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

Earlier onset of North Atlantic hurricane season with warming oceans

随着海洋变暖,北大西洋飓风季提前到来

Truchelut, Ryan E; Klotzbach, Philip J; Staehling, Erica M; Wood, Kimberly M; Halperin, Daniel J; Schreck, Carl J 3rd; Blake, Eric S

Disruption of Fnip1 reveals a metabolic checkpoint controlling B lymphocyte development

Fnip1 的破坏揭示了控制 B 淋巴细胞发育的代谢检查点

Heon Park, Karen Staehling, Mark Tsang, Mark W Appleby, Mary E Brunkow, Daciana Margineantu, David M Hockenbery, Tania Habib, H Denny Liggitt, George Carlson, Brian M Iritani

Gene Expression Profiling of Picogram Amounts of Mouse Universal Reference RNA Amplified Using the Miltenyi Biotec μMACS SuperAmp Technology

利用 Miltenyi Biotec μMACS SuperAmp 技术扩增皮克级小鼠通用参考 RNA,并进行基因表达谱分析。

Burnett, John C; Rossi, John J; Vallandingham, J; Peak, A; Staehling, K; Li, H; Zueckert-Gaudenz, Karin

Histone H3K9 trimethylase Eggless controls germline stem cell maintenance and differentiation

组蛋白H3K9三甲基化酶Eggless控制生殖系干细胞的维持和分化

Xiaoxi Wang, Lei Pan, Su Wang, Jian Zhou, William McDowell, Jungeun Park, Jeff Haug, Karen Staehling, Hong Tang, Ting Xie

Service and Collaboration: Enhancing Project Potential at the Stowers Institute Molecular Biology Facility

服务与合作:提升斯托尔斯研究所分子生物学设施的项目潜力

Stevens, M K; Cope, L D; Radolf, J D; Hansen, E J; Bradford, D; Delventhal, K; Fleharty, B; McDowell, W; Miller, B; Peak, A; Perera, A; Peterson, M; Sanderson, B; Smith, K; Stanley, D; Walton, K; Waugh, K; Weaver, K; Zueckert-Gaudenz, K; Staehling-Hampton, K

Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes

Gdf6 基因相关的眼骨骼表型具有不完全外显率和表型变异性等特征。

Asai-Coakwell, Mika; French, Curtis R; Ye, Ming; Garcha, Kamal; Bigot, Karin; Perera, Anoja G; Staehling-Hampton, Karen; Mema, Silvina C; Chanda, Bhaskar; Mushegian, Arcady; Bamforth, Steven; Doschak, Michael R; Li, Guang; Dobbs, Matthew B; Giampietro, Philip F; Brooks, Brian P; Vijayalakshmi, Perumalsamy; Sauvé, Yves; Abitbol, Marc; Sundaresan, Periasamy; van Heyningen, Veronica; Pourquié, Olivier; Underhill, T Michael; Waskiewicz, Andrew J; Lehmann, Ordan J

A point mutation in the murine Hem1 gene reveals an essential role for Hematopoietic protein 1 in lymphopoiesis and innate immunity

小鼠 Hem1 基因的点突变揭示了造血蛋白 1 在淋巴细胞生成和先天免疫中的重要作用

Heon Park, Karen Staehling-Hampton, Mark W Appleby, Mary E Brunkow, Tania Habib, Yi Zhang, Fred Ramsdell, H Denny Liggitt, Brian Freie, Mark Tsang, George Carlson, Sherree Friend, Charles Frevert, Brian M Iritani

A comprehensive library of histone mutants identifies nucleosomal residues required for H3K4 methylation

一个全面的组蛋白突变体库鉴定出H3K4甲基化所需的核小体残基

Nakanishi, Shima; Sanderson, Brian W; Delventhal, Kym M; Bradford, William D; Staehling-Hampton, Karen; Shilatifard, Ali

Mutations in the MESP2 gene cause spondylothoracic dysostosis/Jarcho-Levin syndrome

MESP2基因突变会导致脊椎胸廓发育不良/Jarcho-Levin综合征。

Cornier, Alberto S; Staehling-Hampton, Karen; Delventhal, Kym M; Saga, Yumiko; Caubet, Jean-Francois; Sasaki, Nobuo; Ellard, Sian; Young, Elizabeth; Ramirez, Norman; Carlo, Simon E; Torres, Jose; Emans, John B; Turnpenny, Peter D; Pourquié, Olivier

RDH10 is essential for synthesis of embryonic retinoic acid and is required for limb, craniofacial, and organ development

RDH10对于胚胎视黄酸的合成至关重要,并且是肢体、颅面和器官发育所必需的。

Sandell, Lisa L; Sanderson, Brian W; Moiseyev, Gennadiy; Johnson, Teri; Mushegian, Arcady; Young, Kendra; Rey, Jean-Philippe; Ma, Jian-xing; Staehling-Hampton, Karen; Trainor, Paul A