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

A case of novel mutation in ANOS1 (KAL1) gene and review of Kallmann syndrome

ANOS1 (KAL1) 基因新突变病例报告及卡尔曼综合征综述

Arora, Sumeet; Yeliosof, Olga; Chin, Vivian L

Evidence That the Etiology of Congenital Hypopituitarism Has a Major Genetic Component but Is Infrequently Monogenic

证据表明,先天性垂体功能减退症的病因具有重要的遗传成分,但很少是单基因遗传。

Jee, Youn Hee; Gangat, Mariam; Yeliosof, Olga; Temnycky, Adrian G; Vanapruks, Selena; Whalen, Philip; Gourgari, Evgenia; Bleach, Cortney; Yu, Christine H; Marshall, Ian; Yanovski, Jack A; Link, Kathleen; Ten, Svetlana; Baron, Jeffrey; Radovick, Sally

Passive transfer of antibodies to the linear epitope 60 kD Ro 273-289 induces features of Sjögren's syndrome in naive mice

被动转移针对线性表位 60 kD Ro 273-289 的抗体可诱导未感染小鼠出现干燥综合征的特征。

Maier-Moore, J S; Kurien, B T; D'Souza, A; Bockus, L; Asfa, S; Dorri, Y; Hubbell, S; Yeliosof, O; Obeso, D; Schoeb, T R; Jonsson, R; Scofield, R H