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

Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

杂合功能缺失变异显著扩展了与 GDF11 缺失相关的表型

Ravenscroft, Thomas A; Phillips, Jennifer B; Fieg, Elizabeth; Bajikar, Sameer S; Peirce, Judy; Wegner, Jeremy; Luna, Alia A; Fox, Eric J; Yan, Yi-Lin; Rosenfeld, Jill A; Zirin, Jonathan; Kanca, Oguz; Benke, Paul J; Cameron, Eric S; Strehlow, Vincent; Platzer, Konrad; Jamra, Rami Abou; Klöckner, Chiara; Osmond, Matthew; Licata, Thomas; Rojas, Samantha; Dyment, David; Chong, Josephine S C; Lincoln, Sharyn; Stoler, Joan M; Postlethwait, John H; Wangler, Michael F; Yamamoto, Shinya; Krier, Joel; Westerfield, Monte; Bellen, Hugo J

Correction: yippee like 3 (ypel3) is a novel gene required for myelinating and perineurial glia development

更正:yippee like 3 (ypel3) 是一个髓鞘形成和神经周胶质发育所必需的新基因

Blanco-Sánchez, Bernardo; Clément, Aurélie; Stednitz, Sarah J; Kyle, Jennifer; Peirce, Judy L; McFadden, Marcie; Wegner, Jeremy; Phillips, Jennifer B; Macnamara, Ellen; Huang, Yan; Adams, David R; Toro, Camilo; Gahl, William A; Malicdan, May Christine V; Tifft, Cynthia J; Zink, Erika M; Bloodsworth, Kent J; Stratton, Kelly G; Koeller, David M; Metz, Thomas O; Washbourne, Philip; Westerfield, Monte

The cone-dominant retina and the inner ear of zebrafish express the ortholog of CLRN1, the causative gene of human Usher syndrome type 3A.

斑马鱼的视锥细胞优势视网膜和内耳表达 CLRN1 的直系同源物,CLRN1 是人类 Usher 综合征 3A 型的致病基因

Phillips Jennifer B, Västinsalo Hanna, Wegner Jeremy, Clément Aurélie, Sankila Eeva-Marja, Westerfield Monte

Identification of differentially expressed genes in the zebrafish hypothalamic-pituitary axis

斑马鱼下丘脑-垂体轴差异表达基因的鉴定

Toro, Sabrina; Wegner, Jeremy; Muller, Marc; Westerfield, Monte; Varga, Zoltan M