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

Glycerophosphodiesters inhibit lysosomal phospholipid catabolism in Batten disease.

甘油磷酸二酯抑制巴顿病中的溶酶体磷脂分解代谢

Nyame Kwamina, Hims Andy, Aburous Aya, Laqtom Nouf N, Dong Wentao, Medoh Uche N, Heiby Julia C, Xiong Jian, Ori Alessandro, Abu-Remaileh Monther

TGFβ-blockade uncovers stromal plasticity in tumors by revealing the existence of a subset of interferon-licensed fibroblasts

TGFβ阻断揭示了肿瘤基质的可塑性,表现为存在一类经干扰素激活的成纤维细胞。

Angelo L Grauel ,Beverly Nguyen ,David Ruddy ,Tyler Laszewski ,Stephanie Schwartz ,Jonathan Chang ,Julie Chen ,Michelle Piquet ,Marc Pelletier ,Zheng Yan ,Nathaniel D Kirkpatrick ,Jincheng Wu ,Antoine deWeck ,Markus Riester ,Matt Hims ,Felipe Correa Geyer ,Joel Wagner ,Kenzie MacIsaac ,James Deeds ,Rohan Diwanji ,Pushpa Jayaraman ,Yenyen Yu ,Quincey Simmons ,Shaobu Weng ,Alina Raza ,Brian Minie ,Mirek Dostalek ,Pavitra Chikkegowda ,Vera Ruda ,Oleg Iartchouk ,Naiyan Chen ,Raphael Thierry ,Joseph Zhou ,Iulian Pruteanu-Malinici ,Claire Fabre ,Jeffrey A Engelman ,Glenn Dranoff ,Viviana Cremasco

Genome sequencing and analysis of the Tasmanian devil and its transmissible cancer

塔斯马尼亚恶魔及其传染性癌症的基因组测序和分析

Elizabeth P Murchison, Ole B Schulz-Trieglaff, Zemin Ning, Ludmil B Alexandrov, Markus J Bauer, Beiyuan Fu, Matthew Hims, Zhihao Ding, Sergii Ivakhno, Caitlin Stewart, Bee Ling Ng, Wendy Wong, Bronwen Aken, Simon White, Amber Alsop, Jennifer Becq, Graham R Bignell, R Keira Cheetham, William Cheng, T

Specific correction of a splice defect in brain by nutritional supplementation

通过营养补充特异性纠正大脑中的剪接缺陷

Shetty, Ranjit S; Gallagher, Cary S; Chen, Yei-Tsung; Hims, Matthew M; Mull, James; Leyne, Maire; Pickel, James; Kwok, David; Slaugenhaupt, Susan A

Loss of mouse Ikbkap, a subunit of elongator, leads to transcriptional deficits and embryonic lethality that can be rescued by human IKBKAP

小鼠 Ikbkap(延伸因子的一个亚基)的缺失会导致转录缺陷和胚胎致死,而人 IKBKAP 可以挽救这一缺陷。

Chen, Yei-Tsung; Hims, Matthew M; Shetty, Ranjit S; Mull, James; Liu, Lijuan; Leyne, Maire; Slaugenhaupt, Susan A

Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa

RP1基因突变导致常染色体显性遗传性视网膜色素变性

Bowne, S J; Daiger, S P; Hims, M M; Sohocki, M M; Malone, K A; McKie, A B; Heckenlively, J R; Birch, D G; Inglehearn, C F; Bhattacharya, S S; Bird, A; Sullivan, L S