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

HttQ111/+ Huntington's Disease Knock-in Mice Exhibit Brain Region-Specific Morphological Changes and Synaptic Dysfunction

HttQ111/+亨廷顿病敲入小鼠表现出脑区特异性形态学改变和突触功能障碍

Kovalenko, Marina; Milnerwood, Austen; Giordano, James; St Claire, Jason; Guide, Jolene R; Stromberg, Mary; Gillis, Tammy; Sapp, Ellen; DiFiglia, Marian; MacDonald, Marcy E; Carroll, Jeffrey B; Lee, Jong-Min; Tappan, Susan; Raymond, Lynn; Wheeler, Vanessa C

Chromosome substitution strain assessment of a Huntington's disease modifier locus

亨廷顿病修饰基因位点的染色体置换株评估

Ramos, Eliana Marisa; Kovalenko, Marina; Guide, Jolene R; St Claire, Jason; Gillis, Tammy; Mysore, Jayalakshmi S; Sequeiros, Jorge; Wheeler, Vanessa C; Alonso, Isabel; MacDonald, Marcy E

HdhQ111 Mice Exhibit Tissue Specific Metabolite Profiles that Include Striatal Lipid Accumulation

HdhQ111小鼠表现出组织特异性代谢物谱,包括纹状体脂质积累

Carroll, Jeffrey B; Deik, Amy; Fossale, Elisa; Weston, Rory M; Guide, Jolene R; Arjomand, Jamshid; Kwak, Seung; Clish, Clary B; MacDonald, Marcy E

Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families

小鼠皮层和多重自闭症家族中16p11.2缺失和重复的转录后果

Blumenthal, Ian; Ragavendran, Ashok; Erdin, Serkan; Klei, Lambertus; Sugathan, Aarathi; Guide, Jolene R; Manavalan, Poornima; Zhou, Julian Q; Wheeler, Vanessa C; Levin, Joshua Z; Ernst, Carl; Roeder, Kathryn; Devlin, Bernie; Gusella, James F; Talkowski, Michael E

Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approaches.

错配修复基因 Mlh1 和 Mlh3 可改变亨廷顿病小鼠的 CAG 不稳定性:全基因组和候选基因方法

Pinto Ricardo Mouro, Dragileva Ella, Kirby Andrew, Lloret Alejandro, Lopez Edith, St Claire Jason, Panigrahi Gagan B, Hou Caixia, Holloway Kim, Gillis Tammy, Guide Jolene R, Cohen Paula E, Li Guo-Min, Pearson Christopher E, Daly Mark J, Wheeler Vanessa C