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

Exploring the Impact of Missing Death Data on Identification of Congenital Malformations in Insurance Claims Data

探讨死亡数据缺失对保险理赔数据中先天性畸形识别的影响

Nickel, Katelin B; Dublin, Sascha; Fuller, Sharon; Osmundson, Sarah S; Colvin, Ryan; Stwalley, Dustin; Kharbanda, Elyse O; Panozzo, Catherine A; Procknow, Sara S; Butler, Anne M

The Corrinoid Model for Dissecting Microbial Community Interactions Across Scales

利用类咕啉模型解析不同尺度下的微生物群落相互作用

Alvarez-Aponte, Zoila I; Procknow, Rebecca R; Taga, Michiko E

Laboratory evolution of E. coli with a natural vitamin B(12) analog reveals roles for cobamide uptake and adenosylation in methionine synthase-dependent growth

利用天然维生素B12类似物对大肠杆菌进行实验室进化,揭示了钴胺素吸收和腺苷酸化在蛋氨酸合成酶依赖性生长中的作用

Mok, Kenny C; Hallberg, Zachary F; Procknow, Rebecca R; Taga, Michiko E

Genetic dissection of regulation by a repressing and novel activating corrinoid riboswitch enables engineering of synthetic riboswitches

通过对抑制性和新型激活性咕啉类核糖开关调控机制的遗传解析,可以设计合成核糖开关。

Procknow, Rebecca R; Kennedy, Kristopher J; Kluba, Maxwell; Rodriguez, Lesley J; Taga, Michiko E

Repurposing Normal Chromosomal Microarray Data to Harbor Genetic Insights into Congenital Heart Disease

利用正常染色体微阵列数据揭示先天性心脏病的遗传学信息

Walton, Nephi A; Nguyen, Hoang H; Procknow, Sara S; Johnson, Darren; Anzelmi, Alexander; Jay, Patrick Y

Modern Malignant Mesothelioma Manifestation

现代恶性间皮瘤的表现

Razzak, Abrahim N; Syed, Ali; Procknow, Elizabeth R; Bequest, Andrea; Jha, Pinky

Cobalamin Riboswitches Are Broadly Sensitive to Corrinoid Cofactors to Enable an Efficient Gene Regulatory Strategy

钴胺素核糖开关对类咕啉辅因子具有广泛的敏感性,从而实现高效的基因调控策略

Kennedy, Kristopher J; Widner, Florian J; Sokolovskaya, Olga M; Innocent, Lina V; Procknow, Rebecca R; Mok, Kenny C; Taga, Michiko E

Emerging mechanisms of elastin transcriptional regulation

弹性蛋白转录调控的新兴机制

Procknow, Sara S; Kozel, Beth A

Clinical and molecular characteristics of a novel rare de novo variant in PPP2CA in a patient with a developmental disorder, autism, and epilepsy

患有发育障碍、自闭症和癫痫的患者中 PPP2CA 中一种新型稀有新生变异的临床和分子特征

Iris Verbinnen, Sara S Procknow, Lisa Lenaerts, Sara Reynhout, Aujan Mehregan, Chris Ulens, Veerle Janssens, Katherine A King

Contribution of metabolic disease to bone fragility in MAGP1-deficient mice

代谢性疾病对MAGP1缺陷小鼠骨骼脆弱性的影响

S E Turecamo ,T A Walji ,T J Broekelmann ,J W Williams ,S Ivanov ,N K Wee ,J D Procknow ,M R McManus ,G J Randolph ,E L Scheller ,R P Mecham ,C S Craft