Showing results (181-190 of 196) with videos related to

Sort By:
Pageof 20
The Journal of the Association of Physicians of India|March 12, 2026
The Mechanism of Action of Mineralocorticoid Receptor Antagonists in Heart Failure with Reduced Ejection FractionR R Mantri, Agam Vora, Asif Hasan, et al.
Microorganisms|December 24, 2021
Mining the Genome of Bacillus velezensis VB7 (CP047587) for MAMP Genes and Non-Ribosomal Peptide Synthetase Gene Clusters Conferring Antiviral and Antifungal ActivitySaravanan R, S Nakkeeran, N Saranya, et al.
Molecular Genetics and Metabolism|June 23, 1998
Molecular analysis and prenatal diagnosis of human fumarase deficiencyE M Coughlin, E Christensen, P L Kunz, et al.
Human Reproduction Open|February 5, 2026
Comprehensive 16S rRNA gene sequencing and meta-transcriptomic analyses of the female reproductive tract microbiota: two molecular profiles with different messagesAlberto Sola-Leyva, Inmaculada Pérez-Prieto, Analuce Canha-Gouveia, et al.
Current Eye Research|November 7, 1999
Retina-derived fetuin (RDF): analysis by immunocytochemistry, reverse transcriptase-polymerase chain reaction and Southern blotH J Sheedlo, R S Krishnamoorthy, T S Nelson, et al.
BMC Public Health|July 31, 2007
The protocols for the 10/66 dementia research group population-based research programmeMartin Prince, Cleusa P Ferri, Daisy Acosta, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|November 8, 2018
Cardiovascular disease management in people with diabetes outside North America and Western Europe in 2006 and 2015M Tabesh, D J Magliano, S K Tanamas, et al.
Lancet (London, England)|July 29, 2008
Prevalence of dementia in Latin America, India, and China: a population-based cross-sectional surveyJuan J Llibre Rodriguez, Cleusa P Ferri, Daisy Acosta, et al.
BMC Public Health|June 26, 2008
The 10/66 Dementia Research Group's fully operationalised DSM-IV dementia computerized diagnostic algorithm, compared with the 10/66 dementia algorithm and a clinician diagnosis: a population validation studyMartin J Prince, Juan Llibre de Rodriguez, L Noriega, et al.
Annals of Neurology|February 3, 2006
AHI1 gene mutations cause specific forms of Joubert syndrome-related disordersEnza Maria Valente, Francesco Brancati, Jennifer L Silhavy, et al.
Pageof 20