Showing results (891-900 of 936) with videos related to

Sort By:
Pageof 94
International Journal of Molecular Sciences|December 11, 2022
Congenital Stationary Night Blindness: Clinical and Genetic FeaturesAngela H Kim, Pei-Kang Liu, Yin-Hsi Chang, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|August 16, 2013
Association of exon 19 and 21 EGFR mutation patterns with treatment outcome after first-line tyrosine kinase inhibitor in metastatic non-small-cell lung cancerVictor H F Lee, Vicky P C Tin, Tim-shing Choy, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 14, 2023
Development of a translatable gene augmentation therapy for CNGB1-retinitis pigmentosaLaurence M Occelli, Lena Zobel, Jonathan Stoddard, et al.
Human Molecular Genetics|August 2, 2014
Analysis of the ABCA4 genomic locus in Stargardt diseaseJana Zernant, Yajing Angela Xie, Carmen Ayuso, et al.
Human Molecular Genetics|August 13, 2016
Catenin delta-1 (CTNND1) phosphorylation controls the mesenchymal to epithelial transition in astrocytic tumorsJin Yang, Alexander G Bassuk, Juliane Merl-Pham, et al.
Ophthalmic Genetics|July 5, 2021
Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndromeAustin D Igelman, Cristy Ku, Mariana Matioli da Palma, et al.
American Journal of Ophthalmology|August 10, 2024
Cross-Sectional Analysis of Outer Retinal Tubulation in Inherited Retinal Diseases: A Multicenter StudyPei-Kang Liu, Winston Lee, Pei-Yin Su, et al.
Pageof 94