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

Matrix metalloproteinase-9 deficiency confers resilience in fibrodysplasia ossificans progressiva in a man and mice.

基质金属蛋白酶-9 缺乏症可使人类和小鼠的进行性骨化性纤维发育不良症具有抵抗力

期刊:Journal of Bone and Mineral Research
影响因子:5.9
doi:10.1093/jbmr/zjae029
Lounev Vitali, Groppe Jay C, Brewer Niambi, Wentworth Kelly L, Smith Victoria, Xu Meiqi, Schomburg Lutz, Bhargava Pankaj, Al Mukaddam Mona, Hsiao Edward C, Shore Eileen M, Pignolo Robert J, Kaplan Frederick S
免疫/内分泌
发表日期：2024
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Polypeptide Substrate Accessibility Hypothesis: Gain-of-Function R206H Mutation Allosterically Affects Activin Receptor-like Protein Kinase Activity

多肽底物可及性假说：功能获得性R206H突变通过变构作用影响激活素受体样蛋白激酶活性

期刊:Biomolecules
影响因子:4.8
doi:10.3390/biom13071129
Groppe, Jay C; Lu, Guorong; Tandang-Silvas, Mary R; Pathi, Anupama; Konda, Shruti; Wu, Jingfeng; Le, Viet Q; Culbert, Andria L; Shore, Eileen M; Wharton, Kristi A; Kaplan, Frederick S
信号转导
发表日期：2023
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Hypoxia-selective allosteric destabilization of activin receptor-like kinases: A potential therapeutic avenue for prophylaxis of heterotopic ossification

缺氧选择性变构去稳定激活素受体样激酶：预防异位骨化的潜在治疗途径

期刊:
影响因子:
doi:10.1016/j.bone.2018.03.027
Lu, Guorong; Tandang-Silvas, Mary R; Dawson, Alyssa C; Dawson, Trenton J; Groppe, Jay C
信号转导
发表日期：2018
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Multi-system involvement in a severe variant of fibrodysplasia ossificans progressiva (ACVR1 c.772G>A; R258G): A report of two patients

进行性骨化性纤维发育不良症（ACVR1 c.772G>A; R258G）严重变异型的多系统受累：两例患者报告

期刊:American Journal of Medical Genetics Part A
影响因子:1.7
doi:10.1002/ajmg.a.37205
Kaplan, Frederick S; Kobori, Joyce A; Orellana, Carmen; Calvo, Inmaculada; Rosello, Monica; Martinez, Francisco; Lopez, Berta; Xu, Meiqi; Pignolo, Robert J; Shore, Eileen M; Groppe, Jay C
发育与干细胞
发表日期：2015
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Functional analysis of alleged NOGGIN mutation G92E disproves its pathogenic relevance.

对所谓 NOGGIN 突变 G92E 的功能分析否定了其致病相关性

期刊:PLoS One
影响因子:2.6
doi:10.1371/journal.pone.0035062
Zimmer Julia, Doelken Sandra C, Horn Denise, Groppe Jay C, Shore Eileen M, Kaplan Frederick S, Seemann Petra
其它
发表日期：2012
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Nucleotide polymorphisms in the canine Noggin gene and their distribution among dog (Canis lupus familiaris) breeds

犬类Noggin基因的核苷酸多态性及其在犬（Canis lupus familiaris）品种中的分布

期刊:Biochemical Genetics
影响因子:1.6
doi:10.1007/s10528-011-9453-5
Ishii, Yuji; Takizawa, Tatsuya; Iwasaki, Hiroshi; Fujita, Yukihiro; Murakami, Masaru; Groppe, Jay C; Tanaka, Kazuaki
发表日期：2012
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In vitro analyses of the dysregulated R206H ALK2 kinase-FKBP12 interaction associated with heterotopic ossification in FOP

体外分析FOP中与异位骨化相关的R206H ALK2激酶-FKBP12相互作用失调。

期刊:Cells Tissues Organs
影响因子:1.9
doi:10.1159/000324230
Groppe, Jay C; Wu, Jingfeng; Shore, Eileen M; Kaplan, Frederick S
信号转导
ALK
发表日期：2011
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Pathogenic mechanisms of tooth agenesis linked to paired domain mutations in human PAX9

人类PAX9基因配对结构域突变与牙齿缺失的致病机制相关

期刊:Human Molecular Genetics
影响因子:3.2
doi:10.1093/hmg/ddp221
Wang, Ying; Groppe, Jay C; Wu, Jingfeng; Ogawa, Takuya; Mues, Gabriele; D'Souza, Rena N; Kapadia, Hitesh
发表日期：2009
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