supported by the National Natural Science Foundation of China(32300730);the Guangdong Science and Technology Department(2023B12120600280);the National Postdoctoral Program for Innovative Talents of China(BX20220365);the China Postdoctoral Science Foundation(2023M734057);the Fundamental Research Funds for the Central Universities(23yxqntd001).
As a key executioner of pyroptosis,Gasdermin D(GSDMD)plays a crucial role in host defense and emerges as an essential therapeutic target in the treatment of inflammatory diseases.So far,the understanding of the mechan...
Supported by the National Natural Science Foundation of China,No.82103173 and No.82460461;Medical Subject Leader of Yunnan Province(General Surgery),No.D-2024029;Yunnan Fundamental Research Project for Excellent Young Scholars,No.202401AW070003;the Young and Mid-aged Academic and Technical Leader Reserve Talent Program of Yunnan Province,No.202205AC160063。
This letter comments on the recently published manuscript by Yu et al,in which the authors revealed a novel mechanism by which the m6A-modified long noncoding RNA kinesin family member 9-antisense RNA 1 promotes stemn...
Objective To evaluate the relationship between the trend of glutamyl transpeptidase(GGT)change and newly developed metabolic syndrome(MS),and to explore the relationship between GGT and MS.Methods The study was a pros...
Supported by Ruian Natural Science Foundation,No.MS2021008.
BACKGROUND Serpin peptidase inhibitor clade H member 1(SERPINH1)was initially recognized as an oncogene implicated in various human malignancies.Nevertheless,the clinical relevance and functional implications of SERPI...
supported by the Shenzhen Science and Technology Program,China(No.KQTD20190929172749226).
Meiosis is the process of producing haploid gametes through a series of complex chromosomal events and the coordinated action of various proteins.The mitochondrial protease complex(ClpXP),which consists of caseinolyti...
supported by the National Natural Science Foundation of China (31872805);the Fundamental Research Funds for Central NonProfit of the Chinese Academy of Agricultural Sciences (CAASZDRW202109 and Y2023PT20);the Nanfan Special Project of the Chinese Academy of Agricultural Sciences (YBXM15).
Plant organ size is an important agronomic trait that makes a significant contribution to plant yield.Despite its central importance,the genetic and molecular mechanisms underlying organ size control remain to be full...
supported by Shanghai Pujiang Program(No.20PJ1413000);the National Natural Science Foundation of China(No.82173106,82130115,81290108033,82004004,and 82074011)。
The management of colorectal cancer(CRC)poses a significant challenge,necessitating the development of innovative and effective therapeutics.Our research has shown that notoginsenoside Ft1(Ng-Ft1),a small molecule,mar...
Liaoning Province Science and Technology Project(grant/award number:2019-BS-221);Shenyang Science and Technology Project(grant/award number:19-112-4-040)。
Background:Alzheimer’sdisease(AD)is a prevalent neurodegenerative disorder causing progressive dementia.Research suggests that microRNAs(miRNAs)could serve as biomarkers and therapeutic targets for AD.Reduced levels ...
supported in part by National Natural Science Foundation of China (#81970194 and#82170176 to XLM);the National Key Research and Development Program of China (#2022YFC2705003 to XLM);Guangzhou Medical University Discipline Construction Funds (Basic Medicine) (Grant No.JCXKJS2022A05 to XLM);Department of Education of Guangdong Province of China (Grant No.2021ZDZX2009 to XLM).
The cell cycle regulator cyclin D3(CCND3)is highly expressed in multiple myeloma(MM)and it promotes MM cell proliferation.After a certain phase of cell cycle,CCND3 is rapidly degraded,which is essential for the strict...
Supported by Postdoctoral program of the Affiliated Hospital of Jining Medical University,No.JYFY303573;Health Commission of Shandong Province,No.202006010928;Academician Lin He New Medicine in Jining Medical University,No.JYHL2018FMS05;Affiliated Hospital of Jining Medical University,No.2018-BS-004.
BACKGROUND Spinocerebellar ataxia recessive type 7(SCAR7)is a rare clinical manifestation beginning in childhood or adolescence.SCAR7 is caused by tripeptidyl peptidase 1(TPP1)gene mutations,and presents with cerebell...