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

Multimodal Imaging Evaluation of Myocardial Involvement in Rare Oculoleptomeningeal Hereditary Transthyretin Amyloidosis

罕见眼脑膜遗传性转甲状腺素蛋白淀粉样变性心肌受累的多模态影像学评估

Hundertmark, Moritz J; Zinkernagel, Martin; Brémova-Ertl, Tatiana; Escher, Pascal; Bauer, Anina; Caobelli, Federico; Banz, Yara; Flammer, Andreas; Martinelli, Michele V; Gräni, Christoph

Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration.

对患有进行性视网膜萎缩的巨型雪纳瑞犬进行全基因组测序,确定 NECAP1 为视网膜退化的新型候选基因

Hitti Rebekkah J, Oliver James A C, Schofield Ellen C, Bauer Anina, Kaukonen Maria, Forman Oliver P, Leeb Tosso, Lohi Hannes, Burmeister Louise M, Sargan David, Mellersh Cathryn S

MKLN1 splicing defect in dogs with lethal acrodermatitis

犬类致命性肢端皮炎的MKLN1剪接缺陷

Bauer, Anina; Jagannathan, Vidhya; Högler, Sandra; Richter, Barbara; McEwan, Neil A; Thomas, Anne; Cadieu, Edouard; André, Catherine; Hytönen, Marjo K; Lohi, Hannes; Welle, Monika M; Roosje, Petra; Mellersh, Cathryn; Casal, Margret L; Leeb, Tosso

A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome

阿哈尔捷金马裸驹综合征中ST14基因的无义变异

Bauer, Anina; Hiemesch, Theresa; Jagannathan, Vidhya; Neuditschko, Markus; Bachmann, Iris; Rieder, Stefan; Mikko, Sofia; Penedo, M Cecilia; Tarasova, Nadja; Vitková, Martina; Sirtori, Nicolò; Roccabianca, Paola; Leeb, Tosso; Welle, Monika M