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M

Marco H. Hofmann

Boehringer Ingelheim
H指数:18
被引数:2,239

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Disentangling effects of the DR and DQ isomers encoded by the HLA class II haplotype DRB1*15:01/DQB1*06:02 to help establish the true risk allele for FVIII inhibitor development in Hemophilia A

区分由HLA-II类单倍型DRB1*15:01/DQB1*06:02编码的DR和DQ异构体的效应,以帮助确定血友病A中FVIII抑制剂发展的真实风险等位基因。

2025-04-090
OA
SOS1 inhibitor BI-3406 shows in vivo antitumor activity akin to genetic ablation and synergizes with a KRASG12D inhibitor in KRAS LUAD

SOS1抑制剂BI-3406显示出类似基因敲除的在体抗肿瘤活性,并能与KRASG12D抑制剂协同作用,用于KRAS LUAD。

2025-03-120
OA
Concurrent SOS1 and MEK suppression inhibits signaling and growth of NF1-null melanoma

同时抑制SOS1和MEK抑制NF1-null黑色素瘤的信号传导和生长

2024-11-010
OAAI
Co-targeting SOS1 enhances the antitumor effects of KRASG12C inhibitors by addressing intrinsic and acquired resistance

共靶向SOS1通过解决内在和获得性耐药增强KRASG12C抑制剂的抗肿瘤作用

2024-08-051
OA
Discovery of BI 7446: A Potent Cyclic Dinucleotide STING Agonist with Broad-Spectrum Variant Activity for the Treatment of Cancer
2023-07-145
PRE
Pharmacodynamic and Antitumor Activity of BI 836880, a Dual Vascular Endothelial Growth Factor and Angiopoietin 2 Inhibitor, Alone and Combined with Programmed Cell Death Protein-1 Inhibition
2023-03-018
OAAI
One Atom Makes All the Difference: Getting a Foot in the Door between SOS1 and KRAS

一个原子就能改变一切: 在SOS1和KRAS之间进门

2021-03-1540
PRE
BI-3406, a Potent and Selective SOS1-KRAS Interaction Inhibitor, Is Effective in KRAS-Driven Cancers through Combined MEK Inhibition

BI-3406是一种有效的选择性SOS1-KRAS相互作用抑制剂,通过联合MEK抑制对KRAS驱动的癌症有效

2021-01-06276
OAAI
Potent induction of a tumor-specific immune response by a cyclic dinucleotide STING agonist
2020-08-155
PRE
BI-3406 and BI 1701963: Potent and selective SOS1::KRAS inhibitors induce regressions in combination with MEK inhibitors or irinotecan

BI-3406和BI 1701963: 有效和选择性的SOS1::KRAS抑制剂与MEK抑制剂或伊立替康联合诱导消退

2020-08-1530
PRE