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

Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy

PRKCI 的罕见变异导致 Van der Woude 综合征和皮周病的其他特征

Robinson, Kelsey; Singh, Sunil K; Walkup, Rachel B; Fawwal, Dorelle V; Vilfort, Kendra M; Koloskee, Amanda; Fashina, Azeez; Adeyemo, Wasiu Lanre; Beaty, Terri H; Butali, Azeez; Buxó, Carmen J; Chung, Wendy K; Cutler, David J; Epstein, Michael P; Gasser, Brooklynn; Gowans, Lord J J; Hecht, Jacqueline T; Mankad, Anuj; Moreno Uribe, Lina; Scott, Daryl A; Shaw, Gary M; Thomas, Mary Ann; Weinberg, Seth M; Liao, Eric C; Brand, Harrison; Marazita, Mary L; Lipinski, Robert J; Murray, Jeffrey C; Cornell, Robert A; Leslie-Clarkson, Elizabeth J

Genetic requirement for Esrp1 and Esrp2 in vertebrate pituitary morphogenesis.

脊椎动物垂体形态发生中 Esrp1 和 Esrp2 的遗传需求。

Carroll Shannon H, Schafer Sogand, Richman Ariella S, Wang Peng, Ahsan Mian Umair, Tsay Lisa, Wang Kai, Liao Eric C

Neural crest and periderm-specific requirements of Irf6 during neural tube and craniofacial development

神经管和颅面发育过程中神经嵴和表皮对 Irf6 的特异性需求

Carroll, Shannon H; Schafer, Sogand; Dalessandro, Eileen; Ho, Thach-Vu; Chai, Yang; Liao, Eric C

Integration of Clinical, Radiographic, Histologic, and Molecular Findings to Diagnose Craniofacial Fibrous Dysplasia

整合临床、影像学、组织学和分子生物学结果诊断颅面纤维性发育不良

Golden, Brandi M; Tucker, Scott K; Carpenter, Marco; Santi, Mariarita; Viaene, Angela N; Peranteau, William H; Swanson, Jordan W; Bartlett, Scott P; Taylor, Jesse A; Liao, Eric C

Genetic requirement for Esrp1/2 in vertebrate pituitary morphogenesis

脊椎动物垂体形态发生过程中Esrp1/2的遗传需求

Carroll, Shannon H; Schafer, Sogand; Richman, Ariella S; Tsay, Lisa; Wang, Peng; Ahsan, Mian Umair; Wang, Kai; Liao, Eric C

Genetic variant classification by predicted protein structure: A case study on IRF6

基于预测蛋白质结构的基因变异分类:以IRF6为例

Murali, Hemma; Wang, Peng; Liao, Eric C; Wang, Kai

Genetic requirement of dact1/2 to regulate noncanonical Wnt signaling and calpain 8 during embryonic convergent extension and craniofacial morphogenesis

dact1/2 基因在胚胎趋同延伸和颅面形态发生过程中调控非经典 Wnt 信号通路和钙蛋白酶 8 的必要性

Carroll, Shannon H; Schafer, Sogand; Kawasaki, Kenta; Tsimbal, Casey; Julé, Amélie M; Hallett, Shawn A; Li, Edward; Liao, Eric C

Nasal Construction in Congenital Arhinia Due to Novel SMCHD1 Gene Variant

先天性无鼻症的鼻部重建,由新型SMCHD1基因变异引起

Bargiela, Marie; Kueper, Janina; Serebrakian, Arman T; Browne, MaKenna R; Brogna, Susan; Peacock, Zachary S; Bojovic, Branko; Shaw, Natalie D; Liao, Eric C

ALX1-related frontonasal dysplasia results from defective neural crest cell development and migration

ALX1相关性额鼻发育不良是由神经嵴细胞发育和迁移缺陷引起的。

Pini, Jonathan; Kueper, Janina; Hu, Yiyuan David; Kawasaki, Kenta; Yeung, Pan; Tsimbal, Casey; Yoon, Baul; Carmichael, Nikkola; Maas, Richard L; Cotney, Justin; Grinblat, Yevgenya; Liao, Eric C

One-Year Experience of Same-Day Mastectomy and Breast Reconstruction Protocol

一年期同日乳房切除和乳房重建方案经验

Specht, Michelle C; Kelly, Bridget N; Tomczyk, Eleanor; Ford, Olivia A; Webster, Alexandra J; Smith, Barbara L; Gadd, Michelle A; Colwell, Amy S; Liao, Eric C