Trends in Neurosciences
For more than 40 years, Trends in Neurosciences (TINS) has been a key resource for insightful reviews and discussions in various areas of neuroscience. Published monthly and peer-reviewed, the journal features articles selected by the Editor and written by top researchers in their fields. TINS showcases groundbreaking developments in brain research, represents the global neuroscience community, and emphasizes the impact of neuroscientific studies on medicine and society.
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Global
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United States
#10310
Science and Education/Biology
#13
Articles
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2 days ago |
cell.com | Ying Liu |Huihui Mei |Li Xue |Chuanli Cheng |Yingtong Wu |Chao Zou | +11 more
During preparation of Figure 2F, an error occurred in Excel that distorted the values of percentage energy from fat. This error has now been corrected online. We, the authors, apologize for any confusion this may have caused and thank Jenni Brand-Miller and Mark Haub, who spotted the problem and drew it to our attention.
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2 weeks ago |
cell.com | Sucharita Sarkar |Ian MacRae |Ian Macrae
Get full text accessLog in, subscribe or purchase for full access. References1. Bobadilla Ugarte, P. ∙ Halter, S. ∙ Mutte, S.K. ... Cyanobacterial Argonautes and Cas4 family nucleases cooperate to interfere with invading DNAMol. Cell. 2025; 85:1920-1937.e102. Bernstein, E. ∙ Caudy, A.A. ∙ Hammond, S.M. ... Role for a bidentate ribonuclease in the initiation step of RNA interferenceNature. 2001; 409:363-3663. Zamore, P.D. ∙ Tuschl, T. ∙ Sharp, P.A. ...
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3 weeks ago |
cell.com | Zilong Zhao |Benxia Hu |Yalan Deng |Melinda Soeung |Jun Yao |Lanxin Bei | +25 more
Keywords sickle cell disease renal medullary carcinoma ferroptosis genomic architecture alteration Hi-C H2S SLC7A11 SMARCB1 immune checkpoint inhibitors CD8+ T cells Introduction Sickle cell disease (SCD), the most prevalent inherited blood disorder,1 arises from the homozygous HbS mutation (GAG>GTG: βGlu6Val), causing hemoglobin abnormalities that make red blood cells (RBCs) assume a sickle or crescent shape.2 Individuals with SCD have RBCs prone to hemolysis, leading to vaso-occlusive...
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3 weeks ago |
cell.com | Zilong Zhao |Benxia Hu |Yalan Deng |Melinda Soeung |Jun Yao |Lanxin Bei | +25 more
Keywords sickle cell disease renal medullary carcinoma ferroptosis genomic architecture alteration Hi-C H2S SLC7A11 SMARCB1 immune checkpoint inhibitors CD8+ T cells Introduction Sickle cell disease (SCD), the most prevalent inherited blood disorder,1 arises from the homozygous HbS mutation (GAG>GTG: βGlu6Val), causing hemoglobin abnormalities that make red blood cells (RBCs) assume a sickle or crescent shape.2 Individuals with SCD have RBCs prone to hemolysis, leading to vaso-occlusive...
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4 weeks ago |
cell.com | Steve Cranford
Main textThe recent global pandemic required an abrupt shift in how science was shared globally, for better or for worse. Virtual meetings were the new normal and have persisted (in a more limited context) past the pandemic's prime. There are numerous pros and cons to moving science online, but is it reflective of a larger trend, merely accelerated by pandemic restrictions?
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