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NARA Subscribed2
Publisher
Springer Nature2
Journal
GeroScience1
Human Genetics1
Publication Year
20211
20101
Goli Compoginis results 2 · Newest (Page 1/1, per page 25)
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Author: Goli Compoginis ×Clear All Filters
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SMAD4 mutations and cross-talk between TGF-β/IFNγ signaling accelerate rates of DNA damage and cellular senescence, resulting in a segmental progeroid syndrome—the Myhre syndromeNARA Subscribed
GeroScience · 2021 · Vol. 43 · Issue 3 · Springer
Renuka Kandhaya-Pillai; Deyin Hou; Jiaming Zhang; Xiaomeng Yang; Goli Compoginis; Takayasu Mori; Tamara Tchkonia; George M. Martin; Fuki M. Hisama; James L. Kirkland; Junko Oshima
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WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterationsNARA Subscribed
Human Genetics · 2010 · Vol. 128 · Issue 1 · Springer
Katrin Friedrich; Lin Lee; Dru F. Leistritz; Gudrun Nürnberg; Bidisha Saha; Fuki M. Hisama; Daniel K. Eyman; Davor Lessel; Peter Nürnberg; Chumei Li; María J. Garcia-F-Villalta; Carolien M. Kets; Joerg Schmidtke; Vítor Tedim Cruz; Peter C. Van den Akker; Joseph Boak; Dincy Peter; Goli Compoginis; Kivanc Cefle; Sukru Ozturk; Norberto López; Theda Wessel; Martin Poot; P. F. Ippel; Birgit Groff-Kellermann; Holger Hoehn; George M. Martin; Christian Kubisch; Junko Oshima
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