Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Liuping Liang"'
Autor:
Pingjiao Chen, Changxing Li, Hongchang Huang, Liuping Liang, Jing Zhang, Qian Li, Qi Wang, Sanquan Zhang, Kang Zeng, Xibao Zhang, Jingyao Liang
Publikováno v:
FEBS Open Bio, Vol 11, Iss 4, Pp 1209-1222 (2021)
Circular RNAs (circRNAs) act as sponges of noncoding RNAs and have been implicated in many pathophysiological processes, including tumor development and progression. However, their roles in cutaneous squamous cell carcinoma (cSCC) are not yet well un
Externí odkaz:
https://doaj.org/article/c8743ba7a517460a8b2ffbc119a18e29
Publikováno v:
Clinical Case Reports, Vol 8, Iss 3, Pp 416-419 (2020)
Abstract We reported the successful treatment with oral methylprednisolone and cyclosporine in combination with topical wound care on a boy with pyoderma gangrenosum presenting as huge and deep ulceration on buttocks and legs.
Externí odkaz:
https://doaj.org/article/8247fb28d86e4779b4e230409fec8922
Autor:
Changxing Li, Jingyao Liang, Pingjiao Chen, Kang Zeng, Rujun Xue, Xin Tian, Liuping Liang, Qi Wang, Minglan Shi, Xibao Zhang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 6, Pp n/a-n/a (2019)
Abstract Background Erythrokeratodermia variabilis et progressiva (EKVP, OMIM 133200) is a rare hereditary disorder characterized by varies from transient, fast moving erythema to persistent brown hyperkeratotic plaques. Recently, mutations in the ge
Externí odkaz:
https://doaj.org/article/d6e8c59abdec4436a8a9d20f6695fb89
Autor:
Jingyao Liang, Changxing Li, Sanquan Zhang, Hongchang Huang, Qian Li, Pingjiao Chen, Jing Zhang, Liuping Liang, Xibao Zhang, Qi Wang, Kang Zeng
Publikováno v:
FEBS Open Bio, Vol 11, Iss 4, Pp 1209-1222 (2021)
FEBS Open Bio
FEBS Open Bio
Circular RNAs (circRNAs) act as sponges of noncoding RNAs and have been implicated in many pathophysiological processes, including tumor development and progression. However, their roles in cutaneous squamous cell carcinoma (cSCC) are not yet well un
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 8, Iss 3, Pp 416-419 (2020)
Clinical Case Reports, Vol 8, Iss 3, Pp 416-419 (2020)
We reported the successful treatment with oral methylprednisolone and cyclosporine in combination with topical wound care on a boy with pyoderma gangrenosum presenting as huge and deep ulceration on buttocks and legs.
Autor:
MENGLEI WANG1, LIUPING LIANG1, LI LI1, KAI HAN1, QIAN LI1, YUSHENG PENG1, XUEBIAO PENG1, KANG ZENG1
Publikováno v:
Molecular Medicine Reports. Jun2017, Vol. 15 Issue 6, p3479-3484. 6p. 3 Charts, 2 Graphs.
Publikováno v:
Molecular Medicine Reports
Pemphigus is an autoimmune disease that causes blisters and erosions in the skin and mucous membranes. The development of pemphigus is associated with the imbalance of T-cell and humoral responses. MicroRNAs (miRNAs) can regulate many cell functions.
Autor:
Minglan Shi, Liuping Liang, Xin Tian, Xibao Zhang, Changxing Li, Kang Zeng, Rujun Xue, Qi Wang, Jingyao Liang, Pingjiao Chen
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 6, Pp n/a-n/a (2019)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Erythrokeratodermia variabilis et progressiva (EKVP, OMIM 133200) is a rare hereditary disorder characterized by varies from transient, fast moving erythema to persistent brown hyperkeratotic plaques. Recently, mutations in the genes gap j
Autor:
Kang Zeng, Liuping Liang, Li Li, Menglei Wang, Xuebiao Peng, Xiaoming Peng, Jing Zhang, Feiyi Cui, Qingxiu Liu, Hao Xiong
Publikováno v:
Molecular medicine reports. 18(1)
Expression of microRNA-338-3p (miR-338-3p) was aberrantly elevated in pemphigus vulgaris (PV), although its role in PV is still unknown. The present study investigated the functional role and possible molecular mechanisms of miR-338-3p in PV. Reverse
Autor:
Chengdan Lai, Zhen Ouyang, Kepin Wang, Liuping Liang, Qi Wang, Xiaoshuai Ren, Sen Yan, Bentian Zhao, Lin Guo, Kang Zeng, Nana Fan, Li Li, Yu Zhao, Liang Huang, Zhaoming Liu, Kai Han, Liangxue Lai, Jiang Fei
Publikováno v:
Human molecular genetics. 26(1)
Atrichia and sparse hair phenotype cause distress to many patients. Ectodermal dysplasia-9 (ED-9) is a congenital condition characterized by hypotrichosis and nail dystrophy without other disorders, and Hoxc13 is a pathogenic gene for ED-9. However,