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JCI Insight|October 5, 2016
Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysisHani Bagheri, Chansonette Badduke, Ying Qiao, et al.Cell|December 9, 1997
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptorC L Freund, C Y Gregory-Evans, T Furukawa, et al.Hypertension (Dallas, Tex. : 1979)|February 12, 2016
Patterns and Correlates of Baseline Thiazide-Type Diuretic Prescription in the Systolic Blood Pressure Intervention TrialTara I Chang, Gregory Evans, Alfred K Cheung, et al.Research Square|May 19, 2025
RPE65 variant p.(E519K) causes a novel dominant adult-onset maculopathy in 83 affected individualsEline Van Vooren, Filip Van den Broeck, Quinten Mahieu, et al.Investigative Ophthalmology & Visual Science|September 23, 2025
RPE65 Variant p.(E519K) Causes a Novel Dominant Adult-Onset Maculopathy in 83 Affected IndividualsEline Van Vooren, Filip Van Den Broeck, Quinten Mahieu, et al.Human Molecular Genetics|November 3, 2018
Loss-of-function mutations in KIF14 cause severe microcephaly and kidney development defects in humans and zebrafishMadeline Louise Reilly, Marijn F Stokman, Virginie Magry, et al.Oncotarget|May 4, 2017
Discovery and characterization of small molecules targeting the DNA-binding ETS domain of ERG in prostate cancerMiriam S Butler, Mani Roshan-Moniri, Michael Hsing, et al.Oncotarget|February 2, 2017
Therapy-induced developmental reprogramming of prostate cancer cells and acquired therapy resistanceMannan Nouri, Josselin Caradec, Amy Anne Lubik, et al.Oncogene|January 17, 2017
Neuropilin-1 is upregulated in the adaptive response of prostate tumors to androgen-targeted therapies and is prognostic of metastatic progression and patient mortalityB W C Tse, M Volpert, E Ratther, et al.Pageof 13