Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Fang-Mei Lu"'
Autor:
Hui-Han Ma, Jun-Ru Wen, Hao Fang, Shan Su, Can Wan, Chao Zhang, Fang-Mei Lu, Ling-Ling Fan, Guang-Liang Wu, Zi-Yi Zhou, Li-Jun Qiao, Shi-Jie Zhang, Ye-Feng Cai
Publikováno v:
Rejuvenation Research. 26:57-67
Autor:
Yu-Min Xu, Fang-Mei Lu, Hong-Cai Xu, Jie Zhang, Shang-Yan Hei, Yu-Hui Qiu, Ye-Feng Cai, Shi-Jie Zhang, Min Zhao
Publikováno v:
Rejuvenation Research.
Autor:
Xing-Hua Xiao, Fang-Mei Luo, E.-Li Wang, Min-Yi Fu, Tao Li, Yue-Ping Jiang, Shao Liu, Jun Peng, Bin Liu
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 150, Iss , Pp 113060- (2022)
Phenotypic transformation and excessive proliferation of pulmonary arterial smooth muscle cells (PASMCs) play an important role in vascular remodeling during pulmonary hypertension (PH). Magnolol (5,5′-diallyl-2,2′-dihydroxybiphenyl) is the major
Externí odkaz:
https://doaj.org/article/7ad13c63eef2476886dfb257de240db3
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Preaxial polydactyly (PPD) is a common congenital abnormality with an incidence of 0.8–1.4% in Asians, characterized by the presence of extra digit(s) on the preaxial side of the hand or foot. PPD is genetically classified into four subtypes, PPD t
Externí odkaz:
https://doaj.org/article/43dfc50d410041e99d6aafcee0c53a53
Autor:
Jie-Yuan Jin, Pan-Feng Wu, Fang-Mei Luo, Bing-Bing Guo, Lei Zeng, Liang-Liang Fan, Ju-Yu Tang, Rong Xiang
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2022)
Background: Preaxial polydactyly (PPD) is one of the most common developmental malformations, with a prevalence of 0.8–1.4% in Asians. PPD is divided into four types, PPD I–IV, and PPD I is the most frequent type. Only six loci (GLI1, GLI3, STKLD
Externí odkaz:
https://doaj.org/article/5bd1882e508d4f69be9747ee1b22d095
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background: Transmembrane protein 231 (TMEM231) is a component of the B9 complex that participates in the formation of the diffusion barrier between the cilia and plasma membrane. Mutations in TMEM231 gene may contribute to the Joubert syndrome (JBTS
Externí odkaz:
https://doaj.org/article/0ba140f824a7427f93e2d06100310f16
Autor:
Yu-Xing Liu, Ai-Qian Zhang, Fang-Mei Luo, Yue Sheng, Chen-Yu Wang, Yi Dong, Liangliang Fan, Lv Liu
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Idiopathic focal segmental glomerulosclerosis (FSGS) is a relatively frequent kidney disorder that manifest clinically as proteinuria and progressive loss of renal function. Genetic factors play a dominant role in the occurrence of FSGS. CD2-associat
Externí odkaz:
https://doaj.org/article/5ea33cf19f7b4c628b45c3256faac43e
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Inherited macrothrombocytopenia (IMTP) is a rare disorder characterized by a reduced platelet count and abnormally large platelets. The main clinical symptom of IMTP is mild bleeding in some patients. At present, more than 30 genes have been identifi
Externí odkaz:
https://doaj.org/article/7841b7336310447689f9da1ee6777fdc
Publikováno v:
Frontiers in Neuroscience, Vol 15 (2021)
Externí odkaz:
https://doaj.org/article/acf54cc95d9a44bfb8dce74a69ae2349
Publikováno v:
Frontiers in Neuroscience, Vol 15 (2021)
Chorea-Acanthocytosis (ChAc), a rare autosomal recessive inherited neurological disorder, originated from variants in Vacuolar Protein Sorting 13 homolog A (VPS13A) gene. The main symptoms of ChAc contain hyperkinetic movements, seizures, cognitive i
Externí odkaz:
https://doaj.org/article/c43d4c5065ab419cb5fea9f1003c9076