Showing results (611-620 of 1,440) with videos related to

Sort By:
Pageof 144
Journal of Biomolecular Structure & Dynamics|September 22, 2001
Research strategies for design and development of NSAIDs: clue to balance potency and toxicity of acetanilide compoundsA K Pal, S Sen, S Ghosh, et al.
Human Reproduction (Oxford, England)|July 26, 2014
Clinical prediction models to inform individualized decision-making in subfertile couples: a stratified medicine approachD J McLernon, E R te Velde, E W Steyerberg, et al.
Nepal Medical College Journal : NMCJ|February 27, 2008
Utility of phenotypic dermal indices in the detection of Down syndrome patientsD Masjkey, S Bhattacharya, S Dhungel, et al.
Life Sciences in Space Research|July 22, 2023
Galactic cosmic ray environment predictions for the NASA BioSentinel missionS Rahmanian, T C Slaba, L A Braby, et al.
Plos One|February 13, 2016
TOPORS, a Dual E3 Ubiquitin and Sumo1 Ligase, Interacts with 26 S Protease Regulatory Subunit 4, Encoded by the PSMC1 GeneBarbara Czub, Amna Z Shah, Giovanna Alfano, et al.
Japanese Journal of Pharmacology|February 20, 1998
Enhancement of membrane damage by saponins isolated from Acacia auriculiformisS P Sinha Babu, D Sarkar, N K Ghosh, et al.
Molecular Vision|June 3, 2011
A novel 1-bp deletion in PITX3 causing congenital posterior polar cataractVanita Berry, Peter J Francis, Quincy Prescott, et al.
American Journal of Human Genetics|April 17, 1999
Connexin46 mutations in autosomal dominant congenital cataractD Mackay, A Ionides, Z Kibar, et al.
Human Molecular Genetics|July 1, 1993
Exclusion of the involvement of all known retinitis pigmentosa loci in the disease present in a family of Irish origin provides evidence for a sixth autosomal dominant locus (RP8)R Kumar-Singh, G J Farrar, F Mansergh, et al.
Genomics|October 1, 1992
The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13)M E Porteous, A Curtis, S Lindsay, et al.
Pageof 144