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

ODAD4-Related Primary Ciliary Dyskinesia: Report of Five Cases and a Founder Variant in Quebec

ODAD4相关原发性纤毛运动障碍:魁北克省五例病例及一个创始变异体的报告

Bourassa, Marie-Hélène; Sillon, Guillaume; Ding, Shuizi; Chioccioli, Maurizio; Lek, Monkol; Ma, Kaiyue; Mejia-Garcia, Alejandro; Gravel, Simon; Vinh, Donald C; Knowles, Michael R; Leigh, Margaret W; Davis, Stephanie D; Ferkol, Thomas; Olivier, Kenneth N; Schecterman, Elizabeth N; Yin, Weining; Sears, Patrick R; Gentzsch, Martina; Boyles, Susan E; Bennett, William D; Zeman, Kirby L; Ostrowski, Lawrence E; Zariwala, Maimoona A; Shapiro, Adam J

Lipid nanoparticle-encapsulated Dnai1 mRNA rescues ciliary activity in primary ciliary dyskinesia mouse cell models

脂质纳米颗粒包裹的Dnai1 mRNA可挽救原发性纤毛运动障碍小鼠细胞模型中的纤毛活动。

Smith, Amanda J; Sears, Patrick R; Hennig, Mirko; Bhattacharjee, Rumpa B; Yin, Weining; Golliher, Hannah; Ishimaru, Daniella; Lombana, T Noelle; Lockhart, David J; Wustman, Brandon A; Ostrowski, Lawrence E

Promoter Deletion Leading to Allele Specific Expression in a Genetically Unsolved Case of Primary Ciliary Dyskinesia

启动子缺失导致原发性纤毛运动障碍病例中等位基因特异性表达,该病例的遗传病因尚未明确

Beaman, M Makenzie; Yin, Weining; Smith, Amanda J; Sears, Patrick R; Leigh, Margaret W; Ferkol, Thomas W; Kearney, Brendan; Olivier, Kenneth N; Kimple, Adam J; Clarke, Shannon; Huggins, Erin; Nading, Erica; Jung, Seung-Hye; Iyengar, Apoorva K; Zou, Xue; Dang, Hong; Barrera, Alejandro; Majoros, William H; Rehder, Catherine W; Reddy, Timothy E; Ostrowski, Lawrence E; Allen, Andrew S; Knowles, Michael R; Zariwala, Maimoona A; Crawford, Gregory E

Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis

隐性遗传的分泌型WFDC2(HE4)缺乏症会导致鼻息肉和支气管扩张

Dougherty, Gerard W; Ostrowski, Lawrence E; Nöthe-Menchen, Tabea; Raidt, Johanna; Schramm, Andre; Olbrich, Heike; Yin, Weining; Sears, Patrick R; Dang, Hong; Smith, Amanda J; Beule, Achim G; Hjeij, Rim; Rutjes, Niels; Haarman, Eric G; Maas, Saskia M; Ferkol, Thomas W; Noone, Peadar G; Olivier, Kenneth N; Bracht, Diana C; Barbry, Pascal; Zaragosi, Laure-Emmanuelle; Fierville, Morgane; Kliesch, Sabine; Wohlgemuth, Kai; König, Julia; George, Sebastian; Loges, Niki T; Ceppe, Agathe; Markovetz, Matthew R; Luo, Hong; Guo, Ting; Rizk, Hoda; Eldesoky, Tarek; Dahlke, Katrin; Boldt, Karsten; Ueffing, Marius; Hill, David B; Pang, Yuan-Ping; Knowles, Michael R; Zariwala, Maimoona A; Omran, Heymut

Mucolytic treatment of chronic rhinosinusitis in a murine model of primary ciliary dyskinesia

在原发性纤毛运动障碍小鼠模型中,黏液溶解剂治疗慢性鼻窦炎

Yin, Weining; Golliher, Hannah L; Ferguson, Amy J; Kimbell, Julia S; Livraghi-Butrico, Alessandra; Rogers, Troy D; Grubb, Barbara R; Kimple, Adam J; Ostrowski, Lawrence E

The role of SPAG1 in the assembly of axonemal dyneins in human airway epithelia

SPAG1在人呼吸道上皮细胞轴丝动力蛋白组装中的作用

Smith, Amanda J; Bustamante-Marin, Ximena M; Yin, Weining; Sears, Patrick R; Herring, Laura E; Dicheva, Nedyalka N; López-Giráldez, Francesc; Mane, Shrikant; Tarran, Robert; Leigh, Margaret W; Knowles, Michael R; Zariwala, Maimoona A; Ostrowski, Lawrence E

Mice with a Deletion of Rsph1 Exhibit a Low Level of Mucociliary Clearance and Develop a Primary Ciliary Dyskinesia Phenotype

Rsph1基因缺失的小鼠表现出黏液纤毛清除功能低下,并出现原发性纤毛运动障碍表型。

Yin, Weining; Livraghi-Butrico, Alessandra; Sears, Patrick R; Rogers, Troy D; Burns, Kimberlie A; Grubb, Barbara R; Ostrowski, Lawrence E

Single-cell transcriptomics reconstructs fate conversion from fibroblast to cardiomyocyte

单细胞转录组学重建了成纤维细胞向心肌细胞的命运转变

Ziqing Liu ,Li Wang ,Joshua D Welch ,Hong Ma ,Yang Zhou ,Haley Ruth Vaseghi ,Shuo Yu ,Joseph Blake Wall ,Sahar Alimohamadi ,Michael Zheng ,Chaoying Yin ,Weining Shen ,Jan F Prins ,Jiandong Liu ,Li Qian

Quantitative Proteomic Analysis of Human Airway Cilia Identifies Previously Uncharacterized Proteins of High Abundance.

人类呼吸道纤毛的定量蛋白质组学分析鉴定出以前未表征的高丰度蛋白质

Blackburn Kevin, Bustamante-Marin Ximena, Yin Weining, Goshe Michael B, Ostrowski Lawrence E

Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype

RSPH1基因突变会导致原发性纤毛运动障碍,并具有独特的临床和纤毛表型。

Knowles, Michael R; Ostrowski, Lawrence E; Leigh, Margaret W; Sears, Patrick R; Davis, Stephanie D; Wolf, Whitney E; Hazucha, Milan J; Carson, Johnny L; Olivier, Kenneth N; Sagel, Scott D; Rosenfeld, Margaret; Ferkol, Thomas W; Dell, Sharon D; Milla, Carlos E; Randell, Scott H; Yin, Weining; Sannuti, Aruna; Metjian, Hilda M; Noone, Peadar G; Noone, Peter J; Olson, Christina A; Patrone, Michael V; Dang, Hong; Lee, Hye-Seung; Hurd, Toby W; Gee, Heon Yung; Otto, Edgar A; Halbritter, Jan; Kohl, Stefan; Kircher, Martin; Krischer, Jeffrey; Bamshad, Michael J; Nickerson, Deborah A; Hildebrandt, Friedhelm; Shendure, Jay; Zariwala, Maimoona A