Cell Press

3 days ago | cell.com | Steve Cranford

Main textPeer review is a little bit of a contentious topic lately, with the proliferation of journal titles being launched and submissions draining the community of time and effort … with little reward or recognition. What used to be somewhat of a gentleman’s agreement between author and journal has turned into the academic equivalent of arranging deck chairs on the Titanic.

3 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.

3 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. ...

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...

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...