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

A Nonketotic Hyperglycinemia Mouse Shows Wide-Ranging Biochemical Consequences of Elevated Glycine, Reduced Folate One-Carbon Charging, and Serine Deficiency

非酮症高甘氨酸血症小鼠表现出甘氨酸升高、叶酸一碳糖化减少和丝氨酸缺乏引起的广泛生化后果

Swanson, Michael A; Jiang, Hua; Kolora, Lakshmi Divya; Molino, Rachel; Reisdorph, Richard; Michel, Cole R; Doenges, Katrina A; Leung, Kit-Yi; Lin, Xiangping; Wong, Frank; Lancaster, Samual; Michael, Basil; Snyder, Michael; Hock, Daniella H; Stroud, David A; Wood, Tim; Binard, Robert; Anderson-Lehman, Laura; Christians, Uwe; Arning, Erland; Friederich, Marisa W; Van Hove, Roxanne A; MacLean, Kenneth N; Greene, Nicholas D E; Van Hove, Johan L K

Deep postnatal phenotyping of a new mouse model of nonketotic hyperglycinemia

对一种新的非酮症高甘氨酸血症小鼠模型进行深入的出生后表型分析

Swanson, Michael A; Jiang, Hua; Busquet, Nicolas; Carlsen, Jessica; Brindley, Connie; Benke, Tim A; Van Hove, Roxanne A; Friederich, Marisa W; MacLean, Kenneth N; Mesches, Michael H; Van Hove, Johan L K

Analysis of differential neonatal lethality in cystathionine β-synthase deficient mouse models using metabolic profiling

利用代谢谱分析胱硫醚β-合成酶缺陷小鼠模型中新生儿死亡率的差异

Gupta, Sapna; Wang, Liqun; Slifker, Michael J; Cai, Kathy Q; Maclean, Kenneth N; Wasek, Brandi; Bottiglieri, Teodoro; Kruger, Warren D

Pcsk9 knockout exacerbates diet-induced non-alcoholic steatohepatitis, fibrosis and liver injury in mice

PCSK9基因敲除会加剧小鼠饮食诱导的非酒精性脂肪性肝炎、肝纤维化和肝损伤。

Lebeau, Paul F; Byun, Jae Hyun; Platko, Khrystyna; Al-Hashimi, Ali A; Lhoták, Šárka; MacDonald, Melissa E; Mejia-Benitez, Aurora; Prat, Annik; Igdoura, Suleiman A; Trigatti, Bernardo; Maclean, Kenneth N; Seidah, Nabil G; Austin, Richard C

Methylene-tetrahydrofolate reductase contributes to allergic airway disease

亚甲基四氢叶酸还原酶与过敏性气道疾病有关。

Eyring, Kenneth R; Pedersen, Brent S; Maclean, Kenneth N; Stabler, Sally P; Yang, Ivana V; Schwartz, David A

Erratum: A de novo 2.78-Mb duplication on chromosome 21q22.11 implicates candidate genes in the partial trisomy 21 phenotype

更正:21q22.11染色体上新发现的2.78 Mb重复序列提示候选基因与21号染色体部分三体表型有关

Weisfeld-Adams, James D; Tkachuk, Amanda K; Maclean, Kenneth N; Meeks, Naomi L; Scott, Stuart A

A de novo 2.78-Mb duplication on chromosome 21q22.11 implicates candidate genes in the partial trisomy 21 phenotype

21q22.11染色体上新出现的2.78 Mb重复序列提示候选基因与21号染色体部分三体表型有关

Weisfeld-Adams, James D; Tkachuk, Amanda K; Maclean, Kenneth N; Meeks, Naomi L; Scott, Stuart A

Constitutive induction of pro-inflammatory and chemotactic cytokines in cystathionine beta-synthase deficient homocystinuria

胱硫醚β-合成酶缺乏型同型半胱氨酸尿症中促炎和趋化细胞因子的组成性诱导

Keating, Amy K; Freehauf, Cynthia; Jiang, Hua; Brodsky, Gary L; Stabler, Sally P; Allen, Robert H; Graham, Douglas K; Thomas, Janet A; Van Hove, Johan L K; Maclean, Kenneth N

Experimental evidence for therapeutic potential of taurine in the treatment of nonalcoholic fatty liver disease.

牛磺酸治疗非酒精性脂肪肝的治疗潜力的实验证据

Gentile Christopher L, Nivala Angela M, Gonzales Jon C, Pfaffenbach Kyle T, Wang Dong, Wei Yuren, Jiang Hua, Orlicky David J, Petersen Dennis R, Pagliassotti Michael J, Maclean Kenneth N

Cystathionine beta-synthase null homocystinuric mice fail to exhibit altered hemostasis or lowering of plasma homocysteine in response to betaine treatment

胱硫醚β-合成酶基因敲除的同型半胱氨酸尿症小鼠在接受甜菜碱治疗后,无法表现出止血功能改变或血浆同型半胱氨酸水平降低。

Maclean, Kenneth N; Sikora, Jakub; Kožich, Viktor; Jiang, Hua; Greiner, Lori S; Kraus, Eva; Krijt, Jakub; Crnic, Linda S; Allen, Robert H; Stabler, Sally P; Elleder, Milan; Kraus, Jan P