日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

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 syndrome

SMAD4 突变和 TGF-β/IFNγ 信号之间的串扰加速了 DNA 损伤和细胞衰老的速度,导致节段性早衰综合征——Myhre 综合征

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

Remission of alopecia universalis in a patient with atopic dermatitis treated with dupilumab

接受度普利尤单抗治疗的特应性皮炎患者的普秃症状缓解

Smogorzewski, Jan; Sierro, Tiffany; Compoginis, Goli; Kim, Gene

WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations

沃纳综合征患者的 WRN 突变:基因组重排、不寻常的内含子突变和种族特异性改变

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 C