Showing results (1421-1430 of 1,658) with videos related to

Sort By:
Pageof 166
Current Medicinal Chemistry|May 29, 2024
Feline Leishmaniasis: Evidence-based Treatments - Challenges to be SolvedCaroline de Jesus Sousa, Joilson Ferreira Batista, Amanda Karoliny Figueredo Brito, et al.
Plos One|October 23, 2020
Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiencyMonica M França, Mariana F A Funari, Antonio M Lerario, et al.
Nature Biotechnology|August 14, 2018
Cas9-mediated allelic exchange repairs compound heterozygous recessive mutations in miceDan Wang, Jia Li, Chun-Qing Song, et al.
Free Radical Biology & Medicine|August 8, 2017
DMAPT inhibits NF-κB activity and increases sensitivity of prostate cancer cells to X-rays in vitro and in tumor xenografts in vivoMarc S Mendonca, William T Turchan, Melanie E Alpuche, et al.
Archives of Endocrinology and Metabolism|February 8, 2018
Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencingFernanda A Correa, Marcela M França, Qing Fang, et al.
Journal of Human Immunity|September 29, 2025
Gut dysbiosis patterns in CVID patients with noninfectious complications observed in a germ-free mouse model through fecal microbiota transplantationJoud Hajjar, Anita Y Voigt, Margaret E Conner, et al.
Clinical Endocrinology|July 31, 2014
Quality of life in a large cohort of adult Brazilian patients with 46,XX and 46,XY disorders of sex development from a single tertiary centreRita Cassia Amaral, Marlene Inacio, Vinicius N Brito, et al.
International Journal of Retina and Vitreous|October 11, 2023
Pseudoaveraging for denoising of OCT angiography: a deep learning approach for image quality enhancement in healthy and diabetic eyesOmar Abu-Qamar, Warren Lewis, Luisa S M Mendonca, et al.
Oncotarget|March 10, 2016
Radiation therapy generates platelet-activating factor agonistsRavi P Sahu, Kathleen A Harrison, Jonathan Weyerbacher, et al.
European Journal of Endocrinology|September 11, 2023
Identification of a second genetic alteration in patients with SHOX deficiency individuals: a potential explanation for phenotype variabilityNaiara C B Dantas, Mariana F A Funari, Antonio M Lerário, et al.
Pageof 166