azizah AM, Elida N, Widowati W. Conditioned medium of IGF1-induced synovial membrane mesenchymal stem cells increases chondrogenic and chondroprotective markers in chondrocyte inflammation. Biosci Rep. 2021 Jul 30;41(7). doi: 10.1042/BSR20202038. PMID: 34143208; PMCID: PMC8255536.
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Serum CYR61 as a potential biomarker for the diagnosis of esophagogastric junction tumor.

Bioscience reports

Chu LY, Zhou JY, Zhao YX, Ou YT, Yang T, Peng YH, Fang WK, Xu YW, Xie JJ.
PMID: 34085702
Biosci Rep. 2021 Jun 25;41(6). doi: 10.1042/BSR20204117.

BACKGROUND: Esophagogastric junction tumor (EGJ) is a rare but fatal disease with a rapid rising incidence worldwide in the late 20 years, and it lacks a convenient and safe method for diagnosis. The present study aimed to evaluate the...

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Chu LY, Zhou JY, Zhao YX, et al. Serum CYR61 as a potential biomarker for the diagnosis of esophagogastric junction tumor. Biosci Rep. 2021;41(6)doi: 10.1042/BSR20204117.
Chu, L. Y., Zhou, J. Y., Zhao, Y. X., Ou, Y. T., Yang, T., Peng, Y. H., Fang, W. K., Xu, Y. W., & Xie, J. J. (2021). Serum CYR61 as a potential biomarker for the diagnosis of esophagogastric junction tumor. Bioscience reports, 41(6), . https://doi.org/10.1042/BSR20204117
Chu, Ling-Yu, et al. "Serum CYR61 as a potential biomarker for the diagnosis of esophagogastric junction tumor." Bioscience reports vol. 41,6 (2021). doi: https://doi.org/10.1042/BSR20204117
Chu LY, Zhou JY, Zhao YX, Ou YT, Yang T, Peng YH, Fang WK, Xu YW, Xie JJ. Serum CYR61 as a potential biomarker for the diagnosis of esophagogastric junction tumor. Biosci Rep. 2021 Jun 25;41(6). doi: 10.1042/BSR20204117. PMID: 34085702; PMCID: PMC8217984.
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Prognostic value of miR-142 in solid tumors: a meta-analysis.

Bioscience reports

Liu R, Zheng S, Yu K, Yu Y, Yu C, Shi W, Ge Q, Ye Z, Shao Y.
PMID: 33600577
Biosci Rep. 2021 Feb 26;41(2). doi: 10.1042/BSR20204043.

Several studies on the prognostic value of microRNA 142 (miR-142) in solid tumors have reported conflicting results. Therefore, the aim of this meta-analysis was to evaluate the relationship between the miR-142 and prognosis in solid tumors. A comprehensive search...

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Liu R, Zheng S, Yu K, et al. Prognostic value of miR-142 in solid tumors: a meta-analysis. Biosci Rep. 2021;41(2)doi: 10.1042/BSR20204043.
Liu, R., Zheng, S., Yu, K., Yu, Y., Yu, C., Shi, W., Ge, Q., Ye, Z., & Shao, Y. (2021). Prognostic value of miR-142 in solid tumors: a meta-analysis. Bioscience reports, 41(2), . https://doi.org/10.1042/BSR20204043
Liu, Rongqiang, et al. "Prognostic value of miR-142 in solid tumors: a meta-analysis." Bioscience reports vol. 41,2 (2021). doi: https://doi.org/10.1042/BSR20204043
Liu R, Zheng S, Yu K, Yu Y, Yu C, Shi W, Ge Q, Ye Z, Shao Y. Prognostic value of miR-142 in solid tumors: a meta-analysis. Biosci Rep. 2021 Feb 26;41(2). doi: 10.1042/BSR20204043. PMID: 33600577; PMCID: PMC7921291.
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Showing 25 to 36 of 820 entries