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Genomics|March 1, 1992
Assignment of the beta-subunit of rod photoreceptor cGMP phosphodiesterase gene PDEB (homolog of the mouse rd gene) to human chromosome 4p16J B Bateman, I Klisak, T Kojis, et al.European Journal of Biochemistry|October 20, 1989
Reconstitution of a light-stimulated adenylate cyclase from retina and Neurospora crassa preparations. Characterization of the heterologous systems using normal and degenerative retinasJ P Muschietti, G M Bianchini, H E Martinetto, et al.Journal of Neonatal-Perinatal Medicine|November 2, 2020
Urinary tract infections in very low birthweight infants: A two-center analysis of microbiology, imaging and heart rate characteristicsN Aviles-Otero, M Ransom, J Weitkamp, et al.International Immunology|February 1, 1992
Binding of low concentration of peptide to H-2Kd produced in insect cells requires mouse beta 2-microglobulin co-expressionF Godeau, J L Casanova, I F Luescher, et al.Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Inflammatory Biomarkers and Physiomarkers of Late-Onset Sepsis and Necrotizing Enterocolitis in Premature InfantsRupin Kumar, Sherry Kausch, Angela K S Gummadi, et al.Experimental Eye Research|February 1, 1996
Screening of the PDE6B gene in patients with autosomal dominant retinitis pigmentosaY Q Gao, M Danciger, D Y Zhao, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 20, 2000
A QTL on distal chromosome 3 that influences the severity of light-induced damage to mouse photoreceptorsM Danciger, M T Matthes, D Yasamura, et al.American Journal of Perinatology|May 29, 2018
Early Pulse Oximetry Data Improves Prediction of Death and Adverse Outcomes in a Two-Center Cohort of Very Low Birth Weight InfantsB A Sullivan, A Wallman-Stokes, J Isler, et al.Physiological Measurement|March 11, 2016
Stochastic modeling of central apnea events in preterm infantsMatthew T Clark, John B Delos, Douglas E Lake, et al.Molecular Vision|November 4, 2000
A homozygous deletion in RPE65 in a small Sardinian family with autosomal recessive retinal dystrophyW J Poehner, M Fossarello, A L Rapoport, et al.Pageof 37