Corrigendum to"SEMA4D acts as a novel oligogenic pathogenic gene of idiopathic hypogonadotropic hypogonadism through the PlexinB1/MET/RND1/RHOA/RAF1/MAPK signaling axis"[Genes&Diseases 10(2023)65-68]
摘要
The authors regret to correct the error in the order of the institute of the first author,which should go as the following.
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2Xiao-Bin Wang,Ping Chen,Xue-Er Yu,Zu-Liang Yao,Ting-Chao Guo,Bo-Chen Pan.Identification of two compound heterozygous GNRHR mutations in two siblings with congenital hypogonadotropic hypogonadism[J].Asian Journal of Andrology,2024,26(1):120-122.
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3Wen-Qing Rao,Zheng Lin,Jian Jiang,Jian-Wen Wang,Zhi-Feng Lin,Rong Fu,Wei-Lin Chen,Yuan-Mei Chen,Xian-EPeng,Zhi-Jian Hu.Esophageal mycobiome landscape and interkingdom interactions in esophageal squamous cell carcinoma[J].Gastroenterology Report,2023,11(1):300-308.
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4XIE Shuwei,SHI Huanbin,WEN Hui,LIU Zhiquan,QIU Jiehua,JIANG Nan,KOU Yanjun.Carbon Catabolite Repressor UvCreA is Required for Development and Pathogenicity in Ustilaginoidea virens[J].Rice science,2024,31(2):203-214.
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5Wei-Xue Jia,Ling-Ling Luo,Wen-Rui Li,Yuan-Yuan Zhang,Ping Cheng,Cheng-Rang Li.The Role of Notch Signaling in Genetic Reticular Pigmentary Disorders[J].International Journal of Dermatology and Venereology,2023,6(3):163-167.
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6Wei-Bin Peng,Yu-Ping Li,Yong Zeng,Kai Chen.Transglutaminase 2 serves as a pathogenic hub gene of KRAS mutant colon cancer based on integrated analysis[J].World Journal of Gastrointestinal Oncology,2024,16(5):2074-2090.
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7Ming-Ran Luo,Si-Ming Dai,Yin Li,Qian Wang,Hao Liu,Peng Gao,Jia-Yun Liu,Jian Chen,Shu-Jie Zhao,Guo-Yong Yin.3M syndrome patient with a novel mutation:A case rep[J].World Journal of Clinical Cases,2024,12(8):1454-1460.
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8ZHU Xinghua,GAN Die,LIU Zhixin.Distributed Least Squares Algorithm of Continuous-Time Stochastic Regression Model Based on Sampled Data[J].Journal of Systems Science & Complexity,2024,37(2):609-628.
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9王啸南,袁琳,胡娜,钟霄毓,林敏,姜逸,陆敏,王晖,陆雄.交泰丸对高脂饮食诱导肥胖小鼠血脑屏障损伤的影响及机制研究[J].中成药,2024,46(6):2058-2062. 被引量：1
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10Jing-Lan Ni,Hua-Ming Wen,Xiao-Sheng Huang,Qian-Wen Li,Jia-Min Cai,Bao-Jian Fan,Jun Zhao.Novel MIP gene mutation causes autosomal-dominant congenital cataract[J].International Journal of Ophthalmology(English edition),2024,17(3):454-465.
