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The FEBS Journal|April 25, 2022
Dietary restriction and lifespan: adaptive reallocation or somatic sacrifice?Matthew D W Piper, Brooke Zanco, Carla M Sgrò, et al.The FEBS Journal|March 18, 2022
Clinical implications of differential functional capacity between tissue-specific human mesenchymal stromal/stem cellsB Linju Yen, Ko-Jiunn Liu, Huey-Kang Sytwu, et al.The FEBS Journal|March 19, 2022
Hedgehog signalling in bone and osteoarthritis: the role of Smoothened and cholesterolAbbi Elise Smith, Elín Sóley Sigurbjörnsdóttir, Eiríkur Steingrímsson, et al.The FEBS Journal|March 19, 2022
Hsp104 N-terminal domain interaction with substrates plays a regulatory role in protein disaggregationAnna Harari, Guy Zoltsman, Tal Levin, et al.The FEBS Journal|March 23, 2022
The atypical sphingosine 1-phosphate variant, d16:1 S1P, mediates CTGF induction via S1P2 activation in renal cell carcinomaMelanie Glueck, Alexander Koch, Robert Brunkhorst, et al.The FEBS Journal|April 12, 2022
Expanding PAM recognition and enhancing base editing activity of Cas9 variants with non-PI domain mutations derived from xCas9Lifang Xie, Yun Hu, Li Li, et al.The FEBS Journal|April 16, 2022
Interleukin-6 signaling requires EHD1-mediated alteration of membrane raftsJoo Hong Woo, Soo Jung Park, Sang Myun Park, et al.The FEBS Journal|September 7, 2018
Thymus autonomy as a prelude to leukemiaRafael A Paiva, Camila V Ramos, Vera C MartinsThe FEBS Journal|October 6, 2018
Defining specific residue-to-residue interactions between the gp120 bridging sheet and the N-terminal segment of CCR5: applications of transferred NOE NMRGautam Srivastava, Adi Moseri, Naama Kessler, et al.Pageof 912