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Refuting the evidence for an earlier birth of the Taklimakan Desert.

Proceedings of the National Academy of Sciences of the United States of America

Sun J, Alloway B, Fang X, Windley BF.
PMID: 26430245
Proc Natl Acad Sci U S A. 2015 Oct 13;112(41):E5556-7. doi: 10.1073/pnas.1517525112. Epub 2015 Oct 01.

No abstract available.

Cite
Sun J, Alloway B, Fang X, et al. Refuting the evidence for an earlier birth of the Taklimakan Desert. Proc Natl Acad Sci U S A. 2015;112(41):E5556-7doi: 10.1073/pnas.1517525112.
Sun, J., Alloway, B., Fang, X., & Windley, B. F. (2015). Refuting the evidence for an earlier birth of the Taklimakan Desert. Proceedings of the National Academy of Sciences of the United States of America, 112(41), E5556-7. https://doi.org/10.1073/pnas.1517525112
Sun, Jimin, et al. "Refuting the evidence for an earlier birth of the Taklimakan Desert." Proceedings of the National Academy of Sciences of the United States of America vol. 112,41 (2015): E5556-7. doi: https://doi.org/10.1073/pnas.1517525112
Sun J, Alloway B, Fang X, Windley BF. Refuting the evidence for an earlier birth of the Taklimakan Desert. Proc Natl Acad Sci U S A. 2015 Oct 13;112(41):E5556-7. doi: 10.1073/pnas.1517525112. Epub 2015 Oct 01. PMID: 26430245; PMCID: PMC4611650.
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Facile preparation and dehydrogenation of unsolvated KB.

Chemical communications (Cambridge, England)

Zheng X, Yang Y, Zhao F, Fang F, Guo Y.
PMID: 28951917
Chem Commun (Camb). 2017 Oct 05;53(80):11083-11086. doi: 10.1039/c7cc06414d.

An efficient synthesis of unsolvated KB

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Zheng X, Yang Y, Zhao F, et al. Facile preparation and dehydrogenation of unsolvated KB. Chem Commun (Camb). 2017;53(80):11083-11086doi: 10.1039/c7cc06414d.
Zheng, X., Yang, Y., Zhao, F., Fang, F., & Guo, Y. (2017). Facile preparation and dehydrogenation of unsolvated KB. Chemical communications (Cambridge, England), 53(80), 11083-11086. https://doi.org/10.1039/c7cc06414d
Zheng, Xiongfei, et al. "Facile preparation and dehydrogenation of unsolvated KB." Chemical communications (Cambridge, England) vol. 53,80 (2017): 11083-11086. doi: https://doi.org/10.1039/c7cc06414d
Zheng X, Yang Y, Zhao F, Fang F, Guo Y. Facile preparation and dehydrogenation of unsolvated KB. Chem Commun (Camb). 2017 Oct 05;53(80):11083-11086. doi: 10.1039/c7cc06414d. PMID: 28951917.
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Pressure induced superconductivity in the antiferromagnetic Dirac material BaMnBi.

Scientific reports

Chen H, Li L, Zhu Q, Yang J, Chen B, Mao Q, Du J, Wang H, Fang M.
PMID: 28487572
Sci Rep. 2017 May 09;7(1):1634. doi: 10.1038/s41598-017-01967-y.

The so-called Dirac materials such as graphene and topological insulators are a new class of matter different from conventional metals and (doped) semiconductors. Superconductivity induced by doing or applying pressure in these systems may be unconventional, or host mysterious...

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Chen H, Li L, Zhu Q, et al. Pressure induced superconductivity in the antiferromagnetic Dirac material BaMnBi. Sci Rep. 2017;7(1):1634doi: 10.1038/s41598-017-01967-y.
Chen, H., Li, L., Zhu, Q., Yang, J., Chen, B., Mao, Q., Du, J., Wang, H., & Fang, M. (2017). Pressure induced superconductivity in the antiferromagnetic Dirac material BaMnBi. Scientific reports, 7(1), 1634. https://doi.org/10.1038/s41598-017-01967-y
Chen, Huimin, et al. "Pressure induced superconductivity in the antiferromagnetic Dirac material BaMnBi." Scientific reports vol. 7,1 (2017): 1634. doi: https://doi.org/10.1038/s41598-017-01967-y
Chen H, Li L, Zhu Q, Yang J, Chen B, Mao Q, Du J, Wang H, Fang M. Pressure induced superconductivity in the antiferromagnetic Dirac material BaMnBi. Sci Rep. 2017 May 09;7(1):1634. doi: 10.1038/s41598-017-01967-y. PMID: 28487572; PMCID: PMC5431619.
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Role of cellular cytoskeleton in epithelial-mesenchymal transition process during cancer progression.

Biomedical reports

Sun BO, Fang Y, Li Z, Chen Z, Xiang J.
PMID: 26405532
Biomed Rep. 2015 Sep;3(5):603-610. doi: 10.3892/br.2015.494. Epub 2015 Jul 27.

Currently, cancer metastases remain a major clinical problem that highlights the importance of recognition of the metastatic process in cancer diagnosis and treatment. A critical process associated with the metastasis process is the transformation of epithelial cells toward the...

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Sun BO, Fang Y, Li Z, et al. Role of cellular cytoskeleton in epithelial-mesenchymal transition process during cancer progression. Biomed Rep. 2015;3(5):603-610doi: 10.3892/br.2015.494.
Sun, B. O., Fang, Y., Li, Z., Chen, Z., & Xiang, J. (2015). Role of cellular cytoskeleton in epithelial-mesenchymal transition process during cancer progression. Biomedical reports, 3(5), 603-610. https://doi.org/10.3892/br.2015.494
Sun, B O, et al. "Role of cellular cytoskeleton in epithelial-mesenchymal transition process during cancer progression." Biomedical reports vol. 3,5 (2015): 603-610. doi: https://doi.org/10.3892/br.2015.494
Sun BO, Fang Y, Li Z, Chen Z, Xiang J. Role of cellular cytoskeleton in epithelial-mesenchymal transition process during cancer progression. Biomed Rep. 2015 Sep;3(5):603-610. doi: 10.3892/br.2015.494. Epub 2015 Jul 27. PMID: 26405532; PMCID: PMC4576489.
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Localized lichen myxedematosus in childhood: what is the accurate diagnosis?.

International journal of dermatology

Fang X, Yang B, Zhou G, Zhang F.
PMID: 27667483
Int J Dermatol. 2017 Mar;56(3):333-336. doi: 10.1111/ijd.13429. Epub 2016 Sep 26.

No abstract available.

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Fang X, Yang B, Zhou G, et al. Localized lichen myxedematosus in childhood: what is the accurate diagnosis?. Int J Dermatol. 2016;56(3):333-336doi: 10.1111/ijd.13429.
Fang, X., Yang, B., Zhou, G., & Zhang, F. (2017). Localized lichen myxedematosus in childhood: what is the accurate diagnosis?. International journal of dermatology, 56(3), 333-336. https://doi.org/10.1111/ijd.13429
Fang, Xiangang, et al. "Localized lichen myxedematosus in childhood: what is the accurate diagnosis?." International journal of dermatology vol. 56,3 (2017): 333-336. doi: https://doi.org/10.1111/ijd.13429
Fang X, Yang B, Zhou G, Zhang F. Localized lichen myxedematosus in childhood: what is the accurate diagnosis?. Int J Dermatol. 2017 Mar;56(3):333-336. doi: 10.1111/ijd.13429. Epub 2016 Sep 26. PMID: 27667483.
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Ubiquitin-specific protease 22 is a deubiquitinase of CCNB1.

Cell discovery

Lin Z, Tan C, Qiu Q, Kong S, Yang H, Zhao F, Liu Z, Li J, Kong Q, Gao B, Barrett T, Yang GY, Zhang J, Fang D.
PMID: 27030811
Cell Discov. 2015;1. doi: 10.1038/celldisc.2015.28. Epub 2015 Oct 13.

The elevated level of CCNB1 indicates more aggressive cancer and poor prognosis. However, the factors that cause CCNB1 upregulation remain enigmatic. Herein, we identify USP22 as a CCNB1 interactor and discover that both USP22 and CCNB1 are dramatically elevated...

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Lin Z, Tan C, Qiu Q, et al. Ubiquitin-specific protease 22 is a deubiquitinase of CCNB1. Cell Discov. 2015;1doi: 10.1038/celldisc.2015.28.
Lin, Z., Tan, C., Qiu, Q., Kong, S., Yang, H., Zhao, F., Liu, Z., Li, J., Kong, Q., Gao, B., Barrett, T., Yang, G. Y., Zhang, J., & Fang, D. (2015). Ubiquitin-specific protease 22 is a deubiquitinase of CCNB1. Cell discovery, 1. https://doi.org/10.1038/celldisc.2015.28
Lin, Zhenghong, et al. "Ubiquitin-specific protease 22 is a deubiquitinase of CCNB1." Cell discovery vol. 1 (2015). doi: https://doi.org/10.1038/celldisc.2015.28
Lin Z, Tan C, Qiu Q, Kong S, Yang H, Zhao F, Liu Z, Li J, Kong Q, Gao B, Barrett T, Yang GY, Zhang J, Fang D. Ubiquitin-specific protease 22 is a deubiquitinase of CCNB1. Cell Discov. 2015;1. doi: 10.1038/celldisc.2015.28. Epub 2015 Oct 13. PMID: 27030811; PMCID: PMC4809424.
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Inhibition of endoplasmic reticulum stress is involved in the neuroprotective effect of aFGF in neonatal hypoxic-ischaemic brain injury.

Oncotarget

Hu Y, Wang Z, Pan S, Fang M, Jiang H, Mao Y, Zhang H, Ji Y, Zhang F, Lin L, Lin Z, Xiao J.
PMID: 28977836
Oncotarget. 2017 Apr 29;8(37):60941-60953. doi: 10.18632/oncotarget.17524. eCollection 2017 Sep 22.

Acidic fibroblast growth factor (aFGF) has been shown to exert neuroprotective effects in experimental models and human patients. In this study, we investigated whether aFGF intranasal-treatment protected against neonatal hypoxic-ischaemic brain injury and evaluated the role of endoplasmic reticulum...

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Hu Y, Wang Z, Pan S, et al. Inhibition of endoplasmic reticulum stress is involved in the neuroprotective effect of aFGF in neonatal hypoxic-ischaemic brain injury. Oncotarget. 2017;8(37):60941-60953doi: 10.18632/oncotarget.17524.
Hu, Y., Wang, Z., Pan, S., Fang, M., Jiang, H., Mao, Y., Zhang, H., Ji, Y., Zhang, F., Lin, L., Lin, Z., & Xiao, J. (2017). Inhibition of endoplasmic reticulum stress is involved in the neuroprotective effect of aFGF in neonatal hypoxic-ischaemic brain injury. Oncotarget, 8(37), 60941-60953. https://doi.org/10.18632/oncotarget.17524
Hu, Yingying, et al. "Inhibition of endoplasmic reticulum stress is involved in the neuroprotective effect of aFGF in neonatal hypoxic-ischaemic brain injury." Oncotarget vol. 8,37 (2017): 60941-60953. doi: https://doi.org/10.18632/oncotarget.17524
Hu Y, Wang Z, Pan S, Fang M, Jiang H, Mao Y, Zhang H, Ji Y, Zhang F, Lin L, Lin Z, Xiao J. Inhibition of endoplasmic reticulum stress is involved in the neuroprotective effect of aFGF in neonatal hypoxic-ischaemic brain injury. Oncotarget. 2017 Apr 29;8(37):60941-60953. doi: 10.18632/oncotarget.17524. eCollection 2017 Sep 22. PMID: 28977836; PMCID: PMC5617396.
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Identification of hMex-3A and its effect on human bladder cancer cell proliferation.

Oncotarget

Huang Y, Fang C, Shi JW, Wen Y, Liu D.
PMID: 28977858
Oncotarget. 2017 May 22;8(37):61215-61225. doi: 10.18632/oncotarget.18050. eCollection 2017 Sep 22.

In this study,

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Huang Y, Fang C, Shi JW, et al. Identification of hMex-3A and its effect on human bladder cancer cell proliferation. Oncotarget. 2017;8(37):61215-61225doi: 10.18632/oncotarget.18050.
Huang, Y., Fang, C., Shi, J. W., Wen, Y., & Liu, D. (2017). Identification of hMex-3A and its effect on human bladder cancer cell proliferation. Oncotarget, 8(37), 61215-61225. https://doi.org/10.18632/oncotarget.18050
Huang, Ying, et al. "Identification of hMex-3A and its effect on human bladder cancer cell proliferation." Oncotarget vol. 8,37 (2017): 61215-61225. doi: https://doi.org/10.18632/oncotarget.18050
Huang Y, Fang C, Shi JW, Wen Y, Liu D. Identification of hMex-3A and its effect on human bladder cancer cell proliferation. Oncotarget. 2017 May 22;8(37):61215-61225. doi: 10.18632/oncotarget.18050. eCollection 2017 Sep 22. PMID: 28977858; PMCID: PMC5617418.
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Correction: Human cytomegalovirus IE1 alters the higher-order chromatin structure by targeting the acidic patch of the nucleosome.

eLife

Fang Q, Chen P, Wang M, Fang J, Yang N, Li G, Xu RM.
PMID: 26974472
Elife. 2016 Mar 14;5:e15893. doi: 10.7554/eLife.15893.

No abstract available.

Cite
Fang Q, Chen P, Wang M, et al. Correction: Human cytomegalovirus IE1 alters the higher-order chromatin structure by targeting the acidic patch of the nucleosome. Elife. 2016;5:e15893doi: 10.7554/eLife.15893.
Fang, Q., Chen, P., Wang, M., Fang, J., Yang, N., Li, G., & Xu, R. M. (2016). Correction: Human cytomegalovirus IE1 alters the higher-order chromatin structure by targeting the acidic patch of the nucleosome. eLife, 5e15893. https://doi.org/10.7554/eLife.15893
Fang, Qianglin, et al. "Correction: Human cytomegalovirus IE1 alters the higher-order chromatin structure by targeting the acidic patch of the nucleosome." eLife vol. 5 (2016): e15893. doi: https://doi.org/10.7554/eLife.15893
Fang Q, Chen P, Wang M, Fang J, Yang N, Li G, Xu RM. Correction: Human cytomegalovirus IE1 alters the higher-order chromatin structure by targeting the acidic patch of the nucleosome. Elife. 2016 Mar 14;5:e15893. doi: 10.7554/eLife.15893. PMID: 26974472; PMCID: PMC4805533.
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Elevated Circulating hsa-miR-106b, hsa-miR-26a, and hsa-miR-29b in Type 2 Diabetes Mellitus with Diarrhea-Predominant Irritable Bowel Syndrome.

Gastroenterology research and practice

Tao W, Dong X, Kong G, Fang P, Huang X, Bo P.
PMID: 27635130
Gastroenterol Res Pract. 2016;2016:9256209. doi: 10.1155/2016/9256209. Epub 2016 Aug 22.

Background and Aims. Although the differential expression of microRNA (miRNA) genes has been identified in many diseases, little information exists concerning the miRNA expression profile in type 2 diabetes mellitus (T2DM) with diarrhea-predominant irritable bowel syndrome (D-IBS). Therefore, the...

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Tao W, Dong X, Kong G, et al. Elevated Circulating hsa-miR-106b, hsa-miR-26a, and hsa-miR-29b in Type 2 Diabetes Mellitus with Diarrhea-Predominant Irritable Bowel Syndrome. Gastroenterol Res Pract. 2016;2016:9256209doi: 10.1155/2016/9256209.
Tao, W., Dong, X., Kong, G., Fang, P., Huang, X., & Bo, P. (2016). Elevated Circulating hsa-miR-106b, hsa-miR-26a, and hsa-miR-29b in Type 2 Diabetes Mellitus with Diarrhea-Predominant Irritable Bowel Syndrome. Gastroenterology research and practice, 20169256209. https://doi.org/10.1155/2016/9256209
Tao, Wenhua, et al. "Elevated Circulating hsa-miR-106b, hsa-miR-26a, and hsa-miR-29b in Type 2 Diabetes Mellitus with Diarrhea-Predominant Irritable Bowel Syndrome." Gastroenterology research and practice vol. 2016 (2016): 9256209. doi: https://doi.org/10.1155/2016/9256209
Tao W, Dong X, Kong G, Fang P, Huang X, Bo P. Elevated Circulating hsa-miR-106b, hsa-miR-26a, and hsa-miR-29b in Type 2 Diabetes Mellitus with Diarrhea-Predominant Irritable Bowel Syndrome. Gastroenterol Res Pract. 2016;2016:9256209. doi: 10.1155/2016/9256209. Epub 2016 Aug 22. PMID: 27635130; PMCID: PMC5011218.
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Abnormal topological organization in white matter structural networks in survivors of acute lymphoblastic leukaemia with chemotherapy treatment.

Oncotarget

Zou L, Su L, Qi R, Bao F, Fang X, Wang L, Zhai Z, Li D, Zheng S.
PMID: 28947994
Oncotarget. 2017 Jul 08;8(36):60568-60575. doi: 10.18632/oncotarget.19104. eCollection 2017 Sep 01.

Previous diffusion tensor imaging (DTI) studies have detected white matter (WM) integrity abnormalities in some specific fibre bundles in acute lymphoblastic leukaemia (ALL) patients with chemotherapy. However, little is known about the changes in the topological organization of the...

Cite
Zou L, Su L, Qi R, et al. Abnormal topological organization in white matter structural networks in survivors of acute lymphoblastic leukaemia with chemotherapy treatment. Oncotarget. 2017;8(36):60568-60575doi: 10.18632/oncotarget.19104.
Zou, L., Su, L., Qi, R., Bao, F., Fang, X., Wang, L., Zhai, Z., Li, D., & Zheng, S. (2017). Abnormal topological organization in white matter structural networks in survivors of acute lymphoblastic leukaemia with chemotherapy treatment. Oncotarget, 8(36), 60568-60575. https://doi.org/10.18632/oncotarget.19104
Zou, Liwei, et al. "Abnormal topological organization in white matter structural networks in survivors of acute lymphoblastic leukaemia with chemotherapy treatment." Oncotarget vol. 8,36 (2017): 60568-60575. doi: https://doi.org/10.18632/oncotarget.19104
Zou L, Su L, Qi R, Bao F, Fang X, Wang L, Zhai Z, Li D, Zheng S. Abnormal topological organization in white matter structural networks in survivors of acute lymphoblastic leukaemia with chemotherapy treatment. Oncotarget. 2017 Jul 08;8(36):60568-60575. doi: 10.18632/oncotarget.19104. eCollection 2017 Sep 01. PMID: 28947994; PMCID: PMC5601162.
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Polyethylenimines modified by amino acids with different charge states and hydrophilic/hydrophobic properties for gene carriers.

Journal of controlled release : official journal of the Controlled Release Society

Zhang Y, Tian H, Guan X, Fang H, Yan N, Chen X.
PMID: 27005165
J Control Release. 2015 Sep 10;213:e41. doi: 10.1016/j.jconrel.2015.05.066. Epub 2015 Aug 19.

No abstract available.

Cite
Zhang Y, Tian H, Guan X, et al. Polyethylenimines modified by amino acids with different charge states and hydrophilic/hydrophobic properties for gene carriers. J Control Release. 2015;213:e41doi: 10.1016/j.jconrel.2015.05.066.
Zhang, Y., Tian, H., Guan, X., Fang, H., Yan, N., & Chen, X. (2015). Polyethylenimines modified by amino acids with different charge states and hydrophilic/hydrophobic properties for gene carriers. Journal of controlled release : official journal of the Controlled Release Society, 213e41. https://doi.org/10.1016/j.jconrel.2015.05.066
Zhang, Ying, et al. "Polyethylenimines modified by amino acids with different charge states and hydrophilic/hydrophobic properties for gene carriers." Journal of controlled release : official journal of the Controlled Release Society vol. 213 (2015): e41. doi: https://doi.org/10.1016/j.jconrel.2015.05.066
Zhang Y, Tian H, Guan X, Fang H, Yan N, Chen X. Polyethylenimines modified by amino acids with different charge states and hydrophilic/hydrophobic properties for gene carriers. J Control Release. 2015 Sep 10;213:e41. doi: 10.1016/j.jconrel.2015.05.066. Epub 2015 Aug 19. PMID: 27005165.
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Showing 25 to 36 of 18716 entries