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

Large variation in availability of Maya food plant sources during ancient droughts

古代干旱期间,玛雅人可食用植物来源的可用性存在很大差异。

Fedick, Scott L; Santiago, Louis S

Detection and toxicity modeling of anthraquinone dyes and chlorinated side products from a colored smoke pyrotechnic reaction

彩色烟雾烟火反应中蒽醌染料和氯化副产物的检测与毒性建模

Dilger, Jonathan M; Martin, Todd M; Wilkins, Benjamin P; Bohrer, Brian C; Thoreson, Kelly M; Fedick, Patrick W

Solubility of hydrocarbon oils in alcohols (≤C(6)) and synthesis of difusel carbonate for degreasing

烃类油在醇类(≤C(6))中的溶解度及用于脱脂的二氟醇碳酸酯的合成

Davis, Matthew C; Fedick, Patrick W; Lupton, David V; Ostrom, Gregory S; Quintana, Roxanne; Woodroffe, Josanne-Dee

Identification and characterization of Aurora kinase B and C variants associated with maternal aneuploidy

与母体非整倍体相关的 Aurora 激酶 B 和 C 变体的鉴定和表征

Alexandra L Nguyen, Diego Marin, Anbo Zhou, Amanda S Gentilello, Evan M Smoak, Zubing Cao, Anastasia Fedick, Yujue Wang, Deanne Taylor, Richard T Scott Jr, Jinchuan Xing, Nathan Treff, Karen Schindler

Deficiency of the alkaline ceramidase ACER3 manifests in early childhood by progressive leukodystrophy

碱性神经酰胺酶ACER3缺乏症在幼儿期表现为进行性脑白质营养不良。

Edvardson, Simon; Yi, Jae Kyo; Jalas, Chaim; Xu, Ruijuan; Webb, Bryn D; Snider, Justin; Fedick, Anastasia; Kleinman, Elisheva; Treff, Nathan R; Mao, Cungui; Elpeleg, Orly

Leukoencephalopathy and early death associated with an Ashkenazi-Jewish founder mutation in the Hikeshi gene

与阿什肯纳兹犹太人创始者 Hikeshi 基因突变相关的白质脑病和早期死亡

Simon Edvardson, Shingo Kose, Chaim Jalas, Aviva Fattal-Valevski, Ai Watanabe, Yutaka Ogawa, Hiroshi Mamada, Anastasia M Fedick, Shay Ben-Shachar, Nathan R Treff, Avraham Shaag, Sherri Bale, Jutta Gärtner, Naoko Imamoto, Orly Elpeleg

Analytical Validation of a Personalized Medicine APOL1 Genotyping Assay for Nondiabetic Chronic Kidney Disease Risk Assessment

用于非糖尿病慢性肾病风险评估的个性化医疗 APOL1 基因分型检测的分析验证

Zhang, Jinglan; Fedick, Anastasia; Wasserman, Stephanie; Zhao, Geping; Edelmann, Lisa; Bottinger, Erwin P; Kornreich, Ruth; Scott, Stuart A

A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic Defects

VPS11 的创始突变导致与自噬缺陷相关的常染色体隐性脑白质病

Jinglan Zhang, Véronik Lachance, Adam Schaffner, Xianting Li, Anastasia Fedick, Lauren E Kaye, Jun Liao, Jill Rosenfeld, Naomi Yachelevich, Mary-Lynn Chu, Wendy G Mitchell, Richard G Boles, Ellen Moran, Mari Tokita, Elizabeth Gorman, Kaytee Bagley, Wei Zhang, Fan Xia, Magalie Leduc, Yaping Yang, Chr

Carrier frequencies of eleven mutations in eight genes associated with primary ciliary dyskinesia in the Ashkenazi Jewish population

阿什肯纳兹犹太人群体中与原发性纤毛运动障碍相关的八个基因中十一种突变的携带者频率

Fedick, Anastasia M; Jalas, Chaim; Treff, Nathan R; Knowles, Michael R; Zariwala, Maimoona A

High-throughput carrier screening using TaqMan allelic discrimination

利用 TaqMan 等位基因鉴别进行高通量携带者筛查

Fedick, Anastasia; Su, Jing; Jalas, Chaim; Northrop, Lesley; Devkota, Batsal; Ekstein, Josef; Treff, Nathan R